STEP 2 Flashcards

1
Q

Bacterial Prostetitis- symptoms- diagnosis- treatment

A

Sypmtoms: Fever, chills, myalgia, pelvic pain (diffuse) Diagnosis: Pyuria, tender prostate, urine cultures + E.coli. Mid-stream urine sampleTreatment: TPM-SMX or fluoroquinolones

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2
Q

Adjustment Disorder

  • Etiology
  • Treatment
A

Caused by an identifiable stressor, within the past 3 monthsRarely lasts more than 6 monthsTreatment: Cognitive or psychodynamic psychotherapy

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3
Q

Anorexia Nervosa vs. Bulimia

A

Anorexia nervosa - Clinical BMI

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4
Q

Reye Syndrome

  • Epidemiology
  • Presentation
  • Blood Labs
A

Children

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5
Q

Trisomy 18- MSAFP- beta-hCG- Estriol- Inhibin A

A

LOW MSAFP- LOW beta-hCG- LOW Estriol- NORMAL Inhibin A

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6
Q

Trisomy 21- MSAFP- beta-hCG- Estriol- Inhibin A

A

LOW MSAFP- HIGH beta-hCG- LOW Estriol- HIGH Inhibin A

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7
Q

Neural Tube or Abdominal wall defect- MSAFP- beta-hCG- Estriol- Inhibin A

A

HIGH MSAFP- NORMAL beta-hCG- NORMAL Estriol- NORMAL Inhibin A

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8
Q

Postpartum blood loss- Etiology (most common)- Treatment

A

Etiology - Uterine AtoniaTreat- bimanual uterine massage, fluid resuscitation, uterine atonic agents: oxytocin, methylergometrine, carboprost

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9
Q

Uremia- Blood concentration causing symptoms- Complication and treatment

A

Symptoms appear at level of 100mg/dL- uremic encephalopathy = indication for hemodialysis

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10
Q

Mitral Stenosis- Auscultation

A

Auscultation: S1 loud, opening snap after S2 @ apex, low pitched diastolic rumble @ apex

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11
Q

Torticollis- epidemiology- presentation- What (lab, scan, procedure) do you order on this patient?

A
  • common condition in children- upper respiratory infection, minor trauma, cervical lymphadenitis, retropharyngeal abscess- x-rays must be obtained
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12
Q

Beta 2 Adrenoceptors- what drug acts on this receptor AND stimulates the release of a metabolic hormone

A

Albuterol - cause release of insulin via activation of beta cells in pancreas

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13
Q

Scaphoid bone fracture- define displaced vs. non-displaced- treatment for each

A

Non-displaced fracture = wrist immobilization

Displaced fracture = surgery

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14
Q

Minimal change disease- pathogenesis

A

Pathogenesis: T-cell mediated injury to podocytes

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15
Q

Acute coronary syndrome- atypical presentation- what lab/scan/procedure do you order?

A

atypical presentation = abdominal pain, nausea, vomiting = women, ELDERLY, diabetes, hx of smokingorder ECG

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16
Q

For Chlamydia and Gonorrhoeae- treatment when nucleic acid amplification test +/– treatment when gram stain +/-

A

if nucleic acid amplification test (+) you don’t have to treat for both if only (+) for 1but if a gram stain (+) for 1 then treat for both

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17
Q

Legionnaires Disease- Presentation- Labs

A

atypical community acquired pneumonia also you get diarrhealabs: hyponatremia, hepatic dysfunction, hematuria, proteinuria, neutrophils, no organisms in sputum stain

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18
Q

Jervell-Lange-Nielsen Syndrome- Genetics- History- Presentation

A

Autosomal recessive, pt. hx, family hx, sudden death, congenital sensorineural deafness, QT prolongation

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19
Q

In elderly pts w/anemia taking NSAIDS or aspirin- Etiology of anemia

A

most common cause = iron deficiency anemia from blood loss in GI tract

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20
Q

Sarcoidosis- Epidemiology - Presentation

A

Most common African American woman 3rd and 4th decade life. Most common effects lungs hilar adenopathy and reticular opacities xray.Symptomatic cough, erythema nodosum, ANTERIOR UVEITIS, and arthritis.

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21
Q

Kleptomania

A

Rare impulse control theft were stolen items have no value or use to the person.Treatment Cognitive behavioral psychotherapy

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22
Q

Syringomyelia- Definition- Associated w/ other disease- Presentation

A

Fluid filled cavity located within the cervical and thoracic spinal cord. Associated with Arnold Chairi malformationtype (1). Presents areflexic weakness in the upper extremities and dissociated sensory loss following a “cape”distribution.

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23
Q

Cyanide toxicity- Occurs in patients treated with too much _________- Or patients who can’t clear that drug because they have this problem _________- How does the drug turn into cyanide?- Presentation

A

Can occur in patients treated with nitroprusside who receive prolonged infusions, higher doses or have underlyingrenal insufficiency. Metabolism nitroprusside releases nitric oxide and cyanide. Cyanide causes altered mental status,lactic acidosis, seizures, and coma.

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24
Q

Chronic Granulomatous disease:- Pathogenesis- Diagnosis

A

Dysfunction of phagocytic cells NADPH oxidase enzyme complex. Diagnosis is made by nitroblue tetrazolium (NBT)slide test.

