Uworld CK Flashcards

(1480 cards)

1
Q

What does the femoral nerve innervate?

A

The anterior thigh for knee extension and hip flexion

Sensation to the anterior thigh and medial leg – via the saphenous branch.

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2
Q

How should hemodynamically stable pts w/suspected splenic injury be managed?

A

They should first undergo a FAST.

  • If normal FAST, but they have high risk features (anemia or guarding)then they should undergo abdominal CT scan w/contrast.
  • If equivocal FAST and stable = CT w/contrast
  • If equivocal FAST and unstable = DPL
  • if DPL positive = laparotomy
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3
Q

How should pts w/massive hemoptysis be managed?

A

Bronchoscopy is the procedure of choice to identify the site of bleeding and attempt intervention.
This is done after establishing a patent airway, maintaining ventilation/gas exchange, and ensuring hemodynamic stability.
Thoracotomy should only be done if bronchoscopy fails.

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4
Q

What are hard signs of vascular injury and how are they managed?

A

Observed pulsatile bleeding
Presence of bruit/thrill over injury
Expanding hematoma
Signs of distal ischemia (absent pulses, cool extremity)
Pts w/any of these signs should undergo urgent surgical repair.

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5
Q

What is the management for SBO?

A

Nasogastric tube, IV fluids, bowel rest, analgesics and surgical exploration (esp. if they aren’t stable or show signs of ischemia and necrosis – metab. acidosis)

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6
Q

Most common complications of cardiac catheterization?

A

Bleeding, hematoma (local or w/retroperitoneal extension), arterial dissection, actue thrombosis, pseudoaneurysm, or AV fistula formation.
Hemorrhage/hematoma normally occur w/in 12 hrs.

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7
Q

Causes, sxs, and dx of a retroperitoneal hematoma:

A

Causes: Recent cardiac cath., anticoagulation.
Sxs: sudden onset HoTN, tachycardia, flat neck veins, and back pain.
This is diagnosed w/a NON-contrast CT of the abdomen/pelvis.

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8
Q

Management of pancreatic pseudocyst:

A

Expectant mgmt. - (NPO,symptomatic therapy) for those without sxs or cxs
Endoscopic drainage - pts w/significant sxs (N/V/abd pain), infected cysts, or evidence of a pseudoaneurysm.

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9
Q

Mgmt of a clavicular fracture:

A

Careful neurovascular exam to r/o injury to the brachial plexus or subclavian artery. Often involves an angiogram – esp. if a bruit is heard.

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10
Q

Ankle-brachial index:

A

Non-invasive test that is sensitive and specific for PAD in symptomatic pts. (intermittent claudication). Usually the first step taken to confirm the diagnosis.
Done by dividing the higher ankle systolic pressure by the higher brachial artery systolic pressure.

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11
Q

What happens to the Left ventricle in states of hypovolemic shock?

A

It will decrease in size d/t low filling volume, and compensate by increasing the ejection fraction (~75%).

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12
Q

Most common causes of massive hemothorax:

A

Traumatic laceration of the lung parenchyma, or damage to an intercostal or internal mammary artery.

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13
Q

Likely post-op complication that would lead to cardiogenic shock?

A

Perioperative MI

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14
Q

What are the interventions for lowering ICP? (5)

A

1- Head elevation: increases venous outflow from brain
2- Sedation: decreases metabolic demand and controls HTN
3- IV Mannitol: Free H2O clearance from brain tissue –> osmotic diuresis
4- Hyperventilation: CO2 washout –> cerebral vasoconstriction
5- CSF drainage: Decreases Vol/P

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15
Q

What anticoagulants are contraindicated in ESRD?

A

LMWH and Xa inhibitors like Rivaroxaban

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16
Q

What is the tx for DVT in patients w/ ESRD?

A

Unfractionated heparin and warfarin. Must start on both and then stop heparin bc warfarin initially causes prothrombotic state.

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17
Q

Who is likely to get bacterial parotitis, how does it present, how can you prevent, most common cause?

A

Post-op patients and the elderly are most likely to get it.
Presents with fever, leukocytosis and parotid inflammation.
Can prevent with adequate fluid intake and oral hygiene.
S. aureus is most common cause

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18
Q

Indications of urgent exploratory laparotomy:

A

Hemodynamic Instability
Peritonitis (rebound tenderness and guarding)
Evisceration (exposed organs)
Blood from NGT or on rectal exam
Also to remove any foreign material such as knives

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19
Q

Signs/Sxs suggestive of meniscal injury:

A

Acute knee pain a/w catching/popping or reduced ROM.

PE may be normal and should be followed by MRI if suspected.

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20
Q

Earliest sign of burn wound infection:

A

Change in appearance – partial thickness injury turns into full-thickness- of the wound, or loss of a skin graft.

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21
Q

Difference in bacteria of burn wound infection:

A

G+ are common directly after injury

G- and fungi are more common >5 days after injury.

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22
Q

What should happen immediately after placing a CVC?

A

Obtain portable CXR to confirm the catheter is in the correct place before catheter use. Catheter should be visualized just proximal to the angle b/w the trachea and R mainstem bronchus.

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23
Q

What is torus palatinus?

A

Fleshy immobile mass on the midline hard palate. It is a congenital growth, and doesn’t require intervention unless it casues sxs or interferes w/speech or eating.

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24
Q

Leriche syndrome:

A

A triad syndrome from aortoiliac occlusion
Bilat. Hip, thigh, and buttock claudication
Absent/diminished femoral pulses – often w/symmetric atrophy of the bilat. LEs from chronic ischemia
Impotence.