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25
Wiskott-Aldrich syndrome (WAS):- Etiology- Presentation- Labs
X-linked recessive. Defect in Wiskott-Aldrich syndrome protein (WASP). Presentation: young boy with eczema, thrombocytopenia, and recurrent infections with encapsulated organisms. At birth may have petechiae, bruises, bleeding from circumcision. or bloody stools. Low IgM, high IgA, and IgE levels. Poor response to polysaccharide antigens, and moderately reduced T-cells and platelets.
26
Chediak-Higashi syndrome:- Labs- Presentation
Characterized by decreased degranulation, chemotaxis, and granulopoiesis. Partial oculocutaneous albinism,neuropathy, hepatosplenomegaly, pancytopenia. Labs neutropenia, and giant lysosomes confirm diagnosis.
27
Leukocyte adhesion defect (LAD):- Pathogenesis- Pathology- Presentation
Defective tethering, adhesion, and targeting of myeloid leukocytes to sites of microbial invasion. Neutrophilia without PMNs in pus. Loss of baby and adult teeth.
28
Hyper- IGE (Job’s) syndrome:- Presentation- Labs
Chronic pruritus dermatitis, recurrent staph infections, elevated IgE levels, eosinophilia and coarse facial features.
29
Chronic Hepatitis B: - Best treatment
Treatment of choice: Tenofovir and then Entecavir.
30
Hepatitis C- Treatment
Treatment: Pegylated interferon plus ribavirin
31
Systemic Lupus erythematosus (SLE):- Pathogenesis of pancytopenia
SLE can cause pancytopenia due to concurrent peripheral immune-mediated destruction of all 3 cell lines.
32
Management of Psychosis:
Second generation antipsychotics such as quetiapine, risperidone, olanzapine, aripiprazole, ziprasidone, andpaliperidone. Clozapine is a second generation antipsychotic that is considered the gold standard treatment for treatment resistantschizophrenia. Cause agranulocytosis.
33
Acute abnormal uterine bleeding:- If patient is stable, what is the first line treatment?
If stable first line treatment is hormonal medication high dose estrogen (conjugated equine estrogen).
34
Cystic fibrosis- Describe the pathophysiology leading to excess bleeding in these patients
Fat malabsorption common leading to vitamin K deficiency. Leads to deficiency in coagulation factors II, VII, IX, andX. also C and S. 1972
35
Lichen sclerosus(lichen sclerosus et atrophicus, LS & A): Define- Epidemiology- Presentation- Physical exam findings- Labs/scans/tests- Treatment
Chronic inflammatory condition of the anogenital region that most commonly affects postmenopausal women andmanifests with vulvar pruritus and discomfort. Exam shows porcelain white atrophic. Must obtain biopsy to R/O vulvar SCC. Treatment is high potency topical corticosteroids.
36
Aortic dissection- Classic presentation- Highest risk factor
Causes chest pain that classically described as sudden, tearing, and radiating to the back. Hypertension is the mostcommon predisposing factor.
37
Acute Respiratory Distress Syndrome (ARDS):- Can be a complication of acute ________- Pathogenesis of ARDS caused by acute _______
Can be caused by acute pancreatitis with increase in serum phospholipase A2 from pancreas. This enzyme leaks intoalveoli and damages surfactant.
38
Wiskott-Aldrich syndrome:- Characterized by a triad of signs & symptoms
Characterized by triad of thrombocytopenia seen in over 90% of patients at diagnosis, eczema, and recurrentinfections.
39
Mid Cycle pain (mittelschmerz):- Presentation- What causes the pain?
Abdominal pain in a young female in the middle of her cycle with a benign history and clinical examination. The painis due to ovulation itself and tends to occur on the side that produces the mature ovum.
40
Duodenal ulcer disease/Peptic ulcer disease:- How does the pain react to eating?- How many % have H.pylori?- Treatment
Epigastric pain relieved with eating as food causes alkali solution to released into the duodenum. Over 90 have H.pylori. Treatment omeprazole and antibiotics amoxicillin plus clarithromycin.
41
Gastric Ulcers- How does the pain react to eating?
Pain is worse with eating
42
Physiologic shunting (V/Q mismatch):- Auscultation- Physical exam = Effect on oxygen saturation with consolidated left lobe hypothetically
Normal upright person ventilation and perfusion greatest at the lung bases and least at apices. In a consolidated leftlobe. A patient will become hypoxic when lying on left side, but have normal O2 sats when lying on right because ofthis principle.
43
Viral Arthritis- Presentation- Labs- Treatment
Presents with symmetric small joint inflammatory arthritis. Distinguished by that fact it tends to resolve within twomonths. Positive inflammatory markers such as ANA and rheumatoid factor may occur. Treatment NSAIDS.
44
Diabetic foot ulcer- Risk factor (most important)- Physical exam
Risk factors diabetic neuropathy is most important contributing factor and can be accessed using a 10g monofilament.Ankle-brachial index (ABI) primarily a measure of large vessel PAD.
45
Renal artery stenosis- Triad of signs/symptoms
Systolic-diastolic abdominal bruit in a patient with hypertension and atherosclerosis is strongly suggestive.
46
Osteomalacia- Pathogenesis- Can be caused by this disease ________- Labs
Due to defective mineralization of organic bone matrix. Can be caused by celiac sprue. Labs show elevated alkalinephosphatase, elevated PTH, hypophosphatemia and hypocalcemia.
47
Emphysematous cholecystitis:- Epidemiology- Pathogenesis
Common form of acute cholecystitis in elderly diabetic males. It arises due to infection of gallbladder wall with gas-forming bacteria.
48
Paget’s disease of the breast:- Presentation- Histopathology
No prior history of skin disease who presents with eczematous rash near the nipple that does not improve with topicaltreatments. Most have underlying adenocarcinoma which show large cells surrounded by a halo-like area.
49
Beta blocker overdose- Presentation- Complications- Treatments
Presents with bradycardia, hypotension, wheezing, hypoglycemia, delirium, seizures, and cardiogenic shock.Intravenous fluids and atropine are first line treatment options. Intravenous glucagon should beadministered in patients with profound or refractory hypotension.
50
Hereditary telangiectasia (Osler-Weber-Rendu syndrome):- Genetics- Pathology- Pathophysiology- Presentation
Autosomal dominant disorder. Characterized by diffuse telangiectasia, recurrent epistaxis, and widespread AVmalformations (AVM). AVM in lungs cause shunt of blood right to left side of heart, leading to chronic hypoxia andreactive polycythemia. Digital clubbing. Possible fatal hemoptysis with recurrent nose bleeds and oral lesions.
51
Chronic myelogenous leukemia (CML):- Genetics- Pathophysiology- Describe leukocyte alkaline phosphatase activity
Low levels of leukocyte alkaline phosphatase (LAP) activity due to abnormal fusion gene t(9;22) (BCR/ABL1) causesdysregulation of tyrosine kinase activity. Leads to decreased apoptosis of myeloid cells and they accumulate highnumbers. They are functionally inactive, so low LAP activity.
52
Primary dysmenorrhea:- Pathophysiology- Treatment
Examination is normal and pain is during the first few days of menses. Pain pathophysiology release of prostaglandinsfrom endometrium causes uterine contractions. Treatment NSAIDS.
53
Cirrhosis- Etiology (most common)
Chronic alcohol abuse and viral hepatitis ( think B and C infection) are the most common underlying cause of cirrhosis.
54
Primary adrenal insufficiency:- Most common Etiology- Cortisol high or low?- ACTH high or low?- Aldosterone high or low?
Most common cause Autoimmune. Cortisol = decreased; ACTH = increased; Aldosterone = decreased
55
Secondary adrenal insufficiency:- Most common Etiology- Cortisol high or low?- ACTH high or low?- Aldosterone high or low?
Most common cause chronic glucocorticoid therapy. Cortisol = decreased; ACTH = decreased; Aldosterone = Normal
56
Lyme disease- Treatment in young children and pregnant/lactating women- Treatment in normal people
Oral amoxicillin is treatment of choice in pregnant and lactating women as well as children age
57
Aspirin-exacerbated respiratory disease (AERD):- Epidemiology- Pathogenesis- Treatment
Seen patients with history of asthmatic or chronic rhinosinusitis with nasal polyposis. Non-IgE mediated reaction thatresults from aspirin induced prostaglandin/leukotriene misbalance. Treatment stop NSAIDS use leukotriene antagonistmontelukast.
58
Acute cardiac tamponade:- Etiology - Presentation- chest x-ray findings
Patient presents with hypotension (UNRESPONSIVE to IV FLUID bolus), tachycardia, and elevated jugular pressure after blunt thoracic trauma. Only takes 100-200mL of fluid, so chest X-ray can sometimes be normal.
59
Criteria for HIV patient vaccinations:- MMR?- Contraindications?
Patients with HIV should receive vaccination for MMR if their CD4 cell count is >200/uL, they have no history ofAIDS-defining illness, and they have no evidence of immunity.Lack of current ART is not a contraindication.Otherwise all other live vaccines are contraindicated.
60
Bacterial sinusitis- Biggest risk factor
The most common predisposing factor for acute bacterial sinusitis is a viral respiratory infection.
61
Primary CNS lymphoma:- Epidemiology- Presentation- Labs, CSF, MRI
Suspect primary CNS lymphoma in an HIV-infected patient with an altered mental status, ((EBV DNA in the CSF)), and asolitary, weakly ring-enhancing periventricular mass on MRI.
62
Viral conjunctivitis- Treatment
Self-limited condition associated with adenovirus and other URI. Treat symptomatic with COOL, MOIST COMPRESSES.
63
Antithyroid drugs propylthiouracil (PTU) and methimazole (MMI):- Complication- Presentation of complication- Treatment- Labs
Can cause agranulocytosis: Patient will complain of fever and sore throat. STOP MEDICATIONS IMMEDIATELY. Recheck WBC count.
64
Chronic beclomethasone use in asthma:- most common adverse effect
Most common adverse effect of inhaled corticosteroid therapy is oropharyngeal thrush.
65
Uterine fibroids- Diagnosis
Work up: Pelvic ultrasound is the prefered initial imaging modality for suspected gynecological tumors. It has a highsensitivity for diagnosing uterine fibroids and ovarian pathology.
66
Brain death- Define- Legal authority
Brain death refers to a total loss of brain function and is legally acceptable definition of death. Family permission is not legally required to discontinue mechanical ventilation in a patient with brain death.
67
Acute coronary syndrome:- How can lidocaine affect the heart?
Although it can decrease the risk of ventricular fibrillation, it may increase the risk of asystole.
68
Glascow Coma scale:- Is determined by measuring what?
Eye Opening; Verbal Response; Motor Response.
69
Endometriosis- Fertility prognosis
At increased risk of impaired fertility or infertility due to chronic inflammation and adhesion formation.
70
Endometriosis- Treatment- Diagnosis (when to diagnose?)
Laparoscopy with visualization and biopsy of implants is the only definitive way to diagnose endometriosis. It isindicated when NSAIDS and hormonal contraceptive therapy have failed.
71
Atypical antipsychotics:- side effects- treatment of side effects
Example: risperidone can cause extrapyramidal side effects and can be treated with anticholinergic medication likebenztropine.
72
Acute pharyngitis children and adolescent:- Diagnosis (gold standard)
Diagnose with rapid streptococcal antigen test (RAST) or throat culture which is gold standard. Antistreptolysin Oantibody is useless for acute infection because antibodies do not present for one month.
73
Premature ovarian failure:- Presentation- Diagnosis - FSH/LH ratio - FSH & LH up or down - Estrogen up or down
Women under age 40 with elevation in FSH for greater than or equal to 3 months of amenorrhea. FSH increased; LH increased; FSH/LH ratio >1.0; estrogen decreased.
74
Anterior cerebral artery stroke:- Presentation
Characterized by contralateral motor or sensory deficits, which are more pronounced in the lower limb than the upperlimb. Urinary incontinence can also be seen occassionaly.
75
What bone problems do immobilized patients have? | What's the treatment?
With high bone turnover as seen in young people and Paget's disease can have increased osteoclast activity leadingto hypercalcemia. Hydration and bisphosphonates are effective treatments.
76
Osteoarthritis 3 criteria
In the setting of knee pain: age >50; crepitus; bony enlargement, bony tenderness, and a lack of warmth/morning stiffness. If three criteria met specificity is 69%.
77
Statin medication recommendation:
Primary prevention in patients age 40-75 with a 10-year risk of atherosclerotic disease ≥7.5%.
78
Anticholinergic toxicity: - Presentation - Common causes
Classic findings are dry skin, dry mouth, constipation, urinary retention, flushing, vision change, and confusion. Often seen in the treatment of Parkinson disease due to treatment of EPS. Trihexyphenidyl and bromocriptine are common culprits.
79
Cushing syndrome:
High- dose dexamethasone does not suppress plasma cortisol levels in patients with ectopic ACTH syndrome.
80
Cushing's Disease
ACTH-producing pituitary adenoma. Partially inhibited by high- dose dexamethasone.
81
Potassium sparing diuretics:
triamterene and amiloride
82
Ascites treatment
``` 1. Sodium and water restriction. 2. Spironolactone. 3. Loop diuretics (not more than 1L/day of diuresis) 4. Frequent abdominal paracentesis (2-4 L/day, as long as the renal function is okay) ```
83
“Fight bite”:
Clenched fist injury to hand from person fist hits opponents teeth. Treatment of choice for prophylaxis is amoxicillin-clavulanate since infection is usually polymicrobial. Also used for dog bites.
84
Stress test for CAD:
Beta blockers, calcium channel blockers, and nitrates are antianginal agents that are healed 48 before performing a cardiac stress test.
85
Systemic lupus erythematosus (SLE) vs. preeclampsia
Hypertension in a pregnant female in the setting of massive proteinuria, malar rash, and a strongly positive ANA titer is most likely due to SLE. Glomerulonephritis in general will cause proteinuria, hematuria, and RBC casts. Not to be confused with what occurs in preeclampsia.
86
Waldenstrom’s macroglobulinemia: - Blood viscosity - Associated Ig - Diagnosis
Characterized by hyperviscosity of blood owing to the excess production of IgM. Two important diagnostic clues: 1. An IgM spike on electrophoresis 2. hyperviscosity.
87
Multiple myeloma: - Blood viscosity - Associated Ig
Immunoglobulins are usually IgG or IgA. No hyperviscosity.
88
Medications that cause cholestasis:
chlorpromazine, nitrofurantoin, erythromycin, anabolic steroids
89
Medications that cause fatty liver:
tetracycline, valproate, and antiretrovirals
90
Medications that cause hepatitis:
halothane, phenytoin, isoniazid, and alpha-methyldopa
91
Medications that cause toxic or fulminant liver failure:
carbon tetrachloride and acetaminophen
92
Medications that cause granulomatous liver:
allopurinol and phenylbutazone
93
Molluscum contagiosum: - Etiology - Epidemiology
Caused by Pox virus. Commonly seen in patient who have CELLULAR IMMUNODEFICIENCY such as HIV and patients on corticosteroids or chemotherapy.
94
Homocystinuria: - Genetics - Presentation
MARFANOID BODY HABITUS that is autosomal recessive. INTELLECTUAL DISABILITY, FAIR complexion, CEREBROVASCULAR ACCIDENTS, megaloblastic anemia, and thrombosis.
95
Fabry disease (α-galactosidase deficiency): - Triad presentation - Complication
Characterized by angiokeratomas, peripheral neuropathy, and asymptomatic corneal dystrophy. At risk for thromboembolic event.
96