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25
What is Extraperitoneal bladder injury? When should this be considered?
Contusion/rupture of the neck, ant. wall, or anterolateral wall of the bladder. Often from pelvic fractures. Get localized pain and gross hematuria. Signs of peritonitis shouldn’t be present (seen in IPBI).
26
Signs and symptoms of necrotizing surgical site infection:
Pain, edema, erythema spreading beyond the surgical site Systemic signs: Fever, HoTN, tachy Par/anesthesia at the wound edges Purulent, cloudy-grey “dishwater drainage” SubQ gas or crepitus
27
Treatment of necrotizing surgical site infections:
Urgent surgical exploration and debridement + parenteral abx
28
What causes the hyperpigmentation/discoloration in stasis dermatitis?
RBC extravasation from the capillaries cause hemosiderin deposition in the tissues.
29
What can be seen on AXR in paralytic ileus?
Gas filled loops in the stomach, SI and LI with no transition point.
30
Common causes of paralytic ileus:
Abdominal surgery is #1 | Others: Retroperitoneal/abd hemorrhage or inflammation, intestinal ischemia, and electrolyte abnormalities.
31
What causes flail chest?
3+ rib fractures in 2+ locations
32
What nerve is most commonly injured in shoulder dislocation, what will it cause?
Axillary nerve is most commonly injured It innervates teres minor and deltoid --> weakened shoulder abduction Provides sensation to lateral shoulder
33
What imaging is indicated for suspected penile fracture? Other indications for this imaging?
Retrograde urethrogram. | Indications for urethrogram: Blood at the meatus, hematuria, dysuria, urinary retention.
34
Shin splints v. Stress fracture:
Stress fractures – have localized point tenderness and activity-related pain, swelling. Often in underweight female athletes Shin splints – diffuse area of tenderness (not point), and is more common in overweight casual runners.
35
What kind of effusion would be expected with a low pleural glucose?
An exudative effusion – typically has glucose <60 mg/dL.
36
What is the light criteria to define an exudative pleural effusion?
Must have at least one of the following (pleural/serum): Pleural fluid protein/serum protein ratio >0.5 Pleural fluid LDH/serum LDH >0.6 Pleural fluid LDH >2/3 of the upper limit of normal for serum LDH.
37
What are empyemas?
Exudative effusions w/low glucose concentration d/t high metabolic activity of leukocytes and bacteria w/in the pleural fluid.
38
What are the different biopsy techniques for central v. peripheral tumors?
Central are done by EBUS (endobronchial US) directed biopsy. | Peripheral are hard to reach via EBUS and are normally done by VATS (Video-Assisted Thoracoscopic Surgery).
39
What lung ca is most likely to cause SVC syndrome?
SCLC
40
Most common locations of lung mets:
Brain, Bone, Adrenals, Liver
41
When is surgical resection indicated for lung ca.?
If the predicted post-op FEV1 is 800mL+
42
What type of skin cancer is more common in males v females?
Basal cell more common in males | Squamous more common in females
43
What are the vaccine recommendations for a patient post-splenectomy? When are they given post-splenectomy?
Give pneumococcal, meningococcal, and H. influenzae vaccines on 14th post-op day
44
Most common surgical txs of Subclavian steal syndrome:
Carotid-subclavian bypass Carotid transposition Percutaneous angioplasty w/ stenting Surgical intervention should only be done in symptomatic patients
45
What is the next best step in mgmt. of a new solitary pulmonary nodule w/out previous images to compare it to?
Obtain chest CT If CT shows intermediate to high chances of malignancy then a PET should be ordered. If PET suggests malignancy then do a biopsy.
46
Common findings a/w Peutz-Jegher:
Polyps in both the small bowel and colon, perioral melanosis, breast malignancy
47
Treatment for anal fissures:
High fiber diet + adequate fluid intake Stool Softeners Sitz baths Topical anesthetics + Vasodilators – Nifedipine, nitroglycerin, etc.
48
Management of spontaneous pneumothorax:
Small (< 2cm) can be managed w/observation and O2 Large + Stable need needle aspiration or chest tube. Unstable – tube thoracostomy
49
Management of tension pneumothorax:
(variant w/ one-way valve causes expansion of pneumothorax during inspiration) Urgent needle decompression or chest tube placement
50
Why is Supplemental O2 used in tx of pneumothorax?
It increases the rate of resorption.
51
Where should a needle be placed to decompress a pneumothorax? What size needle should be used?
A large bore 14-18 gauge needle is inserted in the 2nd or 3rd ICS in midclavicular line, or the 5th ICS in the mid/anterior axillary.
52
Visualization of a dilated common bile duct in the absence of stones is commonly seen in what disorder?
Sphincter of Oddi dysfunction – dyskinesia and stenosis of the sphincter can cause obstruction of flow through the sphincter which mimics a structural lesion. Gold standard for dx: Sphincter of Oddi manometry.
53
Characteristics/Causes of Bile reflux gastritis:
d/t incompetent pyloric sphincter, often following gastric surgery. Allows retrograde flow of bile-rich duodenal fluid into the stomach and esophagus Sxs: Vomiting, frequent heartburn, abdominal pain.
54
Presentation of ruptured ovarian cyst:
Sudden-onset, severe, unilateral lower abdominal pain immediately following strenuous (exercising) or sexual activity. Will see fluid in pelvis on US Hemodynamically unstable pts require immediate surgery.
55
In a patient post-MVA what should an elevated PCWP be suspicious of? What is the next best step? (What does PCWP measure, and what's a normal value?)
Myocardial dysfxn d/t cardiac contusion. These pts need an urgent echo. (PCWP = pulmonary artery occlusion pressure = left atrial pressure. Normal value is 4-12mm)
56
What is the typical course leading to an appendiceal abscess? Sx and Dx tests?
Acute appendicitis with delayed presentation and >5 days of sxs. This often leads to appendiceal rupture with a contained abscess. These pts often have fever and leukocytosis but palpation of the abdomen may be normal. Need to use psoas and other tests to assess for the deep abdominal spaces. CT can be used to confirm Post-op cxs in these pts is extremely high, they should wait 6-8 weeks before removal.
57
Management for duodenal hematomas:
Gastric decompression via NGT and parenteral nutrition. | Surgery or percutaneous drainage only if non-surgical mgmt. fails.
58
Presentation , dx, labs of Emphysematous cholecystitis:
Fever, RUQ pain, N/V, crepitus in abd wall. See air-fluid levels in GB and gas in GB wall. Cultures w/gas-forming Clostridium, or E. coli Labs: UC hyperBRemia (from clostridium-induced hemolysis), slight elevation in aminotransferases
59
Risk factors of emphysematous cholecystitis:
DM, vascular compromise, IMCP
60
Tx of Emphysematous cholecystitis:
Emergent cholecystectomy Broad-spectrum abx w/clostridium coverage (pip-tazo, ertapenem, amp-sulbactam) Bile cultures
61
Immediate (0-2hr) Post-op fever causes:
Prior trauma or infection Blood products Malignant Hyperthermia
62
What is the most likely acid-base disturbance to occur in atelectasis?
Respiratory Alkalosis – pts become hypoxic and hyperventilate to compensate. This decreases the arterial PaCO2, and PaO2. pH will increase.
63
Factors that decrease risk of post-op atelectasis:
Adequate pain control, deep-breathing exercises, directed coughing, early mobilization, and incentive spirometry.
64
How does post-op atelectasis occur? What is the result of these mechanisms?
Post-op changes in lung complicance can lead to shallow inhalations which limit the recruitment of alveoli at the lung bases, and then impaired cough can predispose to small-airway mucus plugging. These both result in hypoxia --> increased RR and low pCO2.
65
Common cause of poor wound healing in alcoholic:
Vit. C deficiency
66
Most common organisms of prosthetic joint infection:
Early <3 months – S. aureus, G- rods, anaerobes (Pseudomonas) Delayed 3-12 months – Coag-neg staph (S. epidermidis), Propionibacterium, Enterococci Late >12 months – S. aureus, G- rods, B-hemolytic strep.
67
What is a cx of eschar formation from a circumferential, full-thickness burn?
It may lead to constriction of venous and lymphatic drainage, fluid accumulation and result in distal acute compartment syndrome.
68
What is abdominal succussion splash, and when is it seen?
It is elicited by placing the stethoscope over the upper abdomen and rocking the pt. back and forth. Seen in gastric outlet obstruction – malignancy, PUD, strictures, etc.
69
What are some cxs of infection w/in the retropharyngeal space?
The retropharyngeal space drains inferiorly to the superior mediastinum. Infection can spread to the carotid sheath --> thrombosis of the IJV and deficits in CNs IX, X, XI, and XII. Extension through alar fascia can cause acute necrotizing mediastinitis.
70
What should be suspected of an extra-axial dural-based brain mass? Tx?
Meningioma. These are treated via surgical resection.
71
What is likely in a pt. w/persistent pneumothorax, and persistent air leak post-chest tube placement? Cause?
Tracheobronchial rupture. This is rare and often follows blunt chest trauma. Other sxs: pneumomediastinum, subcutaneous emphysema.
72
What likely causes esophageal rupture and what will be the findings?
``` Often iatrogenic (w/endoscopy) or esophagitis-related. Findings: pneumomediastinum and pleural effusions. ```
73
Postpericardiotomy Syndrome presentation + Tx?
Presents w/fever, leukocytosis, tachy, and chest pain. Often AI and occurs few weeks after a procedure w/ a pericardium incision. Tx: NSAIDs or steroids, and pericardial puncture if tamponade occurs.
74
Acute Mediastinitis findings and tx:
Often follows cardiac surgery. Sxs: fever, chest pain, leukocytosis, mediastinal widening on CXR Tx: Drainage, surgical debridement, and prolonged abx.
75
Which rotator cuff tendon is most commonly injured?
Supraspinatus – d/t degeneration of the tendon w/age and repeated ischemia induced by impingement b/w the humerus and acromion during abduction.
76
What abx should be given in GB disease?
Ones that cover G- rods and anaerobes Ciprofloxacin + Metronidazole Ampicillin-Gentamycin + Metroniadazole DO NOT pick pip-tazo on tests
77
When should diastolic and continuous murmurs be evaluated?
ALWAYS these are almost always pathological. Midsystolic murmurs in young healthy people don't need further evaluation.
78
What needs to occur pre-op in pts. on Warfarin?
Rapid reversal of anticoagulation, done by infusion of FFP.
79
What should be done to manage acute cholecystitis?
Cholecystectomy within 72 hours
80
What is normal urine output?
800-2000 mL per 24hrs. | Oliguria is <500 mL per 24 hrs.
81
What can post-op pneumonia lead to and how is it managed?
Septic shock – fever, tachy, HoTN, oliguria. Treat w/IVF (0.9% saline) and abx for the underlying infection. If the patient fails to respond or has signs of V-overload w/out improvement in BP then vasopressors (Dopamine) should be started to improve perfusion.
82
Anterior Cord Syndrome presentation? Cause?
Loss of movement, pain and temp Vibration, touch and proprioception still intact. May be a cx of thoracic AA repair, bc there’s decreased blood flow through the radicular aa.
83
What is one of the most common postgastrectomy cxs, and how is it managed?
Dumping syndrome – N/D/V, palpitations, diaphoresis, HoTN Loss of normal pyloric sphincter axn --> rapid emptying of gastric contents Tx: Dietary modification – frequent, small meals, eat slowly, avoid sugars, increase fiber and protein, drink fluids b/w and not during meals.
84
Causes of initial hematuria:
Reflects Urethral damage | Urethritis, Trauma to urethra (caths)
85
Causes of terminal hematuria:
Reflects bladder or prostate damage | Urothelial ca., Cystitis, Urolithiasis, BPH, Prostate ca.
86
Causes of continuous hematuria (7):
Reflects Kidney or ureter damage | Renal mass, Glomerulonephritis, Urolithiasis, PCKD, Pyelonephritis, Urothelial ca., Trauma to kidney
87
Marjolin Ulcer:
SCC arising within a burn wound. SCC may arise in chronically wounded, scarred or inflamed skin. SCC in chronic wounds tends to be more aggressive.
88
Steps in management of complicated diverticulitis:
Fluid collections <3cm – IV abx and observation >3cm – CT-guided percutaneous drainage If sxs are still uncontrolled by 5th day – surgical drainage and debridement Sigmoid resection for pts w/ fistulas, perforation w/peritonitis, obstruction or recurrent attacks.
89
What is a cx of PP mechanical ventilation in a pt w/hypovolemic shock?
Pts in hypovolemic shock have decreased CVP, and the initiation of mechanical ventilation can cause acute loss of RV preload --> loss of CO and cardiac arrest.
90
What are the criteria for initiating long-term O2 therapy in pts. w/COPD?
1. Resting PaO2 <55mmHg or SaO2 <88% on room air | 2. PaO2 <59mmHg or SaO2<89% in pts. w/cor pulmonale, evidence of RHF or Hct >55%.
91
What causes the constitutional symptoms in cardiac myxomas?
Overproduction of IL-6 --> fever, weight loss, or Raynaud phenomenon.
92
Most common causes of hyperkalemia:
Acute or Chronic kidney disease | Medications or disorders that impair the RAAS.
93
Clinical and ECG findings of hyperkalemia:
Chronic may be asx until K+ > 7mEq/L Acute causes sxs at lower levels --> ascending m. weakness, flaccid paralysis ECG changes = peaked Twaves, short QT interval, QRS widening, sine wave w/vFIb
94
Therapy for hyperkalemia and when it should be instituted:
Acute tx: Calcium gluconate or chloride, insulin w/glucose | Should be given to pts. w/ ECG changes, K+ > 7 w/out ECG changes, or rapid K+ d/t tissue breakdown.
95
What is the most common cause of acute limb ischemia post-MI? Mgmt?
Arterial embolus from LV thrombus. | Mgmt: immediate anticoag., vascular surgery consult, and transthoracic echo to screen for thrombus.
96
Classic murmur in Aortic Regurg:
Decrescendo, blowing, diastolic murmur best heard at the L 4th ICS at the sternal border.
97
Murmur in Aortic stenosis:
Systolic, crescendo-decrescendo radiating to the carotids. Best heard in R 2nd ICS at sternal border.
98
Murmur in Mitral regurg:
HoloSystolic, best heard at apex, radiates to axilla.
99
Murmur in mitral stenosis:
Rumbling diastolic with opening snap (closer snap is to S2 worse the stenosis). Best heard at apex.
100
Diagnosis and management of AAA:
Use US for screening/diagnosis NOT arteriogram Anything >3.5cm is considered AAA TX: >3.5cm -- re-screen every 12 mos >4.5cm -- re-screen every 6 mos >5.5cm or growing >0.5cm/6mos -- surgery
101
How to diagnose aortic dissection
Hemodynamically stable pts: CT Angiogram (but can't do in renal failure/elevated Cr) Unstable pts and renal failure: TEE MRA can be used but is not preferred and should also be avoided in pts w/severe kidney disease
102
How to diagnose PVD: | How to identify the lesion location:
``` ABI: >1.4 = calcified vessel, need to do TBI instead 1.0-1.4 = normal 0.9-1 = equivocal, do exercise ABI 0.8-0.9 = Mild 0.4-0.8 = Moderate <0.4 = Severe Can use Doppler US and CTA to find where lesion is ```
103
How to treat PVD:
Use Angioplasty/Stent if the lesion is above the knee or small Use Bypass if lesion is below the knee or large All should f/u with medical tx (Cilostazol, Pentoxyphylline)
104
How to differentiate b/w neonatal conjunctivitis, and treatment:
Onset: <24 hr -- Chemical/Silver Nitrate, tx w/topical erythromycin 2-7d -- Gonorrhea: PURULENT. Tx: Ceftriaxone 5-14d -- Chlamydia: MUCO-Purulent. Tx: Oral Erythromycin
105
How to differentiate between RAS and Primary Hyperaldosteronism:
Both will have HTN and Hypokalemia. Conns: Aldosterone:Renin >20 RAS: Aldosterone:Renin <10
106
How to diagnose esophageal rupture?
Water-soluble contrast upper GI study.
107
How to calculate amount of fluid needed for resuscitation in burn victims:
Parkland formula: | 4 x Weight in Kg x % Area Burned
108
Treatment of hypocalcemia:
IV calcium gluconate
109
Common presentation of atrial myxoma:
Fever, fatigue, night sweats, weight loss. Low-pitched rumbling diastolic murmur heard at the apex that disappears when pt. rolls onto R side (d/t tm obstructing mitral valve). May also have decreased Hb.
110
Where does brain cancer metastasize?
Trick question bitch!!! | It doesnt. It stays in the brain.
111
Diagnostic test for brain tm?
MRI w/contrast is best, then MRI w/o contrast, then CT w/contrast. Once located bx.
112
Brain ca tx?
Resection, radiation, chemo, steroids, seizure ppx.
113
Presentation and Dx of epididymitis:
Spontaneous pain in testicle with relief on elevation. Vertically lying testicle (opposed to horizontal in torsion) Dx w/Doppler US
114
Difference in Epididymitis etiology and tx based on age:
<35 yrs most likely an STD -- tx w/Ceftriaxone + Azithromycin >55 yrs most likely E. coli -- tx w/a fluoroquinolone.
115
Best diagnostic test for kidney stones:
Non-con CT | cant do CT? do US
116
Presentation, Dx, and Tx of Transient synovitis:
Can occur at any age Presents as hip pain following a viral illness. May be so severe that the pt is non-weight bearing. Dx= clinical; Tx= supportive
117
Treatment of a fracture that involves the growth plate in a kid?
Surgery always
118
Ant. v. Post. dislocations of the shoulder:
Both will be adducted. Anterior- from any trauma, even minor, will have external rotation (shows palm of hand) Posterior- from massive trauma, a/w seizures and lightning strikes. Will have internal rotation (shows back of hand).
119
Hard signs of neck injury:
Airway: gurgling, stridor, loss of airway Vasculature: Expanding hematoma, pulsatile bleeding, stroke, shock, flat neck veins
120
Soft signs of neck injury:
Dysphonia Dysphagia SubQ air/emphysema Mild hard signs (hematoma not expanding, bleeding but not pulsatile etc.)
121
Treatment of Spinal Cord syndromes:
Steroids-- dexamethasone | Then diagnose w/MRI
122
Mgmt of pelvic fractures:
Typically external fixation and stabilization w/blood transfusions is enough. Only go to surgery if they are bleeding into the peritoneum. If just bleeding into pelvis don't go.
123
What complication should be investigated for in electrical burns?
Burnt muscle will lead to Rhabdomyolysis so check CK and Creatinine.
124
Rxs that cause hyperkalemia:
TMP-SMX – blocks eNac channel BBs – interfere w/B2 mediated K+ uptake ACEIs, ARBs, Ksparing diuretics – block eNac Digoxin – Inhibits NaK-ATPase Cyclosporine – Blocks aldosterone Heparin – Blocks aldosterone NSAIDs – decrease renal perfusion and K+ delivery to CDs Succinylcholine – extracell leakage of K+ through Ach Rs.
125
Renal effects of TMP-SMX:
Blocks ENac channels --> hyperkalemia. Also competitively inhibits renal tubular creatinine secretion --> artificial increase in serum Cr. GFR does NOT change. Pts should have serial monitoring of K+ to avoid complications.
126
Mgmt of Hypercalcemia:
``` Only severe (>14 mg/dL) or symptomatic pts require treatment. Short term: Normal saline + Calcitonin; Avoid loop diuretics Long term: Bisphosphonate (Zoledronic acid) ```
127
What is the mgmt. and contraindications for chest pain in cocaine use?
Managed with benzos for BP and anxiety Aspirin, Nitroglycerin, and CCBs for pain BBs are contraindicated and Fibrinolytics should be avoided d/t risk of ICH. Cardiac catheterization w/reperfusion done when indicated.
128
What are the different aspiration sites in recumbent v. upright pts?
Recumbent – posterior segment of the upper lobes | Upright – lower lobes or right middle lobe
129
Obesity Hypoventilation Syndrome definition, and other features:
``` Daytime hypercapnia (PaCO2 >45mmHg) in an obese patient (BMI >30), without another explanation for the hypercapnia. Other features: dyspnea, polycythemia, RESP. ACIDOSIS w/renal compensation, pHTN, and cor pulmonale. ```
130
Enoxaparin:
LMWH
131
Factor Xa inhibitors:
Fondaparinux (injection), Rivaroxaban (oral)
132
What defines severe renal insufficiency?
Estimated GFR <30 mL/min/1.73 m2.
133
Expected changes in hyponatremic hypovolemia for: Serum electrolytes Urine electrolytes Enzymes
Decreased serum and urine Na+, Increased renin, aldosterone, and ADH.
134
How do nitrates exert their effect?
Nitrates like nitroglycerin cause venodilation which increases peripheral venous capacitance. They cause systemic vasodilation and decrease cardiac preload --> reduce LV wall stress.
135
What is the first line tx for HTN d/t renal artery stenosis (RAS)?
ACEIs or ARBs. If pts are refractory to therapy then revascularization or stenting may be considered.
136
How will pleural pH change based on the type of effusion?
Normal pleural pH: 7.6 Transudative pH: 7.4-7.55 Exudative pH: 7.3-7.45 pH <7.3 norm. d/t Empyema, pleuritis, tm., pr pleural fibrosis
137
What are the common respiratory findings in Granulomatosis w/Polyangitis?
(aka. Wegener’s) URT: chronic rhinosinusitis, otitis, saddle-nose deformity LRT: tracheal narrowing w/ulceration and CXR w/multiple lung nodules w/cavitation and alveolar opacities.
138
Tx of Uric Acid stones:
Alkalinization of the urine w/oral Potassium Citrate, hydration, and a low-purine diet.
139
How are diuretics related to renal stones?
Furosemide and loop diuretics increase urinary calcium excretion and can cause calcium stones. Thiazides decrease Ca2+ excretion and is used in the tx of calcium stones.
140
What patients have a higher association of angiodysplasia?
Those with advanced renal disease, Von Willebrand, and Aortic stenosis (d/t acquired vWF deficiency).
141
How does Angiodysplasia often present?
Episodic painless GI bleeding – often seen as dark colored stools w/normal bowel movements in between episodes. Will often have signs of anemia as well
142
How is angiodysplasia diagnosed?
Via endoscopy – Upper GI or colonoscopy. | However it is often missed d/t poor bowel prep or location behind a haustral fold.
143
EKG findings in pericarditis:
Diffuse ST elevation with the exception of depression in aVR.
144
First line therapy for Dressler’s syndrome:
NSAIDs
145
Common AEs of inhaled B2-agonists:
Hypokalemia – they drive K+ into cells, causes muscle weakness and can be confirmed w/a BMP. Headache, tremors, and palpitations.
146
Hepatic Hydrothorax – Cause and presentation:
Seen in some pts w cirrhosis and portal HTN. Results from small defects in the diaphragm that allow peritoneal fluid to pass into the pleural space. Occurs more commonly on the right. Causes dyspnea, cough, pleuritic chest pain, and hypoxemia.
147
Hematologic effects of glucocorticoids:
Causes leukocytosis with NP predominance. Mobilizes marginated NPs into the blood, where they are non-fxnl. Decreases LPs and eosinophils.
148
Oliguria:
<250 mL of urine in 12 hrs.
149
Post-op Oligura definition + management?
<0.5 mL/kg/hr – needs immediate assessment w/bladder scan, if urinary retention is present they need a catheter.
150
Scleroderma renal crisis:
Sudden onset of renal failure (w/o previous kidney disease), malignant HTN (HA, blurry vision, N). UA may show mild proteinuria PBS may show microangiopathic hemolytic anemia or DIC w/schistocytes and thrombocytopenia.
151
What is the common finding of a hepatic mass with central scarring on CT scan?
Focal nodular hyperplasia. | Doesn't require tx unless symptomatic -- then resection.
152
What hematologic abnormalities may be seen in Meckel Diverticulum?
Ongoing bleeding from the diverticulum may cause Iron Deficiency anemia
153
CXR shows: pleural effusion w/extensive soft tissue density. Dx? Thoracentesis findings?
Mesothelioma -- extensive soft tissue density = pleural plaques. Thoracentesis will show bloody, exudative effusion.
154
What will be seen on XR of toxic megacolon?
Loss of haustra and dilated bowel. | Use sigmoidoscopy-guided placement of rectal tube to manage.
155
What lab values will be seen with decreased excretion of BR?
Hyperbilirubinemia with predominately conjugated BR. If it is 50-50 Direct-Indirect or predominately indirect then look for another cause of the hyperbilirubinemia (overproduction of BR after transfusion, etc.)
156
Why might alcoholics develop Hypocalcemia?
They are at increased risk for Hypomagnesemia d/t renal tubular loss. W/o magensium PTH cannot be released and therefore Ca2+ levels fall.
157
When is it safe to give anticoagulants post-op?
They can be given 6-12 hrs post-op
158
Tx of hyperaldosteronism:
Spironolactone or other Aldosterone receptor blockers
159
What are ARBs?
ANGIOTENSIN RECEPTOR BLOCKERS!!!!!
160
Management of anal mass:
When thought to be cancer first biopsy to prove cancer, and then use Nigro chemoradiation protocol. If this is not successful in eliminating it completely (90% success rate) then surgery can be used as a last resort in rare cases to remove residual tumor.
161
Causes of fistulas:
``` Foreign body Epithelization Tumors Irradiation Inflammation/IBD Distal obstruction ```
162
What abx should be given in pancreatitis w/proven infection?
Carbapenem
163
When should a pancreatic pseudocyst be drained?
Needs draining if >6cm or if its been present >6 weeks. This indicates complication and high risk of infection. <6cm or 6 weeks you can observe.
164
Colonoscopy schedule:
q10 if clean or hyperplastic q5 if polyp is seen q3 if polyp is CIS or villous q1 if polyp has dysplasia
165
Treatment of urethral injuries:
Anterior- immediate surgical repair | Posterior- suprapubic cystostomy tube and wait for repair
166
What does the cyanide-nitroprusside test detect?
Elevated levels of cystine. Can help confirm the dx of Cystinuria.
167
What metabolic disorder can develop in carcinoid syndrome?
Pellagra (Niacin deficiency). This is d/t the depletion of tryptophan for the preference of conversion to serotonin and 5-HIAA. Tryptophan is needed for both 5-HT and Niacin synth.
168
What metabolic disorder can Isoniazid therapy lead to?
B6/pyridoxine deficiency --> peripheral neuropathy Pellagra/Niacin deficiency --> Diarrhea, Dementia and Dermatitis. D/t interference of tryptophan metabolism (less common, seen in prolonged tx).
169
ABG findings in CHF:
hypoxic, hypercapnic, respiratory alkalosis.
170
What drug therapy is started in pts w/Coronary heart disease to reduce morbidity and mortality?
Dual-antiplatelet therapy: Aspirin + P2y12R blocker (clopidogrel, prasugrel, ticagrelor) BBs ACEIs or ARBs Statins Aldosterone Antagonists (spironolactone, eplerenone)
171
Complications of PEEP:
Alveolar damage, pneumothorax, and HoTN. | Pts. w/underlying lung disease (ARDS, pneumonia, COPD) are especially susceptible.
172
Clinical features of Pneumothorax:
``` Hyperresonance to percussion Diminished breath sounds Decreased tactile fremitus HoTN from decreased VR (collapsed lung compresses the IVC) Tachycardia from impaired RV filling Increased CVP ```
173
Features of obstructive ureterolithiasis:
Severe L lower AbdP radiating to the groin, vomiting, and unremarkable findings on PE. Dx w/US or noncon CT
174
Renal vein thrombosis:
Complication of any nephrotic syndrome, but most commonly a/w membranous glomerulopathy. D/t the loss of antithrombin III in the urine. Presents acutely w/AbdP, fever, hematuria Or more commonly progressive as a gradual worsening of renal fxn, and proteinuria in an asx pt.
175
Clinical presentation of spontaneous bacterial peritonitis:
T > 37.8/100 Abdominal Pain/tenderness Altered mental status HoTN, Hypothermia, paralytic ileus w/severe infection
176
What is spontaneous bacterial peritonitis?
Ascitic fluid infection w/out an obvious intraabdominal surgical etiology. Seen in pts w/cirrhosis.
177
Metabolic AEs of thiazides:
``` Hyperglycemia Increased LDL and TGs Hyperuricemia Hypokalemia Hyponatremia Hypomagnesemia Hypercalcemia ```
178
Tx to rapidly lower K+:
Insulin w/glucose B2-agonists Sodium bicarb in acidotic patients Ca2+ gluconate will stabilize the cardiac membrane, but will not reduce K+
179
Tx to slowly remove K+ from the body:
Diuretics Cation exchange resins Hemodialysis
180
What cardiac issues are associated with malignancies?
Malignancy causes a hypercoagulable state which can lead to massive PE --> RV dysfxn: hemodynamic collapse, syncope, decreased VR, decreased CO. Elevated CVP/JVP
181
What arrhythmia is most specific for Digoxin toxicity?
Atrial tachycardia w/AV block
182
What test is advised for all pts w/suspected gallstone pancreatitis?
RUQ US Then managed w/ERCP to remove the stone Biliary causes of pancreatitis typically present w/ALT > 150
183
How to differentiate b/w osmotic and secretory diarrhea:
Osmotic will have an elevated stool osmotic gap (>125mOsm/kg) Secretory will have a reduced SOG (<50mOsm/kg)
184
Difference between stress and urgency incontinence treatments:
Stress- Lifestyle mods, pelvic floor exercises, pessary, pelvic floor surgery Surgery for stress incontinence can cause urge incontinence later. Urge- Lifestyle mods, bladder training, then antimuscarinics (oxybutynin)
185
Overflow incontinence tx:
Cholinergic agonists, intermittent self-catheterization.
186
If urine osmolality is <100mOsm what should be considered?
Primary polydipsia and malnutrition (beer drinker’s potomania)
187
Difference b/w thrombus and emboli:
Emboli is a fragment that travels and blocks. Thrombus is a blockage that develops in the site it blocks.
188
What ECG findings are consistent with LVH?
High-voltage QRS complexes, lateral ST depression and lateral T wave inversion.
189
Persistent HTN, headaches and nosebleeds in a young pt is concerning of what?
Coarctation of the Aorta—should asses w/ bilateral arm and leg BP readings and pulse checks for brachial-femoral delay.
190
Diagnostic test of choice for PE:
CT angio
191
Most common source of liver mets?
Colorectal cancer—blood from the colon travels through the portal circulation directly to the liver. Lung and breast also commonly met to the liver.
192
What is likely in a young woman with a subauricular systolic bruit?
Fibromuscular dysplasia – causes internal carotid a. stenosis and presents w/recurrent HA, pulsatile tinnitus, TIA and stroke. May also have an abdominal bruit from the RAS --> secondary HTN (leads to hyperaldosteronism) and flank pain.
193
Most common CoD in dialysis pts:
CVD. Also the most common CoD in renal transplant pts.
194
Varying amplitude of QRS complexes suggests what?
Electrical alternans which is highly specific for pericardial effusion. Tx would be emergency pericardiocentesis.
195
Treatment of variant/vasospastic angina:
Prevention w/diltiazem (CCB = potent coronary dilator, but weak systemic dilator) and sublingual nitroglycerin for abortion of an episode. BBs and aspirin are contraindicated in variant angina.
196
What drugs are likely used to tx MDR pyelonephritis?
Aminoglycosides (like Amikacin) bc they treat serious G- organisms which commonly cause pyelonephritis. These may cause ARF in the setting of CKD though. Renal function should be monitored closely.
197
What complication is often secondary to viral pericarditis?
Pericardial effusions – causes electrical alternans on EKG, enlarged cardiac silhouette, distended neck veins and distant heart sounds. PE can vary, but almost all patients have an impalpable PMI
198
What should be done first in mgmt. of suspected cardiac tamponade?
Urgent echo to confirm diagnosis. | Most likely will present with signs of cardiogenic shock
199
What will be seen on pulmonary artery catheterization in the setting of cardiac tamponade?
Elevation and equalization of intracardiac diastolic pressures RA, RV, and PCWP will all resemble LA pressure.
200
What is a positive Kussmaul’s sign and what does it suggest?
Increase in JVD with inspiration | Often positive in RV failure.
201
What are signs of RV MI?
Often in patients w/acute inferior wall MI d/t occlusion of the RCA proximal to the RV brs. Signs/Sxs: chest pain, HoTN, autonomic signs (diaphoresis, V), and EKG findings of ST elevation in leads II, III, and aVF. May also have JVD, +Kussmaul’s sign, and clear lung fields suggestive of RVF Possible bradycardia or AV block bc enhanced AV tone.
202
What special mgmt. is implemented in RVF in addition to standard MI therapy?
Boluses of IVF to improve RV preload and increase LV filling. These pts are preload dependent and anything that reduces preload (nitrates, diuretics) should be avoided.
203
What coronary a. is involved in papillary muscle rupture?
RCA
204
What complications are associated with the LAD coronary?
Free wall rupture LV aneurysm Interventricular septum rupture
205
What coronary vessels can be involved in a IV septum rupture?
LAD (apical septal) | RCA (basal septal)
206
Most common signs/sxs of PE:
Dyspnea, pleuritic chest pain, tachypnea, tachycardia | Often CXR is abnormal, but many cases may have normal CXR
207
Mgmt of BB overdose:
Initially secure airway, IVF, IV atropine. Pts w/refractory or profound HoTN may then require IV glucagon as the next step. This may also treat CCB overdose. Other therapies include: IV Ca2+, vasopressors (E/NE), high dose insulin and glucose, and IV lipid emulsion.
208
Most common cause of constrictive pericarditis in developing countries:
TB
209
Beck’s triad:
HoTN, Distended neck veins, muffled heart sounds – a/w cardiac tamponade Pulsus paradoxus and +hepatojugular reflux are other common signs of tamponade
210
What is responsible for the sxs of cardiac tamponade?
``` Fluid accumulation in the pericardial cavity increases intrapericardial P above the diastolic ventricular P. The sxs (Beck’s triad) are d/t an exaggerated shift of the IV septum toward the LV cavity, this reduces LV preload, SV, and CO. ```
211
Most common cause of sudden cardiac arrest immediately post-MI:
Reentrant ventricular arrhythmias (vFib)
212
How does a ventricular aneurysm present on EKG?
With persistent ST-elevation after a recent MI (5d-3m), and deep Q waves in the same leads.
213
What is a systolic-diastolic abdominal bruit most suggestive of?
Renal artery stenosis.
214
What should be suspected in pts w/diffuse atherosclerosis and resistant HTN?
Renovascular HTN (RAS)
215
Why are IMCPd more likely to develop nocardia infections?
Bc the branching, filamentous growth prevents phagocytosis making host defense dependent on cell-mediated immunity which is often lacking in IMCPd.
216
Tx for nocardiosis:
TMP-SMX txs pulmonary Nocardiosis, may require additional abx like amikacin in severe disease. Carbapenems are added when the brain is involved
217
Who should receive the HAV vaccine?
Pts w/chronic liver disease (HBV, HCV etc) MSM IVDU Travelers to endemic countries
218
Presentation of vitreous hemorrhage:
Sudden loss of vision and onset of floaters. Reduced visual acuity to light perception, loss of fundus details, floating debris and a dark red glow. Diabetic retinopathy is #1 cause
219
What is the best way to monitor a pts response to treatment in DKA and HHS?
Monitor the serum anion gap, or direct assay of beta-hydroxybutyrate
220
What condition classically causes bilateral internuclear ophthalmoplegia?
MS – bilateral lesions in the MLF, bilateral adduction difficulties and nystagmus in the abducted eye.
221
Why do some pts w/celiac disease have negative results on IgA testing?
Many patients have an associated selective IgA deficiency as well. This causes the anti-tissue transglutaminase and anti-endomysial tests to be negative.
222
What MRI changes are associated with alzheimers disease?
Temporal lobe atrophy, mostly in the medial temporal lobes and hippocampi. Parietal may be seen but is much less likely - more likely to be seen in Primary Progressive aphasia Dementia syndrome
223
What will an EKG show in moderate hypokalemia?
Broad, flattened T-waves, U-waves, ST-depression and PVCs | May have some or all
224
When does workup need to be done for a murmur?
Grade III and above systolic murmurs, and all diastolic murmurs. Start w/ echo
225
Why are pts w/Multiple Myeloma at increased risk of infection?
Bc the neoplastic cells infiltrate the bone marrow and impair normal lymphocyte proliferation – ineffective Ab production and hypogammaglobulinemia.
226
What will CSF analysis of Guillain-Barre look like?
Normal except for increased protein.
227
Most commonly isolated organisms to cause brain abscess:
S. aureus and S. viridans
228
What should be used to reduce thromboembolic events in pts w/aFib?
Warfarin or non-VitK antagonist anticoagulants. | These are much more effective than the antiplatelet agents (aspirin, clopidogrel)
229
What is a factorial design?
A study that involves the randomization to different interventions w/additional study of 2+ variables.
230
What is likely to cause chondrocalcinosis?
Pseudogout, which is typically caused by: - hyperPTHism - HypOthyroidism - Hemochromatosis Chrondrocalcinosis = irregular opaque structures in articular cartilage (looks like white stuff IN BETWEEN joint lines)
231
What is Adhesive capsulitis?
When the glenohumeral joint loses its normal distensibility d/t chronic inflammation, fibrosis, and contracture of the joint capsule. Have shoulder stiffnes >> pain, and ROM is markedly reduced both actively and passively.
232
How to distinguish Grave’s from painless (silent) thyroiditis:
Radioiodine uptake. Painless/silent will have decreased uptake Graves will have increased uptake
233
What metabolic/lab abnormalities can hypothyroidism cause?
Hyperlipidemia (decreased LDL-Rs or decreased LDL-R activity) Hyponatremia (d/t decreased free H2O clearance) Asx elevation in creatinine kinase Elevated serum transaminases Macrocytic anemia
234
What can and cannot be calculated in a case-control study?
Odds ratio can- it measures the association between exposed individuals and the controls. Relative risk cannot- it can be calculated in cohort studies that follow individuals over time. The OR generally approximates the RR in case-controls if the disease is rare (low disease prevelance), or the disease incidence (# of new cases) is low --> “rare disease assumption”
235
When do Relative Risk and Odds Ratio approximately equal each other?
In rare disease states.
236
What type of skin cancer is most common in IMCPd?
SCC is common especially in post-transplant patients or those on immunosuppressants. It is also more aggressive in these pts. with increased risk of local recurrence and mets.
237
What complication is a/w neurologic deterioration w/in 2 days after an ischemic stroke?
Hemorrhagic transformation – often when the stroke affects large areas, is d/t an embolic cause or the pt. has been treated with thrombolytics. Often need urgent surgical decompression to treat.
238
When will you see the Jarisch-Herxheimer reaction?
W/in 6-48 hrs of treating a spirochetal disease – mostly syphilis but could be lyme etc.
239
What complications can be prevented by lowering HbA1c/achieving glycemic control in DM?
The microvascular complications – nephropathy and retinopathy – will be reduced. It will have no change on the macrovascular complications – MI, stroke.
240
How to differentiate bed bug rash from scabies:
Scabies are often on the palms, flexor wrist, lateral surface of the fingers and finger webs. It is v pruritic and worse at night. Bed bugs often cause small, punctate lesions in a linear track of clusters. Not commonly on the palms or soles bc of the thickness of the skin.
241
Tx of scabies:
Topical permethrin or oral ivermectin.
242
When is abx prophylaxis indicated for patients w/rheumatic fever valvular defects?
ONLY if they have a history of IE. | If no hx of IE then the risk of developing it following a dental procedure is v low and abx aren’t indicated.
243
How does PCV affect EPO levels?
It causes them to be low bc the constitutively active JAK2 is what causes the overproduction of RBCs and high Hb, not hypoxia.
244
What is Riluzole?
A glutamate inhibitor for ALS. Doesn’t stop progression, but may prolong time to tracheostomy.
245
Most common location of ectopic foci to cause aFib?
Pulmonary veins
246
Best treatment for acute for cluster headaches? And prophylaxis?
Tx: 100% O2 by facemask – most rapid-acting and effective w/out any major AEs. - SubQ sumatriptan can be used if there are no contraindications. Pphx: Verapamil or lithium and should be started asap after the onset of an acute attack.
247
What causes of Hyperthyroidism cause ophthalmopathy?
ONLY graves. If a patient has elevated thyroid hormones and ophthalmopathy then it has to be graves.
248
How to differentiate between Subacute granulomatous (De Quervian) vs. Subacute lymphocytic thyroiditis:
BOTH: - Progress from hyper to hypothyroidism w/ a diffusely enlarged thyroid. - Screen: T3/T4, thyroglobulin (increased), and TSH - Confirm: Increased ESR, decreased iodine uptake - Tx: BB + NSAIDS (MTZ is contraindicated!) for thyrotoxic, levothyroxine for hypothyroid phase Subacute granulomatous = due to infection + painful thyroid +/- jaw pain. Subacute lymphocytic = due to drugs/autoimmune/post-pregnancy + not painful
249
What auto-Abs may be seen in PBC?
Anti-mitochondrial are the most commonly associated. Anti-smooth muscle may also be present but these are more commonly seen in Autoimmune hepatitis.
250
What is goat’s milk deficient in?
Folate
251
What test should be done in a patient with a low Wells score meaning PE is unlikely?
D-dimer – it has high negative predictive value and can exclude the diagnosis of PE. Patients with a high wells score should undergo a CTA, or a V/Q scan if they have contraindications to a CTA.
252
What chromosome is linked to CF?
Chromosome 7 at position F508 is most common.
253
What drug is often a/w an increased risk of PML?
Natalizumab an alpha-4-integrin inhibitor. Often used to treat MS and Crohn’s. It interferes w/LCs, MCs and vascular adhesion of inflammatory cells. Rituximab a CD20 antagonist. Used to treat B-cell NH lymphoma, CLL, RA, and ITP.
254
Most common cranial nerve palsy a/w idiopathic intracranial HTN?
CN VI
255
Medications that can cause idiopathic intracranial HTN:
Growth Hormone Tetracyclines (minocycline, doxy) xs Vit. A and its derivatives: Isotretinoin, ATRA.
256
What FiO2 levels can cause O2 toxicity?
Anything >60%. | When pts are first put on ventilators these levels are often exceeded but should be reduced asap to prevent toxicity.
257
What bone complication can be caused by Celiac and what would the lab findings be?
Osteomalacia – impaired osteoid matrix mineralization. | Have increased AlkPhos and PTH, decreased serum and urinary Ca2+, and 25 OH-D levels.
258
Characteristic radiologic finding of osteomalacia:
Decreased bone density w/thinning of the cortex Bilateral and symmetric pseudofractures (looser zones) Eventually will cause "codfish" vertebral bodies w/a concave shape.
259
Management of tachyarrhythmia causing hemodynamic instability:
Immediate synchronized direct current cardioversion.
260
Initial management for patients with hypertriglyceridemia:
Statin therapy Weight loss Decreased EtOH intake Increased exercise ** Although fibrates decrease TGs these are rarely needed in addition to statins.
261
Treatment of Shingles:
Acyclovir, Famciclovir, Valacyclovir
262
What is Hepatorenal syndrome?
Complication of end-stage liver disease. Characterized by decrease in glomerular filtration w/out another clear cause of renal dysfxn., minimal hematuria (<50 RBCs) and lack of improvement w/volume resuscitation. Pts. develop splanchnic arterial dilation and decrease in vascular resistance, get renal HoPerfusion.
263
Treatment of Painless/Silent thyroiditis:
It is normally self-limiting and doesn’t require therapy, but a BB (propranolol) may be prescribed to control the hyperthyroid sxs.
264
Complications of Metoclopramide and Prochlorperazine:
Both are dopamine antagonists and used as antiemetics. They can cause EPS like acute dystonias, akathisia, and parkinsonism.
265
What is telogen effluvium?
One of the most common causes of hair loss in adults. Follicles undergo widespread shedding and cease growing. Often follows a stressful event – weight loss, pregnancy, major illness/surgery, or psychiatric trauma. In the hair pull test, extraction of >10-15% of fibers suggests TE. Self-limiting but may take up to a year to resolve.
266
Characteristics and treatment of Ehrlichiosis:
Transmitted by tick, causes flu-like illness w/ fever, HA, myalgias, chills, neuro sxs Leukopenia and thrombocytopenia w/elevated liver enzymes and LDH Tx: doxycycline.
267
Rxs that contribute to increased LDL-C levels:
Thiazides Cyclosporine Glucocorticoids Amiodarone
268
Treatment of central retinal a. occlusion:
Emergently treated w/ocular massage and high-flow O2. | Can give thrombolytics if w/in 4-6hrs but must be admin’d intra-ARTERIALLY cannot be given systemically via IV.
269
Presentation of Multiple Myeloma:
Often presents w/anemia and hypercalcemia in a patient with bone pain (chest or back). Classically progresses to renal insufficiency w/bland urinalysis and evidence of granular casts.
270
Treatment of Bacillary angiomatosis:
Oral erythromycin
271
Cause of bilateral trigeminal neuralgia:
MS is one of the only conditions that causes b/l trigeminal neuralgia – d/t demyelination of the nucleus of the CN V nerve or nerve root.
272
Management of Infectious Mononucleosis:
Supportive, and avoidance of sports for >3 weeks (4 if its contact sports) d/t risk of splenic rupture.
273
What test can identify patients w/ Primary adrenal insufficiency (Addison’s)?
ACTH stimulation (cosyntropin test). Should also include 8AM serum cortisol measurement.
274
What has the strongest association with both ischemic and hemorrhagic strokes?
HTN – d/t the shearing force on the intracerebral vascular endothelium, it accelerates AS and promotes thrombi formation.
275
What test is commonly used to compare two means?
The two-sample t test. | In contrast to the chi-squared test which compares categorical data and proportions between two groups.
276
Best initial test to perform on acute stroke patients?
CT w/out contrast – this will rule out hemorrhage the quickest.
277
How to differentiate b/w CML and Leukemoid rxn:
CML: - LAP low - Immature NP precursors = myelocytes > Metamyleocytes - Absolute basophilia Leukmoid: - LAP high - Mature NP precursors = Metamyelocytes > myleocytes - No basophilia
278
EKG leads involved in anterior MI:
LAD blocked | Some or all of V1-V6
279
EKG leads involved in inferior MI:
RCA or LCX blocked ST elevation in leads II, III, and aVF Inferior MIs are a/w HoTN, bradycardia and AV block.
280
EKG leads involved in posterior MI:
LCX or RCA blocked ST depression in V1-V3 ST elevation in I and aVL (LCX) ST depression in I and aVL (RCA)
281
EKG leads involves in lateral MI:
LCX, diagonal vessel blocked ST elevation in I, aVL, V5 and V6 ST depression in II, III, and aVF
282
EKG leads involved in RV MI:
Blocked RCA ST elevation in V4-V6 Occurs in 1/2 of Inferior MIs
283
What is used to confirm the diagnosis of ankylosing spondylitis?
Lumbar XR. | HLA-B27 is not needed – only seen in 5% of patients.
284
Common causes of secondary amyloidosis (AA):
``` Inflammatory arthritis (RA) Chronic infections (bronchiectasis, TB, osteomyelitis) IBD (crohn’s) Malignancy (lymphoma) Vasculitis ```
285
Diagnosis of secondary amyloidosis (AA):
Abdominal fat pad aspiration biopsy
286
Tx of secondary amyloidosis (AA):
Tx underlying condition | Colchicine for prevention and treatment
287
Management of iatrogenic Hyponatremia:
Hypertonic (3%) saline Serial measurement of electrolytes Increase serum sodium
288
What makes a patient automatically not a candidate for lung cancer surgery?
If they have positive LNs from a mediastinal sampling.
289
What is the initial workup for pts. w/HTN?
Basic lab analysis w/urinalysis, chemistry panel, lipid profile, and baseline EKG. In addition a detailed history and physical should be performed
290
Management of torsades de pointes:
In hemodynamically stable pts. first line is Magnesium sulfate. In hemodynamically unstable patients immediate defibrillation needs to be done.
291
DoC for treating Lyme disease:
Doxycycline for most patients – will also treat/prevent coexisting anaplasmosis. In pregnant/lactating women and young children DoC is amoxicillin or cefuroxime
292
Causes of metabolic alkalosis that are responsive to saline:
``` Vomiting Gastric suctioning Diuretics Laxative abuse Volume depletion Urine Chloride <20 mEq/L ```
293
Saline-resistant causes of metabolic alkalosis:
``` Primary hyperaldosteronism Cushing’s Severe hypokalemia (<2mEq/L) Urine chloride >20 mEq/L May see increased Na+ as there is xs mineralocorticoid in these types of metabolic alkalosis and Na+ retention. ```
294
Most effective non-pharmacological intervention to reduce BP:
Weight loss in overweight patients. | DASH diet in others.
295
What should be suspected in a pt w/painless blisters that heal with scarring, and increased skin fragility?
Porphyria cutanea tarda – especially in a patient with HCV. | May also see facial hypertrichosis, and hyperpigmentation.
296
Effect of cirrhosis on thyroid function:
The liver produces thyroid-binding proteins (thyroxine-binding globulin, transthyretin, albumin etc). When the liver fails, total T3 and T4 levels will decrease (because of decreased transport proteins), but free T3 and T4 remain unchanged. So, TSH will be normal looking like the pt. is euthyroid.
297
Common precipitating factors of thyroid storm:
``` Thyroid surgery NON-thyroid surgery!! Acute illness Childbirth Acute iodine load (iodine contrast) ```
298
In diabetic neuropathy what is responsible for the positive v. negative symptoms?
Axonopathy of large nerve fibers causes the negative sxs (numbness, loss of proprioception and vibration sense, diminished ankle reflexes) Axonopathy of small nerve fibers causes the positive sxs (pain, paresthesias, allodynia)
299
NNT equation:
``` NNT = 1/ARR ARR = Risk in control group – Risk in treatment group ```
300
Main complication of prolonged seizures:
Cortical laminar necrosis – can lead to persistent neuro deficits and recurrent seizures.
301
Treatment of Nocardia:
TMP-SMX for pulmonary | Add Carbapenems if brain is involved
302
Rxs that commonly cause folic acid deficiency:
Phenytoin (plus other anti-epileptics), primidone, phenobarbital, TMP, MTX
303
Presentation of pulmonic valve stenosis:
Severe cases present w/RHF in childhood Mild cases have sxs like dyspnea in early adulthood w/ a crescendo-decrescendo murmur that increases on inspiration with a systolic ejection click and widened split S2.
304
What should be given to patients with hypercalcemia d/t bony metastatic lesions?
Bisphosphonate therapy – will stabilize the destructive tumors, reduce risk of pathologic fractures and malignant hypercalcemia.
305
ABG in salicylate toxicity:
Low PaCO2, Low HCO3, and near-normal pH | Bc there is respiratory alkalosis followed by an anion gap metabolic acidosis.
306
Benign paroxysmal positional vertigo:
Episodic dizziness triggered by positional changes d/t crystalline deposits (canaliths) in the semicircular canals that disrupt the flow of vestibular fluid. This is the most common cause of vertigo
307
Dix-hallpike maneuver:
Vertigo and nystagmus triggered by quickly lying back into a supine position with the head rotated 45 degrees. Used to diagnose benign paroxysmal positional vertigo.
308
Tx of Malignant otitis externa:
IV anti-pseudomonal antibiotics, like ciprofloxacin | +/- surgical debridement
309
Gait in Parkinsonism:
Slow, Shuffling, HYPOKINETIC gait. Typically narrow-based.
310
CYP450 Inhibitors:
``` Increase drug effects. Acetaminophen, NSAIDs Abx/Antifungals (metronidazole) Amiodarone Cimetidine Cranberry juice, Ginko, Vitamin E Omeprazole/ PPIs Thyroid Hormone SSRIs (fluoxetine) ```
311
CYP450 Inducers:
``` Decrease drug effects Carbamazepine, phenytoin Ginseng, St. John’s wort Oral contraceptives Phenobarbital Rifampin ```
312
What foods may have an effect on Warfarin?
Brussel sprouts, spinach, or anything else with a good source of Vitamin K. These decrease warfarin’s effect
313
Treatment of Polymyalgia rheumatica:
Glucocorticoids
314
Lab findings in Antiphospholipid antibody syndrome:
paradoxical aPTT prolongation not reversed on plasma mixing studies – d/t the lupus anticoagulation effect. Anticardiolipin Ab Anti-B2-Glycoprotein-I Ab
315
Treatment of Rhino-Orbital-Cerebral mucormycosis:
Surgical debridement + Amphotericin B
316
What complication is seen with Voriconazole use in pts w/Heme malignancies?
Independent risk factor for Mucormycosis
317
Early side effects of levodopa/carbidopa:
``` Hallucinations Confusion Agitation Dizziness Somnolence Nausea ```
318
How would a patient with metastatic testicular cancer likely present?
Testicular tms often met to the retroperitoneal LNs causing low back pain, and the lungs causing dyspnea/cough and pulmonary nodules on CXR. Should be suspected when a young patient presents w/these sxs.
319
Tx of aFib in pts with WPW:
``` Cardioversion or antiarrhythmics like Procainamide AVN blockers (BBs, CCBs, Digoxin, Adenosine) are contra’d bc they can increase conduction through the accessory pathway. ```
320
What levels of pro-insulin are expected to be seen in patients with insulinomas?
Increased levels >5 pmol/L
321
What are some complications of heat stroke?
Rhabdomyolysis Renal failure ARDS DIC – which leads to coagulopathic bleeding and persistent epistaxis
322
Ocular AEs a/w PDE-5 inhibitors:
Blue discoloration of vision | Nonarteritic anterior ischemic optic neuropathy
323
Rx interactions w/PDE-5 inhibitors:
Antihypertensives along with these Rxs can cause severe HoTN, but especially a-blockers like Doxazosin and Nitrates. Both these classes should be avoided.
324
Tx of E. histolytica:
Metronidazole + an intraluminal abx (Paromomycin- an aminoglycoside)
325
When are smudge cells seen?
In cases of CLL – these are pathognomonic.
326
Presentation of CLL:
Often asx, but can have extreme fatigue, B sxs, infection or weight loss. PE shows lymphadenopathy and splenomegaly.
327
What suggests impending respiratory collapse in an asthma exacerbation?
A near normal pH and PaCO2 on ABG – indicates that the ongoing increased work of breathing is unable to maintain adequate ventilation. Resp. mm. fatigue and/or severe air trapping prevent meeting the demands of increased respiratory drive and suggest impending resp. collapse.
328
What valvular pathology can occur 2/2 pacemaker placement?
Tricuspid regurge. | The RV lead passes through the SVC and RA through the tricuspid valve and can damage the valve leaflets.
329
What causes Age-related macular degeneration?
Degeneration and atrophy of the central retina (macula), retinal pigment epithelium, Bruch’s membrane, and choriocapillaries.
330
How will AMD present?
Age-related macular degeneration. Presents w/ progressive loss of central vision with peripheral fields and navigational vision maintained. May develop cataracts after a while.
331
Presentation of Chronic Prostatitis/Chronic pelvic pain syndrome:
Pain in pelvis, perineum, and genitalia. Pain can radiate to the back. Irritative voiding sxs (urgency, hesitancy) Hematospermia, pain w/ejaculation Normal urinalysis and negative culture results Typically NO prostate tenderness.
332
What causes Chronic Prostatitis/CPPS?
Unclear etiology – thought to be noninfectious chronic prostate inflammation.
333
Tx for chronic prostatitis/CPPS:
Abx (quinolones) even though bacteria aren’t thought to cause it. a-blockers (tamsulosin) 5-a-reductase inhibitors (finasteride)
334
How long does it take for Coccidioides to present?
Typically get sxs 7-14 days after inoculation w/ the fungus (mold).
335
Incubation time for Blastomyces?
3-6 weeks!
336
When do you begin tx for HoThyroidism?
When TSH >5
337
Hetrophile antibody test:
Aka monospot – positive in infectious mononucleosis, but there is a 25% false-negative rate during the 1st week of illness.
338
Manifestations of PCV:
``` HTN Erythromelalgia (burning cyanosis in hands/feet) Transient Visual distrubances Aquagenic pruritis Gouty arthritis Bleeding Facial plethora Splenomegaly ```
339
Tx of PCV:
Phlebotomy or Hydroxyurea if increased risk of thrombus
340
What should be given in cases of COPD exacerbation?
``` Inhaled bronchodilators (B2 agonists and anticholinergics), and systemic glucocorticoids. Supplemental O2, Abx, and ventilator support may also be needed. ```
341
How to diagnose Leprosy:
Full-thickness biopsy of skin lesion from an active edge. | It is not culturable.
342
Tx of Leprosy:
Dapsone + Rifampin | Add clofazime if severe/multibacillary
343
What arthritis is non-erosive?
SLE arthritis. It is an inflammatory. All others destroy the bone.
344
What is familial Mediterranean fever?
Genetic disorder causing recurrent episodes of fever often accompanied by pain in abdomen, chest and joints.
345
Febrile Neutropenia common causes and treatment:
G-negs (P. aeruginosa especially) are most common infection in febrile neutropenia. Once blood cultures are taken monotherapy w/an anti-pseudomonal B-lactam should be started – cefepime, meropenem, pip-tazo.
346
How do alcoholics get hypocalcemia?
Often they develop hypomagnesemia which then creates resistance to PTH and decreases PTH secretion leading to hypocalcemia and hypophosphatemia.
347
What Rx is used to diagnose and manage narrow-QRS-complex tachycardia?
Adenosine. | It slows the sinus rate, increases AVN conduction delay or can cause transient AVN block.
348
What should be expected/tested for in unexplained cytopenias?
Chronic HIV infection.
349
What should all patients with presumed ITP be tested for?
HIV and HCV
350
Features of Lewy Body Dementia:
Fluctuating cognition, bizarre, visual hallucinations, and Parkonsonism (giving DA antagonists, 1st-gen antipsychs and risperidone will exacerbate the condition).
351
Most common cause of community-acquired bacterial meningitis:
S. pneumoniae | Can occur w/ or w/o concurrent pneumococcal pneumonia.
352
What is one of the earliest signs of macular degeneration?
Distortion of straight lines so that they look wavy.
353
Lab results of AML:
Cytopenias, elevated LDH, myeloblasts w/auer rods on peripheral smear.
354
What should be thought of in a HIV patient with pulmonary, mucocutaneous and reticuloendothelial findings?
Progressive disseminated Histoplasmosis. Get systemic sxs (fevers, chills, malaise) Weight loss/cachexia Pulmonary – cough, dyspnea Mucocutaneous lesions (papules, nodules) Reticuloendothelial (Hepatosplenomegaly, Lymphadenopathy)
355
Labs in disseminated histoplasmosis:
Pancytopenia Transaminitis Increased LDH + Ferritin
356
Tx of Disseminated Histoplasmosis:
``` Amphotericin B (mod-severe disease) Itraconazole (mild disease/maintenance) ```
357
Most common cause of spontaneous lobar hemorrhage:
Amyloid Angiopathy – most often involves the occipital and parietal lobes.
358
What should pts w/chest pain and suspected ACS be given first in the ED?
Aspirin – as long as the risk of aortic dissection is low.
359
Common AEs of Cyclosporine:
Nephrotoxicity – most common HTN from renal vasoconstriction and Na+ retention Neurotoxicity – HA, visual disturbances, seizure, tremors Glucose intolerance Infection Malignancy – SCC of skin and lymphoproliferative Gingival hypertrophy and hirsutism GI – anorexia, N/V/D
360
Preferred initial test in patients with suspected DVT:
Compression ultrasonography
361
What sites are affected in spondyloarthropathies?
The ligamentous insertion points (enthesitis). | Pain is worse at night and with rest.
362
Causes of chemotx-induced peripheral neuropathy (CIPN):
Vinca alkaloids (Vincristine, Vinblastine) Pb-based analogs (Cisplatin, Carbaplatin) Taxanes (Paclitaxel)
363
What is seen on autopsy of LBD?
Eosinophilic intracytoplasmic inclusions – accumulations of a-synuclein protein. Seen in neurons of the substantia nigra, locus coeruleus, dorsal raphe nucleus, and sustantia innominata.
364
Tx of LBD:
Carbidopa-levodopa for Parkinsonism Cholinesterase inhibitor for cognitive impairement SECOND-gen anti-psychs for psychotic sxs. 1st gens create severe neuroleptic sensitivity in these pts.
365
Euthyroid Sick Syndrome:
Abnormal thyroid fxn tests in any pt. w/an acute, severe illness (post-MI etc) Most common pattern is low free and total T3 with normal TSH and T4.
366
Esophagus ulcers in HIV pts:
Large linear = CMV Vesicles and round/ovoid ulcers = HSV White plaques = Candida
367
What will cause Hyperchylomicronemia?
Aka Type I familial dyslipidemia D/t a defective LPL or apoC-II Often presents with acute pancreatitis
368
Phosphate levels in secondary hyperPTHism:
Normally caused by renal failure – leads to phosphate retention and improper clearing, so increased serum PO4 with decreased Vit D, and Ca2+ and increased PTH. 25-hydroxycholecalciferol (inactive Vit. D storage form) will increase.
369
How should B12 be administered in Pernicious anemia pts?
IM injection – this bypasses enteral absorption which is impaired in these patients.
370
Tx of PE:
Heparin or LMWH (Enoxaparin) then bridge to warfarin Can give tpa in some cases, but is contraindicated in post-op patients. IVC filters can be placed in pts if PE recurs or anticoagulation is strictly contra’d
371
Major risk factors for HBV infection:
Multiple sexual partners and IVDU. HBV is much more likely to present with sxs than HCV. HBV is also much more commonly contracted through sexual contact than HCV.
372
Molluscum contagiosum:
Skin infection from Poxvirus. Characterized by small, pruritic, skin-colored papules w/umbilicated centers. Imaired cell-immunity may lead to a prolonged course w/widely spread papules involving the face. HIV testing should be considered for patients w/MC.
373
Severe cx of Nitroprusside therapy:
Cyanide toxicity – get AMS, lactic acidosis, seizures and coma. Most common in patients w/renal insufficiency.
374
Post-ictal lactic acidosis:
Often follows seizures (esp. tonic-clonic). Raises serum lactic acid d/t skeletal mm. hypoxia. Typically transient/self-limited and resolves w/in 90 min. Mgmt is observation and repeat chemistry panel//ABG after ~2hrs.
375
When should NaHCO3 be given for metabolic acidosis?
When pH < 7.1. | Anything higher may cause myocardial depression and increased lactic acid production.
376
Features of Chronic arsenic poisoning:
Polyneuropathy, pancytopenia, mild transaminase elevation, hypo/hyperpigmentation and hyperkeratosis. Mees lines - horizontal striations of the finger nails is characteristic
377
Tx of acute MS exacerbation:
Glucocorticoids (IV Methylprednisolone) | Plasmapheresis can be considered in pts refractory to steroids.
378
Chronic maintenance tx of MS:
IFN-B or Glatiramer acetate. Both are disease modifying agents and used for chronic tx in pts. w/relapsing-remitting or secondary, progressive forms of MS.
379
Auto-Abs in Scleroderma:
Antinuclear-Ab (most sensitive, but not specific) Anti-topoisomerase I (anti-Scl-70) Ab and anti-RNA pol III (most specific) Anticentromere-Ab (mostly in limited disease/CREST)
380
What does skin infection involving the external ear most likely suggest?
Erysipelas – bc the external ear lacks a lower dermis level which makes cellulitis a v. unlikely diagnosis.
381
Cause and presentation of erysipelas:
S. pyogenes (aka GBS) Warm, tender, erythematous rash w/raised, sharply demarcated borders. May have systemic sxs fever, chills, regional lymphadenopathy.
382
Most common AE w/in 1-6hrs of transfusion:
Febrile nonhemolytic transfusion rxn. -- can be prevented with leukoreduction.
383
When should cells be washed prior to transfusion?
If the pt. has IgA deficiency or had a prior allergic transfusion rxn.
384
What should be given to transplant pts. to prevent opportunistic infections?
TMP-SMX. This prevents PCP, some Listeria and toxoplasma infections. Can be discontinued 6-12 months post-transplant. Some pts. may also receive Ganciclovir for pphx against CMV
385
What is use dependence and what Rxs is it seen with?
It is enhanced pharmacologic effects of a drug during faster heart rates Seen with class I (esp. IC, less so IA) and class IV (CCBs) anti-arrhythmic agents. Class IC cause progressive decrease in impulse conduction w/faster HR – leads to increase in QRS duration. Class IV (CCBs) will see an increase in the PR interval, but no change in the QRS complex.
386
First step in evaluation of Cushing syndrome:
Confirm hypercortisolism w/late-night salivary cortisol assay, 24-hr urine free cortisol, and/or low-dose dexamethasone test. - 2/3 of these tests needs to be + to dx If confirmed, then measure ACTH.
387
Tx of Diffuse esophageal spasm:
CCBs. | Alternatives: Nitrates or TCAs
388
Diagnostic requirements of acute liver failure:
Severe injury with elevated aminotransferases (often >1000) Signs of hepatic encephalopathy Impaired hepatic synthetic fxn (INR > 1.5) **Cirrhosis or underlying liver disease should not be present**
389
Tx of Optic neuritis:
IV corticosteroids.
390
Diagnostic study for suspected aortic dissection:
TEE or CTA – but can’t use CTA in renal disease.
391
Presentation and diagnosis of oropharyngeal dysphagia:
History of difficulty initiating swallowing with cough, choking, or nasal regurgitation. Diagnose with Videofluoroscopic modified barium swallow.
392
Mgmt of caustic ingestion:
Ingestion of alkali substances like sodium hydroxide (lye), can cause immediate chemical burn or liquefactive necrosis. Managed with decontamination and IV hydration. Upper GI endoscopy should be performed w/in first 12-24 hrs to determine extent of damage. Mild injury = supportive measures More severe = tube feedings and possible surgery.
393
What is tonometry and when is it used?
It measures intra-ocular pressure and is used to asses acute ACG.
394
Tx of Trigeminal Neuralgia:
Carbamezapine
395
Preferred tx for hypovolemic hypernatremia:
IV 0.9% saline. | The fluid can be switched to 5% dextrose once the patient is euvolemic.
396
DoC for Osteoporosis:
Alendronate Can’t give to pts. w/GERD so give Zolendronic acid bc its given IV and doesn’t cause reflux esophagitis like Alendronate.
397
What cancers are likely to cause primarily solitary brain mets?
Breast Colon RCCa Lung and melanoma likely to cause multiple mets.
398
Most common ca to met to the Brain?
Lung. Neoplastic cells travel through vasculature and lodge in small-caliber vessels at the gray/white matter jxn. Often cause vasogenic edema as well.
399
MS v. Brain mets on MRI:
MS often has inflammatory white matter lesions. | Brain mets often well-circumscribed lesions at the gray/white matter jxns w/ vasogenic edema.
400
What causes the cyclical fevers in malaria?
Plasmodium-induced RBC lysis.
401
What are Heinz bodies and when are they seen?
Heinz bodies are oxidized/denatured Hb that occurs when there’s a G6PD deficiency (XL-recessive dx).
402
Most frequent source of PEs:
Deep veins of the lower extremities. >90% PEs come from iliac, femoral or popliteal vv. **Exception is patients w/nephrotic syndrome – renal vv. are most common source of PE in these pts.
403
Recommendations for Bladder cancer screening:
Currently there is recommendation against screening d/t its low incidence and poor PPV of current screening tests.
404
Management of Hyperosmolar hyperglycemic state:
Aggressive hydration w/NS IV Insulin (NOT subQ) K+ supplementation.
405
Sxs of ACL injury:
Pain, rapid onset Popping sensation at time of injury Significant swelling w/effusion or hemarthrosis (gross blood on aspiration of joint fluid) Joint instability
406
Common cardiac finding in chronic ankylosing spondylitis:
Aortic Regurgitation.
407
When do HCMP murmurs increase in intensity?
``` With Valsalva (straining phase), abrupt standing, nitroglycerin administration – all d/t decreased preload. They decrease with sustained hand grip, squatting, and passive leg raise. ```
408
Pathogenesis and common causes of phototoxic drug rxns:
D/t production of ROS that then directly damage cell membranes and DNA. Sxs can be seen in both sun-exposed areas as well as non-exposed areas. Common causes: Abx (tetracyclines), Antipsychs (chlorpromazine), Diuretics (furosemide, thiazides), Amiodarone, promethazine, piroxicam.
409
Most common cause of B12 deficiency and possible long-term complication:
Pernicious anemia. | Causes atrophic gastritis which increases risk of gastric cancer and gastric carcinoid tms.
410
Mgmt of frostbite:
Rapid rewarming in 37-39C water bath. Analgesia and wound care Thrombolysis in severe, limb-threatening cases.
411
What medication can help with stone passage?
Tamsulosin or a1-antagonists. They relax ureteral muscles and decrease intraureteral pressure – facilitate stone passage and reduce need for analgesics.
412
Tx of PCT:
Serial phlebotomy or hydroxychloroquine along w/mgmt. of underlying causes (HCV).
413
Tx plan for patients with RA:
All pts should be started on DMARDs as soon as possible to prevent further joint damage. Started on non-bio DMARDs first (MTX is DoC) and then if no improvement, step-up to a biologic DMARD after 6 mo. Then NSAIDs and glucocorticoids can be added for symptom relief.
414
DMARDs:
Nonbiologic: MTX (Initial DoC), Hydroxychloroquine, sulfasalazine, leflunomide, azathioprine Biologics: Etanercept, infliximab, adalimumab, tocilizumab, rituximab.
415
What can ingestion of home distilled liquor cause?
Lead poisoning. Often distill alcohol through parts w/lead soldering.
416
Best tx of Anaphylaxis:
IM epinephrine
417
What is likely to be the cause of NPH?
Decreased CSF absorption
418
What is pathognomonic for rhabdomyolysis on urine analysis?
3+ blood with no RBCs on microscopy. Bc the myoglobin is making it positive for blood.
419
What causes Graves ophthalmopathy?
T cell activation and stimulation of orbital fibroblasts by TSH-R auto-Abs leading to expansion of orbital tissues.
420
What is a complication of supplemental O2 in advanced COPD patients?
CO2 retention and worsened hypercapnia d/t 1- Increased dead space perfusion – V/Q mismatch 2- decreased affinity of oxy-Hb for CO2 3- reduced alveolar ventilation. Can cause increased lethargy and confusion and lead to seizure.
421
What should the goal O2 saturation be in pts. w/advanced COPD?
SaO2 90-93% or PaO2 60-70mmHg | Will decrease chance of CO2 retention.
422
Heme abnormalities in Chronic renal failure:
Platelet dysfxn is the most common cause of abnormal hemostasis in pts. w/CRF. Get abnormal bleeding and bruising in uremic coagulopathy PT, aPTT, and platelet count will be normal, but BT is prolonged. DDAVP is DoC. **DON’T give platelet transfusion bc the new platelets will quickly become inactive
423
What comorbidities are a/w PCOS?
``` Metabolic syndrome (diabetes, HTN) Obstructive sleep apnea Nonalcoholic steatohepatitis Endometrial hyperplasia/cancer **Scren for DM w/oral glucose tolerance tes ```
424
Most common cause of Acute Liver Failure:
Acetaminophen toxicity
425
What is the preferred tx for Diabetic gastroparesis?
Metoclopramide – it is a prokinetic and antiemetic.
426
Tetrad that characterizes Neuroleptic malignant syndrome:
Mental status change Rigidity Fever Autonomic dysregulation
427
How to differentiate b/w NMS and Rx-Induced Parkinsonism:
Only NMS will have autonomic instability and fever. Also more likely to see mental status changes. Both will have tremors, rigidity, and gait abnormalities.
428
Pathophys of Cyanide toxicity:
Cyanide binds cytochrome oxidase and inhibits mitochondrial oxidative phosphorylation. Cells shift to anaerobic metab w/decreased ATP production – lactic acidosis. Thiocyanate accumulation causes the neuro sxs.
429
Treatment of Cyanide toxicity:
Sodium Thiosulfate
430
What would cause refractory hypokalemia?
Hypomagnesemia is one of the most common causes. Intracellular Mg inhibits K+ secretion by renal outer medullary K+ channels in the CT of the kidney; So when Mg is low K is secreted in xs.
431
What lab values will be seen in hyperthyroidism d/t exogenous intake?
Low TSH High fT3 and T4 Low radioactive iodine uptake Low serum Thyroglobulin
432
What thyroid condition will give you an elevated ESR?
Subacute (DeQuervain’s) thyroiditis.
433
Most likely cause of Culture negative urethritis?
Chlamydia
434
Effects of UGI bleeding on BUN/Cr:
Pts. w/upper GI bleeding, but not lower, may have increased BUN:Cr d/t increased urea production (from intestinal Hb breakdown) and increased urea reabsorption (d/t hypovolemia). No changes are seen with creatinine.
435
Meningococcal vax schedule:
Regular – Primary vaccine age 11-12, then booster at age 16-21 High-risk patients – Vaccinate/booster even if age >18 for pts w/complement deficiency/asplenics, college students in residential housing (<21yo), military recruits, travelers to endemic areas, exposure to community outbreaks.
436
When should epidural glucocorticoid injections be used for low back pain?
In patients with lumbosacral radiculopathy who haven’t responded to initial tx. NOT helpful for nonradicular pain.
437
Heme effects of ParvoB19:
Transient pure red cell aplasia | Aplastic crises in pts w/underlying heme disease.
438
Arthritis of ParvoB19:
Non-destructive (like SLE) | Acute, symmetric – affects hands (MCP, PIP, and wrists), knees, and ankles.
439
Most common behavioral risk for TB:
Substance abuse
440
Common findings in invasive aspergillosis:
Triad of fever, chest pain and hemoptysis Pulmonary nodules (yes plural) with halo sign (surrounding ground-glass opacities) Positive cell wall biomarkers (galactomannan, beta-D-glucan)
441
Mgmt of DKA:
NORMAL (0.9%) saline and regular insulin infusion. Can add dextrose 5% once glucose is <200 mg/dL Add K+ if serum K+ is < 5.2 mEq/L
442
AE of EPO therapy:
HTN – may lead to HTN crises esp. in pts who receive large doses or experience a rapid rise in Hb concentration.
443
Dialysis disequilibrium syndrome:
D/t osmotic shifts during hemodialysis – causes changes in neuro status d/t cerebral edema. May cause HA and N.
444
What is salvage therapy?
A form of treatment for a disease when a standard tx fails. | Ex: Radiation for prostate ca. recurrence after radical prostatectomy fails.
445
Lab values in steroid abuse:
Erythrocytosis/increased erythropoiesis – elevated Hb Cholestasis Hepatic failure Dyslipidemia Slight elevation in Creatinine (d/t increased mm. mass)
446
Lab values in Klinefelter syndrome:
Low/no testosterone High FSH and LH Azoospermia
447
What risk is increased in pts w/plantar puncture wounds through footwear?
Osteomyelitis d/t Pseudomonas.
448
What adjunctive therapy can be used to tx PCP?
In addition to TMP-SMX corticosteroids may be used and have been shown to reduce mortality in severe cases. Indications: PaO2 <70 or A-a gradient >35 on room air.
449
What is an external hordeolum, what causes it, what is used to tx?
Hordeolum = stye. Its an acute inflamm. disorder of the eyelash follicle or tear gland. Often d/t S. aureus, but can be sterile. Tx: warm compresses. If it persists or is v. large may consider I+D.
450
Typical features of cerebellar hemorrhage:
Occipital HA (may radiate to neck/shoulders) Neck stiffness (d/t extension of blood into 4th ventricle) N/V Nystagmus Ipsilateral hemiataxia
451
First-line tx of Reactive arthritis:
NSAIDs. | Abx are not used.
452
Pulse in severe aortic stenosis:
Pulsus parvus et tardus | Delyaed/Slow-rising and diminished/weak carotid pulse.
453
Winter’s Formula:
PaCO2 = 1.5 (HCO3-) + 8 +/- 2
454
What are conduction abnormalities in pts. w/IE suspicious of?
Perivalvular abscess – most commonly seen with aortic valve involvement. These are seen in almost 30-40% of patients with IE.
455
Postconcussive syndrome:
Follows TBI (hrs to days) Sxs: HA, confusion, amnesia, difficulty concentrating or multitasking, vertigo, mood alteration, sleep disturbance, and anxiety. Typically resolves w/in weeks to few months w/symptomatic tx.
456
What Rx increase risk of Exertional heat stroke?
Anticholinergics, antihistamines, phenothiazines, and TCAs.
457
Mgmt of exertional heat stroke:
Rapid cooling – ice water immersion preferred Fluid resuscitation Electrolyte correction No role for antipyretics
458
Anticholinergic toxicity presentation:
Hyperthermia, tachycardia, dry skin, nonreactive mydriasis (Dilation w/ineffective accommodation), and decreased bowel sounds. MOF/dysfxn is uncommon
459
What anti-DM medication is most likely to result in weight loss?
GLP-1 Receptor agonists (Exenatide, Liraglutide). | Pioglitazones (TZDs) and Sulfonylureas are likely to cause weight gain.
460
How to differentiate diarrhea in AIDS pts:
All can cause weight loss Cyrptosporidium (CD4<180) – severe watery diarrhea, low fever Micro/Isosporidium (CD4<100) – watery diarrhea, crampy AbdP fever RARE MAC (CD4<50) – watery diarrhea HIGH FEVER (> 39/102) CMV (CD4<50) – small volume diarrhea, only one that can be bloody/hematochezia, AbdP, low fever
461
When is asterixis seen?
Hepatic encephalopathy Uremic encephalopathy CO2 retention
462
Indications for Urgent Dialysis:
AEIOU Acidosis – metabolic acidosis (pH < 7.1 and refractory to tx) Electrolyte abnorms – symptomatic/severe hyperkalemia (EKG changes, arrhythmias, K>6.5) Ingestion – toxic alcohols (MeOH, ethylene glycol), salicylate, Lithium, Na-valproate, carbamazepine Overload – V overload refractory to diuretics Uremia – symptomatic, encephalopathy, pericarditis, bleeding
463
What is hemi-neglect syndrome?
Caused by a lesion to the R/non-dominant parietal lobe, responsible for spatial organization. Characterized by ignoring the L side of a space, and possible anosognosia
464
What are common BRAF inhibitors?
Vemurafenib and Dabrafenib
465
Adalimumab MoA and conditions it treats:
TNF-a inhibitor. | Txs IBD, RA, ankylosing spondylitis and psoriasis
466
What dx procedure should be done for pts. w/painless, gross hematuria?
Cystoscopy – to evaluate for bladder cancer.
467
Acid-Base abnormalities a/w salicylate toxicity:
Combined Respiratory alkalosis and an anion-gap metabolic acidosis
468
Clinical associations with FSGS:
AfAm + Hispanic ethnicity, obesity, HIV, heroin use
469
What post-MI cx is likely to cause biventricular failure?
Interventricular septum rupture aka VSD.
470
Aminoglycoside toxicity:
Can damage the cochlear cells – ototoxicity Gentamicin especially can also damage the motion-sensitive hair cells in the inner ear to cause selective vestibular injury (vestibulopathy) w/or w/o ototoxicity.
471
What should be done before initiating trastuzumab therapy?
Trastuzumab = HER2 inhibitor Baseline assessment of cardiac fxn by echo. It is cardiotoxic.
472
2 Primary manifetations of Chagas disease:
Megacolon/megaesophagus and cardiac disease.
473
What patients should metformin be avoided in?
Acutely ill pts w/ARF Pts predisposed for hypoxia (CVD, CKD, COPD) Liver failure Sepsis All these conditions increase risk of lactic acidosis
474
Lab findings in PSGN:
UA: Protein+, Blood+, RBC casts +/- Serum: decreased C3 and C4, increased Anti-DNase B, anti-AHase (antihyaluronidase), ASO, and anti-NAD
475
First line therapy for Raynaud?
Dihydropyridine CCBs (Nifedipine, Amlodipine) – just like vasospastic angina
476
What criteria must be met to receive pphx for Lyme dx?
Must meet all 5! 1- Tick is adult or nymphal Ixodes scapularis 2- Tick attached for >36hrs or engorged 3- Pphx started w/in 72hrs of removal 4- Local B. burgdorferi infection rate >20% 5- No contra’d to doxycycline
477
Effects of hypopituitarism on aldosterone:
There are no significant effects. | Adrenal aldosterone is mainly regulated by the RAAS and is not affected by low ACTH.
478
Tx of toxic megacolon:
IVF, BS Abx, and bowel rest. | IBD-induced should be treated w/IV corticosteroids
479
AEs of MTX:
Pancytopenia, folic acid deficiency, nausea, stomatitis, rash, hepatotoxicity, ILD, alopecia and fever.
480
Difference b/w case control and retrospective cohort:
Case control compares a group w/disease v w/o and tries to find risk factors Retrospective cohort finds a group w/ a risk factor v a group w/o the risk and sees if the disease developed in each group.
481
Most appropriate diagnostic tests for acute HBV infection:
HBsAg and anti-HBc bc they’re both elevated during initial infection, and anti-HBc will remain elevated during the window period.
482
What is the most common tx of homocysteinemia?
Folate and B6. Need B6 as cofactor for cystathionine B-synthase which catalyzes homocysteine to cystathionine. If documented B12 deficiency then cobalamin is addcled.
483
Diagnosis of Dermatomyositis:
Increased CPK, aldolase, LDH Anti-RNP, anti-Jo1 and anti-Mi2(anti-helicase) Abs Can do EMG or mm./skin bx if uncertain Should screen for malignancy once diagnosed.
484
Typical features of CJD:
Rapidly progressive dementia, myoclonus, and sharp, triphasic, synchronous discharges in EEG.
485
What are Hollenhorst plaques and when are they seen?
Bright, yellow, refractile plaques in the retinal a. seen on fundoscopy. These are seen in atheroembolism/cholesterol embolism and indicate a more proximal source (Internal carotid).
486
What is a mediastinal mass w/elevated AFP and B-hCG diagnostic of?
A nonseminomatous germ cell tumor. | If found a testicular US should be performed to exclude a sm. primary tm there.
487
What could pulsatile tinnitus in a young woman be concerning of?
Fibromuscular dysplasia with involvement of the carotid or vertebral aa. Or Idiopathic Intracranial HTN
488
Treatment of Paget disease:
Bisphosphonates
489
What conditions are a/w Pseudogout?
Hemochromatosis Hyperparathyroidism Trauma/Overuse/Surgery
490
What is the main measure of association in case controls?
Exposure odds ratio
491
When is prevalence odds ratio calculated?
In cross-sectional studies
492
Tx for severe hypovolemic hypernatremia:
Isotonic 0.9% saline. Once the volume deficit has been restored pts can be switched to half-normal 0.45% saline to better replace the free water deficit. Goal rate of plasma Na+ correction is no more than 1mEg/L/hr to prevent cerebral edema. Less severe cases can be treated w/5% dextrose in 0.45% saline
493
Most common cause of hypernatremia?
Hypovolemia
494
What is Ichthyosis vulgaris?
Chronic, inherited skin disorder characterized by diffuse dermal scaling. Caused by mutations in flaggrin gene.
495
Situational syncope:
Form of reflex/neurally mediated syncope a/w triggers – micturition, cough, defecation. Triggers cause alteration in ANS response and lead to cardioinhibitory, vasodepressor or mixed response. Increased PSNS and decreased SNS
496
Aspirin-exacerbated respiratory disease:
Non-IgE mediated, psuedoallergic Rx reaction. Seen in pts. w/hx of asthma, chronic rhinosinusitis w/nasal polyposis. Characterized by bronchospasm and nasal congestion following aspirin ingestion.
497
Post-exposure pphx in HBV unvax’d pts:
Immediate HB vaccine and HB immune globulin with follow up serology.
498
HSV retinitits in an IMCP’d pt:
Rapidly progressing b/l necrotizing retinitis – “acute retinal necrosis syndrome.” Initial sxs: keratitis, conjunctivitis w/eye pain, followed by rapid vision loss. Fundoscopy: widespread, pale, peripheral lesions and central necrosis of the retina. VZV may also cause this same type of retinal necrosis.
499
Most common cause of corneal blindness in the US:
HSV infection.
500
CMV retinitis:
Most common ocular cx in HIV pts. Typically painless (unlike HSV) Fundoscopy: fluffy or granular retinal lesions near the retinal vessels and assoc. hemorrhages. No conjunctivitis or keratitis like in HSV.
501
What is sympathetic ophthalmia?
“Spared eye injury” Immune-mediated inflammation of one eye after a penetrating injury to the other eye. Typically see anterior uveitis, but panuveitis, papillary edema, and blindness may develop. Pathophys is thought to be the uncovering of “hidden antigens.”
502
Cxs of Subarachnoid hermorrhage:
``` Re-bleed (first 24hrs) Vasospasm (>3days – use nimodipine to prevent) Hydrocephalus/increased ICP Seizures Hyponatremia (from SIADH) ```
503
Serum measurement of what has a high sensitivity of diagnosing CHF?
BNP. Elevated levels of BNP correlate w/the severity of LV dysfunction and help differentiate dyspnea 2/2 CHF from other causes.
504
What conditions are a/w Nephrotic syndrome 2/2 AA amyloidosis?
Chronic inflammatory conditions: RA, IBD | Chronic Infections: Osteomyelitis, TB
505
Risk factors for Fluoroquinolone associated tendinopathy:
Age >60, normal BMI, female, concurrent oral corticosteroid use, recent transplant.
506
Anti-mitochondrial Abs:
Seen in PBC – high sensitivity and specificity
507
Typical presentation of Idiopathic Intracranial HTN:
Holocranial HA Vision changes (blurry/diplopia) Pulsatile Tinnitus
508
When is Papilledema a contraindication to LP?
Only when the pt has evidence of obstructive/non-communicating hydrocephalus +/- a space-occupying lesion, or midline shift.
509
What does the pronator drift test assess?
UMN or pyramidal/corticospinal tract disease.
510
What are signs of pyramidal tract injury?
Pronator drift, focal weakness, spasticity, hyperreflexia, and Babinski sign.
511
What is most likely a/w pts describing a “curtain drawn down” over the eye?
Retinal detachment. | May also be seen in amaurosis fugax/central retinal a. occlusion.
512
Lung cancer screening:
Can be done w/annual low-dose CT for patients 55-80 with >30 pack year smoking history. CXR has not been shown to reduce mortality as a screening method.
513
Murmur heard in HCMP:
Harsh crescendo-decrescendo systolic murmur heard best at the apex and lower left sternal border.
514
Valvular abnormalities a/w bicuspid aortic valve:
In younger patients: Aortic regurg | In older: aortic stenosis
515
How to calculate the corrected Ca2+ level:
Corrected Ca2 = Measured Ca2 + 0.8 (4-Albumin)
516
Tx for Syphillis in a Pen-Allergic patient:
Oral Doxycycline for 14 days | Pen desensitization should be avoided if possible.
517
What abx therapy should be started in prostatitis while awaiting urine cultures?
TMP-SMX or Fluoroquinolone for acute | Fluoroquinolone for chronic.
518
Role of PEEP in respiratory distress:
PEEP prevents alveolar collapse and may also reopen some alveoli that have already collapsed, reducing shunting. High PEEP will improve oxygenation and directly counteract a mechanism by which ARDS causes hypoxemia. High PEEP may improve mortality in pts. w/severe ARDS.
519
When should hypercoagulability testing be done?
In pts <45 with a 1st time unprovoked DVT/PE Pts w/recurrent DVT/PE Pts w/unusual sites of thrombi (cerebral, mesentery, portal vv.)
520
Manifestations of HITT:
Thrombocytopenia – normally with platelets <60K. d/t RES removal of ab-coated platelets. Thrombus – HIT Abs activate platelets and cause aggregation w/ release of procoagulant factors.
521
What is required for dx of malignant HTN?
Severe HTN w/retinal hemorrhages, exudates, or papilledema. | Malignant nephrosclerosis is often seen, but not always present and not required for diagnosis.
522
What differentials present with low DLCO?
Obstructive spirometry – Emphysema Restrictive – ILD, Sarcoidosis, asbestosis, heart failure Normal – Anemia, PE, pHTN
523
What differentials present with Normal DLCO?
Obstructive – Chronic bronchitis, asthma | Restrictive – MSK deformity, Neuromuscular disease.
524
What differentials present w/Increased DLCO?
Obstructive – asthma Restrictive – morbid obesity Normal – pulm hemorrhage, polycythemia
525
What is the management for pts w/Epidural spinal cord compression?
Emergent MRI, IV glucocorticoids (given 1st before confirmation w/MRI), and Neurosurgery consult.
526
Common presentation of pancreatic cancer:
Most occur in the head and compress the pancreatic duct and common bile duct --> painless jaundice. Backup of bile leads to intra- and extrahepatic biliary duct dilation and nontender distended GB. Jaundice can lead to pruritus, pale stools, and dark urine.
527
What is Felty syndrome?
RA – erosive jt disease/deformity, rheumatoid nodules, vasculitis (mononeuritis multiplex, necrotizing skin lesions) Neutropenia Splenomegaly. Often are anti-CCP and RF +, have v. high ESR.
528
What causes the myopathy a/w Cushing syndrome?
Direct catabolic effects of cortisol on sk.mm. which leads to muscle atrophy. NOT d/t an electrolyte imbalance.
529
How to diagnose CO poisoning:
ABG – check carboxyHb levels, EKG and cardiac enzymes is Ischemia or CAD.
530
How to diagnose acromegaly:
First test IGF-1, if elevated confirm w/ glucose suppression test – normal pts. glucose will rapidly suppress GH secretion. In acromegaly it will not decrease and may even have a paradoxical increase.
531
Treatment of Neurosyphillis:
IV penicillin for 10-14d (Not IM PenG like primary)
532
1st line tx for Chemo-Induced N/V:
5HT3R antagonists – odansetron
533
Common precipitating factors for HHS:
Hyperosmolar hyperglycemic state Infection (most common) Meds (Steroids, thiazides, pentamidine, atypical antipsychs.) Injury/Acute Illness Interruption of insulin tx HHS typically develops over days – weeks.
534
What causes the neurologic sxs in HHS?
Confusion to coma can occur and are primarily d/t the high serum osmolality (norm. >320 mOsm) HHS pts typically have pseudohyponatremia and therefore this is not a cause of neuro sxs
535
Nephropathy with dense intramembranous deposits that stain for C3 but not Igs:
``` Membranoproliferative glomerulonephritis type 2 aka Dense deposit disease. IgG Abs (C3 nephritic factor) directed against C3 convertase of the alt. complement pathway lead to persistent complement activation and kidney damage. ```
536
What type of ulcers are typically seen on plantar surface of foot/toes?
Diabetic foot ulcers – tested for w/monofilament test. | In contrast arterial ulcers are often at v tip of toes but not plantar surface.
537
Causes and risk factors of GBS:
Most common cause is C. jejuni. Others – HHVs, Mycoplasma, H. influenzae. Pts. at higher risk: Lymphoma, Sarcoidosis, SLE, recent HIV infection, and recent immunization.
538
Preferred tx for Pen-susceptible IE:
IV aqueous penicillin G or IV ceftriaxone for 4 wks. | PO abx aren’t recommended.
539
Tx of Ethylene glycol poisoning:
Fomepizole (competitive inhibitor of Alcohol DH) or EtOH. These prevent further breakdown into toxic metabs. Bicarb can help alleviate acidosis Hemodialysis may be required.
540
What does methylene blue tx:
Methemoglobinemia
541
Osteitis deformans:
Paget disease
542
Effect of serum albumin on Ca2+:
Decreases in albumin will cause a decrease in total serum Ca2+ bc about half of total blood Ca2+ is bound to it. Ionized Ca2+ is hormonally regulated though and remains stable, so Ca2+ levels must be corrected based on albumin levels.
543
What Meds should always be considered in the differential dx of peripheral edema?
Dihydropyridine CCBs (Amlodipine and Nifedipine)
544
How to differentiate embolic v. thrombotic ischemic strokes:
Thrombotic are a/w AS risk factors, and sxs may alternate w/periods of improvement. Emboli are a/w hx of cardiac disease and the onset is abrupt and normally maximal at the start. Will see multiple infarcts in different vascular territories.
545
pH effects on serum Ca2+:
Increased extracellular pH (alkalosis) causes H+ to dissociate from albumin, freeing up space for more ionized Ca2+ to bind. This leads to a decrease in ionized Ca2+, though total Ca2+ levels remain unchanged. Causes signs/sxs of hypocalcemia – crampy pain, paresthesias, carpopedal spasm etc. Seen in pts w/PE for example who get resp. alkalosis from hyperventilation.
546
What are the potential causes of hypocalcemia w/elevated PTH?
Endo: Vit.D def., CKD Inflammatory: Pancreatitis, Sepsis Oncology: Tumor lysis syndrome
547
Rxs that cause hypocalcemia:
Ca-chelators, Bisphosphonates, phenytoin
548
Features of Pyruvate Kinase deficiency:
Chronic hemolysis, hepatosplenomegaly, skin ulcers and pigmented gallstones. Not triggered by stress/drugs like G6PD. Seen as hemolytic anemia in a newborn.
549
Attributable risk percent calculation:
The risk percentage that can be explained by a particular exposure or risk factor ARP = (Risk in exposed – risk in unexposed)/ Risk in exposed ARP = (RR-1)/RR (If a group has 4x risk w/an exposure the ARP=4-1/4=75%)
550
Tx for Exercise Induced Bronchoconstriction:
SABA 10-20min before exercise | Those who exercise daily can try ICS or antileukotriene agents.
551
What is Polymyalgia Rheumatica?
Seen commonly in pts w/temporal arteritis Presents w/morning stiffness, pain and decreased RoM in the shoulders, neck and hip girdle. Stiffness > Pain Have normal muscle strength Increase in ESR, normal CRP and creatinine kinase. Tx w/glucocorticoids.
552
What are tophi?
Tumors formed in soft tissues by urate crystal deposition. | White in appearance and can ulcerate and drain a chalky material.
553
Mgmt of Diabetic foot infections:
Wound debridement and empiric IV abx (pip-tazo + vancomycin) to cover the polymicrobial nature of these infections.
554
Features of Interstitial cystitis:
Aka Bladder pain syndrome A/w psychiatric and pain disorder (fibromyalgia) Presents as bladder pain w/filling, relief w/voiding, increased freq, urgency and dyspareunia. Pain can be exacerbated by exercise, EtOH and sex Normal UA Tx: not curative, can give Amytiptyline, pentosane polysulfate sodium, and analgesics for acute exacerbations.
555
Tx of Toxoplasmosis:
Sulfadiazine and Pyrimethamine + Leucovorin | PPhx w/TMP-SMX
556
Endocrine causes of recurrent pregnancy loss:
``` Thyroid disease PCOS DM Hyperprolactinemia **Celiac (not an endocrine dx) can also cause it ```
557
CA-MRSA Pneumonia:
A common cause of secondary bacterial pneumonia that complicates the flu. Often seen in young people. Get severe, necrotizing pneumonia that’s rapidly progressive and often fatal. Sxs: high fever, productive cough w/hemoptysis, leukopenia, and multilobar cavitary infiltrates. CXR: multilobar (often midlung) infiltrates b/l and thin-walled cavities.
558
Behcet disease:
Seen in young adults of Turkish, middle east or Asian descent. Get recurrent painful oral aphthous ulcers, genital ulcers, eye lesions (uveitis), skin lesions (erythema nodosum, acneiform lesions) and thrombosis. May also get pathergy – exaggerated skin ulceration w/ minor trauma (needlestick)
559
What Rx-Combo is likely to reduce the risk of CCB-assoc. peripheral edema?
CCB + ACEI
560
Features of PCP:
Elevated LDH! With diffuse reticular infiltrates on imaging. Normally indolent in HIV but can cause acute respiratory failure in IMCP’d Presents w/fever, dry cough and decreased O2 levels.
561
CVS manifestations of Primary HyperPTHism:
HTN, arrhythmias, ventricular hypertrophy and vascular/valvular calcification. Significant HTN a/w HyperPTHism should be worked up for MEN2 and pheochromocytoma.
562
What should victims of smoke inhalation be treated for?
CN toxicity and CO toxicity.
563
What is the likely mechanism of lactic acidosis in smoke inhalation victims?
CN toxicity – it binds Ferric iron in Cytochrome oxidase a3 of electron transport chain which blocks oxidative phosphorylation and promotes anaerobic metab – lactic acidosis.
564
Features of Sideroblastic anemia:
Microcytic anemia w/dimorphic RBC population (both normo- and hypochromic RBCs) Will have normal Fe levels and decreased TIBC to differentiate from Fe-def anemia. Caused by B6/pyridoxine deficiency.
565
Derm associated cx of M. penumoniae infection:
SJS
566
What infection is a/w aged seafood?
Aka cured fish – get foodborne Botulism
567
Tx of Botulism:
Equine serum heptavalent botulinum antitoxin
568
Findings suggestive of severe AS:
Sxs of fatigue, exertional lightheadedness, syncope Diminished/delayed carotid pulse – parvus et tardus Mid to Late-peaking systolic murmur Presence of soft and single S2. Early peaking of the murmur suggests mild-mod AS – these pts are typically asx.
569
Cxs of PBC:
Malabsorption, fat-soluble vitamin deficiencies Severe hyperlipidemia w/xanthelasmas Metabolic bone disease – osteoporosis, osteomalacia (w/normal levels of Ca and Vit. D - bone dx isn't from malabsorption) HCCa.
570
Hyperlipidemia a/w PBC:
HDL elevation out of proportion to LDL. | Does not increase the risk of AS.
571
Where is bile absorbed?
In the ileum. | Pts w/ileal disease (Crohn’s) can get bile salt malabsorption/bile salt diarrhea
572
Effects of HoVolemia on Na+ values:
HoVolemia can cause hyponatremia as well, but many patients have normal serum Na+ levels, and some may even have hypernatremia. However all patients w/V depletion will have decreased urine Na+ d/t RAAS activation and aggressive Na+ reabsorption in the kidney.
573
Most common causes of bloody diarrhea:
E. coli (esp. if fever is absent) Shigella (a/w fever) Campylobacter
574
What types of shock will see an increase in SVR (afterload)?
Hypovolemic and Cardiogenic. Septic shock the SVR decreases Differentiate Cardio v. Hypovolemic based on increase in preload (RA pressure, and PCWP) in cardiogenic and decreased preload in hypovolemic.
575
Mgmt of acetaminophen toxicity:
For pts who present early (<4hrs from ingestion) gastric decontamination (activated charcoal) and measurement of acetaminophen levels should be obtained. Then based on levels and time since ingestion it can be determined if N-acetylcysteine should be admin’d Pts can be asx during first 24hrs post-ingestion.
576
Tx recommendations in pregnant women w/suspected APS:
PPhx w/Aspirin and LMWH to prevent arterial and venous thromboses and pregnancy loss.
577
Tachycardia-mediated cardiomyopathy:
Presents w/progressive dyspnea, decreased exercise tolerance, aFib w/RVR, and LV systolic dysfxn. Dx: EKG, Echo, and exclusion of other causes of LV dysfxn. Tx: Aggressive rate or rhythm control
578
Tx of Latent TB:
9 mo of Isoniazid + Pyridoxine | Latent TB is dx’d w/positive PPD and negative CXR/no sxs.
579
What is Melanosis coli characteristic of?
Laxative abuse – seen on colonoscopy Dark brown discoloration of the colon w/pale patches of lymph follicles “alligator skin” Can disappear if laxatives are stopped. Histo will show pigment in the MPs of the lamina propria
580
Tx for Giardia:
Metronidazole
581
Features of Putaminal (BG) hemorrhage:
Putaminal hemorrhages almost always involve adjacent internal capsule – contralateral hemiparesis and hemianesthesia + conjugate gaze deviation toward side of the lesion (from damage to frontal eye field efferents in ant. limb) Common site of HTN intraparenchymal brain hemorrhage.
582
Pontine hemorrhage features:
Deep coma and total paralysis w/in mins. Pinpoint reactive pupils.
583
Primary Pphx of esophageal variceal hemorrhage:
Nonselective BBs (Propranolol/nadolol), or endoscopal ligation.
584
Best investigation for pleural effusion:
Thoracocentesis, except in pts w/clear evidence of CHF – they undergo trial of diuretic therapy first.
585
Characteristics of Acute Interstitial Nephritis:
Maculopapular rash, fever, new Rx exposure, +/- arthralgias. Mostly caused by Rxs – Pens (Naficilin common), TMP-SMX, cephalosporins, NSAIDs, omeprazole Labs: AKI, pyuria, hematuria, WBC casts, eosinophilia Renal bx: inflammatory infiltrates and edema
586
Infectious causes of Acute Interstitial Nephritis:
Legionella, TB, Streptococcus | These are uncommon causes. Rxs are most common cause of AIN.
587
Cxs of Paget disease:
Giant cell tm and osteosarcoma
588
What can Beta-D-glucan be useful in diagnosing?
Fungal infections – esp. candida and aspergillus
589
Cxs of Giant Cell arteritis:
Permanent vision loss d/t anterior ischemic optic neuropathy from arteritis and aortic aneurysm.
590
How does prevalence affect PPV and NPV?
Increased prevalence increased PPV and decreases NPV | Decreased prevalence increases NPV and decreases PPV
591
What are the contributing factors to orthostatic HoTN in the elderly?
Decreased baroreceptor sensitivity, arterial stiffness, decreased NE content of SNS nerve endings, and reduced sensitivity of the myocardium to SNS stimulation.
592
Characteristics of Myasthenic crisis:
Increased generalized and oropharyngeal weakness, resp insufficiency/dyspnea Risk factors: Infection, surgery, pregnancy/birth, tapering immunosuppressants, Rxs – aminoglycosides, BBs. Tx: Intubation, Plasmapheresis, IVIG and corticosteroids. Daily AchEIs used in MG mgmt. should be held to prevent xs airway secretions and risk of aspiration.
593
What are the features of De Quervain tenosynovitis and who is it commonly seen in?
Inflammation of the abductor pollicis longus and extensor pollicis brevis tendons – tenderness elicited w/direct palpation on the radial side of the wrist at the base of the hand. Finkelstein test may also elicit pain. Classically seen in new mothers who hold the babies w/ the thumb outstretched.
594
Dx of Polymyositis:
Elevated m. enzymes – CK, aldolase, AST Auto-Abs – ANA, anti-Jo-1 Bx – Endomysial infiltrate and patchy necrosis
595
Effects of RAI therapy in Grave’s disease:
Resolution of Hyperthyroidism in 6-18 weeks, but most develop permanent hypothyroidism in mos-yrs following. May also worsen Graves ophthalmopathy d/t increased titers of Thyroid stimulating Auto-Abs.
596
What skin conditions are a/w HIV infection?
Sudden-onset severe psoriasis Recurrent herpes zoster Disseminated molluscum contagiosum Severe seborrheic dermatitis
597
What conditions are a/w severe Seborrheic dermatitis?
HIV and Parkinson
598
What are the indication for parathyroidectomy in PHPT?
Symptomatic hypercalcemia! Age <50 Cxs – osteoporosis, nephrolithiasis/calcinosis, CKD (GFR < 60) Elevated risk of Cxs – Ca2+ >1 mg/dL above norm., urinary Ca2+ excretion >400 mg/day
599
What should be suspected in an elderly pt. w/anemia + thrombocytopenia?
CLL – esp. if lymphadenopathy and hepatosplenomegaly are present. Cxs: recurrent infections common, AIHA, Secondary malignancy (Richter transformation – AML) Dx w/flow cytometry
600
How to differentiate b/w an adrenal and ovarian androgen producing-tm:
Testosterone and DHEAS levels. If only testosterone is elevated – ovaries (most common) If both elevated – Adrenals, DHEAS is only produced in adrenals. Testosterone is produced in both.
601
Diagnosis of Parkinson:
Clinically – need 2/3 cardinal signs: Rest tremor, rigidity, bradykinesia.
602
Mgmt to reduce liver damage in HCV:
Avoid EtOH, HBV/HAV vax.
603
Most common murmur heard at 1st R-ICS and features associated:
Supravalvlar AS – normally d/t congenital LV outflow tract obstruction. Systolic murmur v. similar to normal AS. May present w/unequal carotid pulses, differential BP in upper extremities, and palpable thrill in suprasternal notch.
604
Rxs used in HCV treatment:
Ledipasvir, Sofosbuvir
605
1st line tx of Bullous Pemphigoid:
High-potency topical glucocorticoids – Clobetasol Topical is 1st choice even in extensive disease. Oral systemic steroids are not a/w with better outcomes and should be avoided unless topical is highly unpractical
606
What does randomization of a trial prevent?
Confounding
607
Middle Mediastinal masses:
Bronchogenic cysts, tracheal tms, pericardial cysts, lymphoma, LN enlargement, and aortic aneurysms of the arch. Thymomas are in the anterior mediastinum.
608
Common presentation of HSV keratitis:
Dendritic ulcers are most common, corneal vesicles, pain, photophobia, blurred vision, tearing and redness. Common in pts w/xs sun exposure, outdoor occupations, fever or IMCPd.
609
Features of Anterior Cord Syndrome:
Norm d/t anterior spinal a. trauma. Bilateral hemiparesis – damage to lateral corticospinal tract Diminished b/l pain and T – lateral spinothalamic tract (1-2 levels below injury bc decussation) Intact b/l proprioception, vibration and light touch – dorsal column intact bc supplied by posterior spinal aa.
610
Mgmt of HCMP:
Avoidance of volume depletion, BBs and CCBs (Non-Dihydropyridines ONLY), and surgery for persistent sxs.
611
What should patients with new-onset aFib be screened for?
Occult hyperthyroidism as an underlying cause – get TSH and free T4 levels.
612
Most common cause of death in acute liver failure:
Cerebral edema – coma, brain stem herniation, death.
613
Indications for liver transplant in patients w/ALF:
Grade III or IV hepatic encephalopathy PT > 100 Cr >3.4 mg/dL
614
What type of conjunctivitis will have a reappearing discharge after wiping?
Bacterial | Viral and allergic conjunctivitis will not.
615
Adult Still Disease:
uncommon inflammatory disorder – recurrent high fevers, arthritis/arthralgias, salmon colored macular or maculopapular rash. ESR may be v elevated
616
Empiric abx tx for Bacterial meningitis according to risk group:
Age 2-50: Vanc (S. pneumo) + 3rd gen cephalosporin (N. men) Age >50: Vanc. + ampicillin (listeria coverage) + 3rd-gen cephalosporin IMCPd: Vanc + ampicillin + cefepime (GNR) Neurosurgery/Penetrating trauma: Vanc + Cefepime
617
Malaria pphx:
Mefloquine started >2 weeks prior to travel, throughout and then 4 weeks after returning from an endemic country. Chloroquine-resistant countries: Mefloquine, Doxycycline or Primaquine Chloroquine-Sensitive (Carib/S.Am): Chloroquine
618
Common causes of crystal-induced AKI:
``` Acyclovir Sulfas MTX Ethylene glycol Protease Inhibitors Uric acid – tm lysis syndrome Causes renal tubular obstruction ```
619
Features of Lithium toxicity:
Tremor, hyperreflexia, ataxia, seizures, V/D
620
Features of phenytoin toxicity:
Horizontal nystagmus, cerebellar ataxia, and confusion
621
Senlie purpura:
aka solar or actinic purpura. Non-inflammatory disorder most common in elderly, but can present in younger w/xs sun D/t loss of elastic fibers in perivascular connective tissue. Have residual brownish discoloration from hemosiderin deposition and many ecchymotic areas.
622
What is pseudobulbar palsy?
Regurgitate liquids through the nose – from b/l damage to corticobulbar pathways.
623
Features of Osler-Weber-Rendu Syndrome:
Aka Hereditary hemorrhagic telangiectasia AD disease w/diffuse telangiectasis (ruby-colored papules that blanch w/pressure), recurrent epistaxis, and widespread AVMs.
624
Why might pts w/Osler-Weber-Rendu have increased Hct?
If a pulmonary AVM is present. Will shunt blood from the R – L heart causing chronic hypoxemia, digital clubbing, and reactive polycythemia. Pulmonary AVMs can lead to massive, sometimes fatal hemoptysis.
625
Treatment of Dermatitis herpetiformis:
Dapsone – has anti-inflammatory and immunomodulatory properties. Long-term tx is gluten-free diet.
626
Mgmt of patients with thromboembolic events:
If there is a clear provoking factor or there is a family hx suggesting the source workup should be done for these. If there are no clear provoking factors then patients should undergo age-appropriate ca-screening to check for malignancy as the source of hypercoagulability.
627
Light criteria for transudative pleural effusions:
Protein pleural/serum <0.5 | LDH pleural/serum <0.6; Pleural LDH <2/3 upper limit of normal serum LDH.
628
Causes of transudative pleural effusion:
Hypoalbuminemia – cirrhosis, nephrotic synd. | CHF
629
Causes of exudative pleural effusion:
Infection (parapneumonic, TB, fungal, empyema) Malignancy PE **Infectious or inflammatory causes – cytokine release and increased capillary permeability.
630
Features of TB effusion:
Moderate lymphocytosis V. elevated protein >4g/dL Elevated LDH Tend to occur on the R and have low pleural pH and glucose.
631
Shy-Drager Syndrome:
Aka multiple system atrophy – degenerative disease characterized by: Parkinsonism Autonomic dysfxn – postural HoTN, abnorm sweating, bowel/bladder disturbances, abnorm salivation/lacrimation, impotence, and gastroparesis Widespread neurologic signs – cerebellar, pyramidal or LMN.
632
Diagnostic studies to asses for esophageal perforation:
CT – esophageal wall thickening, mediastinal air fluid level | CXR or CT (late) – wide mediastinum, pneumomediatinum, pneumothorax, air around paraspinal mm., pleural effusion
633
What kind of Rx is Memantine and what is it used for?
A glutamate inhibitor of the NMDA receptor. | Used to tx mod-severe alzheimers
634
What year did blood and organs start being screened for HCV?
1992 – anyone before this needs testing.
635
When are BBs contra’d in the tx of acute MI?
When there is presence of pulmonary edema – acute decompensated HF.
636
What is “ugly duckling sign?”
A lesion that is substantially different from others in a patient who has multiple pigmented lesions. Has ~90% sensitivity for melanoma
637
Tx of Bacillary angiomatosis:
Doxycycline or erythromycin + ART
638
Rxs that cause pill-esophagitis:
Abx – tetracyclines Anti-inflammatory agents – aspirin and many NSAIDs Bisphosphonates – alendronate, risedronate Others – potassium chloride, iron
639
Endoscopic appearance of pill-esophagitis:
Circumferential deep ulceration w/relatively normal surrounding mucosa. Normally in mid-esophagus.
640
Pupillary axn that can worsen glaucoma:
DILATION!!! | Anything that can dilate the pupil – ATROPINE – is contraindicated in glaucoma.
641
Infections that can cause acute pancreatitis:
Legionella Aspergillus CMV Less common viruses: HSV, Mumps, HBV, Coxsackie
642
Initial tx of chronic venous insufficiency:
Leg elevation, exercise, and compression stockings
643
Plasma aldosterone:renin value suggestive of primary hyperaldosteronism:
>20
644
Associated neoplasms of Lynch syndrome:
Colorectal ca., endometrial and ovarian
645
Associated neoplasms of FAP:
Colorectal ca., desmoids & osteomas, brain tms.
646
Associated neoplasms of von Hippel-Lindau:
Hemangioblastomas, RCCa (clear cell), Pheochromocytoma.
647
Pulmonary effects of A1AT deficiency:
Causes panacinar emphysema with the majority of destruction involving the lower lobes. Likely to present w/progressive SoB and cough w/mucoid sputum. Worse w/exertion. CXR: b/l basilar lucency Smokers present in their 30s, nonsmokers in their 40s
648
What is a common precipitant of SIADH?
Any type of pulmonary pathology. HIV pts are especially prone to develop SIADH – may occur after episode of PCP. Suspect in any patient w/hypotonic, hyponatremic, euvolemia. Infusion of NS may worsen hyponatremia in SIADH.
649
What is acrochordon?
Skin tag
650
Explanation for large amounts of blood on UA, but only few (0-1) RBCs on micro:
Myoglobinuria. | UA isn’t able to differentiate from Hb and Mb so use micro to distinguish between hemoglobinuria and myoglobinuria.
651
Tx of cancer-related anorexia/cachexia syndrome:
DoC – Progesterone analogues (Megestrol acetate) 2nd line – corticosteroids Cannabinoids have benefit in HIV cachexia but not cancer related.
652
Features of lateral Medullary syndrome:
aka Wallenberg syndrome – most sxs ipsilateral Vertigo, falling to side of lesion, diplopia, nystagmus, difficult sitting upright, limb ataxia Abnormal facial sensation or pain Dysphagia, aspiration, hoarseness Horner’s syndrome, hiccups, lack of autonomic respiration
653
Earliest renal abnormality present in pts w/DM:
Glomerular hyperfiltration
654
Risk factors for C. diff infection:
Recent abx Hospitalization PPIs – gastric acid suppression
655
What immune complexes are seen in HCV-cryoglobulinemia?
Complexes are formed from: HCV, anti-HCV IgG, IgM anti-IgG Abs (Rheumatoid factor) and complement.
656
What endocrine complication can TB lead to?
Chronic primary adrenal insufficiency
657
Granulomatous diseases that can lead to adrenal insufficiency:
TB, Histoplasmosis, Coccidiomycosis, Cryptococcosis and Sarcoidosis
658
DTR in polymyositis:
NORMAL! Differentiates it between other causes of muscle weakness – Hypothyroidism (delayed), and Lambert Eaton (absent)
659
Features of Trichinellosis:
``` Intestinal stage (w/in 1wk of ingestion) – asx, or AbdP, N/V/D Muscle Stage (up to 4wks after) – myositis, fever, subungual splinter hemorrhages, periorbital edema, eosinophila, elevated CK and leukocytosis. Clinical dx w/characteristic triad of periorbital edema, myositis and eosinophilia ```
660
Typhoid fever presentation:
Progressive 1st week – fever 2nd – abdominal pain and salmon-colored rash 3rd – hepatosplenomegaly and abdominal complication, intestinal bleeding/perforation.
661
Effects on mixed venous O2 saturation in different types of shock:
Both Hypovolemic and Cardiogenic will have decreased MvO2 d/t decreased tissue perfusion. Septic shock will have increased MvO2 d/t hyperdynamic circulation and an inability of the tissues to adequately extract O2.
662
What kind of shock can be seen in mineralocorticoid deficiency?
Distributive shock – norm from primary adrenal insufficiency. Will have HoTN from low aldosterone levels and low SVR a/w hyperkalemia and hyponatremia.
663
Stroke therapy w/in 3-4.5hrs of onset:
IV Alteplase
664
Tx for stroke pts w/out prior antiplatelet tx:
Aspirin
665
Tx for stoke pts on aspirin:
Aspirin + Dipyridamole OR clopidogrel
666
Tx for stroke pts w/aFib:
Long-term ACs – Warfarin, dabigatran, rivaroxaban
667
What antiplatelet agents are effective in reducing the risk of early recurrence of ischemic stroke?
ONLY ASPIRIN | Should be given w/in 24hrs to all pts w/ischemic stroke
668
Complicated v. Uncomplicated Parapneumonic effusions:
Parapneumonic effusion = neutrophil dominate pleural effusion Uncomplicated pleural analysis – pH > 7.2, Glucose > 60, WBC < 50K Complicated – pH <7.2, Glucose <60, WBC > 50K Both will have negative pleural fluid gram stain and culture Tx: abx for both, drainage also for complicated
669
How to differentiate empyema v complicated parapneumonic effusion:
Empyema will have frank pus on paracentesis and gram stains are typically positive for them as well. Both require abx + drainage by chest tube
670
Characteristics of pleural effusion 2/2 PE:
Exudative, and bloody. Typically have normal pH and glucose levels.
671
Lab values a/w Chikungunya:
Lymphopenia, thrombocytopenia, elevated liver enzymes
672
What does a positive hepatojugular reflux signify?
A failing right ventricle – it cant accommodate an increase in VR w/abdominal compression. Most common causes: Constrictive pericarditis, RV infarction, and restrictive cardiomypoathy
673
When should abx be initiated in COPD exacerbations?
If they have 2+ cardinal sxs (increased dyspnea, increased cough, sputum production). Or if mechanical ventilation is required.
674
What abx are used in COPD exacerbation?
Macrolides, respiratory fluoroquinolones (levofloxacin, moxifloxacin) or penicillin/B-lactamase inhibitors (amoxicillin-clavulanate)
675
Dacrocystitis:
Infection of the lacrimal sac. Acute cases characterized by sudden onset pain and redness in the medial canthal region. Often can express purulent discharge from the area. S. aureus and GBS are the main causes.
676
What should be suspected in a patient with a pure motor stroke?
Lacunar infarct – especially if they have HTN. | Lacunar infarcts are from a combo of microatheroma formation and lipohyalinosis.
677
Primary pphx of esophageal varices:
Nonselective BBs. Endoscopic ligation can be done in pts w/contraindications to BBs Endoscopic sclerotherapy is used only for actively bleeding varices, not as pphx
678
What causes an anaphylactic rxn post-transfusion?
Host autoIgG-Abs against IgA. Happens in IgA deficient individuals.
679
Which COPD patients have a lower threshold to start LTOT?
Pts w/Cor Pulmonale, evidence of RHF, or Hct >55%
680
Clinical associations of Minimal change disease:
NSAIDs and lymphoma
681
Most common form of nephrotic syndrome in pts/w Hodgkin lymphoma:
Minimal change
682
Most common form of nephrotic syndrome a/w malignancies:
Membranous glomerulopathy. | Except lymphoma – minimal change disease, and MM – amyloidosis.
683
How to differentiate between primary and secondary adrenal insufficiency:
Primary – d/t AI destruction of adrenal gland will see hyperpigmentation and mineralocorticoid deficiency, HoTN etc. Eosinophilia and hyperplasia of lymphoid tissues (tonsils) are also common findings. Secondary – d/t destruction of the pituitary gland will not have these effects and will only present w/signs of glucocorticoid and androgen deficiency.
684
First test to order in suspected SLE pts?
ANA titers – v. sensitive (95-100%) Should be first no matter what sxs they present with. If positive, then others can be ordered (anti-smith, anti-dsDNA etc)
685
How does lymphoma lead to hypercalcemia?
Increased Vit. D. Will have increased Ca2+ absorption, decreased PTH, and increased PO4
686
Tx of Uncomplicated cystitis:
Nitrofurantoin for 5d – avoid if suspected pyelo TMP-SMX for 3d Fosfomycin single dose If complicated use fluoroquinolones Only do Uculture if pts fail initial therapy
687
Tx of Pyelo:
Outpatient – Fluoroquinolones | Inpatient – IV abx (fluoros, aminoglycosides +/- ampicillin)
688
How to diagnose Patellofemoral syndrome:
Clinical – patellofemoral compression test. | Often see increased pain with squatting, running and using stairs.
689
Tx for restless leg syndrome:
1st line – dopamine agonists (pramipexole) | 2nd – Alpha-2-delta calcium channel ligands (gabapentin enacarbil)
690
Secondary causes of restless leg syndrome:
``` Fe-def anemia Uremia (ESRD, CKD) DM MS, Parkinson Pregnancy Rxs (antidepressants, metoclopramide) ```
691
What Rx-combo should be added to reduce mortality in AfAms w/LVF?
Hydralazine and nitrates
692
What does a hx of recent URI followed by sudden onset cardiac failure suggest?
Dilated cardiomyopathy most likely 2/2 acute viral myocarditis Coxsackie B is most common; Others – parvo, HHV6, adeno, and enteroviruses.
693
What will be seen on echo of DCMP?
Dilated ventricles w/diffuse hypokinesia and a low EF (systolic dysfxn).
694
How to differentiate b/w a stone in the cystic v. common bile duct based on labs:
Both will cause elevations in BR, AST, ALT and possibly amylase, but only common bile duct occlusion would be expected to cause obstructive jaundice w/scleral icterus and v. high AlkPhos levels.
695
VIPoma v. Carcinoid syndrome:
Both cause very similar sxs, but VIPoma will be tm in pancreas, and Carcinoid is typically in the SI. Carcinoid more likely to cause bronchospasm and cardiac cxs.
696
When should tetanus-Ig be given as post-exposure pphx?
Only if the wound is dirty or severe AND the pt is unimmunized, uncertain, or has < 3 tetanus toxoid doses as a child. All other cases only require Td booster
697
Lab findings a/w atheroembolism:
aka cholesterol crystal embolism Elevated serum Cr, eosinophilia (d/t IL-5 activation), hypocomplementemia UA may also show eosinophiluria.
698
Features and tx of TTP:
Decreased ADAMTS13 – uncleaved vWF multimers – platelet trapping and activation. Causes hemolytic anemia w/schistocytes, renal failure, neuro sxs and fever Tx w/plasma exchange, glucocorticoids, and rituximab
699
Definition of Massive PE:
PE complicated by HoTN and/or acute right heart strain. Syncope tends to only occur w/massive PEs, and likely to see JVD and RBBB on EKG. Signs/sxs of cardiogenic shock common.
700
CVS effects of acromegaly:
Cardiomyopathy, HTN – concentric LV hypertrophy, HF, valvular disease (mitral & aortic regurg)
701
Pphx for migraines:
CCBs, propranolol, TCAs | Sumatriptans are used to abort episodes
702
Rare cx in HIT:
Adrenal hemorrhage. Should be suspected in pts w/shock in the setting of a drop in Hb after being diagnosed w/HIT. Pts should undergo CT scanning right away.
703
What differentiates HIT from other hypercoagulable states?
It effects both the arterial and venous systems. Others preferentially affect the venous system. *Anti-phospholipid syndrome also commonly effects both systems
704
How to dx Necrotizing fascititis:
Urgent surgical exploration. Imaging is not adequate enough and shouldn’t delay surgical intervention.
705
Tx of Babesiosis:
Atovaquine + Azithromycin for mild to moderate cases | Clindamycin + Quinine in severe cases
706
Tx of H. pylori:
PPI + Clarithromycin + Amoxicillin | In pen-allergic pts, metronidazole is sub’d for amoxicillin
707
Definitive diagnosis of diverticulitis:
CT w/ oral and IV contrast
708
Nitazoxanide:
An antiparasitic used to tx C. parvum in immunocompetent hosts. Should only be used in HIV pts if they are already initiated on ART and their CD4 counts aren’t increasing and clearing the infection.
709
What Rxs are used in HTN-urgencies to lower BP over hours?