Krabbe disease: - Genetics - Pathogenesis - Presentation
Autosomal recessive lysosomal storage disorder caused by galactocerebrosidase deficiency. Clinical features intellectual disability, blindness, deafness, paralysis, neuropathy, and seizures.
97
Phenylketonuria: - Etiology - Pathogenesis - Presentation
Inborn error of metabolism that results from a deficiency of phenylalanine hydroxylase. Clinical features intellectual disability, fair complexion, eczema, and a musty body odor.
98
Tay-Sachs disease: - Etiology - Pathogenesis - Presentation
Autosomal recessive gangliosidosis caused by a deficiency of β-hexosaminidase A. Clinical features intellectual disability, weakness, seizures, and presence of a cherry- red macula on examination.
99
Gestational diabetes mellitus: - Screening done when? - Target glucose levels @ 1 and 2 hours - First line treatment - Second line treatment
Screen weeks 24-28. Target blood glucose levels: Fasting ≤95 mg/dL; 1-hour postprandial ≤140 mg/dL; 2-hour postprandial ≤120 mg/dL. First line treatment: dietary modification; Second line treatment: Insulin, oral agents (metformin, glyburide)
100
Gestational diabetes mellitus newborn risks
Polycythemia (hct >65%), hyperviscosity, organomegaly, macrosomia, hypoglycemia
101
Panic disorder: - Comorbidities - Treatment
Comorbidities include MAJOR DEPRESSION, agoraphobia, bipolar disorder, and substance abuse. Higher rates of suicide attempts. Tx: SSRI
102
Fibromuscular dysplasia: - Pathology - Presentation
Noninflammatory and nonsclerotic condition primarily effectting renal arteries causing hypertension. Can affect carotid and vertebral with TIA like symptoms. Can hear carotid bruit.
103
Acute decompensated heart failure (ADHF): - Presentation - Treatment
Presents with acute pulmonary edema. Tx: Oxygen, assisted ventilation, aggressive intravenous diuresis (furosemide), and possible vasodilator therapy.
104
Unilateral cervical lymphadenitis: - Epidemiology - Etiology - Treatment
Acute, unilateral cervical adenitis in children is typically caused by streptococcal or staphylococcal infection. The treatment consists of clindamycin plus incision and drainage.
105
Torsades de pointes (TdP): - Define - Treatment
Polymorphic ventricular tachycardia that occurs in the setting of congenital or acquired prolonged QT interval. Tx: Immediate defibrillation is indicated in hemodynamically unstable patients with TdP, while intravenous magnesium is the first-line therapy for stable patients with recurrent episodes of TdP.
106
Acute type A aortic dissection: - Diagnosis - Treatment
Must get a TEE, so you can rapidly diagnose and treat. Surgical emergency!
107
Single photon emission CT scan:
Tool to evaluate CAD and indicates inducible ischemia when a reversible defect is noted on stress and rest. Antiplatelet therapy, beta blockers, and life style modification.
108
Insulinoma:
Beta cell tumor: elevated levels of insulin, c-peptide, and proinsulin.
109
Parapneumonic effusions:
When the pH of the pleural fluid is less than 7.2, the probability is very high that this is an empyema and must be drained.
110
Metronidazole:
Should not drink alcohol because of disulfiram-like reaction.
111
Somatic symptom disorder:
Involve one or more somatic complaints (including pain) that are distressing or result in significant disruption of life, with excessive thoughts, feelings, or behaviors related to these symptoms and lasting ≥6 months.
112
Vitamin D Toxicity - Etiology - Presentation
Toxicity mainly due to hypercalcemia and includes constipation, abdominal pain, polyuria, and polydipsia.
113
Pneumonia pathophysiology oxygen exchange:
Hypoxia in pneumonia causes areas of V/Q mismatch that manifests as increase in the alveolar-arterial oxygen gradient.
114
Daughters of women who took diethylstilbestrol during pregnancy: - Risks - Pathology
Increased risk of developing CLEAR CELL ADENOCARCINOMA of the vagina and cervix. Daughters and sons with in utero exposure also have structural anomalies of the reproductive tract (HOODED CERVIX, T-shaped uterus, small uterine cavity, vaginal septae, vaginal adenosis)
115
Labor pre eclampsia magnesium sulphate treatment:
Depression of the deep tendon reflexes is the earliest sign of magnesium sulfate toxicity. STOP the MAGNESIUM SULPHATE infusion and administration of CALCIUM GLUCONATE.
116
HIV patient with Pneumocystis pneumonia (PCP):
Trimehoprim-sulfamethoxazole (TMP-SMX) is drug of choice. Corticosteroids decrease mortality in severe PCP infections and should be given if PaO2 ≤70 mmHG or A-a gradient ≥35 mmHg on room air.
117
Hematuria suggests on timing during stream:
Initial hematuria suggests urethral damage. Terminal hematuria indicates bladder or prostatic damage, and total hematuria reflects damage in the kidney or ureters. Clots are not usually seen with renal causes of hematuria.
118
Congenital diaphragmatic hernia management:
Newborn with concave abdomen and barrel shaped chest with absent breath sounds on one side needs emergency intubation with cautious ventilations
119
Chronic hepatitis C asymptomatic presentation and extrahepatic sequelae:
Presents with fatigue and nonspecific symptoms. Patients transaminases wax and wane. Extrahepatic sequelae can include essential mixed cryoglobulinemia, porphyria cutanea tarda, and membranoproliferative glomerulonephritis.
120
HIV ophthalmologic problems:
In HIV patients, both HSV and VZV can cause severe,acute retinal necrosis associated with pain, keratitis, uveitis, and fundoscopic findings of peripheral pale lesions and central retinal necrosis. CMV retinitis is painless.
121
Cerebellar hemorrhage:
Patients typically have headache, neck stiffness, gait ataxia, and no hemiparesis
122
Putamen hemorragia:
Most common cause is hypertension. Next to internal capsule, so leads to hemiparesis.
123
Pontine hemorragia:
Coma due to disruption of reticular activating system, and quadriplegia that develops within a few minutes. Pinpoint pupils, but may react strongly to light with no horizontal movement. Decerebrate rigidity.
124
Adrenal tuberculosis:
Patient who presents with clinical features of adrenal insufficiency and calcifications in the adrenal glands.
125
Diabetic neuropathy:
Presents with alterations in sensation, including loss of proprioception. When motor findings are present and patient has hyperactive reflexes and an upgoing plantar reflex (UMN) you need to get an MRI of spine for epidural abscess or cord compression.
126
Tea and toast diet is associated with what:
Folic acid deficiency. Folic acid is heat sensitive and deficiency cause macrocytic anemia.
127
Thalamic stroke (Dejerine-Roussy syndrome):
Caused by a stroke involving the VPL nucleus of the thalamus, which transmits sensory information from the contralateral side of the body. Classically presents with contralateral hemianesthesia that can be accompanied by transient hemiparesis, athetosis, or ballistic movements.
128
Midbrain and medulla strokes have in common:
Classically involve the nuclei of the cranial nerves.
129
Schizoaffective disorder:
Characterized by a significant mood episode (depressive or manic) with concurrent psychotic symptoms in addition to a period of psychosis without mood symptoms of at least 2 weeks.
130
Chloroquine resistant Plasmodium falciparum:
Common in Sub-Saharan Africa, the Amazon basin, and Southern and Southeast Asia. Tx chemoprophylaxis is mefloquine, atovaquone-proguanil.
131
Hyperemesis gravidarum:
Patients with multifetal gestation or molar pregnancy are at increased risk for hyperemesis gravidarum therefore an ultrasound should be performed in pregnant women with severe vomiting.
132
Autosomal dominant polycystic kidney disease (ADPKD):
Clues to diagnosis: hypertension, palpable bilateral abdominal masses and microhematuria. Remember intracranial berry aneurysm is a common complication. No screening recommended.