Oral captopril, furosemide, or clonidine. | Nifedipine or IV meds like labetalol should be avoided bc they’ll lower it too quickly.
710
How to calculate corrected Na+ in hyperglycemia:
Corrected Na+ = measured Na + (serum glucose – 100)/100 x 1.6
711
First line tx of Torsades de pointes:
Magnesium sulfate
712
Tx of perianal disease in Crohn’s:
Mild to moderate tx’d w/metronidazole | Mod-severe tx’d w/anti-TNFa Rxs like infliximab or adalimumab
713
Initial test in suspected Paget’s disease:
Xray
714
Tx of Goodpasture’s:
Plasmapharesis, then cyclophosphamide and steroids can be used to keep inflammation suppressed.
715
How to differentiate spinal stenosis from herniated disc:
Radiculopathy is usually unilateral in disc herniation and b/l in stenosis.
716
Most common renal stones in Hyperparathyroidism:
Calcium phosphate
717
What should pts w/HIT be switched to instead of heparin?
Direct thrombin inhibitors like Bivalirudin
718
Tx of DIC:
FFP – need for platelets and low fibrinogen level. | In pts w/normal fibrinogen and low platelets, platelet transfusion is enough.
719
Tx of ITP:
glucocorticoids
720
Tx of TTP:
plasma exchange
721
Manifestations and mgmt. of tumor lysis syndrome:
Mostly in aggressive heme malignancies Severe electrolyte abnormalities – hyperkalemia, hyperphosphatemia, hyperuricemia and HYPOcalcemia AKI d/t uric acid/calcium phosphorus Cardiac arrhythmias Tx – continuous telemetry and aggressive electrolyte monitoring/tx Pphx – IVF, allopurinol or rasburicase
722
MoA and AE of Hydroxychloroquine:
TNF and IL-1 suppressor. | Can cause retinopathy, pts need periodic eye exams while taking this Rx.
723
Risk factors for Ascending v. Descending aortic aneurysms:
Ascending (60%) are d/t cystic medial necrosis (occurs w/aging) or CT disorders (ED and Marfan). Descending (40%) usually d/t atherosclerosis – risk: HTN, hypercholesterolemia & smoking
724
Features and cause of Cauda Equina Syndrome:
Compression of spinal nerve roots, leads to LMN signs. B/l, severe radicular pain w/saddle hypo/anesthesia and hypo/areflexia Get asymmetric motor weakness. Contrast to conus medullaris syndrome w/symmetric motor weakness, hyperreflexia and perianal hypo/anesthesia
725
Tx of CAP and HAP:
CAP – Ceftriaxone and azithromycin | HAP – Vancomycin and Pip-Tazo
726
Manifestations of Chromium deficiency:
Impaired glucose control in Diabetics
727
Manifestations of Cu deficiency:
Brittle hair, Skin depigmentation, Neuro dysfxn (ataxia, periph neuropathy), sideroblastic anemia and osteoporosis
728
Manifestations of Selenium deficiency:
Thyroid dysfxn, Cardiomyopathy, immune dysfxn
729
Manifestations of Zinc deficiency:
Alopecia, pustular skin rash (perioral and extremities), hypogonadism, impaired wound healing, impaired taste, immune dysfxn.
730
Deficiency of what can cause impaired taste?
Zinc
731
How to differentiate b/w Central and Nephrogenic DI:
Central typically don’t have an intact thirst mechanism so have decreased intake and significant hypernatremia >150 Nephrogenic have normal/near normal Na+ and intact thirst mechanism
732
When are target cells seen?
Often in B-thalassemia. | B-thal minor pts are typically asx and require no tx.
733
What is the most likely vessel occluded in a stroke pt w/urinary incontinence?
The anterior cerebral artery.
734
Most common trigger of COPD exacerbation:
URI
735
Pphx of Spontaneous bacterial peritonitis:
Fluroroquinolones | Tx when you already have it: 3rd gen ceph (cefotaxime)
736
Classic EKG findings of PE:
S1Q3T3 Prominent S in lead 1, Q in lead III, and inverted T in lead III. Only occur in a minority of cases though. aFib is commonly a/w PE though
737
Most common ear pathology in AIDS:
serous otitis media d/t auditory tube dysfxn, characterized by presence of middle ear effusion w/out evidence of acute infection. Otoscopy – dull tympanic membrane that is hypomobile Conductive hearing loss most common sx
738
What is Ludwig Angina (causes, sxs, tx):
Rapidly progressive cellulitis of the submandibular space. Mostly d/t dental infections in the molar roots. Typically polymicrobial – need aerobic and anaerobic coverage Sxs: rapidly develop systemic sxs (fever, chills, malaise), and local compressive (mouth pain, drooling, dysphagia, muffled voice, airway compromise) May have crepitus. IV abx – amp-sulbactam, clindamycin and removal of infected tooth
739
PE signs of pulmonary HTN:
L parasternal lift/RV heave Loud P2, right-sided S3 Pansystolic murmur of tricuspid regurgitation JVD, ascites, peripheral edema, hepatomegaly
740
What is LVEDV?
PRELOAD!!! | Mitral regurg increases preload, and so does increased blood volume d/t renal Na+ and H2O retention in heart failure.
741
Murmur heard w/Tricuspid regurgitation:
Holosystolic and increases in intensity w/inspiration.
742
What differentiates R-sided systolic murmurs from all others?
Augmentation of intensity with inspiration. | Only R-sided systolic murmurs will change w/inspiration.
743
What is central cord syndrome?
Often a result of hyperextension injuries in elderly w/pre-existing degenerative spinal changes. Characterized by weakness more pronounced in the upper extremities than lower. May have complete loss of movement and sensation in UEs.
744
What is posterior cord syndrome?
A/w b/l loss of vibratory and proprioceptive sensation. Often w/weakness, paresthesias and urinary incontinence or retention. MS and vascular disruption are most common causes.
745
How does Acetazolamide tx IIH?
It inhibits choroid plexus carbonic anhydrase which decreases CSF production.
746
What studies are considered Observational, Experimental, Review?
Observational: Cohort, Corss-sectional, Case-control, Case-study Experimental: Randomized control, nonrandomized design Review: Meta-analysis
747
What is considered a positive bronchodilator response?
>12% increase in FEV1
748
Difference in immune response to the pneumococcal vaccines:
PPSV23 is a polysaccharide vax. It alone can’t be presented to T-cells so it induces a relatively T-cell-independent B-cell response. PCV13 is a conjugate vax and induces a T-cell-dependent B-cell response. PCV13 produces a more effective response.
749
What is Metolazone?
A thiazide Diuretic
750
What Thyroid tx will worsen ophthalmopathy?
RAI bc increased TRABs are released Pts. w/moderate to severe ophthalmopathy should undergo thyroidectomy instead of RAI. Glucocorticoids can prevent complications in pts w/mild ophtalmopathy
751
Features of malignant biliary obstruction:
Conjugated hyperBRemia, elevated AlkPhos, painless jaundice, and systemic sxs.
752
Organisms that alkalinize the urine:
Proteus and Klebsiella. Often have pH>8 | E. coli will not cause alkaline urine bc it doesn’t produce urease
753
What is the tx for Cervicofacial Actinomyces?
Penicillin for 2-6mos | May need surgery if fistulas form
754
What would increase the risk of HACEK IE?
Periodontal infection, poor dentition, and dental procedures.
755
How to differentiate b/w glomerular and non-glomerular hematuria:
Glomerular will have microscopic > gross hematuria w/Blood and protein + RBC casts and dysmorphic RBCs on UA Non-glomerular has Gross > micro hematuria w/blood, no protein and normal appearing RBCs on UA.
756
Differences in renal cysts:
On CT/MRI simple renal cysts will have absence of contrast enhancement and smooth thin walls. These do not require any tx (esp in asx pts) Malignant renal cysts will have irregular walls, contrast enhancement and need follow-up
757
When are BBs contra’d in MI pts?
If they have bradycardia or cardiogenic shock
758
What is a GI complication of uric acid stones?
Ileus d/t a vagal reaction caused by ureteral colic. Not just uric acid stones. Can be anything causing renal/ureteral colic. Should get CTabdo, US, or IV pyelography to dx underlying stones and tx to resolve ileus.
759
Preventative migraine Rxs:
Topiramate, Divalproex sodium, TCAs, BBs
760
Abortive migraine Rxs:
Triptans, NSAIDs, Acetaminophen, Antiemetics (metoclopramide, prochlorperazine), Ergots
761
In pts w/suspected MG but negative acetylcholine-R Abs, what should be checked?
Muscle-specific TK Abs
762
What type of acid-base disorder is likely seen in shock?
Primary metabolic acidosis d/t lactic acidosis 2/2 hypoperfusion.
763
Nerve injuries a/w humeral fractures:
Spell ARM proximally to distally Axillary – humeral neck Radial – mid shaft or anterolaterally displaced supracondylar Median – anteromedially displaced supracondylar
764
Main cause of traveler’s diarrhea?
ETEC | Presents w/bloating, watery nonbloody stools that are foul smelling
765
Mgmt of esophageal full-thickness tears:
Operative repair.
766
When do you hear S3?
Heard during rapid ventricular filling in diastole. D/t turbulent blood flow to the ventricles d/t increased volume Normal: Children, young adults, pregnancy Abnormal: Age >40, heart failure, RCMP, High-output states
767
When do you hear S4?
Heard immediately after atrial contraction as blood is forced into a stiff ventricle. Normal: healthy older adults Abnormal: younger adults, children, ventricular hypertrophy, ACUTE MI!
768
Mgmt of Hypovolemic hypernatremia:
Symptomatic pts get NS until euvolemic and then switch to 5% dextrose Asx pts get 5% dextrose from beginning If euvolemic they just get free H2O supplementation
769
Most common cause of febrile neutropenia & tx:
GNR – esp Pseudomonas. | Tx w/Pip-Tazo
770
What are the features of Milk-Alkali Syndrome?
Pathophys: xs intake of Ca leads to renal vasoconstriction and decreased GFR w/renal loss of Na+ and H2O and reabs of HCO3-. Sxs: N/V/Constipation, polyuria, polydipsia, neuropsych sxs Labs: Hypercalcemia, metab alkalosis, AKI, suppressed PTH Tx: NS then furosemide
771
Most common electrolyte abnormality in primary adrenal insufficiency:
Hyponatremia - leads to increased renin activity Must be corrected w/a mineralocorticoid like Fludrocortisone
772
Contraindications to the Yellow Fever Vaccine:
Egg allergy AIDS w/CD 4 <200 IMCP’d – especially those a/w thymus disorders or recent stem cell transplant Immunosuppressive therapy – TNF antagonists, high-dose steroids, etc
773
What are PVCs and how are they treated?
Premature ventricular contractions – wide, distorted QRS. | Tx: asx pts do not need therapy. Those w/sxs need escalating doses of BBs or CCBs
774
Features of PVCs (4):
QRS >0.12 seconds Bizarre morphology not resembling any conduction abnormality T wave in opposite direction of QRS axis Compensatory pause
775
What is Calciphylaxis?
Aka calcific uremic arteriolopathy Arteriolar and soft tissue calcification Local tissue ischemia & necrosis NO vasculitis
776
Risk factors of calciphylaxis (5):
``` ESRD Hypercalcemia, hyperphosphatemia Hyperparathyroidism Hypomagnesemia (Mg inhibits extraosseous calcification) Obesity/DM Oral anticoagulants (warfarin) Vitamin K deficiency ```
777
Clinical manifestations of calciphylaxis:
Painful nodules and ulcers Soft tissue calcification on imaging Skin bx: arterial calcification/occlusion, subintimal fibrosis
778
What is the most specific diagnostic test for osteomyelitis?
Bone bx and culture. | Should be done before starting abx
779
What nerve is commonly compressed by the inguinal ligament?
The lateral femoral cutaneous nerve (L2, 3)
780
What should be used to tx UTIs in children?
Typically 3rd gen cephalosporins – cefixime
781
What are the common features/sxs of Sick sinus syndrome?
Bradycardia – fatigue, dyspnea on exertion, lightheadedness, confusion, and syncope/presyncope If atria is affected – aFib/atrial arrhythmias, or bradycardia-tachycardia syndrome.
782
What causes Sick sinus syndrome?
Typically d/t age-related degeneration of the cardiac conduction system w/fibrosis of the SAN. Characterized by inability of the SAN to generate an adequate HR.
783
What are the features of Benzo withdrawal?
Tremulousness, hallucinations, and elevated VS (HTN, tachycardia). Severe cases pts may develop seizures
784
What is gamma gap, and what would a large one suggest?
Gamma gap Is the difference b/w total protein and albumin. | Large gamma gaps can be seen in Waldenstrom macroglobulinemia and Multiple myeloma.
785
Major internal manifestations of Waldenstrom Macroglobulinemia:
Hyperviscosity syndrome Neuropathy Bleeding Hepatosplenomegaly Lymphadenopathy Cryoglobulinemia and renal insufficiency – a nephritic syndrome “sausage-link” (dilated, segmented, tortuous) retinal vv.
786
Lab values a/w Waldenstrom Macroglobulinemia:
Anemia Gamma gap Elevated ESR **If cryoglobulinemia develops, may show hypocomplementemia**
787
Screening test for Waldenstrom macroglobulinemia:
Serum electrophoresis – will show IgM spike. Peripheral smear will show rouleaux (like in MM) And BM bx will show >10% clonal B cells (differentiates from the >10% plasma cells in MM).
788
Sxs experienced in Waldenstrom macroglobulinemia:
``` Vision changes Headaches (bi-temporal common) Vertigo Dizziness Ataxia Rarely stroke or coma may occur ```
789
How is a urethral diverticulum likely to present?
As a tender anterior vaginal wall mass. May lead to dyspareunia or a palpable mass on pelvic exam. If urine and debris collect inside it can lead to a purulent discharge, dysuria, or postvoid dribbling. Diagnosis confirmed w/MRI.
790
What is considered normal labor progression in the active phase of labor?
When the cervix dilates 1+ cm every 2hours.
791
How is chronic bacterial prostatitis likely to present?
``` In young and middle age men Recurrent UTIs (w the same organism) +/- prostatic tenderness and swelling (often absent) Pain with ejaculation Hx of abx tx w/transient improvement ```
792
How is Chronic bacterial prostatitis dx’d and tx’d?
Dx: pyuria & bacteriuria on UA. Bacteria in prostatic fluid. UA before prostatic massage has less bac than after massage Tx: Fluoroquinolones (Cipro) for 6wks
793
What will cause xs collagen deposition in the bone marrow?
Myelofibrosis – deposits xs collagen or reticulin in the BM | Presents w/fatigue, fevers, and HPT-SP-megaly.
794
What effect will Down syndrome have on muscle tone?
Babies are v hypotonic – possibly protruding tongue and floppy body and extremities.
795
What are some common disorders that present with hypotonia in infancy?
``` Down Syndrome Cretinism/Hypothyroid Fragile X Prader-Willi Infantile Botulism ```
796
What are the most common bacteria that cause Epiglottitis?
H. influenzae Strep. spp. (S. pneumo, S. pyogenes) S. aureus
797
What is the tx of epiglottitis?
Broad spectrum abx: Ceftriaxone – targets H. influ and Strep. Spp. Vancomycin – targets S. aureus (including MRSA
798
What is chronic exertional compartment syndrome?
Increased pressure within a muscle group during exercise – often seen in young athletes. Will not have point tenderness or bone tenderness.
799
How will injury to the interosseous ligaments present?
Aka a high ankle sprain – presents w/acute anterolateral ankle pain often following rotational force on a dorsiflexed ankle. Often have associated fibular fracture
800
What is medial tibial stress syndrome?
Shin splints
801
How are anterior shoulder dislocations typically caused?
By a blow to the externally rotated and abducted arm.
802
How do anterior shoulder dislocations often present?
With flattening of the deltoid prominence Protrusion of the acromion Anterior axillary fullness (bc humeral head is now here) Arm abducted and externally rotated
803
What nerve is most commonly injured in shoulder dislocations and what deficits will be seen?
Axillary n. It innervates: Teres minor Deltoid – weakened abduction Sensory innervation of lateral shoulder – numbness
804
What does the radial n. innervate and how is it most commonly injured?
Primary innervation of the wrist and digit extensors. Sensation to posterior arm, forearm and dorsolateral hand. Most commonly injured in mid-humeral fractures and from improperly fitted crutches.
805
What is responsible for the biceps reflex?
Mediated by C5 and C6 spinal nerves, via the musculocutaneous n.
806
Damage to what nerve causes scapular winging?
The long thoracic n. which innervates the serratus anterior.
807
What would indicate neuroimaging in a child w/a HA?
Coordination difficulties Presence of numbness/tingling/focal neurologic signs Hx of HA that awakens from sleep Hx of increasing HA frequency
808
1st line mgmt. of migraines in peds pts:
Acetaminophen or NSAIDs + counsel the fam.
809
What will the crystals look like on UA in cystinuria?
Hexagonal crystals
810
What does the urinary cyanide-nitroprusside test detect?
Elevated levels of cystine
811
When is complete bedrest recommended in pregnancy?
NEVER – has not been proven to be effective and increases risk of thromboembolisms.
812
What is the initial mgmt. of mixed incontinence?
A voiding diary – helps classify the predominant type of incontinence and determine tx.
813
What are some of the features unique to Ehlers-Danlos syndrome?
Skin manifestations – transparent/hyperextensible skin, easy bruising, poor healing, velvety w/atrophy and scarring Abdominal and inguinal hernias Uterine prolapse High arched palate
814
What are some of the features unique to Marfan syndrome?
``` Tall w/long extremities Pectus carinatum Progressive aortic root dilation Lens and retinal detachment Spontaneous pneumothorax ```
815
Genetics a/w Ehlers-Danlos and Marfan syndromes:
Both AD inheritance ED – COL5A1 and COL5A2 mutations Marfan – FBN1 mutation
816
What are the chronic cxs a/w Giardiasis?
Malabsorption – lactose intolerance Profound weight loss Vitamin deficiencies **NOT a/w GBS**
817
How is CMV transmitted?
Through contact w/infected bodily fluids (urine, saliva, breast milk)
818
What are the stimuli for ADH secretion?
``` Osmotic: Serum osmolality >285mOsm Nonosmotic: Nausea Pain Physical/emotional stress HoTN HoVolemia Hypoxia HoGlycemia ```
819
What is Exercise-associated hyponatremia?
Phenomenon in athletes who participate in prolonged exercise – most often caused by ingestion of xs hypotonic fluids which triggers SIADH. Sxs: lethargy, N, seizures, profound confusion
820
What are common associations with erythema multiforme development?
Infections – HSV and Mycoplasma Rxs – sulfonamides Malignancies Collagen vascular disease
821
Rxs that often trigger hemolysis in G6PD deficiency:
``` Dapsone Isobutyl nitrite Nitrofurantoin Primaquine Rasburicase Sulfonamides TMP-SMX ```
822
Presentation of Infantile botulism:
Age <12mos Constipation, poor feeding, hypotonia Oculobulbar palsies (absent gag reflex, ptosis) Symmetric, descending paralysis Autonomic dysfxn (decreased salivation, fluctuating HR/BP)
823
What is herpes zoster oticus?
Aka Ramsay Hunt Syndrome – reactivation of VZV from geniculate ganglion w/spread to CN VIII 2 defining manifestations: erythematous, vesicular rash on the auditory canal or auricle and ipsilateral facial droop/paralysis Other sxs: vertigo, N/V, hearing/taste disturbances
824
How to differentiate central from peripheral vertigo:
Peripheral – horizontal +/- vertical/torsional nystagmus; walking usually preserved, may have hearing loss or tinnitus. Central – purely vertical/torsional nystagmus, severe postural instability, no hearing loss/tinnitus, often has other neuro signs.
825
Causes of central v. peripheral vertigo:
Central – Stroke, MS, migraine, CNS tm, cerebellar infarction Peripheral – BPPV, Meniere's, vestibular neuritis, acoustic neuroma
826
What would gamma-tetramers on Hb-electrophoresis represent?
Alpha-thalassemia/Hb Barts
827
What would lab evaluation in Hb Barts look like?
Low MCV Increased RBCs Target cells on peripheral smear
828
What might prevertebral calcifications on a spinal XR indicate?
AAA – calcifications seen in the aorta.
829
What cardiac cxs are a/w Turner syndrome?
Bicuspid aortic valve, aortic root dilation, aortic coarctation and HTN. Pregnancy increases risk of dissection in Turner pts.
830
What are common sxs of snake bites?
Hemoglobinuria, bleeding, mm. paralysis, severe local pain and swelling, and discoloration w/in hrs of the bite.
831
How to differentiate brown recluse from black widow bites:
Black widow – N/V w/in hrs of the bite, then muscle pain, abdominal rigidity, and muscle cramps. Ulceration uncommon. Brown recluse – deep skin ulcer w/an erythematous halo and necrotic center progressing to an eschar.
832
What should pts with Restless Leg Syndrome be screened for?
Fe-def anemia
833
What is the target BP reduction in HTN-emergencies?
Reduce BP by 20-25% or get DBP less than 100 mmHg within mins or hrs
834
What are recommended agents for lowering BP over hrs in HTN-urgency?
Oral captopril, furosemide, or clonidine
835
How does chlamydial pneumonia often present?
In infants 3-16wks. Often are sick for several weeks and appear nontoxic and afebrile, but are tachypneic w/prominent cough. Over 50% have conjunctivitis as well Often have eosinophilia on CBC
836
What is the criteria for introducing a 5-a-reductase inhibitor to treat BPH?
Evidence of prostatic enlargement or PSA >1.5. | If these criteria aren’t met then use an a-blocker, PDE-5 inhibitor, or antimuscarinic for BPH
837
Recommended tx for a mallet fracture (forced flexion injury of DIP):
Splinting the DIP in extension for about 8weeks.
838
What is active phase protraction and what is the most common cause?
Active phase protraction is when the cervix dilates <1cm every 2 hrs. Commonly caused by cephalopelvic disproportion
839
How do the two different types of Vulvar Lichen Planus present?
``` Erosive variant (most common): Erosive, glazed lesions w/white border, vaginal involvement +/- stenosis, associated oral ulcers Papulosquamous variant: Small pruritic papules w/purple hue Both present in women age 50-60 w/vulvar pain or pruritus, and dyspareunia ```
840
What are some common Lab abnormalities seen in lead poisoning?
``` Anemia Elevated venous lead level Elevated serum zinc protoporhpyrin Hyperuricemia (from impaired purine metab) Elevated Cr (nephrotoxicity) Basophilic stippling on peripheral smear ```
841
What is increased QRS-complex voltage consistent with?
LV hypertrophy
842
What is retinal arteriovenous nicking, and what is it indicative of?
When the retinal venules are narrowed at the intersection points w/arterioles and then bulge on either side. Consistent w/hypertensive retinopathy
843
What is isolated ambulatory HTN?
Aka masked HTN Pts often present w/normal BP readings in the clinical setting but have consistently high BP throughout the day and night. They are often only caught once there is evidence of HTN end-organ damage. Dx w/ambulatory pressure monitoring
844
Who has greatest risk of developing osteosarcoma?
Pts w/mutations in RB1 or TP53 So typically have hx of previous ca. (Retinoblastoma in RB1 and leukemia, breast, brain, or adrenocortical tms in TP53/Li Fraumeni synd.)
845
Tx of Spinal Epidural abscess:
BSA – vanc + ceftriaxone | Aspiration/surgical decompression
846
Classic triad of Spinal Epidural Abscess:
Fever Focal/Severe back pain Neuro sxs – motor/sensory change, bowel/bladder dysfxn, paralysis
847
Rx causes of Osteoporosis (7):
``` Glucocorticoids Heparin Phenytoin Carbamazepine PPIs Aromatase Inhibitors Medroxyprogesterone (depot) ```
848
Endocrine causes of osteoporosis:
Hyperthyroidism (accelerated bone turnover) Hyperparathyroidism (PTH increases bone breakdown) Hypercortisolism (inhibit bone formation) Hypogonadism (decreased estrogen)
849
What type of bone lesions would cause an increase in ALP?
Osteoblastic lesions Osteolytic lesions would not increase ALP and therefore there should not be a rise in disorders that cause pure osteolytic lesions – Multiple myeloma, RCCa
850
Tx of Viral or Idiopathic acute pericarditis:
NSAIDs + Colchicine
851
What virus causes Croup?
Aka Laryngotracheitis – caused by Parainfluenza virus
852
What is mixed connective tissue disease and what are the lab findings?
AI disorder w/variable features of: SLE, Systemic Sclerosis and Polymyositis Lab findings: Anti-U1 ribonucleoprotein, ANA, RF, anti-CCP, elevated CK, anemia/cytpoenias
853
What effect does chronic hyperglycemia have on the renal arterioles?
Causes dilation of the renal afferent arterioles and constriction of the efferent arterioles – glomerular hyperfiltration and Diabetic nephropathy.
854
What could early deceleration in head growth signify?
Rett Syndrome These pts also have breathing abnormalities characterized by alternating episodes of hyperventilation and hypoventilation/apnea, and retropulsion (rocking back and forth).
855
Features of anaphylactic blood transfusion rxn:
HoTN Rapid onset of shock, angioedema/urticaria & resp. distress Happens w/in sec-min of transfusion Caused by recipient anti-IgA Abs (seen in pts w/IgA deficiency) Tx: IM Epi, antihistamines, vasopressors +/- high-dose steroids
856
Features of Transfusion-related acute lung injury:
HoTN, Resp. distress & signs of noncardiogenic pulmonary edema Happens w/in 6hrs of transfusion Caused by donor anti-leukocyte Abs
857
Features of primary HoTN rxn caused by blood transfusion:
Transient HoTN often in pts on ACEIs Happens w/in min of transfusion Caused by bradykinin in blood products
858
Features of transfusion-transmitted bacterial infection (TTBI):
Greatest in pts receiving platelet transfusions (bc platelets are stored at room temp) High fever (>39C), HoTN, rigors, tachycardia (>120bpm), DIC, septic shock Happens w/in approx. 30 min. of completing transfusion Tx: stop transfusion, IVF, blood cultures, and BSAbx
859
How would Candidal otitis externa present and what is used to tx?
With pruritus and white flaky debris in the ear canal. | Tx: Clotrimazole
860
DoC for acute otitis media:
Amoxicillin | If tx failure happens tx w/Amoxicillin-Clavulanate (Augmentin)
861
What are common sxs of HME?
Human monocytic erlichiosis Nonspecific sxs – HA, myalgias, cough, rash Labs – leukopenia, thrombocytopenia, elevated transaminases Seen in S. US, caused by Lone Star tick Tx w/Doxycycline
862
When should pts w/Hb between 8-10 be transfused?
If they meet any of the following criteria: Symptomatic anemia Acute and ongoing blood loss Acute coronary syndrome w/ischemia
863
What would a combo of increased VLDL and TGs indicate?
Type IV familial dyslipidemia Caused by xs hepatic VLDL production. Often leads to acute pancreatitis
864
What could create a false positive for amphetamines?
Atenolol/Propranolol Buproprion Nasal Decongestants
865
What opioids will not show up on urine drug screens?
Semisynthetics – Hydrocodone, hydromorphone, oxycodone Synthetics – Fentanyl, meperidine, methadone, tramadol Only morphine and its metabolites (heroin, codeine) are detected
866
What Rxs may create a false positive for PCP?
``` Dextromethorphan Diphenhydramine Doxylamine Ketamine Tramadol Venlafaxine ```
867
What are common presenting sxs of C. neoformans infection?
Fever, malaise, umbilicated skin lesions (resembles molluscum) Increased ICP w/enlarged ventricles, HA/N/V, abducens n. palsy
868
What is multifocal atrial tachycardia and what are its common causes?
Rapid, irregular pulse w/ 3+ P-wave forms and atrial rate >100/min on EKG Typically asx Common causes: exacerbation of pulmonary disease/COPD, electrolyte disturbance/hypokalemia, catecholamine surge (sepsis) Norm. tx is just to correct underlying issue
869
What are the indications for aortic valve replacement?
Severe AS and 1+ of the following: Onset of sxs (angina, syncope, etc.) - symptomatic pts w/severe AS have a high risk of SCD LVEF <50% (regardless of sxs) Undergoing other cardiac surgery (CABG, etc.) Only pts. who are truly asx and have severe AS w/LVEF >50% can be monitored w/serial echos instead of undergoing valve replacement.
870
Criteria to dx severe aortic stenosis:
Aortic jet velocity >/= 4.0 m/sec OR Mean transvalvular pressure gradient >/= 40mmHg *Valve area is normally <1 cm but this isn’t required to dx*
871
What is the most common cause of vesicovaginal fistula worldwide?
Obstructed labor
872
Features of delirium tremens:
Onset w/in 48-96hrs | Sxs: Confusion, agitation, fever, tachycardia, HTN, diaphoresis, hallucinations
873
Differentiation of pseudoaneurysm from AV fistula:
AV fistula – no palpable mass, but continuous bruit and palpable thrill over the region. May have decreased distal pulses in the region. Pseudoaneurysm – pulsatile mass with an audible systolic (not continuous) bruit.
874
What are the skin conditions often a/w HIV infection?
Sudden-onset severe psoriasis Recurrent herpes zoster Disseminated molluscum contagiosum Severe seborrheic dermatitis (also a/w Parkinson)
875
What are the features of secondary varicocele?
Pathophys: extrinsic compression (renal or retroperitoneal mass) of the IVC; Or venous thrombosis Clinical features: “bag of worms” mass, persists when supine, Prepubertal onset on R (often Wilms), Older onset on L (often RCCa) Mgmt: Abdominal US in children, CT Abd in adults (investigate for cause – Wilms tm, RCCa etc.)
876
Features of urethral stricture:
M>F Often caused by: urethral trauma (catheter), urethritis, or radiotherapy Sxs: weak/spraying stream, incomplete emptying, irritative voiding (dysuria, frequency) Will typically have normal UA and high PVR
877
What are the features and mgmt. of superficial dehiscence?
Separation of the skin and subQ tissue w/intact rectus fascia. Often in overweight/obese pts. Have scant serosanguineous discharge without signs of infection Mgmt: regular dressing changes
878
When should a toddler’s legs be straight?
By 18mos. From 6-18mos: physiologic genu varum 4yrs: physiologic genu valgum 7+yrs: straight legs
879
Characteristics of nasopharyngeal carcinoma:
Endemic to Asia, and linked to EBV reactivation. Risks: diet (salty fish), smoking, genetics May present w/obstruction – congestion, epistaxis, HAs; CN palsies, otitis media; Neck mass – cervical LAD
880
Surgical indications for severe mitral regurgitation:
Surgery if LVEF 30-60% regardless of sxs | Surgery is successful valve repair is highly likely in pts w/sxs & LVEF <30% or asx & LVEF >60%
881
What is referred otalgia and what is it commonly a/w?
Ear pain without an otic origin. Often a/w: dental disease, TMJ disorders, and mucosal head and neck SCCa. Almost never due to a central CNS cause
882
What is the most common cancer of late adolescence (15-19)?
Hodgkin lymphoma
883
Xray findings in Osteoarthritis v RA:
OA – Narrowed joint space and osteophytes | RA – periarticular erosions and soft tissue swelling
884
Ottawa ankle rules (when x-ray of the ANKLE is required):
If pain at the malleolar zone AND Tender at post. margin/tip of medial malleolus; or Tender at post. margin/tip of lateral malleolus; or Unable to bear weight 4 steps (2 on each foot)
885
Ottawa ankle rules (when x-ray of the FOOT is required):
If pain at the midfoot zone AND Tender at the navicular; or Tender at the base of the 5th metatarsal; or Unable to bear weight 4 steps (2 each foot)
886
What allows for severe chronic AR pts to remain asx in the short term?
Eccentric hypertrophy allows for increased LV compliance as well as increased LV contractility to sustain increased SV and maintain CO.
887
What is blepharospasm?
A form of focal dystonia involving recurrent forceful contraction of the eyelid muscles – commonly affected by sensory input/triggered by bright lights. When a/w spasm of the lower face it’s called Meige syndrome
888
What are the HTN guidelines for mgmt.?
Elevated BP (120-129)/<80 – only lifestyle changes Stage I HTN (130-139/80-89) – Lifestyle + 1 anti-HTN Rx Stage II HTN (140+/90+) – Lifestyle + 2 anti-HTNs
889
Clinical features of Asbestosis:
Presentation – prolonged asbestos exposure, sxs developing 20+ yrs after exposure, progressive dyspnea, basilar fine crackles, clubbing. Diagnosis: pleural plaques on chest imaging; imaging, PFTs, and histo consistent w/pulmonary fibrosis
890
What are the systemic manifestations a/w RA (7)?
Pericarditis Scleritis Felty syndrome – RA w/splenomegaly & neutropenia Still’s disease – RA w/fever, rash and splenomegaly Interstitial lung disease Caplan syndrome – RA plus pneumoconiosis Sjogren’s syndrome
891
What is the most common tx of Pediatric UTIs?
3rd-gen Cephalosporin (Cefixime)
892
What are some of the common features to suggest Cervical Myelopathy?
LMN signs at the level of the lesion – weakness and atrophy in the arms UMN signs below the lesion – gait dysfxn, and hyperreflexia in the legs
893
What are common risk factors for PCP pneumonia?
HIV with low CD4 count | Chronic glucocorticoid
894
What is the most common location for Epidural spinal cord compression?
Thoracic #1, then lumbosacral
895
What are the AEs of MTX therapy?
Hepatotoxicity Stomatitis – painful oral ulcers Cytopenias
896
Tx of Paget:
Bisphosphonates
897
What is likely in a patient that can walk on their toes but not heels?
Peripheral n. compression of the common peroneal n. Will have: unilateral foot drop numbness/tingling over dorsum and lateral shin impaired ankle dorsiflexion and great toe extension (can’t walk on heels) preserved plantar flexion (can walk on toes)
898
What are the AEs of the anti-thyroid Rxs?
Thionamides – agranulocytosis MTZ: 1st-trimester teratogen, cholestasis PTU: Hepatic failure, ANCA-associated vasculitis
899
What are the hallmarks of secretory diarrhea?
Larger daily stool volumes (>1 L/day) Diarrhea that occurs even during fasting and sleep Reduced stool osmotic gap
900
What are the common txs of acute migraine episodes?
SubQ tripans (contraindicated in CAD) Antiemetics (D2 antagonists – Prochlorperazine) ** BBs have no role in abortive/acute mgmt. of migraine **
901
Injury to which nerve will cause numbness and burning pain over the lateral aspect of the thigh?
Lateral femoral cutaneous n. Often compressed by the inguinal ligament No motor fibers, so no weakness Risks: obesity, increased lumbar lordosis (pregnancy), DM
902
What is Chromogranin A a marker for, and when will it be elevated?
It is a marker for well-differentiated neuroendocrine tms. | Can be elevated in: carcinoid tms, hyperthyroidism, chronic atrophic gastritis, and chronic PPI tx.
903
What kind of arrhythmia is Carotid massage used for?
Helps to terminate PSVT – a regular, narrow-complex tachycardia. It increases PSNS activity which helps directly slow AVN conductivity Not used in the tx of aFib Contraindications: recent TIA/stroke, carotid bruit
904
What are risk factors for atraumatic splenic rupture?
Heme malignancy – leukemia/lymphoma Infection – CMV, EBV, Malaria Inflammatory diseases – SLE, pancreatitis Splenic congestion – cirrhosis, pregnancy Medications – anticoagulation, G-CSF
905
How is gallstone pancreatitis managed?
ERCP | Elective cholecystectomy should be performed but only after the pancreatitis and cxs are cleared.
906
Findings of anterior cord syndrome:
B/l hemiparesis at level of cord injury and below – damage to lateral corticospinal tracts Loss of b/l pain and temp. – lateral spinothalamic tract injury Intact b/l proprioception, vibration and light touch
907
Difference b/w narrow and wide-complex tachycardia:
Narrow complex = supraventricular tachycardia | Wide complex = ventricular tachycardia
908
EKG features of Narrow-complex tachycardia:
aka SVT | Have narrow QRS complexes w/no discernable P-waves bc they’re buried w/in the QRS complex.
909
How to dx diverticulitis:
CT w/contrast
910
What age should mammogram start being the diagnostic imaging test of choice for breast lesions?
30 and older! | Women under 30 should get US first.
911
What parasite is a/w rectal prolapse?
Trichuriasis or Whipworm When there is a heavy parasite load it can cause rectal prolapse. Heavy loads can also affect a child’s growth and cognition
912
What are some cxs a/w Enterobiasis infection?
In high worm burden can get abdominal pain.fullness or N/V | Rare cxs: UTIs/vulvovaginal pruritus in girls, eosinophilic enterocolitis and appendicitis.
913
What is considered a wide QRS complex?
QRS >.12s or 3 small boxes on EKG strip
914
What is the LDL goal in patient with KNOWN coronary artery disease?
LDL <100mg/dL Known CAD = previous MI, angina, etc. Disease equivalents to known CAD = DM, Cerebrovascular disease, AAA, PAD.
915
Difference in site of pain for testicular torsion and inguinal hernia:
Torsion – Scrotal pain Hernia – Groin pain Both can be from increased abd pressure, exercise, etc. Site is one of main differences
916
What is a cx of testicular torsion and how is it identified?
Testicular necrosis can occur w/ >12hrs torsion/ischemia – can lead to nonviability. Will be seen as heterogenous echotexture on US.
917
Most common cause of community-acquired bacterial meningitis:
S. pneumoniae | Often secondary to dissemination, and may occur w/or w/out pneumococcal pneumonia
918
What are some common sites for SCC of the skin to arise in?
Within chronically wounded, scarred or inflamed skin | Overlying a focus of osteomyelitis, radiotherapy scars, and venous ulcers
919
What kind of infection is ringworm?
It is a Dermatophyte infection – Tinea Corporis Aka this is a fungal, NOT parasitic infection and needs to be tx’d 1st line w/topical anti-fungals (Clotrimazole, terbinafine) Dermatophyte infection involving the scalp (tinea capitis), diffuse or refractory cases are tx'd w/oral anti-fungals (griseofulvin, terbinafine)
920
Tx of Polymyalgia Rheumatica:
Low-dose corticosteroids
921
Indications for gastric bypass:
BMI >40 | BMI >35 + comorbid conditions
922
What is the cause of physiologic hydronephrosis in pregnancy?
High progesterone levels cause ureteral dilation and decreased peristalsis. As the uterus enlarges it also compresses the ureters at the pelvic brim worsening the hydronephrosis.
923
Signs of pHTN:
L parasternal lift, RV heave Loud P2, R-sided S3 Pansystolic murmur of tricuspid regurg, JVD, ascites, peripheral edema, hepatomegaly
924
How to differentiate LVF from RVF based on S3:
RVF S3 is best heard at the L-lower sternal border on end-inspiration LVF S3 is best heard at the apex on end-expiration
925
What are the common manifestations of Tumor Lysis Syndrome?
Severe electrolyte abnormalities – increased PO4, K+, uric acid, and v. high LDH Hypocalcemia (d/t the hyperphosphatemia binding all the Ca2+) AKI – d/t uric acid/calcium phosphorus Cardiac arrhythmias
926
Pphx of Tumor Lysis Syndrome:
IV fluids and Allopurinol or Rasburicase
927
When would you see pencil cells on peripheral smear?
Iron deficiency
928
What are the features and triggers of Microscopic colitis?
MC is a chronic, immune-mediated colitis. Features: watery, non-bloody diarrhea (secretory), fecal urgency & incontinence, nocturnal diarrhea (classic sign) Less common sxs: abdP (50%), fatigue and wt. loss. Triggers: smoking, Rxs – NSAIDs, PPIs, SSRIs, Ranitidine
929
How to dx Microscopic colitis and differentiate the 2 types:
Dx w/colonoscopic bx – lymphocytic infiltration of lamina propria Collagenous type – thickened subepithelial collagen band Lymphocytic type – high levels of intraepithelial lymphocytes (>20 for every 100 epithelial cells)
930
Mgmt of Microscopic colitis:
Remove possible triggers, antidiarrheal Rxs, Budesonide
931
What thyroid cancer arises from the parafollicular cells?
Medullary thyroid carcinoma – overproduces calcitonin Calcitonin levels correlate w/the risk of metastasis and recurrence and should be measured at the time of dx and then serially after tx. CEA also correlates w/disease progression and should be monitored w/calcitonin
932
What should be the first step in evaluation of hypospadias?
Karyotype analysis. It is often indicative of a disorder of sex development (androgen receptor mutation, etc.). May represent virilization of an XX female, or undervirilization of an XY male.
933
What are the common pulmonary features of RA?
Interstitial lung disease w/pulmonary nodules | Exudative pleural effusions – v. low glucose (<50mg/dL), v. high LDH (>700), and low pH resembling bacterial empyema.
934
What are the most common causes of pleural effusions w/very low glucose (<50)?
RA Empyema Malignancy TB
935
Common risk factors of brain abscess:
``` Cyanotic heart disease (ToF) Sinusitis Mastoiditis Otitis media Dental Infection **most commonly caused by S. aureus or S. viridans** ```
936
How to differentiate Viral v. Bacterial acute rhinosinusitis:
Viral – no fever, or early resolution of fever Mild sxs (mild facial pain, etc.) Improvement & resolution by day 5-10 Bacterial – fever 3+ days, OR New/recurrent fever after initial improvement, OR Persistent sxs 10+ days
937
Tx of acute rhinosinusitis:
Intranasal saline, saline irrigation, NSAIDs | Need abx if bacterial
938
Most common causes of a positive hepatojugular reflux:
Constrictive pericarditis RV infarction Restrictive cardiomyopathy
939
What does leukocyte esterase in the urine signify?
Significant pyuria
940
What does nitrite positive urine signify?
Presence of enterobacteriacae (converts urinary nitrates to nitrites)
941
What is the expected dipstick finding in acute pyelonephritis?
Pyuria, significant bacteriuria – positive for nitrites and esterase
942
Tx of Actinomyces:
Penicillin (oral) is DoC; Severe cases may require IV pen or surgery
943
What causes the diarrhea/steatorrhea in Zollinger-Ellison syndrome?
Excess gastric acid in the SI causes diarrhea and then steatorrhea can develop d/t inactivation of pancreatic enzymes and injury to the mucosal brush border.
944
How to calculate and interpret the SAAG:
Serum-to-ascites albumin gradient Calculated by subtracting peritoneal fluid albumin from serum albumin SAAG >/= 1.1: Indicates portal HTN – cardiac ascites, cirrhosis, Budd-Chiari syndrome SAAG < 1.1: absence of portal HTN – TB, peritoneal carcinomatosis, pancreatic ascites, nephrotic syndrome
945
Tx of Bell’s Palsy:
Oral Corticosteroids
946
When should topical/rectal Mesalamine be used in tx of UC?
In patients with mild disease that doesn’t extend beyond the mid-sigmoid colon.
947
What is pathognomonic for Chediak-Higashi syndrome?
Peripheral smear showing giant granules in the neutrophils.
948
Tx of tension HAs:
NSAIDs are 1st line | HAs refractory to NSAIDs, or rebound HAs can be treated with TCAs
949
Mgmt of ASCUS in a patient 21-24:
Immediate HPV testing/reflex HPV testing or repeat pap in 1 year.
950
How long must pts be on PPIs before considered refractory to tx?
12 weeks!
951
Tx of Lyme disease in a child <8yrs:
Amoxicillin or Cefuroxime
952
How long should Fluoxetine be dc’d before initiating another serotonergic med?
5 weeks – has longer t1/2 than the other SSRIs which only need 2 weeks
953
What arteries are commonly affected by FMD?
Preferentially affects the renal and internal carotids Less common the vertebral, iliac, or mesenteric are affected. Leads to arterial stenosis, aneurysm or dissection
954
Most common presenting sx of FMD:
Recurrent HA – d/t carotid a. stenosis or aneurysm
955
What PE maneuvers can assess for appendiceal abscess?
Psoas sign, obturator sign, and rectal tenderness. Obturator and rectal tenderness also test for pelvic appendix Psoas sign also tests for retrocecal appendix. All of these maneuvers assess the deep abdominal spaces
956
Which benzo is most likely to result in seizures following abrupt dc?
Alprazolam – short t1/2
957
Difference b/w diagnostic tests of choice for Diverticulitis v. Diverticulosis:
Diverticulosis – barium enema is test of choice | Diverticulitis – Contrast CT is test of choice (barium enema and colonoscopy are contraindicated until rupture is r/o)
958
Difference in presentation of Proximal v. Mid/Distal SBOs:
Proximal – present w/early vomiting, abd discomfort, and abnorm contrast filling on XR Mid or distal – present as colicky abd pain, delayed vomiting, prominent abd distention, constipation-obstipation, hyperactive BS, and dilated loops of bowel on abd XR
959
What are Ladd’s bands?
Congenital adhesions seen in children
960
What causes the bleeding and possible anemia in Meckel diverticulum?
Ectopic gastric mucosa secretes HCl acid which causes surrounding small-bowel ulceration and subsequent bleeding.
961
What is one way to differentiate Niacin from Riboflavin deficiency?
Both cause dermatitis and glossitis. Only riboflavin will cause normocytic-normochromic anemia Only niacin will cause neuro and GI sxs
962
What is the timeline for fat embolism?
24-72 hrs following the inciting event
963
Risk factors of cerebral palsy:
Prematurity | Low birth weight
964
Why does prematurity increase the risk of Cerebral Palsy?
Premature infants are more likely to have periventricular leukomalacia (white matter necrosis from ischemia/infarction) and intraventricular hemorrhage Both of these are a/w CP
965
Time course of post-MI cxs:
RVF – Acute Papillary muscle rupture – acute, or w/in 3-5 days Interventricular septum rupture – acute or w/in 3-5 days Free wall rupture – w/in 5 days-2 weeks LV aneurysm – up to several mos.
966
What findings on CXR would suggest Bronchiectasis?
Linear atelectasis Dilated and thickened airways Irregular peripheral opacities
967
How is VUR diagnosed?
Voiding cystourethrogram
968
Abx used for GBS+ patients w/penicillin allergy at low-risk for anaphylaxis?
Cefazolin
969
What patients require immediate defibrillation?
Vfib or pulseless ventricular tachycardia | VT w/a pulse needs cardioversion not defibrillation
970
When should atropine be given to pts w/bradycardia?
If persistent bradyarrhythmia + one: HoTN or signs of shock Acute mental status changes Chest discomfort concerning for cardiac ischemia Acute heart failure If no response to atropine: transcutaneous pacing, IV dopamine or IV epinephrine
971
What are the main organisms that cause central line-associated bloodstream infections?
``` #1: Coagulase negative staph. Others: S. aureus, gram negs. (Klebsiella, pseudomonas), and Candida ```
972
How to differentiate Obesity hypoventilation syndrome from ILD:
OHS will have a normal DLCO whereas ILD will have decreased DLCO Only ILD will have cough and bibasilar crackles
973
What are the NOACs?
Non-vitamin K antagonist oral anticoagulants Rivaroxaban Dabigatran Apixaban Edoxaban **Should be given to patients w/aFib and a mod-high risk of thromboembolic events**
974
Tx of Spontaneous bacterial peritonitis:
``` Empiric abx (3rd gen cephalosporins – Cefotaxime) Fluoroquinolones are used for pphx ```
975
Precipitating factors of Hepatic Encephalopathy:
``` Drugs (sedatives, narcotics) Hypovolemia (diarrhea) Electrolyte changes (hypokalemia) Increased Nitrogen load (GI bleed) Infection (pneumonia, UTI, SBP) Portosystemic shunting/TIPS ```
976
What type of shock would be seen in acute Fe poisoning?
All three can occur Hypovolemic shock – from GI losses Distributive shock – vasodilation Cardiogenic shock – direct injury to myocardium
977
Complications of acute Fe poisoning:
Hepatic necrosis Shock GI bleeding – scarring and obstruction
978
What are the most important prognostic factors for astrocytomas?
Patient age Functional status Tumor grade – increased atypia/anaplasia, mitoses, neovascularity and necrosis are all considered worse prognoses
979
What is the worst astrocytoma?
Grade IV – aka Glioblastoma multiforme | It has neovascularity and necrosis w/a high degree of anaplasia and many mitoses
980
Most common brain tm in adults?
Astrocytoma (subcategory of glioma)
981
How to differentiate CML from CLL:
CML has marked leukocytosis of predominately neutrophil origin CLL has marked leukocytosis of predominately lymphocyte origin
982
Where do you see smudge cells?
CLL “crushed little lymphocytes”
983
What preceding infection is likely to cause a brain abscess in the temporal lobe or cerebellum?
Otitis media or mastoiditis
984
What preceding infection is likely to cause a brain abscess in the frontal lobe?
Sinusitis or dental infection
985
What effects will renal tubular necrosis have on volume status?
It can be seen in pts w/severe HoTN and impaired renal perfusion – HYPERvolemic hyponatremia w/urine Na>20
986
How to differentiate between types of Hypovolemic Hyponatremia:
Must have serum Na < 135 and signs/sxs of Hypovolemia 1. Extrarenal losses (D/V, burns, pancreatitis): urine NA <20 2. Renal losses (diuretics, mineralocorticoid deficiency): urine Na >20 3. Decreased effective circulating volume (CHF, cirrhosis)
987
Conditions which require pphx against bacterial endocarditis:
High-risk cardiac conditions: Prosthetic heart valve Previous IE Structural valve abnormality in a transplanted heart Unrepaired cyanotic congenital heart disease Repaired CHD w/residual defect
988
First step in evaluating dizziness:
Classification of sxs into 1/3 categories: Vertigo – sensation of spinning Presyncope – feeling like about to faint Disequilibrium – a sense of imbalance
989
Most common UA findings in pts w/Multiple Myeloma:
UA will often be normal with little/no proteinuria (it detects albumin but not the monocloncal protein)
990
Most common cause of renal insufficiency in pts w/MM:
Myeloma cast nephropathy – the monoclonal light chains clog the renal tubules and cause intratubular cast formation and toxicity.
991
What does the PCWP measure?
It reflects L atrial pressures
992
What would the results of cardiac catheterization in a patient w/a PE show?
``` Cardiac output: decreased RA pressure: increased RV pressure: increased Pulmonary a. pressure: increased PCWP: normal ```
993
Who is likely to get septic arthritis from gram negative bac?
IVDU Severe IMCP Advanced age Sexually active young adults (N. gonorrhea)
994
Most common coagulopathy in malignancy:
DIC | Often in gastric, breast and lung cancer pts.
995
What valvular abnormality is caused by chordae tendonae degeneration?
Mitral regurgitation | NOT aortic regurg.
996
When would hyposegmented neutrophils be seen on PBS?
In Myelodysplastic syndrome | Get granulocytes – hyposegmented/hypogranular NPs and ovalomacrocytosis – dysplastic RBCs
997
What investigation should be done in pts. w/widened mediastinum on CXR post-trauma?
A TEE or Chest CT w/contrast to look for ruptured aorta | A TTE will not adequately visualize the thoracic aorta and should not be performed
998
What is thyroid acropachy?
Nail clubbing in the setting of hyperthyroidism | Uncommon, but specific finding of Graves disease (like ophthalmopathy)
999
How is lid lag described on PE?
Sclera seen above the iris on downward gaze
1000
Respiratory effects of opioid poisoning:
Decreased RR and tidal volume – decreased minute ventilation and CO2 retention – respiratory acidosis
1001
What causes ovarian hyperstimulation syndrome?
Overexpression of VEGF in the ovaries leads to b/l enlarged and cystic ovaries w/increased vascular permeability (increased Doppler flow) which causes 3rd spacing – ascites and pulmonary edema
1002
Conditions associated with Pyoderma gangrenosum:
IBD Inflammatory arthritis/RA Malignancy
1003
Malignancies that may secrete PTHrP and lead to hypercalcemia:
``` Squamous cell of: lung, head and neck Renal cell carcinoma Breast Bladder Ovarian ```
1004
What is drug-induced acne and what are common causes of it?
``` Acute papular inflammatory rash – has monomorphic papules and lacks comedomes. Seen in any age group Rxs: Glucocorticoids/steroids Androgens Immunomodulators (azathioprine, EGFR inhibitors) Anticonvulsants (phenytoin) Antipsychotics Anti-TB Rxs (Isoniazid) ```
1005
Cxs of cardiac myxoma:
Embolization – stroke, acute limb or mesenteric ischemia, etc. Sudden cardiac death d/t impaired CO.
1006
How does b/l choanal atresia present?
Shortly after birth with cyanosis that worsens during feeding and improves when crying. May also have noisy breathing/stertor Unable to pass a catheter from the nares into the oropharynx. Often a/w CHARGE syndrome
1007
How does unilateral choanal atresia present?
As chronic nasal discharge during childhood.
1008
What are the sxs of a Left ventricular aneurysm?
Progressive enlargement of the LV can cause: Heart failure Refractory angina Ventricular arrhythmias Mural thrombus w/systemic arterial embolization Mitral annular dilation w/MR
1009
When is Clopidogrel used?
Clopidogrel and ticlopidine are ADP-R inhibitors – inhibit platelet aggregation. These are only used to tx arterial thromboses – MI and Stroke. They have no use in the tx of venous thrombosis (DVT, PE)
1010
What bug is most commonly a/w pediatric seizures in the setting of acute bacterial gastroenteritis?
Shigella spp. The seizures are typically self-limited with a quick return to baseline (unlike seizures a/w Reye syndrome or hyponatremia) If the seizure occurs a week after the diarrhea has resolved, likely HUS
1011
What are the long term cxs of Mitral Stenosis?
MV narrowing causes LA enlargement which causes increased LAP during ventricular diastole This leads to elevated pulmonary artery pressure and pHTN Ultimately causes RHF
1012
What abnormalities would be seen on PBS in CMV infection?
Atypical lymphocytes - -have granulated LCs
1013
Difference between pitting and non-pitting edema:
Pitting edema is caused by low protein in the ISF – Liver failure (hypoalbuminemia), nephrotic syndrome, and Congenital/Congestive HF Nonpitting edema is d/t high protein in the ISF – lymphatic network dysgenesis/congenital lymphedema
1014
How should minimal bright red blood per rectum be managed?
<40y/o and no red flags – anoscopy 40-49 w/out red flags – sigmoidoscopy or colonoscopy >50 or red flags – colonoscopy
1015
By what age do most SCD patients have functional asplenia?
5 years old
1016
What are helmet cells?
Schistocytes
1017
Recommended tx for splenic abscess:
Splenectomy Abx alone have 50% mortality rate If poor surgical candidate may consider percutaneous drainage instead
1018
Tx of severely enlarged tonsillitis/pharyngitis in Infectious Mononucleosis:
Corticosteroids – decreases the airway edema and risk of acute airway obstruction
1019
What are children who develop premature adrenarche at risk for?
PCOS, type 2 DM, and metabolic syndrome – risk increases in obese children. Obesity is also a risk factor for premature adrenarche – adipose triggers xs insulin production which stimulates adrenals to produce androgens
1020
Tx of gallstone ileus:
Surgical removal of stone and simultaneous or delayed cholecystectomy
1021
How to distinguish b/w gallstone ileus and emphysematous cholecystitis:
Both will have penumobilia Gallstone ileus – colicky, diffuse abdP, bloating, distention, inability to pass flatus or stool, HoTN. These patients will have HYPERactive bowel sounds d/t mechanical obstruction Emphysematous cholecystitis – RUQ pain, fever, septic sxs These patients may have HYPOactive bowel sounds d/t paralytic ileus
1022
What age group is at increased risk for developing Listeria meningitis?
Those >50 years | Must add Ampicillin coverage for anyone >50 (in addition to the normal Vancomycin + 3rd gen-ceph)
1023
What should be added to the tx regimen of Meningitis in addition to empiric abx?
Dexamethasone – helps prevent the neuro cxs (deafness, focal deficits) a/w S. pneumo meningitis in adults and H. influenzae in children If cultures r/o s. pneumo or H.flu as the cause it should be dc’d
1024
When should Cefepime be part of the tx regimen for meningitis?
If the person is IMCP’d or it occurs after neurosurgery/penetrating skull trauma It’s a 4th gen-ceph and covers: S. pneumo, N. meningitidis, GBS, H. influenzae, MSSA and Pseudomonas
1025
What is one of the leading causes of new-onset urinary incontinence in the elderly?
UTIs – may cause concurrent delirium w/o systemic signs/sxs (fever, etc.) Should obtain UA to r/o this before other investigations
1026
B vitamins:
``` B1 – Thiamine B2 – Riboflavin B3 – Niacin B5 – Pantothenic acid B6 – Pyridoxine B7 – Biotin B9 – Folate B12 – Cobalamin ```
1027
What causes the pulmonary edema seen in preeclampsia/HELLP syndrome?
``` Systemic HTN leads to: Increased afterload – increased pulmonary capillary P Decreased renal function Increased vascular permeability Hypoalbuminemia ```
1028
What are the current guidelines recommended for PCI in pts w/acute STEMI?
Reperfuse w/PCI if: W/in 12hrs of symptom onset AND w/in 90min from first medical contact to device time at a PCI capable facility OR w/in 120min from first contact to device time at non-PCI capable facility
1029
What is dead space ventilation?
It is the ventilation of areas of the lung that are not perfused with blood – effected in PE, etc. Pneumonia does not interfere w/pulmonary vasculature and does not cause significant alterations in dead space ventilation.
1030
When is a tube thoracostomy not enough to manage hemothorax?
In patients who have: An initial bloody output >1.5L Persistent hemorrhage – >200mL/hr for >2hrs Continuous need for blood transfusion to maintain hemodynamic stability **Patients with any of these factors need emergent thoracotomy**
1031
What is the current recommendation for Td/Tdap vaccination in adults?
Adults should get Td booster every 10 years, with a one-time dose of Tdap in place of the Td booster. Pregnant women should get Tdap with every pregnancy.
1032
Lab values seen in G6PD deficiency:
Hemolysis – decreased Hb and haptoglobin, increased BR and LDH PBS – bite cells and Heinz bodies Negative Coombs test Decreased G6PD levels, but may be normal during an attack!
1033
What causes the short stature in Turner’s and how is it tx’d?
Short stature is caused by absence of X chromosome | Tx’d w/GH even though GH levels are typically normal
1034
What may be seen on US in a threatened abortion?
Subchorionic hematoma
1035
How should hemodynamically stable v. unstable pts w/evidence of renal trauma be evaluated?
Stable patients: US and contrast-CT of abdomen and pelvis. | Unstable: IV pyelography prior to surgical evaluation
1036
What are the risk factors of chronic venous stasis?
Obesity Advanced age Varicose veins Hx of DVT
1037
What will be seen on imaging in a patient w/Complex regional pain syndrome?
XR: Patchy demineralization/osteopenia | Bone scintigraphy: increased uptake in the affected limb
1038
What is sialadenosis and what patients are at risk for it?
It is a benign, non-tender, non-inflammatory swelling of the salivary glands – a/w abnormal autonomic innervation of the glands w/accumulation of secretory glands in the acinar cells. Patients at risk: Advanced liver disease (alcoholic and non), altered dietary patterns and malnutrition (DM, bulimia) No mgmt. necessary except to tx underlying condition
1039
Tx of Neurocysticercosis:
Antiparasitics – albendazole Corticosteroids Antiepileptics – phenytoin if seizures
1040
When should a CT be ordered in a patient w/vertigo?
Vertigo may indicate an underlying stroke or hemorrhage, so a noncontrast CT is needed if patients have 1+ of the following: Prominent stroke risk factors – hyperlipidemia, HTN, DM New-onset HA Neurologic signs/sxs
1041
Most common congenital heart defect in Down Syndrome:
Complete AV septal defect—failure of endocardial cushions to merge
1042
How should warfarin anticoagulation be reversed prior to urgent surgery?
1 – Immediately dc warfarin 2 – administer Prothrombin complex concentrate (contains vitK-dependent cofactors + normalizes INR <10 min) 3 – Give IV vitamin K **If PCC is unavailable can give FFP (IV colloid) but it is less effective**
1043
What are the sxs of Pelvic congestion syndrome?
A dull, ill-defined pelvic ache that worsens w/intercourse or long periods of standing. Pain is often relieved by menses
1044
What causes Friedrich ataxia?
Trinucleotide expansion (normally GAA) in the frataxin gene
1045
What is acute cerebellar ataxia?
Typically post-infectious – presents w/acute onset of ataxia, nystagmus, and dysarthria 1-3wks post-viral illness. Reflexes, proprioception and vibration NOT affected. Most commonly in children <6 Used to be highly a/w varicella but is decreasing now w/vaccine (can occasionally see it after getting VZV vaccine). Coxsackie and herpes viruses most common Usually resolves w/supportive care in <2 weeks
1046
Tx of Friedrich ataxia:
Supportive – PT and psychosocial support. No Rxs to tx it
1047
Most common organisms to cause brain abscess:
S. aureus S. viridans Less commonly – anaerobes
1048
What causes aFib in patients with Mitral stenosis?
Dilated left atrium and increased pressures within it.
1049
What is the problem in factor V Leiden?
It causes a resistance to activated protein C Most common thrombophilia in white people (2nd most common is mutation in prothrombin)
1050
What is a common imaging finding in pts w/Idiopathic intracranial HTN?
Empty sella
1051
What are some common causes of functional asplenia where you would see Howell-Jolly bodies?
Sickle cell disease Sarcoidosis – and other infiltrative disorders of the spleen Splenic congestion – thrombosis, etc.
1052
Typical presentation of Friedrich ataxia:
Neurologic dysfxn – spastic weakness, loss of vibration and proprioception, ataxia Cardiomyopathy – HCMP Diabetes (frataxin is highly expressed in the pancreas) Skeletal abnormalities – kyphoscoliosis, pes cavus (high arched feet)
1053
Difference in mgmt. of exertional v. non-exertional heat stroke:
Exertional – rapid cooling, ice-water immersion, IVF, etc. | Non-exertional – evaporative cooling: spraying lukewarm water and blowing w/fans etc.
1054
Cxs of Zenker diverticulum:
Tracheal compression Ulceration w/bleeding Regurgitation Pulmonary aspiration
1055
Who is at greatest risk for developing Cholangiocarcinoma and what lab values will be seen?
Risk is greatest in pts w/fibropolycystic liver disease and primary sclerosing cholangitis (90% a/w UC) Labs will show cholestatic liver enzyme pattern: Hyperbilirubinemia, mild increase in ALT/AST, increased ALP & GGT, and often CEA and CA 19-9 are elevated
1056
What will be seen on abdominal imaging in Cholangiocarcinoma?
Intrahepatic or common bile duct dilation. Common bile duct may be normal depending on the level of the lesion. EUS or ERCP are needed for tissue bx after this is seen
1057
Clinical signs of traumatic AV fistula:
Widened pulse pressure Strong peripheral arterial pulsation (brisk carotid upstroke) Systolic flow murmur Tachycardia Flushed extremities/site affected will be erythematous and more flushed LVH w/displaced PMI
1058
Physiologic changes in a patient w/traumatic AVF:
The fistula shunts large amounts of blood and causes: Decreased SVR Increased preload Increased CO This will cause a compensatory increase in HR and SV to meet O2 requirements of peripheral tissues. Ultimately leads to high output heart failure`
1059
What are the common lab values seen in HCC?
Large increases in AFP and ALP (esp. if mets to the bone) | AST/ALT may be normal or mildly elevated.`
1060
What type of bone lesions are a/w HCC?
HCC mets to the bone cause a mixed osteolytic and osteoblastic pattern
1061
Clinical features of Langerhans cell histiocytosis:
Lytic bone lesions (skull, jaw, femur-often diaphysis) Skin lesions (purplish papules, eczematous rash) LAD, hepatosplenomegaly Pulmonary cysts/nodules (present w/cough) Central DI May have recurrent otitis media w/mass involving mastoid bone
1062
What are the common infectious complications seen in atopic dermatitis?
Impetigo Eczema herpeticum Molluscum contagiosum Tinea corporis
1063
What is hepatopulmonary syndrome and what are the likely findings?
Syndrome that results from intrapulmonary vascular dilations in the setting of chronic liver disease. Patients often have platypnea (increased dyspnea when upright) and orthodeoxia (decreased O2 saturation when upright)
1064
What is postoperative endophthalmitis and how will it present?
Most common form of endophthalmitis – bacterial or fungal infection w/in the eye (mostly the vitreous) Occurs w/in 6wks of surgery Presents w/swollen eyelids and conjunctiva, hypopyon, corneal edema, exudates in the anterior chamber and decreased visual acuity.
1065
Risk factors and complications of Hidradenitis suppurativa:
Risks – Obesity, tobacco use and Fhx | Cxs – Contractures, lymphatic obstruction, fistula
1066
How to differentiate b/w rotator cuff tear and impingement/tendinopathy:
Impingement or tendinopathy will have pain w/abduction and external rotation, subacromial tenderness and normal ROM w/positive impingement tests Tear will present similar but may have less pain and more weakness – weakness w/abduction and external rotation and positive drop arm test
1067
What are the common cxs of PPROM?
Preterm labor Intraamniotic infection Placental abruption Umbilical cord prolapse
1068
When would you not use B-agonists to tx hyperkalemia?
If the patient has active coronary artery disease (angina etc.) – they can cause tachycardia and precipitate angina.
1069
Cxs of cholesteatomas:
Hearing loss Cranial n. palsies Vertigo Infections – brain abscess, meningitis
1070
Common causes of cylothorax:
Tramua – cardiothoracic surgery Congenital malformations Syndromes – Down syndrome, Noonan syndrome Malignancy
1071
Major AEs of Metoprolol:
``` Bradyarrhythmias Acute worsening of HF Bronchoconstriction Fatigue Depression Weight gain Sexual dysfxn ```
1072
What enzyme is deficient in hereditary fructosemia and how will it present?
Aldolase B deficiency Presents in infancy after the introduction of fruits and vegetables leads to accumulation of fructose-1-phosphate Sxs: V, poor feeding and lethargy. May lead to seizures or encephalopathy if fructose isn’t removed from the diet
1073
Enzyme deficient in Galactosemia and presentation:
Galactase-1-phosphate uridyl transferase in RBCs Presents in first few days of life w/jaundice, hepatomegaly and failure to thrive after consumption of breast milk or formula
1074
What are the current screening guidelines for DM in asx pts?
Screen in pts w/sustained BP >135/80 (whether tx’d or untx’d) Screen in all pts 45+ and those at any age w/addn’l risk factors (BMI >25, hx of gDM, Fhx, etc)
1075
What is responsible for the development of male external genitalia and prostate?
DHT which is converted from testosterone via 5-a-reductase 5-aR deficiency will therefore lead to normal internal male genitalia (testes) and external female (blind-ending vagina) which become virilized during puberty (clitoromegaly)
1076
Why don’t patients w/5 a-R deficiency have breast development?
Because they still have responsive androgen receptors (unlike AIS) so the increased levels of testosterone bind and inhibit estrogen from binding and stimulating breast proliferation.
1077
What are the sxs of hypokalemia?
Sxs depend on the severity but may include: Weakness, fatigue, and mm. cramps Flaccid paralysis, hyporeflexia, tetany Arrhythmias (K <2.5 norm) – aFib, TdP, Vfib can all occur
1078
How do the nasal polyps a/w CF appear on PE?
Translucent shiny, grey or yellow masses that obscure the nasal turbinates. Present bilaterally
1079
What GI complications can occur in CF?
Blockage of pancreatic ducts – pancreatic insufficiency and CF-related diabetes Blockage of the biliary tree – biliary cirrhosis from increased pressure and subsequent fibrosis
1080
What does peak airway pressure in a ventilated patient measure?
Total airway resistance + plateau pressure | plateau pressure inversely measures lung compliance and = elastic pressure + PEEP
1081
What would cause an increase in peak pressure without a change in plateau pressure in a ventilated patient?
``` Increased peak and normal plateau means total resistance has increased Causes: Bronchospasm Mucus plug Biting endotracheal tube ```
1082
What would cause an increase in both peak and plateau pressure in a ventilated patient?
``` Increase in plateau signifies decreased lung compliance or increased elasticity Causes: Pneumothorax Pulmonary edema Pneumonia Atelectasis R mainstem intubation ```
1083
How are plateau pressure and PEEP measured?
Plateau is calculated by performing the end-inspiratory hold maneuver PEEP is calculated by performing the end-expiratory hold maneuver
1084
What are the cofactors for PTH secretion?
Magnesium and Vitamin A | In alcoholism there is hypomagnesemia which leads to decreased PTH and therefore hypocalcemia
1085
What causes Hypocalcemia in alcoholism?
Alcoholics have decreased magnesium which leads to decreased PTH secretion and ultimately hypocalcemia
1086
What causes Myasthenia Gravis?
Abs against the acetylcholine Rs on the motor endplate – plenty of Ach gets released, but it cannot bind to the Rs bc they’re blocked. *Lambert eaton blocks release of Achth*
1087
How to diagnose HTN in pediatric population:
Measure BP on 3 separate occasions at least 1 week apart.
1088
Defect in which cells will leave a child at greatest risk for TB?
T cells, specifically Th1 cells. | Often seen in IL-12 receptor deficiency – unable to produce/activate Th1 cells
1089
What causes acne?
``` Pilosebaceous follicles (holocrine glands) on the face have increased sebum, keratin and bacteria that lead to: Obstruction – causing comedomes Inflammation – causing papules/pustules, nodules and cysts ```
1090
What are apocrine glands and where are they found?
They are sweat glands found in the axilla, groin and areola | They are scent glands – why we smell when we sweat
1091
What is the most common cause of acquired ataxia and how will it present?
Alcoholic cerebellar degeneration It effects LE > UE and leads to gait resembling EtOH intoxication “reeling from one side to the other” MRI will show atrophy of cerebellar vermis
1092
Most frequent pathogens to cause infection in Multiple Myeloma:
S. pneumoniae | Gram negatives
1093
What will be seen on fundoscopy in optic neuritis?
Pallor of the optic disc or hyperemia and swelling | Depends on time of exam
1094
When should cervical conization be done?
When CIN grade 2 or 3 is found on colposcopy | In young women observation is preferred for CIN-2
1095
What is anemia of prematurity and how will it present?
Seen in preterm infants d/t impaired EPO production, short RBC lifespan and iatrogenic blood sampling Normally asx, but may have tachycardia, apnea, and poor weight gain
1096
Lab findings in anemia of prematurity:
Low Hb and Hct Low reticulocytes (bc decreased EPO) Normocytic, normochromic RBCs Tx: minimize blood draws, Fe supplements, transfusions
1097
What pediatric patients are at risk for Wilm’s tm. and hepatoblastoma?
Patients with Beckwith-Wiedemann syndrome, as well as those with isolated Hemi-hyperplasia (WAGR complex and Denys-Drash are also at risk for Wilm’s tm.) Both need to undergo frequent screening w/US and AFP measurements
1098
What are the features of Denys-Drash syndrome?
Early-onset nephrotic syndrome (diffuse glomerulosclerosis) leading to kidney failure in childhood Male pseudohermaphroditism or ambiguous genitalia w/undescended testes in 46XY pts - Females typically have normal genitalia Wilms tumor (develops in 90% of cases)
1099
What malignancy is commonly a/w Sjogren syndrome?
Non-hodgkin lymphoma
1100
What signs should raise suspicion of HIT?
Heparin exposure >5d and any of the following: Platelet count reduction >50% from baseline Arterial or venous thrombosis Necrotic skin lesions at heparin injection sites Acute systemic (anaphylactoid) reactions after Heparin *sxs may manifest sooner in pts previously exposed to Heparin*
1101
Causes of Hyperthyroidism w/decreased RAI uptake:
Painless/silent Thyroiditis (nontender goiter) Subacute/granulomatous thyroiditis aka De Quervain (tender goiter) Iodide exposure Exogenous thyroid hormone
1102
What is the MoA of hyperthyroidism with decreased RAIU?
It is d/t release of preformed thyroid hormone, so the thyroid gland is underworking in these states and not being stimulated.
1103
What is the most common congenital cyanotic heart disease in the neonatal period?
Transposition of the great vessels
1104
What is the only cyanotic congenital heart disease that might present w/o a murmur?
Transposition of the great vessels It requires a VSD, PDA or PFO to survive in the neonatal period, and a VSD and PDA will both present with murmur but if the patient has a PFO then there will be no murmur
1105
What conditions are a/w Erythema Nodosum?
``` Strep Infection Sarcoidosis TB Endemic fungal diseases – Histoplasmosis IBD Behcet disease ```
1106
Mgmt of Toxic megacolon (d/t C. diff):
Bowel rest, NGT Aggressive abx tx: Oral vancomycin and IV metronidazole d/c anything that contributes to decreased GI motility (opiates) Lack of response/deterioration often need surgery – subtotal cholectomy
1107
What is iliotibial band syndrome and how will it present?
It is an overuse injury and will cause lateral pain w/tenderness at the lateral femoral condyle
1108
What are the effects of Na+ on Ca2+ absorption?
Increased Na+ intake enhances Ca2+ excretion in the urine – hypercalciuria and increases the risk of developing calcium stones. Low Na+ intake promotes Na+ and Ca2+ reabsorption. Therefore pts w/renal calculi should be advised to follow a low-Na diet w/normal dietary Ca2+ intake
1109
What would promote hyperoxaluria and Ca-Oxalate stone formation?
``` Decreased Ca2+ intake – leads to free Oxalate absorption in the gut and hyperoxaluria Increased Vitamin C intake Malabsorption syndromes (Crohn, CF) that have increased intestinal FAs that form salts w/Ca2+ and lead to increased Oxaluria reabsorption ```
1110
When is amnioinfusion contraindicated?
In a patient w/prior uterine surgery
1111
How to differentiate Histoplasma from Coccidioiomycosis based on CXR:
Histoplasma is typically bilateral, focal, reticulonodular or miliary infiltrates and b/l hilar or mediastinal LAD Coccidiodes is typically a unilateral infiltrate w/ipsilateral hilar LAD
1112
When do hemothoraces require emergent surgical thoracotomy?
If chest tubes (tube toracostomy) put out immediate bloody drainage >1.5L
1113
Preferred imaging modality to assess for an empyema:
Chest US – can assess volume and location of fluid + presence or absence of loculated fluid.
1114
Most common cause of acute v. subacute unilateral LAD in children:
Acute – S. aureus and S. pyogenes (tender LN) Subacute – MAC and other non-TB mycobacteria (non tender LN) *acute in poor dentition is most commonly caused by anaerobes (prevotella)*
1115
Most common cause of acute v. subacute bilateral LAD in children:
Acute – Adenovirus and other URIs | Subacute – CMV and EBV
1116
What is the difference b/w PMR and Polymyositis?
PMR has pain and stiffness in muscles, but NO weakness. Have increased ECR and CRP, but CK, aldolase, etc are all normal Polymyositis has severe weakness, but pain is mild/absent and no stiffness. Will have increased CK, aldolase, AST and ANA/Anti-Jo-1 Abs. Need muscle bx to dx this but not PMR
1117
Tx of Peri-infarction pericarditis:
Aka early post-MI pericarditis (not Dressler) Tx is supportive – should avoid anti-inflammatory meds (NSAIDs, steroids) bc they’ll disrupt healing and increase risk of other cxs (free wall rupture, etc)
1118
What kind of malabsorption is Lactose intolerance?
Carbohydrate malabsorption | No problems w/fat absorption in these pts so have negative acid steatocrit tests
1119
What is the most common cause of hearing impairment in children?
Conductive loss d/t repeated ear infections
1120
What effect does hyperthyroidism have on Ca2+?
Increased Thyroid hormone increases osteoclast activity and bone resorption – hypercalcemia and decreased PTH. Ultimately leads to hypercalciuria as well and increases risk of Ca-stones.
1121
DoC for tocolysis <32 weeks gestation:
Indomethacin | Contraindicated >32 weeks d/t risk of closing the PDA
1122
What causes febrile non-hemolytic transfusion rxn and how does it present?
Small amounts of leukocytes remain in red cell concentrate after being separated from whole blood and plasma, and when stored the leukocytes release cytokines that cause sxs when transfused. Sxs: transient fevers, chills, and malaise w/o hemolysis Will have negative Coombs/direct antiglobulin test and negative free Hb
1123
What is the timeline for acute hemolytic transfusion rxns and how will they present?
Presents w/in 1 hour of transfusion w/fever, chills, flank pain, and hemoglobinuria which can progress to renal failure and DIC. Will have a positive direct coombs/antiglobulin test and plasma free Hb >25
1124
Using whole blood increases the risk of what kind of rxn?
Whole blood contains lots of leukocytes and increases the risk of febrile non-hemolytic rxn It is rarely used bc of this, and normally only for cases of acute massive hemorrhage (trauma)
1125
What do plasma mixing studies tell you about increased PT or aPTT?
In patients w/prolonged pt or aptt plasma mixing studies differentiate b/w coagulation factor deficiencies or coagulation inhibitors: Coagulation corrects w/mixing study – there is a deficient coagulation factor Coagulation does not correct w/mixing – there is an inhibitor present
1126
What is one of the most common coagulation inhibitors in females?
Lupus anticoagulant – a type of antiphospholipid Ab. | It prolongs the aPTT and will not correct w/plasma mixing studies, but will correct w/the addition of phospholipids
1127
What coagulation study would be prolonged in pts taking Xa inhibitors?
Thrombin time (PT and aPTT should be normal)
1128
How should patients with long QT syndrome (Jervell-Lange-Nielsen, etc.) be treated?
BBs + Pacemaker – if hx of syncope or sxs (lightheadedness, palpitations, etc.)
1129
How will pts w/Galactokinase deficiency present?
With cataracts – otherwise asx
1130
When is diagnostic peritoneal lavage used?
Typically only in unstable pts w/equivocal FAST results, or if CT/US are unavailable
1131
What is the significance of endometrial cells being found on Pap test?
Endometrial cells on pap test mean that the endometrial lining is shedding. In women <45yrs this is not reported on results bc it’s a normal finding esp if in the 1st 10 days of the menstrual cycle Women >45 yrs this is concerning for an abnormality and might signify endometrial hyperplasia/ca and these women need an endometrial bx to investigate
1132
Tx of Invasive Aspergillosis:
1-2wks of IV Voriconazole + an Echinocandin (Capsofungin) | Then can be transitioned to prolonged oral tx of Voriconazole alone
1133
Predominant MoA for ventricular arrhythmias in the immediate post-MI period:
Reentry – most commonly leads to Vfib and sudden cardiac arrest These are called phase 1a ventricular arrhythmias and occur w/in 10min of coronary occlusion
1134
What are the immunologic responses seen in IE?
Positive Rheumatoid factor (possibly d/t Ab production) Immune complex-mediated glomerulonephritis (get hematuria and RBC casts) Cutaneous lesions – osler nodes (painful fingertip nodules) Roth spots – edematous/hemorrhagic lesions of the retina
1135
What needs to occur in pregnant women w/a non-reactive NST?
Must be followed up w/a BPP or CST – they are equivalent to each other, but CST is contraindicated in any woman where labor is contraindicated (placenta previa, prior myomectomy, etc.)
1136
What are the cxs of Biliary cysts?
Cysts may transform into cholangiocarcinoma and require surgical resection. Older children may present w/the normal sxs (jaundice, acholic stools, dark urine, abd pain, etc.) with pancreatitis superimposed on top of it.
1137
What effects will maternal Listeria infection have on a baby?
If infection during 1st trimester – often causes fetal death, may lead to premature birth Perinatal – can cause newborn infections that are typically severe w/fever, Granulomatosis infantiseptica: disseminated abscesses in multiple organs (liver, spleen, lungs, kidneys, brain) and skin lesions.
1138
When would you see a pendular knee reflex?
In cerebellar degeneration – commonly seen in EtOH-induced cerebellar degeneration
1139
What kind of lesion would the presence of clonus suggest?
Lesion in the pyramidal tracts – UMN lesion
1140
When should a baby be able to sit unsupported?
By 7mos | At 6mos they should be able to sit propped on their hands and unsupported for a few moments
1141
What features of ureterolithiasis would warrant a Urologic consult?
``` Signs of urosepsis – fever, chills, tachycardia, etc. Anuria Acute kidney injury Pain refractory to analgesics Large stones (10+ mm) Stones that do not pass w/in 4-5 weeks ```