133
Obstructive uropathy:
Causes flank pain, low volume voids with or without occasional high volume voids, and if bilateral renal dysfunction.
134
Interstitial nephritis:
Most frequently occurs as a drug reaction. Patient present with fever, rash, acute renal dysfunction, and eosinophiluria with white blood cell casts.
135
Glomerulonephritis:
Presents with hematuria, red blood cell casts, acute renal failure, hypertension, and edema.
136
Chagas disease (Trypanosoma cruzi):
Primarily affects the heart (cardiomyopathy, RBBB) and gastrointestinal tract (megacolon, megaesophagus). First line treatment Benznidazole.
137
Strongyloidiasis:
Presents with urticaria, abdominal pain, and respiratory problems (dry cough, dyspnea, wheezing). First line treatment ivermectin.
138
Onchocerciasis (“river blindness”)
Causes ocular lesions and dermatitis. Treatment is ivermectin.
139
Empyema
Most commonly occurs in the setting of untreated pneumonia due to bacterial seeding of a pleural effusion. Most common bacteria are Streptococcus pneumoniae, Staphylococcus Aureus, and Klebsiella pneumonia.
140
Management of placenta previa:
Depends on the severity of bleeding and the age of the pregnancy. Complete placenta previa requires delivery by cesarean section. If mother and baby are stable SCHEDULED cesarian section.
141
By age 12 months height and weight and developmental:
Weight should TRIPLE and height should INCREASE 50%. Walking independently, using a 2-finger pincer grasp, saying a few words other than “mama” and “dada” and imitating the actions of others.
142
By age 9 months developmental milestones: gross motor; fine motor; language; social/cognitive.
Pulls to stand and cruises; 3-finger grasp and holds bottle or cup; Says “mama” and “dada”; Waves “bye” and plays pat-a-cake
143
By age 6 months developmental milestones: gross motor; fine motor; language; social/cognitive.
Sits momentarily propped on hands (unsupported by 7 months); Transfers objects hand to hand and raking grasp; Responds to name and babbles; Stranger anxiety.
144
By age 4 months developmental milestones: gross motor; fine motor; language; social/cognitive.
Sits with trunk support and begins to rolling; Hands mostly open and reaches midline; Laughs and turns to voice; Enjoys looking around
145
By age 2 months developmental milestones: gross motor; fine motor; language; social/cognitive.
Lifts head/chest inprone position; Hands unfisted 50% of time, tracks pasat midline; Alerts to voice/sound and coos; Social smile and recognizes parents.
146
Rheumatoid arthritis at increased risk for:
Developing osteopenia, osteoporosis, and bone fracture. Management adequate physical activity, optimization of calcium and vitamin D intake, minimization of corticosteroid therapy, and consideration for bisphosphonate treatment.
147
Acute liver failure:
Most often due to acute viral hepatitis, ACETAMINOPHEN TOXICITY, and ischemic hepatopathy. Characteristic findings include the acute onset of markedly elevated transaminases ( often in the thousands), reduced hepatic synthetic function, and encephalopathy.
148
Galactosemia characteristics and metabolic disorder:
Newborn or young infant with failure to thrive, bilateral cataracts, jaundice, and hypoglycemia. GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE DEFICIENCY leads to ELEVATED BLOOD GALACTOSE.
149
Galactokinase deficiency:
Presents with cataracts only, otherwise asymptomatic.
150
Circumstantiality:
Thought process deviate from original subject but eventually return to it.
151
Tangentiality:
Thought process in which there is abrupt, permanent deviation from the current subject. This new thought process is minimally relevant at best and never returns to the original subject.
152
Loose association:
Best described as the lack of a logical connection between the thoughts or ideas of an individual. It tends to be more severe form of tangentiality in which one statement follows another but there is no clear association between the sentences.
153
Preservation
Repetition of words or ideas during a conversation.
154
Flight of ideas:
Loosely associated thoughts that rapidly move from topic to topic.
155
Contact lens-associated infectious keratitis:
Medical emergency: causes painful, red eye and opacification and ulceration of the cornea. Most case are due to Gram-negative organisms such as Pseudomonas and Serratia, but can be from gram-positive, fungi, and amoebas. Tx with topical broad spectrum antibiotics.
156
Pneumoperitoneum
Radiograph reveals intraperitoneal air between the liver and diaphragm. This is surgical emergency.
157
Secondary pneumothorax:
Should be suspected in COPD patients presenting with catastrophic worsening of their respiratory symptoms and is usually due to dilated alveolar blebs that rupture air into the pleural space.
158
Patient with metabolic acidosis:
Calculate the anion gap: AG = Na - (HCO3 + Cl) KARMEL: K — Ketoacidosis; A — aspirin; R — Renal failure; M — Methanol; E — Ethylene glycol; L — Lactic acidosis
159
Multiple myeloma:
An elderly patient with bone pain, renal failure, and hypercalcemia. Renal insufficiency most likely due to obstruction of the distal and collecting tubules by large laminated casts containing PARAPROTEINS (mainly Bence Jones protein).
160
External cephalic version:
Can be attempted in women with breech pregnancies at ≥37 weeks gestational age if there are no contraindications to vaginal delivery, and fetal well-being has been established.
161
Chronic myeloid leukemia (CML):
Reciprocal translocation of chromosome 9 and 33 can form the Philadelphia chromosome containing BCR/ABL fusion gene. Tyrosine kinase inhibitors are key treatments. Non-receptor tyrosine kinase.
162
Acute promyelocytic leukemia (APML):
Retinoic acid receptor is involved. Tx: All-retinoic acid.
163
Neonatal bilious emesis:
Signifies bowel obstruction and requires immediate X-ray to evaluate the need for emergency surgery or further diagnostic study. Contrast studies (enema) should be performed in stable patients to determine the level of obstruction.
164
Mullerian agenesis:
Phenotypically and genotypically female. They experience breast development and body hair growth at puberty but do not menstruate due to a congenitally absent or underdeveloped uterus, cervix, and upper vaginia.
165
Biliary atresia:
Newborns with CONJUGATED hyperbilirubinemia and hepatosplenomegaly require immediate evaluation for biliary atresia. Evaluated with ultrasound.
166
HIV medication didanosine:
Induced pancreatitis
167
HIV medication abacavir:
related hypersensitivity syndrome.
168
HIV medication nevirapine:
associated liver failure.
169
HIV medication NRTIs:
lactic acidosis
170
HIV medication NNRTIs:
Steven-Johnson syndrome.
171
Solitary brain metastasis:
Surgical resection is recommended in patients with good performance status and stable extracranial disease In patients with multiple metastases, whole brain radiation therapy is typically used.
172
Factitious thyrotoxicosis:
Results from ingestion of exogenous thyroid hormone. Signs and symptoms of thyrotoxicosis without goiter or exophthalmos. TSH low; elevated T3/T4. Radioactive iodine uptake is low in these patients. Diagnosis is made by low serum thyroglobulin levels.
173
Clavicular fracture:
If a bruit is heard need an angiogram to rule out injury to the underlying vessel.
174
Pseudogout:
Diagnosed by the presence of rhomboid, positively birefringent crystals in synovial fluid analysis, and radiographic evidence of chondrocalcinosis.
175
Gout:
Monosodium urate crystal deposition. Crystals are needle shaped and negatively birefringent on synovial fluid analysis.
176
Most common crystal found in renal calculi:
Calcium oxalate
177
Struvite