1142
What are the 3 main categories of Diabetic Retinopathy?
1. Background/Simple retinopathy: consists of microaneurysms, hemorrhages (dot & blot), exudates (hard) and retinal/macular edema (what causes visual impairment) 2. Pre-proloferative: w/cotton wool spots 3. Proliferative/malignant: consists of newly formed vessels
1143
What is erythromycin use in neonates a/w?
Pyloric stenosis | Should avoid use in all children <1mo.
1144
What are the risk factors for ovarian cancer?
Endometriosis and Fhx | delayed menarche and early menopause are protective
1145
What causes unilateral pain in the middle of the menstrual cycle?
Mittelschmerz – rupture of the ovarian follicle releases the egg and the small amount of blood released at this time can irritate the peritoneum. Typically occurs on days 10-14 of the menstrual cycle (this starts counting from the 1st day of the previous menses)
1146
What are the common adult causes of osteomalacia?
``` Malabsorption (IBD, CF, etc.) Bypass surgery Celiac sprue Chronic liver disease Chronic kidney disease (RTA type 2) ```
1147
Most common skin malignancy in pts on chronic immunosuppressive tx:
SCC – esp. if they’re on immunosuppressants for organ transplant Often aggressive w/local recurrence, regional mets, and perineural invasion
1148
What are broad casts and when would they be seen?
Seen in chronic renal failure Arise in the dilated tubules of enlarged nephrons that have undergone compensatory hypertrophy in response to reduced renal mass. Waxy casts (shiny, and translucent) are also seen in chronic renal disease
1149
When are RBC casts found in the urine?
In glomerulonephritis or vasculitis (malignant HTN, etc.)
1150
What does the progesterone withdrawal test evaluate for?
Secondary amenorrhea – will determine if amenorrhea is from low estrogen (no withdrawal bleed).
1151
Characteristics of the tremor a/w Parkinson’s:
Resting tremor that decreases w/voluntary movement. | Also have pill-rolling tremor
1152
What type of tremors will be worse w/goal-directed movement?
Essential tremors | Intention tremors d/t cerebellar dysfxn.
1153
What causes the bounding peripheral pulses in septic shock?
The Cardiac Index and SV both increase to compensate for the intravascular hypovolemia and this creates an increased pulse pressure which manifests as bounding peripheral pulses (like in AR) This happens in the early phase of sepsis/the hyperdynamic phase
1154
What Rxs should be used to treat patients w/accessory pathways (WPW)?
``` Class IA – Procainamide, Quinidine, Disopyramide Class III (K+ channel blockers) – Amiodarone, Sotalol, Dofetilide, Ibutilide ```
1155
What is likely the cause of a painless corneal abrasion?
Abrasion in a patient who has damage to the V1 (ophthalmic) branch of the trigeminal n. Common causes of trigeminal dysfxn: tumor, trauma, prior zoster infection.
1156
How would a corneal abrasion be expected to present?
Severe eye pain (from V1 sensory innervation), photophobia w/reluctance to open the eye, and possible sensation of foreign body in the eye. May have decreased visual acuity and pupillary dysfxn. Will see corneal staining defect on fluorescein exam
1157
How should patients w/neurogenic bladder be managed to avoid catheter-assoc. UTIs?
Clean intermittent catheterization – decreases risk of infection, performed every 4-6 hours Another option is subrapubic catheterization
1158
What medications can be used to tx Kleptomania?
SSRIs, opioid antagonists, lithium and anticonvulsants. | Should also use CBT
1159
How would cholecystitis and cholangitis be differentiated on US?
Cholecystitis will show gallbladder wall thickening and edema/pericholecystic fluid (no obstruction, just inflammation) Cholangitis will show dilation of the intrahepatic ducts and common bile duct (obstruction leading to infection)
1160
What is a common complication of gallstone pancreatitis?
Acute cholangitis – should be suspected in anyone w/gallstone pancreatitis who has fevers, RUQ pain, jaundice, AMS, and HoTN. Must do ERCP stat to relieve obstruction to prevent development of sepsis and death
1161
Who is at highest risk of developing severe infections with Vibrio vulnificus?
Patients with liver diseases (cirrhosis, hepatitis) as well as DM. Hemochromatosis is especially a risk bc the free iron is a growth catalyst for the bacteria
1162
How will infection w/V. vulnificus present and how is it tx’d?
It is rapidly progressive and presents in <12hrs most of the time with: Septicemia – septic shock and bullous lesions Cellulitis – hemorrhagic bullae and necrotizing fasciitis (much quicker presentation than most causes of nec.fasc. – s.aureus/s.pyogenes) Tx: IV ceftriaxone + doxycycline in anyone w/even suspected illness bc highly fatal
1163
What are the major and minor criteria for Acute rheumatic fever?
Major: (JONES) Joints- migratory arthritis (esp. in the wrists, ankles and knees) <3 – Carditis (friction rub, long PR, diffuse ST elevation) Nodules – subcutaneous/erythema nodosum Erythema marginatum Sydenham chorea Minor: Fever, arthralgias, elevated ESR/CRP, prolonged PR interval
1164
Why do OCPs cause HTN?
Estrogen causes increased angiotensinogen synthesis during hepatic 1st-pass metabolism
1165
Why does a-Thalassemia major cause Hydrops fetalis?
These fetuses have no a-chains for Hb and instead form gamma tetramers (HB Barts) y-tetramers have >10x more affinity for O2 than normal HbA and bind all the O2 and don’t release it to the tissues This causes severe hypoxemia leading to high-output HF and subsequent hydrops fetalis
1166
What conditions are a/w Hydrops fetalis?
``` Achondroplasia Turner syndrome Parvo B19 infection a-Thalassemia major/Hb Barts Rh alloimmunization ```
1167
Diseases a/w the different gene losses in a-Thalassemia:
1 gene loss (aa/a-): a-Thalassemia minima – asx, silent carrier 2 losses (aa/--) or (a-/a-): a-Thal minor – mild microcytic anemia 3 losses (a-/--): Hb H disease – chronic hemolytic anemia 4 losses (--/--): Hb Barts/Hydrops fetalis – High-output HF, anasarca, death in utero can only get babies like this from 2 parents w/cis losses (aa/-- or a-/--)
1168
How does secondary syphilis often present?
Weeks to months after initial exposure: Systemic sxs – fever, malaise, sore throat, HAs Widespread LAD – cervical, axillary, inguinal, epitrochlear Oral lesions – often seen as grey mucous patches Condylomata lata – raised grey genital papules Diffuse maculopapular rash – begins on trunk and spreads to extrems. and involves palms and soles
1169
How to differentiate Syphilis from RMSF based on the rash:
Secondary syphilis – will have a centrifugal rash that starts on the trunk and spreads out to involve palms and soles RMSF – will have centripetal rash that starts on extremities and palms/soles and then moves in to involve the trunk
1170
What is chronic hyperthyroid myopathy?
Myopathy that manifests as proximal muscle weakness weeks to months after the onset of hyperthyroidism May have muscle atrophy early on, but usually there is no muscle tenderness Tx of the hyperthyroidism often improves the myopathy **May also see myopathy in Hypothyroidism**
1171
What stage of labor can neuraxial anesthesia have an effect on?
It can lengthen the second stage – 10cm dilation until fetal delivery It will have no effect on the first stage/latent and active phases
1172
What post-MI pts are at greatest risk for SCD?
Those w/prior MI complicated by LV systolic dysfxn and ejection fraction <30% These patients often have normal systolic fxn or improved fxn w/proper therapy, but those who do not improve w/meds and still have <30% EF need an implantable cardioverter-defibrillator
1173
What are the common manifestations of cardiac sarcoidosis?
``` Conduction defects – complete AV block is most common Restrictive CMP (early manifestation) Dilated CMP (late) Valvular dysfxn Heart failure ```
1174
When should oral abx be given to children w/AOM?
All children <6mo | 6+ mos only need abx if they have: high fever, severe pain, or bilateral disease
1175
What are the extraarticular features a/w Ankylosing spondylitis?
Patients may develop: Anterior uveitis IBD Cardiac involvement w/aortic regurgitation
1176
What are the characteristics of the rash in disseminated gonoccal infection?
Vesiculopustular rash – rarely involves the face
1177
When is rouleaux formation seen?
In conditions that cause elevated serum protein – MM, Waldenstrom, Connective tissue diseases, etc.
1178
How long post-partum before women can be prescribed combined OCPs?
3+ weeks | Cannot prescribe <3 weeks
1179
How does the disease course differ for PCP in HIV pts v.non-HIV IMCP’d?
Typically causes an indolent disease in HIV pts. Immunosupressed pts w/o HIV often develop acute respiratory failure w/tachypnea, dyspnea, hypoxia leading to respiratory alkalosis, dry cough and fever Pts on prolonged glucocorticoid tx (esp if combined w/other immunosuppressants) should be on TMP-SMX pphx
1180
Where would lesions be expected to be seen in Korsakoff syndrome?
Anterior and medial thalami, and corpus callosum
1181
What neuropathologic findings are seen in Wernicke encephalopathy?
Mamillary body atrophy and dorsomedial thalamic neuron loss
1182
What is the mgmt. of prepatellar bursitis?
Must do fluid aspiration for cell count, gram stain and culture. About 1/3 of cases are infectious and need abx If infection is r/o then can manage w/NSAIDs
1183
What will be seen in exercise testing of a patient w/Sick sinus syndrome?
Chronotropic incompetence – inadequate HR response to exercise These patients need pacemakers
1184
What infections are patients w/Hemochromatosis at increased risk for?
Listeria V. vulnificus Yersinia enterocolitica
1185
What are the msk, endocrine and cardiac manifestations of Hemochromatosis?
MSK: arthralgia, arthropathy, choncrocalcinosis Endo: DM (“bronze diabetes”), Hypothyroidism, secondary hypogonadism Cardio: Restrictive or Dilated CMP, and conduction abnormalities (sick sinus syndrome)
1186
What are the PDA-dependent congenital heart diseases (5)?
``` Coarctation of aorta Transposition of the great arteries Hypoplastic LH syndrome Total anomalous pulmonary venous connection Tricuspid atresia ```
1187
What extrarenal features are seen in AD-PCKD?
``` Cerebral aneurysms Hepatic and pancreatic cysts Mitral valve prolapse, aortic regurg, HTN Colonic diverticulosis Ventral and inguinal hernias ```
1188
Risk factors for Psoas abscess:
HIV, IVDU, DM, Crohn’s | Diverticulitis and vertebral osteomyelitis are also risk factors bc they can be causes of direct spread.
1189
What are the risk factors and common findings in chronic pulmonary aspergillosis?
Risks: lung disease/damage (cavitary TB) Findings: 3+ months of wt. loss, productive cough (may have blood-tinged sputum), hemoptysis, and fatigue. Cavitary lesions may contain debris and fluid, or a fungus ball – Aspergilloma Dx: positive aspergillus IgG serology
1190
How to differentiate Type I Cryoglobulinemia from Mixed (Types II and III):
Type I: often asx, may have hyperviscosity (blurry vision), thrombosis (Raynaud), skin findings (Livedo reticularis, purpura) - Seen in lymphoproliferative or heme diseases (MM) - NORMAL complement levels, and negative RF Mixed: Often have systemic sxs, renal (HTN, glomerulonephritis), Pulm (dyspnea, pleurisy), Skin (palpable purpura, leukoclastic vasculitis), and liver involvement - Seen w/chronic HCV, HIV, and SLE - LOW complement, often v. low C4, elevated transaminases, and positive RF
1191
Tx of Essential tremor:
1st line: BBs – Propranolol Anticonvulsants – Primidone (can be used alone or in combo w/the BBs) Small amounts of EtOH Benzos – Clonazepam
1192
What will be seen on CXR in Takayasu arteritis?
Aortic dilation and widened mediastinum – CT/MRI will show wall thickening and narrowing of the lumen
1193
What will be the lab findings in acute mesenteric ischemia?
Leukocytosis Elevated amylase and phosphate Metabolic acidosis (d/t elevated lactate) Elevated Hb (hemoconcentration)
1194
What is spondylothisthesis and in what age is it most common?
It is a fracture of the pars interarticularis (spondylosis) and then slippage of a vertebral body. Most common in adolescents (10-19) during growth spurts d/t increased physiologic lumbar lordosis and decreased bone mineralization. Pain w/extension of spine, and athletes w/repetitive extension (gymnastics, ballet, diving) are at greatest risk
1195
How should billous emesis be managed in children?
Stop feeds, NGT decompression, IVF then do AbXR – if no evidence of free air, distal obstruction (dilated loops of bowel) or duodenal atresia (double bubble) then need to get an upper GI series/barium swallow
1196
What are common causes of asterixis?
Hepatic encephalopathy Uremic encephalopathy Hypercapnia Each requires unique mgmt. and careful review of labs and hx should be done to determine the cause before initiating tx.
1197
What screening tests are part of the routine newborn care?
Comprehensive newborn screen – metabolic/genetic disorders Hyperbilirubinemia Hearing screen Pre and Post-ductal pulse ox (tests for CHD) Hypoglycemia in select populations
1198
What antidote may be used as a mucolytic in CF patients?
N-acetylcysteine
1199
What is required to diagnose Bipolar II?
``` Hypomanic episode(s) and at least 1 MDE No psychotic features (requirement to be hypomanic) if psychotic features are present it is automatically mania/BP-I MDE may happen in BP-I but is not required for the diagnosis ```
1200
What will be heard on cardiac auscultation in aortic dissection?
New aortic regurgitation
1201
What would be the expected clinical presentation of a lesion in the vertebrobasilar system?
Vertebrobasilar vessels supply the brain stem – lesions would cause: Alternate syndromes w/contralateral hemiplegia and ipsilateral cranial n. involvement Possible ataxia
1202
What is the difference in presentation of a stroke involving the MCA of the dominant v. non-dominant lobe?
``` Both will present w/contralateral motor and somatosensory deficits worse in the face/UEs, and homonymous hemianopia/quadrantanopia Dominant lobe lesions (L) often present w/aphasia Nondominant lobe (R) often present w/hemineglect or anosognosia (lack of awareness of illness) ```
1203
What is the most common electrolyte abnormality in chronic alcoholism?
Hypomagnesemia
1204
How might hypophosphatemia present?
Typically only have sxs in severe deficit but may cause weakness, rhabdomyolysis, paresthesias, and respiratory failure.
1205
What is the tx of actinic keratosis?
Fluorouracil cream
1206
What would the results of a Hb electrophoresis show in a and B thalassemia minors?
a-minor will show normal results | B minor will show increased HbA2
1207
What is the Mentzer index and how can it differentiate b/w types of anemia?
Mentzer index is the ratio of MCV/RBC Mentzer index < 13 is seen in a- and B-Thal minors (decreased MCV/normal or high RBCs) Mentzer index > 13 is seen in Fe-def anemia (decreased MCV/decreased RBCs)
1208
What can be used as an alternative antidote to Methylene blue?
Methylene blue is the antidote for methemoglobinemia, but is sometimes unavailable or contra’d (G6PD def.) High-dose ascorbic acid/Vit. C can be used in these cases
1209
What are periarticular erosions on XR indicative of?
RA
1210
What drugs might cause pancreatitis?
``` Diuretics – furosemide, thiazides IBD rxs – sulfasalazine, 5-asa Immunosuppressants – azathioprine, 6-MP HIV rxs – didanosine, pentamidine, PIs, NRTIs Abx – metronidazole, tetracycline, sulfas Anti-epileptics – valproate GLP-1 agonists (exenatide/liraglutide) Cannabis (only illicit drug to cause it) ```
1211
What lab value will suggest biliary pancreatitis?
ALT > 150 | This is helpful when no stone is seen on US (in cases where the stone may have already passed)
1212
What is the most likely cause of statin-induced myopathy?
Statins decrease coenzyme Q10 synthesis involved in muscle cell energy production which most likely causes the myopathy a/w these Rxs
1213
What would cause loss of pain and temp in the ipsilateral face and contralateral trunk and limbs?
Wallenberg/lateral medullary syndrome – d/t occlusion of the PICA - Will have motor function of face intact, but will have bulbar sxs Lateral pontine syndrome – d/t occlusion in the AICA - Will have loss of facial motor function, but no bulbar sxs Both vessels are brs. of vertebral a.
1214
A lesion in what vessel is the only one that will cause hoarseness and dysphagia as part of the stroke syndrome?
Lesion in PICA (br. of vertebral a.) – these effects are d/t its supply of the nucleus ambiguus Only a lesion of the PICA will cause loss of gag reflex, hoarseness and dysphagia
1215
When should coronary angiography be done as the first diagnostic test?
In patients w/high (>90%) pretest probability of ischemic heart disease: Typical angina in men 40+ or typical angina in women 60+
1216
What is required to classify typical/classic angina?
Must have all three of the following: 1. Typical location (substernal), quality and duration 2. Provoked by exercise or emotional stress 3. Relieved by rest or nitroglycerin Atypical is 2/3 and <2 is considered non-anginal
1217
What kind of heart failure is prolonged HTN a risk for?
Diastolic LHF
1218
What are the ocular cxs of PDE-5 inhibitors?
Blue discoloration of vision | Nonarteritic anterior ischemic optic neuropathy
1219
What is the BP goal in diabetics?
DM w/signs of nephropathy: <130/80 DM w/o signs of nephropathy < 140/90 - this is also the goal BP for all pts age <60, or who have CKD all pts age 60+ goal is <150/90 whether they have DM or not
1220
What is the etiology of serum sickness-like reaction?
It is a type III HS rxn w/immune-complex formation Occurs 1-2 wks after tx w/B-lactams (penicillin, amoxicillin, cefaclor) or TMP-SMX May also be seen in acute HBV infection
1221
Most common cause of gross lower GI bleeding in adults:
Diverticulosis
1222
What is the diagnostic test of choice when CLL is suspected?
Flow cytometry – will show a clonality of mature B cells | LN or BM biopsy are typically not needed, but can help dx HL and NHL
1223
What is the early-morning cortisol test used for?
Primary adrenal insufficiency – will show low or low-normal levels This test is NOT useful in assessing hypercortisolism in suspected Cushing’s
1224
What are the features and tx of Chronic prostatitis/chronic pelvic pain syndrome?
Non-infectious chronic prostate inflammation (separate dx from chr. bac. prostatitis) Sxs: pain in low back, pelvis, perineum and genitalia; irritative voiding sxs, hematospermia, and pain w/ejaculation Will have no/mild prostate tenderness and a sterile UCx Mgmt: a-blockers, abx (Cipro – esp. if hx of UTI), and 5-a-reductase inhibitors
1225
What neurotransmitters does tetanus toxin prevent release of?
Inhibitory neurotransmitters GABA and glycine
1226
What is the timeline of presentation in order for a patient to be considered for alteplase therapy?
Must present w/in 3-4.5hrs of sx onset and not have any contraindications to thrombolytic therapy
1227
What is the recommended mgmt. of a Hydatidiform mole?
Suction curettage and then weekly B-hCG levels until it is undetectable. - if these levels increase or plateau = gestational trophoblastic neoplasia Once undetectable check monthly levels for 6mo (must use contraception during this time) - if B-hCG becomes detectable again = gestational trophoblastic neoplasia Once clear for 6mo pts can attempt pregnancy again
1228
What is the therapeutic Magnesium range for treating preeclampsia?
5-8mg/dL | Mg2+ becomes toxic at concentrations >8`
1229
What are the Centor criteria and who are they used for?
Centor criteria predicts likelihood of Strep throat in adults only, should NOT be used in preadolescents and children. Criteria: fever by hx, tender anterior cervical LAD, tonsillar exudates, absence of cough 0-1 – no testing or tx for strep 2-3 – rapid strep test (pen or amox if +) 4 – Empiric penicillin or amoxicillin or do rapid test
1230
What Rxs are a/w causing exacerbations of Myasthenia Gravis?
Abx: Fluoroquinolones, aminoglycosides, azithromycin Anesthetics: neuromuscular blocking agents Cardiac meds: BBs, procainamide Others: Mag sulfate, penicillamine Tapering immunosuppressants can also cause exacerbations
1231
What surgery is a particular risk for exacerbation of Myasthenia Gravis?
Thymectomy – aka one of its tx options
1232
What are the common clinical findings in neonatal HSV infection?
Pathogenesis: vertical transmission intrauterine, perinatal, or postnatal Skin/membranes: mucocutaneous vesicles, keratoconjunctivitis - cutaneous sxs may be absent in CNS or disseminated infections CNS: seizures, fever, lethargy, temporal lobe hemorrhage/edema Disseminated: sepsis, hepatitis, pneumonia
1233
What patient population is Otosclerosis most likely to effect?
Young adults 20s-30s w/female predominance | abnormal remodeling of the otic capsule – stapes becomes fixed to the oval window
1234
What are the common sxs a/w Herpetic whitlow?
Norm. have mild prodrome of fever/malaise, and then development of grouped vesicles on an erythematous base typically on the hand – often have tingling, burning and pain Some pts have epitrochlear and axillary LAD
1235
What are common findings in burn wound sepsis?
``` May have some or all of the following: Temperature <97.7 or >102.2 Progressive tachycardia >90bpm Progressive tachypnea >30/min Refractory HoTN (SBP <90) Oliguria AMS Unexplained hyperglycemia Thrombocytopenia ```
1236
What is the tx of TCA overdose?
O2 and intubation if necessary IVF Activated charcoal if pts present w/in 2 hrs and there are no signs of ileus IV Na-HCO (alleviates depressant axn on myocardial Na channels)
1237
What finding a/w Raynaud is suggestive of the presence or future development of a CTD?
Abnormalities such as dilated or dropout vessels in the nailfold capillaries
1238
Who should undergo carotid endarterectomy?
Symptomatic pts (previous TIA or stroke in distribution of affected vessel w/in last 6 mos) w/high-grade carotid stenosis (>70%) Asymptomatic pts w/stenosis >80% Everyone else should get aspirin + other meds to control their risk factors (including asx pts w/stenosis up to 80%)
1239
How to differentiate XLA from CVID:
XLA – low B cells (lymphocytes – Tcells) and low numbers of all immunoglobulin classes Presents in infancy/early childhood CVID – normal B cells w/decrease in all immunoglobulin classes Presents w/less severe sxs than XLA and after adolescence
1240
What is the best way to secure an airway in an unstable cervical spine injury?
Still orotracheal intubation – can stabilize the neck w hand during procedure, its quick, and there isn’t that much movement
1241
What is the pathophys of secretory diarrhea and what are its common causes?
Occurs when luminal ion channels are disrupted in the GIT and results in a state of active secretion Common causes: bacteria (Cholera), viruses (Rota), congenital disorders of ion transport (CF), early ileocolitis, and postsurgical changes
1242
What cxs can occur in pts w/only sickle cell trait?
Hematuria/papillary necrosis (most common) Hyposthenuria Splenic infarction (esp. at high altitudes) Venous thromboembolism Priapism Exertional rhabdomyolysis Will have normal Hb, retic count, RBC indices and morphology
1243
Renal cxs in sickle cell trait:
``` Hematuria – mostly from papillary ischemia or necrosis Renal medullary carcinoma UTIs Hyposthenuria Distal renal tubular acidosis ```
1244
What are the features of postdural puncture HA?
Occurs after LP or neuraxial anesthesia – dural puncture causes CSF leakage, low CSF pressure and slight herniation of brain/brainstem Positional HA worse when upright, improves when supine Neck stiffness Photophobia, diplopia Hearing loss and tinnitus *mostly self-limited but severe sxs can be tx’d w/epidural blood patch*
1245
What is alcoholic neuropathy and how does it present?
EtOH is a neurotoxin and results in axonal neuropathy w/a reduction in the number of small myelinated and unmyelinated fibers. May occur alone or a/w thiamine def. Features: symmetric distal polyneuropathy in stocking glove pattern, paresthesia, burning pain, numbness, loss of DTRs (starting w/ankle), low of light touch and vibration, and gait ataxia Tx: EtOH cessation, thiamine to prevent secondary neuropathies, gabapentin and TCAs for pain
1246
What will be seen on imaging in Colonic ischemia?
CT scan: Colonic wall thickening and fat stranding (although may have only nonspecific findings) Endoscopy: Edematous and friable mucosa
1247
Difference between colonic and mesenteric ischemia:
Colonic – mostly d/t low blood flow/HoTN or non-occlusive ischemia w/underlying atherosclerotic disease. Effects watershed regions most (splenic flexure and rectosigmoid jxn) Mesenteric – d/t atheroembolic or thrombotic events causing occlusive ischemia of the small bowel typically (jejunum, ileum, duodenum)
1248
What Rxs are used to tx Frontotemporal Dementia?
SSRIs and Trazodone can both help the neuropsychiatric sxs
1249
What should be done in patients w/suspected blunt cardiac injury?
Continuous cardiac monitoring w/echo (TTE or TEE in intubated/unstable pts) and EKG for 24hrs to detect arrhythmias that may occur
1250
What are the CVS hemodynamic effects of Thyrotoxicosis?
Systolic HTN and increased PulseP Increased contractility and CO Decreased SVR Increased myocardial O2 demand
1251
What is one of the most common causes of acute renal failure in hospitalized patients?
CONTRAST INDUCED NEPHROPATHY!!! always pay attention when there is imaging done in pts w CKD and then worsening of renal failure Can prevent w/IVF pre-procedure and by holding NSAIDs
1252
What are the 2 main toxic products of combustion that can harm pts w/inhalation smoke injuries?
``` Hydrogen Cyanide (aka cyanide toxicity) Carbon monoxide – carboxyhemoglobin **methemoglobinemia does NOT occur 2/2 inhalational smoke exposure and is actually used to tx the cyanide poisoning that may occur** ```
1253
What will be seen on coagulation studies in severe B12 def causing pancytopenia?
Normal results. | Severe deficiency can cause decrease in all cell lines, but coagulation will be normal
1254
Cardiac causes of hemoptysis:
Mitral stenosis/acute pulmonary edema
1255
Timeline difference b/w Crystal-induced AKI and AIN:
Crystal-induced typically occurs w/in 24-48hrs of starting a drug and is often asx AIN usually occurs 7-10d after starting a Rx and rash + eosinophilia, etc.
1256
What kind of infections does Kingella kingae cause and what abx is often used to treat them?
Septic arthritis, osteoarthritis, bacteremia and endocarditis Most infections are found in children They are aerobic gram neg. and often tx’d w/Ceftriaxone
1257
What cx of appendicitis is significantly increased after laparoscopic procedures v. laparotomy?
Intra-abdominal abscess – often found sub-phrenic causing hiccups, pleural effusions and SoB
1258
What is the mgmt. of Primary Ovarian Insufficiency?
Estrogen therapy and Progestin added if there is an intact uterus
1259
What is the most common mechanism of leukopenia and thrombocytopenia in SLE?
Immune-mediated destruction
1260
How can a large PE be differentiated from RV MI?
PE is more likely to cause tachycardia, dyspnea, and syncope RVMI is more likely to cause bradycardia and arrhythmias Both can cause RV dysfxn, increased CVP and decreased LV preload and CO
1261
When should Penicillin desensitization be done to tx Syphilis?
If other txs (Doxycycline) are contraindicated – like in pregnancy If it has progressed to Neurosyphilis/Tertiary stage (CVS/aortitis effects, gummas) All other pts. w/severe penicillin allergies can receive Doxycycline instead
1262
What does the Secretin stimulation test diagnose?
Gastrinoma/ZES Normal G cells in the stomach are inhibited by Secretin, but gastrinoma cells are stimulated by it. Secretin will not cause a rise in gastrin levels in any other causes of hypergastrinemia besides ZES/gastrinoma
1263
How is Seborrheic dermatitis tx’d?
Topical antifungals (ketoconazole, selenium sulfide) – malassezia spp. are thought to play a role in its pathogenesis
1264
What stroke syndrome is least likely to cause Hemiparesis?
Cerebellar – almost all others will cause paresis/paralysis
1265
What stroke syndrome is most likely to cause seizures?
Cerebral lobar strokes
1266
What are the most common causes of Steppage gait?
L5 radiculopathy or neuropathy of the common peroneal n.
1267
What are the soft signs of extremity vascular trauma?
``` Hx of hemorrhage Diminished pulses Bony injury Neurologic abnormality These should be investigated w/imaging (CT, US, Angio) if the pt. is stable and there are no hard signs present ```
1268
Mgmt of Neonatal Varicella exposure:
Give VZIG if exposure or if mother developed infection 5d pre- or 2d post-delivery If varicella infection develops tx w/Acyclovir (safe in pregnancy and infancy)
1269
What renal pathology does HBV infection increase the risk for?
Membranous nephropathy – a nephrotic syndrome. Thought to be d/t HBeAg deposits in the glomeruli (membranoproliferative glomerulonephritis has also been a/w HBV but is much less common)
1270
What is a common source of nosebleeds in pregnancy?
Pyogenic granulomas of the anterior nasal septum. Pregnant women have an increased incidence of these.
1271
Most common organisms cultured from peritoneal fluid in SBP:
E. coli and Klebsiella
1272
Risk factors for Hydatidiform mole:
Extremes of maternal age Previous Hx of mole Vitamin A def. (seen post Roux-en-Y surgery)
1273
How will viral myocarditis likely present?
Post-URI w/fatigue, dyspnea, elevated JVP and cardiomegaly on CXR Typically have audible S3 and bibasilar rales w/pulmonary vascular congestion on imaging.
1274
What is seen on UA in hemoglobinuria?
Will be dipstick positive for blood but there will be absent RBCs on microscopy bc the heme is lysed from the RBCs and excreted in the kidneys but the whole RBC is not intact in the urine (hematuria)
1275
Anti-DM Rxs used in pregnancy:
Insulin is 1st choice, but Metformin and Glyburide may also be used, but these both cross the placenta
1276
Mgmt of Aortic Dissections:
``` Pain control w/Morphine, and IV BBs should be started right away, then: Type A (involving the ascending aorta) need immediate surgical repair Type B (only descending involved) can be managed w/pain and tight BP control unless there are signs of organ malperfusion, (mesenteric ischemia, etc.) then these need surgery asap as well ```
1277
What are the common lab findings and mgmt. of acute mesenteric ischemia?
Labs: leukocytosis, elevated amylase and phosphate, elevated Hb (hemoconcentration) and metabolic acidosis (elevated lactic acid) Mgmt: immediate operative evaluation, or dx w/CT-angio. Then need bs-abx and anticoagulation
1278
What kind of arthritis does Lyme disease cause?
A mono-articular migratory arthritis. Most commonly involves the knee, but only involves 1 joint at a time and then may resolve and affect another joint later.
1279
What is EPO?
A cytokine
1280
Endocrine causes of recurrent pregnancy loss:
Thyroid disease (anti-TPO Abs a/w miscarriage in both euthyroid and hypothyroid women) PCOS DM Hyperprolactinemia Celiac dx (not an endocrine cause, but remember it)
1281
How long should a pt. be seizure free before considering dc of anti-epileptics?
>2 years | Must slowly taper and then dc
1282
What is the tx of Carcinoid syndrome?
Octreotide for sxs and prior to surgery/anesthesia | Surgery for liver mets
1283
What products do carcinoid tms secrete?
Histamine 5-HT and 5-HIAA VIP
1284
What are the CVS features of DM-autonomic neuropathy?
Tachycardia, impaired exercise tolerance | Postural HoTN w/loss of diurnal BP variation
1285
What is the role of ADH in ADPCKD?
Tubular destruction leads to a mild nephrogenic DI which then increased ADH levels. The high ADH levels may promote renal cyst growth, so Vasopressin-2-R antagonists (tolvaptan) have been shown to slow progression of the disease.
1286
What causes aFlutter?
Reentrant circuit around the tricuspid annulus
1287
What are the clinical features of Neurofibromatosis 1?
Café-au-lait macules (1st cutaneous finding-often in infancy), axillary and inguinal freckling, Lisch nodules and neurofibromas Pseudoarthrosis Pheochromocytoma These pts are at increased risk for neurologic disorders: cognitive deficits, learning disabilities, seizures, intracranial neoplasms (astrocytomas, brainstem gliomas), and optic pathway gliomas
1288
What are the features of Tuberous sclerosis?
Neurocutaneous disorder w/benign tumors in multiple organs – intracardiac rhabdomyomas Angiofibromas, ash-leaf spots and shagreen patches (thick leathery skin, dimpled like an orange peel)
1289
What are the features of Sturge-Weber syndrome?
Triad of port-wine stain on the face, ocular disease (visual deficits or glaucoma), and leptomeningeal capillary-venous malformations. Often have seizures from the malformations
1290
When does renal biopsy need to be performed in the pediatric population?
Kids >10 w/nephrotic syndrome Kids of all age w/nephritic syndrome Patients <10 w/minimal change that don’t respond to steroids
1291
How should pulseless electrical activity be managed?
This is a rhythm on the monitor w/o a palpable pulse or measurable BP Mgmt: CPR x 2min, IV access, Epi every 3-5min, possible advanced airway. Continue this until there is a shockable electrical rhythm or the underlying causes have been reversed
1292
What is Lemierre Syndrome?
Infection caused by Fusobacterium necrophorum – affects young immunocompetent pts. Typically starts w/tonsillitis (but may be 2/2 dental work or mastoiditis) then the bacterium invades the lateral pharyngeal space and causes IJV thrombosis and infection
1293
What is the typical presentation of Lemierre syndrome?
A prolonged duration (1+ week) of sore throat w/high fever, rigors, dysphagia and neck pain w/swelling along the SCM (IJ thrombosis) Once the IJ is infected septic thromboembolic can seed other organs – esp. the lungs, see nodules and cavitation on imaging
1294
What are the common effects of Growth Hormone?
``` Hyperglycemia Sodium retention HTN Swollen hands Joint and muscle pain ```
1295
What would be the expected hormone levels in exercise-induce hypothalamic amenorrhea?
Decreased: GnRH, LH, FSH and Estrogen | Normal TSH and PRL
1296
What would be used to make the diagnosis of Mallory-Weiss syndrome?
Upper GI endoscopy – can confirm dx and tx persistent bleeding This is a mucosal tear w/bleeding (contrast to Boerhaave which is transmural and EGD is contraindicated)
1297
How is thyroglobulin used as a tumor marker?
Thyroglobulin is produced by normal thyroid tissue and differentiated thyroid cancer – papillary, follicular Once patients have undergone Thyroidectomy w/RAI tx they should have no Thyroglobulin production. A rise in its concentration would signify recurrence of the cancer
1298
What is often used as bs-coverage in PID?
Cefoxitin + Doxycycline | Metronidazole may also be used as part of the regimen
1299
Patients with what condition have increased sensitivity to lactate infusions?
Patients w/Panic Disorder | Lactate infusion can provoke panic attacks in susceptible pts.
1300
What should be suspected in a neonate w/direct hyperbilirubinemia and hepatomegaly?
Biliary atresia
1301
Tx of Bacterial Vaginosis in pregnant pts:
Metronidazole or Clindamycin is the tx regardless of pregnancy status
1302
What are the characteristics and common locations of Tophi?
Tophi are nodular deformities filled w/chalky material, often found on the ears, tendons and periarticular tissues of the digits. Unlike acute gout tophi are normally painless. In pts w/gout who develop tophi a urate-lowering Rx (allopurinol) is required
1303
What is the gold standard for diagnosing DM in pts w/PCOS?
Oral glucose tolerance test | This is more sensitive for detecting glucose intolerance than the standard DM screening tests (fasting glucose, HbA1c)
1304
When is BRCA mutation testing indicated?
In pts w/Fhx of ovarian ca. at any age and a personal or Fhx or breast cancer <50. Not indicated for Fhx of endometrial cancer
1305
What are the most common inciting factors of Hepatorenal syndrome?
Spontaneous bacterial peritonitis | GI bleeding
1306
What is the tx of Hepatorenal syndrome?
``` Address precipitating factors and return liver fxn to normal Liver transplantation Splanchnic vasoconstrictors (Midodrine, octreotide, NE) and albumin ```
1307
Most common cause of chronic mitral regurg in developed countries?
MVP – murmur may be more consistent w/severe mitral regurg (holosystolic radiating to axilla) in late stage instead of the classic mid/late systolic click
1308
How will changes in K+ affect patients w/cirrhosis?
Hypokalemia is a common precipitant to hepatic encephalopathy and even slight decreases require prompt repletion. This commonly occurs after the initiation of diuretics which deplete K+ and cause low intravascular volume despite total volume overload Metabolic alkalosis (increased HCO3-) is often a/w hypokalemia which also exacerbates HE by increasing conversion of NH4+ to NH3
1309
What are the common inherited forms of Pheochromocytoma?
VHL gene w/Von hippel-Lindau RET gene – MEN type 2 NF1 gene – Neurofibromatosis Type I
1310
What test can be performed to assess ovarian fxn?
Day 3 FSH testing – during the follicular phase As ovarian reserve and fxn decline, estradiol and inhibin dencrease – negative feedback leads to increased FSH as ovarian fxn decreases
1311
When would hypertrophic osteoarthropathy be seen?
It is a paraneoplastic syndrome a/w intrathoracic malignancy + other pulm diseases (CF) Polyarthropathy a/w digital clubbing and periostosis (xs bone formation)
1312
Important diagnostic clues for Psoriatic arthritis:
Involvement of the DIPS and nail changes – pitting and onycholysis (separating of the nail from nailbed) Often presents as asymmetric oligoarthritis or symmetric polyarthritis May have seronegative spondyloarthritis or aggressive/destructive arthritis mutilans Psoriatic arthritis manifestations are increased in pts positive for HLA-B27 or w/involvement of the nails
1313
Tx of acne:
Always start w/topical retinoids, salicylic or glycolic acid For mild inflammatory can start topical retinoids + benzoyl peroxide Next step add topical abx Next add oral abx Last resort for unresponsive severe nodular/cystic acne can replace other Rxs w/oral isotretinoin
1314
What clinical picture should a biliary leak be suspected with?
A patient w/low-grade fever, RUQ tenderness, N/V, leukocytosis and obstructive-appearing liver enzymes (elevated BR and ALP) w/normal-appearing biliary ducts or mild dilation on imaging 2-10d post-cholecystectomy (or other biliary surgeries)
1315
How to tell if there’s a statistically significant difference b/w 2 groups based on CIs:
If the CIs of 2 different groups do not overlap (A = 1-2 and B = 3-4) then that suggests there is a statistically significant difference b/w the two groups
1316
Manifestations of early Lyme disease:
Erythema Migrans Systemic sxs: malaise, fatigue, arthralgia Regional LAD Neuro: meningitis, CN palsy (often b/l facial n. palsy), radiculoneuritis CVS: AV block **most pts 1st present w/erythema migrans (80%) but some may present w/early disseminated signs such as Neuro signs and/or carditis** All of these sxs may occur alone or in combinations
1317
What should be suspected in a patient w/flu-like sxs and b/l facial palsy?
Lyme disease
1318
What tm markers are commonly increased in testicular cancer?
AFP and B-hCG
1319
Common causes of Intertrigo:
Candida #1 (will also form satellite lesions w/vesicles, papules or pustules) S. aureus + others
1320
What will present as segmented hyphae on KOH prep?
Dermatophyte infections
1321
What is the most common congenital infection worldwide?
CMV – it is also one of the only ones a/w microcephaly