Magnesium ammonium phosphate may be found in the renal calculi of patients with UTI caused by urease-producing organisms (Klebsiella, Proteus).
178
Opioid withdrawal
Tx: Inpatients should be treated with methadone if they are being treated for another medical problem other than addiction.
179
Benzodiazepine overdose difference from opioids:
During benzodiazepine intoxication, pupil size tends to be normal, with only mild respiratory depression.
180
Sustained monomorphic ventricular tachycardia (SMVT):
Hemodynamically unstable electrical cardioversion. Hemodynamically stable give amiodarone.
181
Prior to starting lithium:
Calcium, renal function, and thyroid function should be monitored.
182
Autoimmune hemolytic anemia (AIHA):
Positive direct Coomb’s test.
183
Aminoglycosides:
Aminoglycosides are antibiotics used to treat serious gram-negative infections. They are potentially nephrotoxic and renal functions must be monitored closely. AMIKACIN.
184
Emergency contraception:
The copper intrauterine device is the most effective precoital and postcoital contraceptive, with up to 99% efficacy. OCPs are less effective.
185
Cardiac tamponade:
Catastrophic complication of acute aortic dissection. Suspected in patients with hypotension, tachycardia, distended neck veins, and pulsus paradoxus.
186
Patients with narrow-QRS-complex tachycardia:
Intravenous adenosine is useful in the initial diagnosis and management. It slows the sinus rate, increases atrioventricular (AV) nodal conduction delay, or can cause a transient block in AV node conduction. Good for identifying P waves. Terminates PSVT sometimes.
187
Association between diabetes mellitus with nose and sinus infections with what organism:
mucormycosis (Rhizopus species).
188
Increased extracellular pH (respiratory alkalosis) causes dissociation:
Of hydrogen ions from albumin, allowing increased binding of calcium and a drop in unbound (ionised calcium. Ionized calcium is the physiologically active form, and decreased levels can result in clinical manifestations of hypoglycemia.
189
Delusional disorder:
Involves one or more delusions and the absence of other psychotic symptoms in an otherwise high functioning individual.
190
Babesiosis disease:
Caused by parasite Babesia and is transmitted by Ixodes tick. Evidence of hemolysis in a patient who was splenectomised highly suspicious. Diagnosed Giemsa-stained thick and thin blood smear.
191
Hypertension in overweight people:
Weight lose is the most effective nonpharmacologic measure to decrease blood pressure in overweight individuals.
192
Glomerular hematuria characteristics:
Urine studies reveal proteinuria, dysmorphic red blood cells (RBCs) or RBC cast.
193
Nonglomerular hematuria characteristics:
More common. Gross hematuria with normal-appearing red blood cells (RBCs) but without significant proteinuria.
194
Adrenal insufficiency due to hypopituitarism:
Not associated with hypoaldosteronism. Aldosterone is independent of ACTH secretion by pituitary gland.
195
Persistent pneumothorax after patient has sustained blunt chest trauma:
Suggests tracheobronchial rupture. Findings include pneumomediastinum and subcutaneous emphysema.
196
Mechanism of pain relief in patient with chest pain treated with nitroglycerin:
Dilation of veins (capacitance vessels) which leads to decrease ventricular preload.
197
Immediate postpartum period what is normal:
Low-grade fever, leukocytosis especially first 24 hours and vaginal discharge are normal findings. The vaginal discharge (lochia) is initially bloody, then serous and finally white to yellow in color days following delivery.
198
When lochia is foul smelling and/or uterus is tender:
Start empiric antibiotics.
199
Urine chloride level:
<20mEq/L (saline responsive) | >20mEq/L (saline resistant)
200
Erythema Nodosum (EN) characteristics and found in what diseases:
Condition of painful, subcutaneous, pretibial nodules. Symptom of more serious diseases including sarcoidosis (get chest x ray especially in AAF), TB, histoplasmosis, recent streptococcal infection, and IBD.
201
Incomplete abortion findings and unstable vs stable:
Vaginal bleeding, a dilated cervical os, and partial expulsion of products of conception. Hemodynamically unstable: Surgical evacuation (D & C). Hemodynamically stable: Expectant management, prostaglandins (misoprostol), or surgical.
202
Threatened abortion characteristics:
Vaginal bleeding, closed os, and fetal cardiac activity.
203
Missed abortion:
No vaginal bleeding, closed cervical os, no fetal cardiac activity or empty sac.
204
Inevitable abortion:
Vaginal bleeding, dilated os, products of conception may be seen or felt at or above cervical os.
205
Complete abortion:
Veginal bleeding or none, closed cervical os, and products of conception completely expelled.
206
Most common complication in post thyroidectomy:
Hypoparathyroidism caused by the removal of 3 ½ parathyroid glands causes low PTH with resultant hypocalcemia and elevated phosphorus levels.
207
Lumbar spinal stenosis:
Common cause of back pain in patients over 60 years of age. Characterized by back pain radiating to the buttocks and thighs that interferes with walking and lumbar extension.
208
Seronegative spondylarthritis (ankylosing spondylitis):
Characterized by progressive limitation of back motion and most often occurs in young men. Back pain and stiffness are typically worst in the morning and improves as day progresses.
209
Acute arterial occlusion (limb ischemia):
Classically presents with “5 Ps” (pain, pallor, pulselessness, paresthesia, and paralysis). Immediate anticoagulation and referral for vascular surgery.
210
Mallory-Weiss syndrome:
Tears occur in the distal esophagus at the gastroesophageal junction after repeated bouts of retching and vomiting. Do not confuse with Acute erosive gastritis from severe hemorrhagic erosive lesions of the gastric mucosa.
211
Cat bite treatment:
Wounds can be infected with Pasteurella multocida, so prophylactic treatment with 5 day course of amoxicillin/clavulanate.
212
Fanconi Anemia etiology and characteristics:
Autosomal recessive or X-linked disorder of chromosomal breaks usually diagnosed before age 16. Causes congenital marrow failure, with short stature, microcephaly, abnormal thumbs, and hypogonadism. Skin can be hypopigmentes or hyperpigmented, cafe au lait spots, and large freckles. Strabismus, low set ears, chronic, ear infections.
213
Mitral stenosis characteristics:
Causes pulmonary congestion which leads to symptoms such as exertional dyspnea, nocturnal cough, and hemoptysis. Atrial fibrillation occurs due to atrial dilation. Especially common in patients who had rheumatic fever.
214
Variant angina (Prinzmetal's angina):
Causes chest pain by coronary vasospasm. Treatment is calcium channel blocker. Nonselective β-blockers and aspirin should be avoided because they can promote vasoconstriction.
215
ABO incompatibility:
Occurs generally in a group O mother with a group A or B baby. Less severe than Rh(D) incompatibility.
216
Chronic cough that worsens at night and does not improve with antihistamines:
Possible asthma must check PFTs.
217
Factorial design study:
Involve randomization to different interventions with additional study of 2 or more variables.
218
Symptomatic pulmonary embolism most common cause:
The proximal deep veins (iliac, femoral and politeal veins) are the source of >90% of acute PEs.
219
Meniscal tear compared to ligament tear:
Both case the patient feels a popping sensation during an acute event, but the swelling that occurs with meniscal tear until 12 to 24 hours. Ligament tears swell almost immediately
220
Correlation coefficient (r):
Shows the strength and direction (positive, negative) of linear association between 2 variables. It does not imply causality. An r=-0.25 for HDL to carotid intima thickness would mean they are inversely proportional.
221
In postmenopausal women the initial work up of an adnexal mass: What is contraindicated:
Should include transvaginal ultrasonography and a serum cancer antigen (CA)125 level which has good sensitivity and specificity for malignant adnexal mass. Needle aspiration for cytology is contraindicated due to possible cancer spread.
222
First-trimester maternal-fetal transmission of the rubella virus:
Teratogenic. Congenital rubella syndrome is characterized by the triad of cataracts, patent ductus arteriosus, and snesoneural hearing loss. Prevent by MATERNAL VACCINATION before conception. Must have IgM and IgG to know if current infection or previous immunity.
223
Stab wounds near artery veins can cause:
``` Arteriovenous fistulas (AVF) which can lead to high-output cardiac failure by shunting the blood from the arterial to venous side, thereby increasing cardiac preload. Hypoxia of tissues drives this. Doppler ultrasound to diagnose. ```
224
Paroxysmal supraventricular tachycardia (PSVT) characterized by:
Heart rates between 160-220 beats per minute. Results from accessory conduction pathways through the AV node. Vagal maneuvers and medication (adenosine) that decrease conduction through the AV node often revolve the PSVT.
225
Glucose-6-phosphatase deficiency(Type I glycogen storage disease & Von-Gierke's disease):Characteristics
Appearance is a doll-like face (fat cheeks), thin extremities, short stature, and protuberant abdomen (due to enlarged liver and kidneys) in a 3-4 month old. Hypoglycemic seizures may occur.
226
Developmental milestones toddlerhood 12 months: Gross Motor; Fine motor; Language; Social/Cognitive.
Stands well, walks first steps independently throws ball; 2-finger pincer grasp; Says first words (other than “mama” & ”dada”); Separation anxiety, follows 1-step command with gestures
227
Developmental milestones toddlerhood 18 months: Gross Motor; Fine motor; Language; Social/Cognitive.
Runs, kicks ball; builds tower of 2-4 cubes, removes clothing; 10-25 word vocabulary, identifies ≥1 body part; Understands “mine”, begins pretend play.
228
Developmental milestones toddlerhood 2 years: Gross Motor; Fine motor; Language; Social/Cognitive.
Walks up/down stairs with both feet on each step, jumps; Builds 6-cube tower, copies a line, turns pages; 50+ word vocabulary, 2-word phrases; Follows 2-step command, parallel play, begins toilet training.
229
Developmental milestones toddlerhood 3 years: Gross Motor; Fine motor; Language; Social/Cognitive.
Walks up/down stairs with alternating feet, rides tricycle; copies a circle, uses utensils; 3-word sentences, speech 75% intelligible; Knows age/gender, imaginary play.
230
Developmental milestones toddlerhood 4 years: Gross Motor; Fine motor; Language; Social/Cognitive.
Balance & hops on 1 foot; Copies a square; Identifies colors, speech 100% intelligible; Cooperative play.
231
Developmental milestones toddlerhood 5 years: Gross Motor; Fine motor; Language; Social/Cognitive.
Skips, walks backward; Copies a triangle, ties shoelaces, independent dressing/bathing, prints letters; Counts to 10, 5-word sentences; Has friends, complete toilet-training.
232
Guillain-Barre syndrome CSF findings:
Protein elevated (45-1000) albuminocytologic dissociation; WBC normal; RBC normal; Glucose normal.
233
Prolactin production is stimulated by:
Serotonin and TRH, and inhibited by dopamine. Hypothyroidism may result in amenorrhea and galactorrhea. Prolactin inhibits GnRH release thus decreasing FSH and LH.
234
Hashimoto’s thyroiditis are at increased risk for what cancer:
Lymphoma of the thyroid. anti-thyroperoxidase (TPO) antibodies.
235
Thyroid cancers of epithelial origin include: which one is C-cell origin:
Follicular, papillary and anaplastic; C-cell origin is medullary.
236
Management of hypercalcemia Severe: Important effects on body:
Severe (calcium >14mg/dL) or symptomatic: Short term (immediate treatment) Normal saline hydration plus calcitonin. Long-term treatment bisphosphonates (zoledronic acid). Remember hypercalcemia induces urinary salt wasting, which results in significant volume depletion.
237
Massive postoperative pulmonary embolism (PE): Typical presentation:
Patient with hypotension, jugular venous distension, and new-onset right bundle branch block (RBBB)
238
Treatment of stable chronic angina:
First line therapy Beta blocker: Metoprolol, decreases myocardial contractility & HR. Improves survival. Calcium channel blockers can be added if angina persists. Causes peripheral & coronary vasodilation. Nitrates, Aspirin, Statin, lifestyle.
239
Patients with persistent tachyarrhythmia (narrow or wide-complex) causing hemodynamic instability managed:
Immediate synchronized DC cardioversion. Stable patients get vagal maneuvers (carotid sinus massage) and/or adenosine.
240
Vipoma is a rare tumor affecting: Describe VIPoma syndrome: Diagnosis:
The pancreatic cells that produce vasoactive peptide (VIP). VIPoma syndrome (pancreatic cholera) with watery diarrhea, muscle weakness/cramps (due to hypokalemia), and hypo- or achlorhydria (due to decreased gastric acid secretion). Stool studies show secretory diarrhea, VIP levels are >75pg/mL confirms.
241
Which of the three main treatments for Graves disease worsens eye disease initially:
Radioactive iodine (RAI) due to thyroid cell death and release of excess thyroid hormone.
242
Hemineglect syndrome is characterized by:
Ignoring the left side of a space, and involves the right (non-dominant) parietal lobe.
243
McCune-Albright syndrome:
Rare condition characterized by precocious puberty, cafe au lait spots and multiple bone defects (polyostotic fibrous dysplasia). Can have other endocrine disorders.
244
Post-splenectomy patients are at increased risk for sepsis from:
Encapsulated organisms due to impaired antibody-mediated opsonization in phagocytosis. S. pneumoniae, N. meningitidis, and H. influenzae.
245
Restless legs syndrome (RLS): Treatment and mechanism.
First line: Dopamine agonist (pramipexole, ropinirole) | Alternative: Alpha-2-delta calcium channel ligands (gabapentin)
246
In the treatment of a patient using both sildenafil and an alpha-blocker (doxazosin):
It is important to give the drugs with at least a 4-hour interval to reduce the risk of hypotension.
247
Tricyclic antidepressant overdose: Treatment: Mechanism:
Can present with CNS, cardiac, and anticholinergic findings. Sodium bicarbonate is used to treat cardaic toxicity (QRS>100msec and ventricular arrhythmias). Sodium bicarbonate increases serum pH and extracellular sodium, therby alleviating the cardio-depressant action on sodium channels.
248
First degree AV block:
With normal QRS duration delay at AV node and require no further evaluation. Prolonged QRS duration likely have a conduction delay below the AV node and should have electrophysiology testing.
249
Sickle cell kid with sepsis most common species:
S. pneumoniae, H. influenzae.
250
Acute cholecystitis primary inciting event:
A gallstone obstructing the cystic duct with subsequent inflammation and infection.
251
Hypertensive intracranial hemorrhages occur most commonly:
In the basal ganglia, thalamus, pons, and cerebellum. Evolves over minutes to hours with focal neurologic symptoms compared to subarachnoid hemorrhages complain of severe HA do not have focal deficits.
252
Gastric outlet obstruction can be caused by ingestion:
``` Of acid (caustic substance) causes pyloric strictures to form. This presents as early satiety, nausea, nonbilious, vomiting and weight lose. ```
253
Herpetic whitlow:
Common viral infection of the hand by HSV 1 or 2 and is self limiting. Healthcare workers especially dentist are at risk for it. Remember multinucleated giant cells in the Tzanck smear confirms diagnosis.