1322
What are some relative contraindications to NSAIDs in acute gout attacks?
Pts. taking anticoagulants (increase risk of bleeding) and those w/heart failure (can acutely worsen HF) In these pts. Colchicine or steroids should be used for acute attacks But shouldn’t use colchicine in elderly or w/severe renal dysfxn, and steroids are not preferred in DM
1323
How does ocular rosacea present and how is it treated?
It is seen in the majority of pts w/rosacea and may appear on its own w/out skin findings. Involves the cornea, conjunctiva and lids and often has recurrent chalazia Sxs: burning or foreign body sensation/”dirt in eyes sensation", blepharitis, keratitis, conjunctivitis, and corneal ulcers Tx: Mild – lid scrubs, topical abx (metro, erythro), and ocular lubricants; Severe may require systemic abx and topical immunosuppressive agents
1324
What is seen in the clinical presentation of Acute Liver Failure?
Generalized sxs – fatigue, lethargy, anorexia, N RUQ abd pain Pruritus and jaundice – from hyperbilirubinemia Renal insufficiency Thrombocytopenia Hypoglycemia Signs of HE – somnolence, disorientation, asterixis
1325
What is the most common neural tube defect?
Myelomeningocele
1326
What might be the fetal effects of maternal cigarette smoking?
FGR, intra-uterine fetal demise, and cleft lip/palate
1327
What is a severe cx of basal ganglia hemorrhages?
Uncal herniation – hemorrhage compresses part of the temporal lobe (uncus) laterally and downward against the tentorium cerebelli.
1328
What are sxs of an uncal herniation?
Aka transtentorial herniation CN-III palsy – dilated, nonreactive pupil ipsilateral to the side of herniation (d/t direct compression) Contralateral extensor/decerebrate posturing, coma and respiratory compromise (d/t compression of the midbrain) Often occur after hemorrhagic strokes 2/2 HTN
1329
What are sxs of a cerebellar tonsillar herniation?
Neck tilt, flaccid paralysis, coma, BP instability, and respiratory arrest all d/t tonsillar herniation and compression of structures through the foramen magnum
1330
What can be done in pts w/increased risk for pulmonary cxs in the post-op period to decrease their risk?
Pre-op PT w/aerobic exercise, and inspiratory muscle training can significantly reduce the risk of atelectasis and pneumonia Smoking cessation 8+ weeks pre-op is also of benefit
1331
Besides infections, what are some cxs of Wiskott-Adrich syndrome?
Bc they have microthrombocytopenia they are at increased risk for bleeding. May have just petechiae/purpura or more severe bleeding like hematuria, hematochezia, or intracranial hemorrhage
1332
What are the features of Chediak-Higashi syndrome?
Lysosomal defect – impaired phagocytosis | Signs/Sxs: Albinism, peripheral neuropathy, recurrent skin and soft-tissue pyogenic infections, giant granules in NPs
1333
Why might pts w/Hypercalcemia present w/signs of dehydration?
Hypercalcemia induces nephrogenic DI – polyuria and volume depletion. This is why NS is the first line tx of hypercalcemia – restores intravascular volume and promotes urinary Ca2+ excretion
1334
When should glucocorticoids be used to tx hypercalcemia?
When the hypercalcemia is d/t extrarenal calcitriol production – Lymphomas and granulomatous diseases (sarcoid)
1335
What are the target INR ranges for pts taking Warfarin w/a mechanical prosthetic valve?
Mitral valve: INR 2.5-3.5 | Aortic valve: INR 2.0-3.0
1336
What are the clinical features of mechanical prosthetic valve thrombosis?
Inadequate coagulation (#1 risk factor) Mitral valve risk > aortic valve Obstructive thrombus mimics valvular stenosis—get rapid onset dyspnea, pulm edema w/crackles, lightheadedness HF, cardiogenic shock Systemic thromboembolic events (stroke, limb ischemia)
1337
Most common cause of persistent nasal obstruction in childhood:
Adenoid hypertrophy – have signs/sxs of chronic upper airway obstruction: Nasal congestion refractory to medical mgmt., recurrent sinus and ear infections, mouth breathing, sleep disturbances/snoring d/t apnea May also have mucopurulent nasal discharge, postnasal drip, and elongated/flattened facial features Concurrent tonsillar hypertrophy is common
1338
What are the cxs of Ventricular aneurysms post-STEMI?
``` Progressive LV enlargement – HF Refractory angina Ventricular arrhythmias Systemic arterial embolization – stroke, mesenteric ischemia, UE or LE ischemia Mitral annular dilation – MR ```
1339
What are the features of Beriberi?
High-output heart failure and peripheral neuropathies | Caused by Thiamine/B1 deficiency
1340
Contraindications to the two types of IUD:
Levonorgestrel – active liver disease, breast ca., active pelvic infection Copper – Wilson disease, Cu allergy, Menorrhagia, Acute pelvic infection
1341
Risk factors and most common causes of Pyelonephritis in pregnancy:
Risks – asx bacteriuria, DM, age <20, Tobacco use | Common pathogens – E. coli (most common), Klebsiella, Enterobacter, GBS
1342
What are signs of cervical ca. tm extension?
Low back pain from pelvic extension Lymphedema from obstruction of lymphatics and BVs Hydronephrosis from obstruction of ureters
1343
What are potential cxs of chronic hypoparathyroidism?
Nephrocalcinosis Cataracts Deposition of Ca2+ in the basal ganglia (may cause EPS) *cxs are higher in those w/hyperphosphatemia and a Calcium x Phosphorus product >55, this increases risk of soft tissue calcification*
1344
What are the risk factors for retained placenta?
Gestational age 24-27wks Stillbirth Placenta accreta Hx of prior retained placenta
1345
What is the difference b/w Type I and II Chemo-induced cardiomyopathy?
Type I: a/w anthracyclines (Doxorubicin). Causes myocyte necrosis and destruction w/fibrosis. Causes asx decline in LV systolic fxn which progresses to overt HF. Unlikely to be reversible Type II: a/w Trastuzumab. Causes myocardial stunning/hibernation w/o myocyte destruction. Get asx LV systolic dysfxn. Often reversible when Rx is dc’d
1346
Risk factors for penile cancer:
Age >60, HPV, phimosis, cigarette smoking | Most are SCC
1347
What is pulmonary cachexia?
Phenomenon of loss of lean muscle mass a/w chronic pulm. Disease (mostly advanced COPD) Suggested by BMI <20 or >5% wt. loss Occurs in 20-40% of COPD pts and leads to impaired balance, increased susceptibility to lung infections and increased mortality. Development of the disorder correlates w/disease severity.
1348
What is pHTN and what are the causes of pulmonary venous HTN?
pHTN = mean pulm. arterial P 25+ at rest Causes of venous pHTN: L heart disease (LV dysfxn, AR/S, MR/S, etc.), chronic lung disease/hypoxemia, chronic thromboembolic disease, other – hematologic, systemic or metabolic disorders
1349
What kind of pHTN do connective tissue diseases cause?
CTDs (SLE, RA, sclerosis) cause narrowing and obliteration of the small arterioles and alveolar capillaries which leads to pulmonary ARTERIAL HTN.
1350
What is an osteoclastoma?
Giant cell tumor
1351
What is the likely presentation and outcome of a constitutionally small infant?
Prenatally will be seen as estimated fetal wt. <10% for gestational age, but then will have normal Doppler a. US during follow-up and appropriate interval growth via US Outcome is normal neonatal course and no adverse outcomes. Often seen in women w/low pre-pregnancy wt. and short stature
1352
What are the long-term cxs of infants w/FGR?
Neuro cxs: delayed cognitive development, motor dysfxn, behavioral probs (ADHD) Growth failure Childhood obesity and Metabolic syndrome
1353
What value is considered small for gestational age in a term infant?
2500g or 5lb 8oz
1354
How is incisional hematoma managed?
For large symptomatic hematomas the incision needs to be opened to evacuate the clot, obtain hemostasis and then reclosed. Incisional hematomas can be a nidus for bacterial growth, bc of their stagnant fluid, and increase the risk of surgical site infection (cellulitis, abscess)
1355
What ophthalmologic disease is a/w gradual peripheral vision loss?
Open-angle glaucoma | On fundoscopy see: Enlargement of the optic disc/cupping, increased cup:disc ration, and elevated IOP
1356
What are the cxs seen in infants of DM mothers w/hyperglycemia in the 1st trimester?
Congenital heart disease Neural tube defects Small L colon syndrome Spontaneous abortions
1357
What are the cxs seen in infants of mothers w/Hyperglycemia in the 2nd and 3rd trimesters?
Polycythemia Organomegaly Neonatal hyperglycemia Hypocalcemia (d/t PTH suppression, but norm asx) Macrosomia – shoulder dystocia, brachial plexopathy, clavicle fracture, perinatal asphyxia
1358
Most common causes of DRESS syndrome?
Allopurinol and Anti-epileptics (Phenytoin, Carbamazepine) Less commonly abx – sulfas, minocycline, vancomycin Long latency from Rx initiation to rxn – 2-8wks Possible cross-reactivity b/w herpesvirus lymphocytes and drug antigens – most pts have Ab evidence of HHV6 reactivation during DRESS syndrome
1359
How will Ogilvie syndrome present on imaging?
Aka acute colonic pseudo-obstruction | Colonic dilation w/oral contrast visualized throughout the entire colon – suggesting no anatomical obstruction
1360
What will be the clinical presentation of Ogilvie syndrome (acute colonic Pseudo-obstruction)?
Abdominal distension, pain, N/V Constipation/obstipation or paradoxical diarrhea Increasing dilation may lead to ischemia/perforation – guarding, rigidity, extreme tenderness Partial/total colonic dilation w/o anatomic obstruction on CT
1361
What spp. of Malaria have a dormant phase?
P. vivax – seen in Non-african countries. Need tx w/Chloroquine and Primaquine (kills hepatic hypnozoites) P. falciparum – seen in Africa doesn’t have a dormant phase
1362
Where is Choriocarcinoma most likely to met?
Lungs – dyspnea/ARDS | Vagina – bloody or purulent vaginal discharge, vascular/friable nodule on pelvic exam
1363
Features of chronic ischemic colitis:
Chronic abd pain, bloody diarrhea, weight loss, and colonic strictures May see mucosal atrophy and granulation tissue on colonic biopsy
1364
What are the risk factors and features of Myelodysplastic syndrome?
Hematipoietic stem cell neoplasm Risks: advanced age, hx of chemo or radiation Causes dysplasia and cytopenias – typically decrease in all cell lines Anemia – weakness and fatigue Granulocytopenia – infections and hyposegmented NPs Thrombocytopenia – bleeding and bruising Cx: transformation to AML
1365
How to differentiate Hairy cell leukemia from the chronic leukemias:
All may cause massive splenomegaly Hairy cell – pancytopenia (d/t fibrosis of bone marrow: dry tap) CLL – lymphocytosis CML – leukocytosis **Myelofibrosis may also cause massive splenomegaly w/pancytopenia**
1366
What pulmonary sxs does Listeria cause?
NONE! You’re thinking of legionella, they’re different Listeria = GI and Neuro; G+ aerobic rod Legionella = GI then pulmonary; G- aerobic rod
1367
What are the clinical features and tx of Legionella?
G- aerobic rod, a/w travel and hospital Spreads via aerosolized water droplets from contaminated source (ac, ventilator) Get GI sxs first (D/V, cramps), then fever (>101.8), relative bradycardia for fever (70s norm) and then pulmonary sxs are delayed and show last Often have Hyponatremia and patchy unilobar or interstitial infiltrates Tx: Resp fluoroquinolone (levo) is DoC, newer macrolides (azithro) are 2nd choice
1368
AEs of oral Isotretinoin tx:
``` Teratogenic – spontaneous abortion, fetal malformations Hyperlipidemia Chelitis (dry, cracked lips), dry skin Myalgias Pseudotumor cerebri ```
1369
What causes testicular torsion
Twisting of the spermatic cord d/t inadequate fixation of the lower pole of the testis to the tunica vaginalis – compression of pampiniform plexus and reduced venous outflow
1370
When will women start menstruating post-partum?
Formula feeding: 8-14 weeks | Exclusive breastfeeding: >6mos (variable)
1371
Common causes of SIADH:
CNS disturbance – stroke, hemorrhage, trauma Meds – Carbameazepine, SSRIs, NSAIDs, Cyclophosphamide, Lung disease (pneumonia) Ectopic ADH secretion (SCLC) Pain and/or nausea
1372
Most common type of fibroid to cause heavy/prolonged menstrual bleeding:
Submucosal; Intramural may as well, but less common. Subserosal will not.
1373
What is the best diagnostic step to confirm uterine fibroids?
Sonohysterography – saline infusion US
1374
What does omental caking on CT signify?
Intra-abdominal carcinomatosis
1375
What are common causes of Uric acid stones?
Uric acid stones are relatively uncommon (5-10%) Increased serum uric acid levels: gout, tumor lysis syndrome Chronic HCO3- loss: diarrhea, dehydration
1376
What is the tx of Waldenstrom macroglobulinemia?
Plasma exchange – to remove the xs serum IgM
1377
When would ultrafiltration be used?
In pts. w/massive volume overload whose condition doesn’t respond to aggressive diuretics
1378
What is the most common form of lung cancer?
Adenocarcinoma
1379
How to tell different types of lung ca. based on CXR:
Squamous cell – often a single, upper lobe, cavitary lesion. Typically the only type to cause a cavitary lesion Adenoca. – peripheral nodule Bronchoalveolar – typically a solitary peripheral nodule, but may have multiple nodules or lobar consolidation SCLC – central (hilar, perihilar) mass, often w/mediastinal LAD
1380
What type of hernia may extend into the scrotum?
Indirect inguinal – protrudes through deep inguinal ring into inguinal canal d/t patent processus vaginalis (lat. to inferior epigastrics) Direct – protrude through weakness in transversalis fascia/inguinal canal floor (med. To inferior epigastrics). Has no route into the scrotum.
1381
What is the tx of Condylomata accuminata in pregnancy?
Topical trichloroacetic acid Imiquimod and podophyllin resin are contraindicated d/t teratogenicity Excisional removal is avoided d/t increased anesthetic and surgical risks Viral culture does not need to be done bc it won’t change mgmt.
1382
What pattern of pain suggests Ureterolithiasis obstruction at the UVJ?
Severe flank pain that radiates to the perineum, penis, scrotum, or inner thigh
1383
What imaging studies should be done when Pancreatic ca. is suspected?
If jaundice is present – abdominal US | No jaundice – CT
1384
What is likely to cause jejunal atresia and how will it present?
Jejunal and ileal atresia likely d/t vascular insults in utero that cause necrosis and resorption of fetal intestine Common causes: maternal vasoconstrictive meds, tobacco or cocaine abuse Presents w/bilious emesis, abdominal distension and “triple bubble” sign on xray and gasless colon typically w/in first 24hrs
1385
Tx of Acute Cholangitis:
Abx covering enteric bacteria | ERCP drainage w/in 24-48hrs
1386
What are common secondary causes of RLS?
``` Fe-def anemia Uremia – ESRD, CKD DM MS or Parkinson Pregnancy Drugs – antidepressants, metoclopramide ```
1387
Tx of RLS:
DA-agonists (Pramipexole, Ropinirole) are 1st line a-2-d calcium channel ligands (Gabapentin) may be preferred in pts w/comorbid insomnia, chronic pain syndrome or anxiety Opioids are last choice for refractory sxs
1388
What are the features of Medication overuse HA?
Near-daily HA in the setting of regular use of acute HA medications Occurs in pts w/a preexisting HA disorder (migraine) and sxs must be present for 3+ mos The pts underlying HA disorder may worsen or they may develop a new HA pattern Sxs frequently mimic tension-type or migraine-type HA and are commonly present upon awakening
1389
What are the feats. and tx of tissue-invasive CMV disease?
Mostly affects immunosuppressed, esp. after solid organ transplant Can cause: pneumonitis, gastroenteritis (w/hematochezia), hepatitis, and meningoenceohalitis Tx: dc any immunosuppressants and start anti-virals – IV ganciclovir for severe disease, oral valganciclovir for pts w/minimal signs
1390
What are the 2 ways to improve oxygenation in pts on ventilators?
Needs to be done in pts who have PaO2 <60: Increase PEEP – prevents alveolar collapse and decreases hypoxemia Increase FiO2 – delivers higher amounts of O2 to the lungs, but should be decreased to <60% as soon as possible
1391
What are the ways to improve ventilation in pts. on ventilators?
Should be done in pts w/high levels of PaCO2: Increase the respiratory rate Increase the tidal volume Both will increase the minute ventilation and decrease the PaCO2
1392
1st line therapy for pts w/RAS:
1st line for both unilateral and bilateral RAS is ACEIs or ARBs b/l RAS should only dc ACEIs if there is >30% increase in Cr after starting the Rx Revascularization should be avoided and only done in refractory cases
1393
Neurovascular injuries seen in supracondylar humeral fractures:
Most common pediatric elbow fracture – FOOSH w/elbow hyperextension Anterolateral displacement – radial n. injury Anteromedial displacement – brachial a. or median n. injury Posteromedial displacement (rare) – ulnar n. injury; happens w/fracture during elbow flexion
1394
Mgmt of acute v. chronic hyponatremia:
Acute (<48hrs) – poorly tolerated and pts at high risk for brain herniation. Pts w/ANY sxs of elevated ICP should get 3% NS boluses to rapidly correct serum Na+ (neural adaptations haven’t occurred at this point, so low risk of osmotic demyelination) Chronic (48+ hrs) – better tolerated so 3% NS is reserved for severe hyponatremia (<120), severe sxs, or concurrent intracranial pathology (mass, stroke, etc)
1395
What is the difference in pathology of the types of pHTN Systemic sclerosis can cause?
Primary paHTN d/t hyperplasia of the intimal sm. mm. of the pulm. aa. The lung parenchyma will be unaffected w/normal FEV1 and FEV1/FVC ratio as well as a normal CXR -This type is more common in the limited cutaneous type/CREST syndrome Secondary pHTN caused by ILD (alveolar spaces filled w/fibroblasts) may also occur and will present w/a restrictive pattern on spirometry and reticular opacities on CXR - More common in the diffuse cutaneous type
1396
First line tx of Idiopathic intracranial HTN:
Acetazolamide +/- Furosemide
1397
What are common PE and lab findings in vertebral osteomyelitis?
PE: Exquisite focal tenderness on percussion of affected spinous processes, increased muscle spasm and decreased ROM, +/- fever Labs: WBC count may be normal or elevated, BCx positive in majority of pts, ESR and CRP usually v. elevated
1398
What are some disorders that increase the risk of pediatric thromboembolic events?
Homocystinuria – presents w/Marfan habitus, fair complexion, developmental delay, lens dislocation, and hypercoagulability. Cystathionine synthase def. Fabry disease – presents w/angiokeratomas, peripheral neuropathy, asx corneal dystrophy, increased risk for renal and heart failure as well as thromboembolic events. a-Galactosidase def.
1399
What are the common lab findings in Hodgkin Lymphoma?
CBC and PBS are often completely normal, however Reed-Sternberg cells, when seen, are pathognomonic
1400
What is the only type of pathology that will cause increased breath sounds on auscultation?
``` Consolidation (lobar pneumonia) – will cause increased tactile fremitus as well as increased breath sounds seen as crackles and egophony present Everything else (pleural effusion, pneumothorax, emphysema, atelectasis, etc) will cause decreased or absent breath sounds and decreased tactile fremitus ```
1401
When should congenital fetal heart block be suspected?
In pts w/SLE or Sjogren syndrome w/anti-Ro (anti-SSA) Abs. | These may cross the placenta and cause heart block presenting as fetal bradycardia (<110) on NST.
1402
Tx and most common causes of acute bacterial rhinosinusitis:
1. Nontypeable H. influenzae (~50%) 2. S. pneumoniae (~25%) 3. Moxarella catarrhalis Tx: Amoxicillin +/- Clavulanate
1403
Bacteremia with what bacteria should prompt a screening colonoscopy?
Clostridium septicum – can cause bacteremia and acalculous cholecystitis Streptococcus bovis (group D strep.) – this should also prompt TTE d/t risk of IE These are both a/w colon cancer and when found should prompt screening colonoscopy
1404
What type of screening exams should be prompted after finding Candida bacteremia?
Ophthalmologic evaluation – even in asx pts bc it commonly causes fungal endophthalmitis
1405
What are the neurotropic effects of the Mumps virus?
Aseptic meningitis (norm benign) and sensorineural hearing loss (often transient but may lead to deafness)
1406
Common acid-base disturbance seen in Laxative abuse:
Metabolic alkalosis – unlike most other causes of diarrhea that cause metabolic acidosis Facticious diarrhea can also cause acidosis, but the finding of alkalosis in a pt. w/diarrhea should raise suspicion for laxative abuse
1407
What Rxs are known to increase Lithium levels?
ACEIs, NSAIDs, Tetracyclines, Metronidazole, Thiazides | + anything that decreases renal perfusion will decrease Li clearance and increase risk of toxicity.
1408
What are common causes of constrictive pericarditis?
``` Idiopathic pericarditis Prior cardiac surgery (CABG, valve surgery) Mediastinal irradiation TB Malignancy Uremia ```
1409
What will be seen on imaging of constrictive pericarditis?
Pericardial calcifications and thickening of the pericardium
1410
What is a pericardial knock?
Mid-diastolic sound heard in constrictive pericarditis
1411
How will pts likely present w/Constrictive pericarditis?
Fatigue and dyspnea on exertion Signs of RHF: peripheral edema, ascites, increased JVP, may have hepatic congestion and hypoalbuminemia May hear pericardial knock (middiastolic murmur) on auscultation Pulsus paradoxus, Kussmaul’s sign
1412
What causes Vasovagal syncope?
Abrupt PSNS activation leads to a cardioinhibitory response that manifests as bradycardia w/sinus arrest This causes abrupt decrease in cerebral perfusion leading to syncope
1413
What protein is coded for by the NF2 gene?
Merlin | NF1 tumor suppressor gene encodes protein neurofibromin
1414
What is retinitis pigmentosa?
Inherited degenerative disease of retinal photoreceptor cells that causes b/l tunnel vision and eventually binocular blindness usually begins w/night blindness and may lead to scotoma (central vision loss) a/w A-betalipoproteinemia Fundoscopy: bone spicule-shaped deposits around maucla
1415
What are the cxs of McCune Albright Syndrome?
It causes overproduction of all pituitary hormones: Peripheral precocious puberty (LH, FSH) Thyrotoxicosis (TSH) Acromegaly (GH) Cushing syndrome (ACTH) Recurrent fractures d/t polyostotic fibrous dysplasia
1416
What are the common features of Tick-Borne paralysis and how is it differentiated from GBS?
Progressive ascending paralysis over hrs-days; may be more localized/pronounced in one extremity Sensory exam is usually normal No fever or prodromal illness (GBS has this) CSF analysis is normal (contrast to GBS – high protein few cells) Caused by neurotoxin release from a tick, must feed for 4-7d before toxin release Search for and removal of tick results in improvement w/in an hr and complete recovery w/in days NO ANS dysfxn (tachycardia, urinary retention) like seen in GBS
1417
Sxs of GVHD:
Typically develop w/in 100d of transplant (bone marrow is highest risk) Maculopapular rash – can be painful and become confluent, may resemble SJS Profuse, watery diarrhea – secretory pattern (persistent, occurs at night, even when fasting) Liver inflammation – damage to biliary tract epithelium w/increased BR, ALP and transaminases
1418
How to differentiate HCCa caused by a Hepatic adenoma and Cirrhosis:
Hepatic adenomas rarely undergo malignant transformation, but when they do there is no associated decompensated liver failure bc only one small part of the liver has lost its fxn Cirrhosis caused HCCa will have liver failure bc the entire organ has been affected Both can have a palpable liver nodule and cause cachexia, anorexia, wt. loss, etc.
1419
At what gestational age do tocolytics become contraindicated?
34+ weeks At this point in time the risks of the tocolytics for the mother and fetus outweigh the risks of premature delivery Pts in preterm labor <37wks and >34 wks need steroids, abx, and delivery (route depends on status of fetus and mother) They are always contraindicated in PPROM though, if membranes rupture prior to onset of labor (regular contractions) they can’t be given
1420
What are the features of Stress-induced CMP?
Aka Takotsubo CMP/apical ballooning syndrome/broken heart syndrome Transient systolic dysfxn of apical/mid segments of the LV w/hyperkinesis of the basal segments Causes balloon-like appearance of the LV in systole Seen in older adults in response to intense physical/emotional stress or acute medical illness
1421
What is the only MEN syndrome that would cause parathyroid adenomas?
MEN1 | MEN2 only causes primary hyperparathyroidism by parathyroid hyperplasia, MEN1 can cause adenomas or hyperplasia
1422
What conditions should Succinylcholine be avoided in and why?
Succinylcholine is a depolarizing NM blocker and binds post-synaptic Ach-Rs to cause influx of Na+ and efflux of K+ Pts w/upregulation of Ach-Rs or who are already at risk for hyperkalemia should not receive this bc can cause cardiac arrhythmias Exs: Crush Injuries (rhabdo), Burn injury, Disuse muscle atrophy, denervation – stroke, GBS, critical illness polyneuropathy **use non-depolarizers for these pts (vecuronium, rocuronium)**
1423
What anesthetic can lead to adrenal insufficiency?
Etomidate – it inhibits 11B-hydroxylase
1424
What pts should Propofol be avoided in?
Those w/ventricular systolic dysfxn | It can cause severe HoTN d/t myocardial depression
1425
What would be seen on FHR tracing w/a nuchal cord?
Variable decels
1426
What would Benzene exposure cause?
Aplastic anemia d/t chromosomal breakage. | Benzene is found in solvents, polishes and gasoline
1427
Cxs of Severe Pancreatitis:
``` Severe acute pancreatitis = pancreatitis + 1 or more organ failure Pseudocyst Peripancreatic fluid collection Necrotizing pancreatitis ARDS GI bleeding Acute renal failure ```
1428
What is the mgmt. of CIN3?
If age >25 and not pregnant need immediate: Cone biopsy +/- LEEP and cryoablation Then need pap w/HPV test 1 and 2 yrs post-procedure
1429
What are the risks a/w Porphyria cutanea tarda?
``` HCV HIV Xs EtOH Estrogen use Smoking ```
1430
How will porphyria cutanea tarda present?
Mostly skin mainfestations – blisters, bullae and scarring on sun-exposed skin, increased skin fragility on the dorsal surfaces of the hands, and facial hypertrichosis May have hypo/hyperpigmentation Scarring and calcification similar to scleroderma Mild elevation of liver enzymes and Fe overload
1431
How would paraneoplastic myelopathy present?
It is lesion against the spinal cord and will present w/flaccid or spastic paraplegia or quadriplegia, sensory deficits +/- urinary or fecal retention/incontinence
1432
What is the most common cause of gastric MALTomas?
H. Pylori infection!!!! Causes 90% of tms All pts w/MALTomas should be tested for H. pylori and undergo eradication tx, for those w/early-stage, which causes most tms to go into complete remission *Sjogren and Hashimoto also increase risk of MALToma*
1433
What kind of cancers are pts. w/Pernicious anemia at risk for?
Gastric adenocarcinoma and gastric carcinoids | NO risk for MALTomas
1434
How will the UA differ in glomerular v. nonglomerular hematuria?
Glomerular have microscopic > gross hematuria and will have blood and protein on UA w/RBC casts and dysmorphic RBCs Nonglomerular have gross > micro hematuria and UA will have blood, no protein and normal appearing RBCs (non-glomerular is more common)
1435
Most common causes of nonglomerular hematuria:
``` Nephrolithiasis Cancer (RCCa, prostate) PCKD Infection – cystitis Papillary necrosis ```
1436
Common causes of renal papillary necrosis:
``` Mnemonic: NSAID NSAIDs Sickle cell Analgesic abuse (long-term abuse) Infection (pyelo) Diabetes ```
1437
What characteristic of CF bronchiectasis helps differentiate it from other causes?
Upper lung lobe involvement – CF is the main cause of bronchiectasis involving the upper lobes Infection w/Pseudomonas is also characteristic
1438
Mothers with what blood types are capable of causing a neonatal ABO incompatibility?
A (against baby B or AB blood), B (against A or AB), or O (against everything) AB mothers have no Abs against the other bloodtypes and will not cause hemolysis
1439
What are the common presenting features of Thyroid lymphoma?
Mostly occurs in pts w/Hashimoto and high anti-TPO Abs Rapidly progressive thyroid enlargement +/- mild tenderness, hoarseness and dysphagia Retrosternal extension is common and compresses surrounding vasculature – get JVD, and facial plethora, worse w/raising the arms. B sxs may also be present – night sweats, fatigue, wt. loss, fever
1440
What might be seen on imaging in a mitral stenosis?
EKG – “p mitrale” (broad, notched P waves), atrial tachyarrhythmias (aFib), RVH (tall R waves in V1 and V2) Echo – MV thickening and calcification, decreased mobility and coexisting MR
1441
What test should be done to diagnose suspected tracheobronchial ruptures?
Bronchoscopy CT scan can detect large injuries but misses small tears Most pts require surgery
1442
What are the sxs of Trochanteric bursitis?
Unilateral hip pain that is worse w/external pressure to the upper lateral thigh (like when you sleep on your side) external rotation and with resisted hip abduction
1443
What bugs should be suspected when urine pH is >8?
Urease producing: Proteus (most common) and Klebsiella
1444
What is the recommended workup for a thyroid nodule?
First get TSH levels Low – do RAI scan low uptake requires further workup (FNA, US) high uptake just tx hyperthyroidism High or Normal – do US and consider FNA based on the findings
1445
What are common precipitants of recurrent episodes of Herpes simplex keratitis?
Excessive sun exposure/outdoor occupation, fever or immunodeficiency
1446
How should oligohydramnios be managed in late and post-term pregnancies?
Oligohydramnios or a non-reactive NST individually are indications for immediate delivery Position of fetus, and status of it and the mother determine method – vag v c-section
1447
How to differentiate sepsis/infection post liver-transplant and acute rejection:
Infection is more likely to cause rapid-onset hemodynamic instability, high fever and significant leukocytosis Rejection occurs <90d post-transplant and will cause fever, RUQ pain, and elevation in liver fxn tests but leukocytosis and rapid hemodynamic instability are less common
1448
Timeline of infections post-liver transplant:
<1mo: Bacteria from op-cxs (hepatic abscess, biliary leak, wound infection) or hospitalization (catheter, external drain) Months 1-6: Opportunistic pathogens (CMV, Aspergillus, TB) >6mo: Immunosuppressants at lower doses so typical community acquired infections most common
1449
What is ventricular remodeling and what can prevent it post-MI?
Remodeling gradually causes dilatation of the LV w/thinning of the ventricular walls. Get globular shaped LV Prevent w/ACEIs started w/in 24hrs of an MI
1450
What are the common presenting features of Gaucher disease?
Onset may be delayed and present in mid-late adolescents Bone marrow infiltration – anemia and thrombocytopenia Splenomegaly – typically severe and more prominent than hepatomegaly Bony pains d/t skeletal involvement – often mistaken for “growing pains” May have osteopenia and pathologic fractures following minimal trauma Failure to thrive – height and weight <5th percentile Delayed puberty (tanner stage I in a 16yo)
1451
How will an infant w/posterior urethral valves present?
In the neonatal period with decreased/absent urine output Distended abdomen and weight gain (rather than the normal loss) d/t retained urine Postnatal respiratory distress d/t lung hypoplasia from oligohydramnios in utero Often missed in those who don’t follow-up prenatal care
1452
Most common causes of Duodenal ulcers:
H. pylori | NSAIDs
1453
What causes the myopathy a/w Cushing syndrome?
Catabolic effects on skeletal muscle which leads to muscle atrophy Get progressive proximal mm. weakness and atrophy w/o pain. LE more involved ESR and CRP will be normal
1454
What diseases will have a decreased absorption of D-xylose?
Small intestinal mucosal disease (Celiac) | malabsorption d/t enzyme deficiencies will have normal absorption (CF, lactose)
1455
What is the inheritance pattern and comorbidities a/w Myotonic dystrophy?
AD inheritance of trinucleotide repeat (CTG) Comorbidities: arrhythmias, cataracts, balding, testicular atrophy/infertility Presentation: onset 12-30; facial weakness, hand grip myotonia, dysphagia (risk of aspiration pneumonia). May have ptosis, frontal balding, and generalized muscle wasting
1456
Common causes of adrenal hemorrhage:
Pts on anticoagulants w/acute stress (sepsis) | Hemorrhagic necrosis w/systemic infections: meningococcemia or pseudomonas sepsis
1457
What causes adrenoleukodystrophy?
Accumulation of VLCFAs within the adrenal glands leads to adrenal insufficiency Only affects males, females are carriers
1458
What electrolyte disturbances are seen in refeeding syndrome?
Increased insulin occurs d/t carbohydrate ingestion (IV or enteral) This causes increased cellular uptake and decreased serum levels of: K+, PO4, Mg2+, and Thiamine Phosphate is the primary deficient electrolyte bc its needed to make ATP Deficiencies in Mg2+ and K+ cause cardiac arrhythmias Thiamine deficiency causes Wernicke Aggressive nutrition w/o adequate electrolyte replacement – cardiopulmonary failure
1459
Lab/Imaging findings in ILD:
CXR – reticular/nodular opacities CT – fibrosis, honeycombing, traction bronchiectasis PFTs – normal or increased FEV1/FVC, decreased DLCO, decreased TLC, decreased RV Resting ABG – normal or mild hypoxemia; Exertion will cause significant hypoxemia V/Q mismatch and Increased A-a gradient
1460
What is Miller-Fisher syndrome and how will it present?
It is a variant of GBS and will also present post-infection w/the same organisms It is d/t Anti-Gq1b Abs (highly sensitive for MFS) that attack peripheral nerves Will cause rapid-onset ophthalmoplegia, diplopia, ptosis, cerebellar-like ataxia (dysmetria) and areflexia Ophtho signs may be unilateral with the areflexia and extremity weakness bilateral Paralysis is less common in MFS than classic GBS CSF analysis and mgmt. are the same as classic GBS
1461
What would cause decreased or absent response to vaccination in an adult?
CVID
1462
Who is most at risk for CA-MRSA and how is it tx’d?
CA-MRSA preferentially attacks young patients w/influenza – severe, destructive, secondary necrotizing pneumonia Often causes leukopenia instead of leukocytosis Most pts need to be tx’d in the ICU w/IV abx – Vancomycin or Linezolid
1463
What are common abx used for anaerobe coverage (esp. in aspiration pneumonia)?
Clindamycin Metronidazole + Amoxicillin (high failure when metro is used as monotx) Amoxicillin + Clavulanate Carbapenems
1464
How to differentiate Tabes Dorsalis from Subacute Combined Degeneration:
Both affect dorsal columns – sensory ataxia from decreased proprioception and vibration sense w/+Romberg Tabes dorsalis – Argyll robinson pupils + nerve root involvement: decreased Pain/T and hypo/areflexia SACD – lateral corticospinal tract involvement: spastic paresis and hyperreflexia
1465
How to tell cauda equina and conus medullaris syndromes apart:
Cauda equina – asymmetric motor weakness, hypo/areflexia and b/l severe radicular pain Conus medullaris – symmetric motor weakness, hyperreflexia and sudden-onset severe back pain **contrast both to Spinal cord compression when there is typically no pain and numbness can begin higher up – umbilical area, etc.**
1466
What Rxs are contraindicated or should be avoided in pts w/RVMI?
Nitrates – decrease RV preload and cause profound HoTN and cardiogenic shock Diuretics – volume depletion and HoTN Opiates – venous dilation and decreased RV preload BBs – sometimes appropriate, but contraindicated in pts w/bradycardia or cardiogenic shock
1467
When should amyloid cardiomyopathy be suspected?
In pts w/unexplained CHF, proteinuria (>300mg/d), and LV hypertrophy w/o hx of HTN This is a cause of restrictive CMP and RHF sxs seem to predominate Echo: concentric LV hypertrophy, nondilated LV cavity, LA enlargement and preserved EF Other sxs: anemia, thrombocytopenia, hepatomegaly, thickened skin, peripheral neuropathy
1468
Difference in mgmt. of hernias:
All symptomatic hernias should undergo surgical resection Asx femoral hernias – elective surgical resection (high risk of incarceration and strangulation) Asx inguinal hernias – can be reassured and observed (low risk of incarceration)
1469
Mgmt of hepatic adenomas:
asx and <5cm – stop OCPs | Sxs or >5cm – surgical resection
1470
What are common lab findings in Wilson disease and how is it tx’d?
Increased AST and ALT only may occur – w/AST being almost 2x higher than ALT ALP, BR, and GGT may all be completely normal Tx: Chelators – D-penicillamine, trientine; Zinc – will interfere w/Cu absorption
1471
How will CNS tms manifest based on their location?
Supratentorial: Increased ICP, weakness, sensory changes, and seizures - Astrocytoma, Glioblastoma, Craniopharyngioma ``` Posterior fossa (infratentorial): Increased ICP, cerebellar dysfxn – dysmetria, ataxia, clumsiness - Astrocytoma, Ependymoma, Medulloblastoma ``` Brainstem: ataxia, clumsiness, CN palsies Spinal cord: back pain, weakness, abnormal gait - Ependymoma (much less common than post. fossa)
1472
What are the most common posterior fossa tms in children and what structures do they arise from?
``` #1 – Ependymoma: arises from the ependymal cell lining of the ventricles and spinal cord. #2 – Medulloblastoma: arises from the cerebellar vermis ```
1473
What causes Meniere’s disease?
Elevated endolymphatic pressure and volume, likely d/t defective resorption of endolymph Sxs: low-freq tinnitus in affected ear, episodic vertigo (may have N/V, lightheaded), sensorineural hearing loss in affected ear
1474
Most common cause of urethritis in men:
Gonococcus – contrast to chalmydia being most common in women
1475
Tx of bacterial vaginosis:
Metronidazole or Clindamycin (topical or oral)
1476
What are the sxs of an uncal herniation?
Compression of contralat. crus cerebri – ipsilateral hemiparesis (same side of hemorrhage) Compression of CN III – mydriasis (early), ptosis and down-n-out gaze (late) of ipsilateral eye Compression of PCA – contralateral homonymous hemianopsia (opposite eye of CN III defects) Compression of reticular formation – altered level of consciousness, coma **seen in basal ganglia hemorrhages 2/2 HTN and epidural hematomas**
1477
What should be suspected in Non-pupil sparing CN III palsies?
Non-pupil sparing palsies are most often caused by mass effect. They should be assumed to be d/t aneurysm until proven otherwise and need immediate MRA or CTA of the head Pupil-sparing (doesn’t affect the PSNS fibers on the outside of the n., only motor in the center) Are most often d/t microvascular ischemia – DM, HTN. HLD, advanced age. These can be observed in most cases and worked up by risk factors
1478
Abnormal proliferation of what type of cells leads to epithelial ovarian ca.?
It can be d/t abnormal proliferation of: ovarian, fallopian/tubal, or peritoneal cells. All three will cause lg. ovarian tm. causing ascites and solid mass w/thick septations on US
1479
How will Phenytoin toxicity present?
Acute toxicity: signs of cerebellar dysfxn – horizontal nystagmus, ataxia/wide-based gait, dysmetria, slurred speech, paresis; N/V and hyperreflexia Severe toxicity: AMS (lethargy, confusion), coma, paradoxical seizures (unlike most anti-epileptic toxicities), and death Rapid phenytoin infusion can also result in HoTN and bradyarrhythmias **susceptible to toxicity in renal or hepatic dysfxn or when taken w/Valproate, and Rxs that inhibit CYP-450**
1480
What will be seen on echo in LV aneurysm?
Thin and dyskinetic myocardial wall