254
The most common cause of sudden cardiac arrest in the immediate postinfarction period in patients with acute MI:
Reentrant ventricular arrhythmias (ventricular fibrillation).
255
Hypokalemia signs and ECG findings:
Causes weakness, fatigue, and muscle cramps. ECG may show U wave, flat and broad T waves, and premature ventricular beats.
256
Epidural spinal cord compression initial management:
Intravenous glucocorticoids (decreases vasogenic edema) and MRI.
257
Amaurosis fugax:
Characterized by visual loss that is transient and usually monocular. “Curtain falling down.” Most common cause RETINAL EMBOLI from the CAROTID ARTERY.
258
Most common causes of viral meningitis are the:
Non-polio enteroviruses, such as echoviruses and coxsackie viruses.
259
Aspirin intoxication triad and typical blood gas analysis:
Triad of fever, tinnitus, and tachypnea (stimulates respiratory center in the medulla). Adults with aspirin toxicity develop a mixed respiratory alkalosis and anion gap metabolic acidosis. pH 7.39; PaCO2 20; HCO3 12.
260
Normal pH in acid base disturbance signifies:
A mixed respiratory and metabolic acid-base disorder.
261
Lithium exposure in the first trimester:
Increases the risk of cardiac malformations including septal defects and possibly Ebstein’s anomaly
262
Lithium exposure during the second and third trimester:
May cause goiter and transient neuromuscular dysfunction.
263
Mammograms should be performed every:
2 years starting at age 50 in women till age 74 at average risk for breast cancer. Not recommended after 75.
264
Thyrotoxic myopathy can present with:
Proximal muscle weakness with or without muscle atrophy can occur in 60-80% of patients with untreated hyperthyroidism and correlates to the duration of the hyperthyroid state.
265
Myasthenia Gravis (MG) presentation and comorbid disease:
Fatigable muscle weakness that primarily involves the extraocular and bulbar musculature is the most consistent with MG. Approximately 15% have a Thymoma, so screening with a chest CT recommended.
266
Dermatomyositis mechanism and presentation:
Idiopathic inflammatory myopathy with immune mediated muscle injury that can be due to paraneoplastic syndrome in malignancy. Patient typically have symmetrical proximal muscle weakness and erythematous rash over the dorsum of the fingers (Gottron’s sign) and/or upper eyelids (heliotrope eruption).
267
Lambert-Eaton key findings on PE:
DIMINISHED or ABSENT DEEP TENDON REFLEXES. Proximal muscle weakness, autonomic dysfunction (dry mouth).
268
Sarcoidosis can have elevated serum:
Angiotensin converting enzyme (ACE) levels.
269
Syndrome of inappropriate antidiuretic hormone secretion: What do lab values show and what is treatment?
Low plasma osmolarity especially Na (hyponatremia) with an inappropriately elevated urine osmolality and urine sodium concentration.
270
Acute cholecystitis management:
May be treated with observation and supportive care initially, followed by laparoscopic cholecystectomy within 72 hours during same hospitalization.
271
Distinguishing between dementia and normal changes of aging:
Impairment of daily functioning is seen in dementia.
272
Premature ovarian failure characterized by and treated with:
Amenorrhea, hypoestrogenism, and elevated gonadotropins (increased serum FSH & LH). Patients lack oocytes. Infertility is treated with in vitro fertilization with donor oocytes for women who desire pregnancy.
273
Laxative abuse is characterized by:
Frequent, watery, nocturnal diarrhea. Diagnoses can be confirmed with characteristic biopsy of dark brown discoloration of the colon with lymph follicles shining though pale patches (melanosis coli).
274
Chorioamnionitis Treatment:
Intravenous broad spectrum antibiotics (ampicillin, gentamicin, clindamycin). Oxytocin to accelerate labor. This is not a reason for cesarean delivery.
275
Standard obstetric indications for cesarean delivery:
Fetal distress, breech presentation, multiple prior cesarean deliveries.
276
Hyperosmolar hyperglycemic state: Etiology: Symptoms:
Type 2 diabetics are prone to the development of a hyperosmolar hyperglycemic state without ketoacidosis. Decreased consciousness is the most common symptom, and other neurologic abnormalities such as blurred vision.
277
Breath holding spells are episodes: What should they be evaluated for:
Of apnea that are precipitated by frustration, anger, or pain. Age 6 months-2 years. Patients should be evaluated for iron deficiency anemia. CBC
278
CMV retinitis treatment:
Ganciclovir or foscarnet
279
Attributable risk percent (ARP) formula:
ARP =(RR-1)/RR | RR = Relative Risk
280
Digitalis toxicity causes what type of arrhythmia:
Leads to ectopy and increased vagal tone. Atrial tachycardia with AV block occurs from combination of these two digitalis effects and is relatively specific for digitalis.
281
Systemic and topical corticosteroids can induce: Skin finding:
An acneiform eruption characterized by monomorphous, erythematous follicular papules distributed on the face, trunk and extremities. Comedones are characteristically absent.
282
Hazard ratio (HR) interpretation:
A hazard ratio <1 indicates that an event is more likely to occur in the control group A hazard ration >1 signifies that an event is more likely to occur in the treatment group. A ratio close to 1 implies little difference between the 2 groups.
283
Mobitz Type I vs Mobitz Type II:
Mobitz Type I: Atrioventricular block has PROGRESSIVE PROLONGATION of PR interval leading to a NON-CONDUCTED P WAVE and a dropped QRS complex. Problem is conduction in the AV node. Mobitz Type II: PR interval is always CONSTANT with no progressive prolongation and ((QRS complex drops suddenly)). Due to a block in the His-Purkinje system below AV node. Can lead to third degree block.
284
Adults who have frequent contact with children (school teacher, daycare worker) disease risk:
Parvovirus can cause an acute symmetric arthritis of the hands (MCP, PIP, and wrist), knees, and ankle joints. Onset is 10 days unlike RA symptoms 6 weeks. Morning stiffness 1 hour RA, and only 10-15 minutes Parvo .
285
Atrial fibrillation (AF) with rapid ventricular response (RVR): Treatment:
Rate control should be attempted initially with beta blockers or calcium channel blockers. Immediate synchronised electrical cardioversion is indicated in hemodynamically unstable patients.
286
The patient’s pulsatile abdominal mass is most likely: Test:
An abdominal aortic aneurysm (AAA). Abdominal ultrasound is the study of choice for diagnosis.
287
All patient with chronic hepatitis C infection should get: This includes:
Immunized against A and B if they are not immune. Including pregnant women. Vaccines are inactivated (killed). Safe.
288
Hyperkalemia time to treat:
Initial evaluation is with ECG. Acute therapy is given for patients with ((ECG changes, potassium ≥7.0 mEq/L without characteristic ECG changes, or rapidly rising POTASSIUM due to tissue breakdown)).
289
Alpha-1 antitrypsin deficiency test positive for:
They stain with the periodic acid-Schiff (PAS) reaction and resist digestion to diastase.
290
Glucagonoma often presents with:
Nonspecific symptoms and require a high index of suspicion to make the diagnosis. Patients presenting with mild diabetes mellitus or hyperglycemia with NECROTIC MIGRATORY ERYTHEMA, diarrhea, anemia, and weight lose. Glucagon >500 pg/mL. Get abdominal imaging.
291
Stress incontinence is characterised by: Mechanism: Diagnosis: Treatment:
The loss of small amounts of urine with increased intra-abdominal pressure, as occurs with laughing, coughing, and sneezing. Urine leakage occurs from ineffective closure of urethral sphincter. Inserting cotton swab demonstrating angle >30° upon increase abdominal pressure. Kegel exercises and urethropexy.
292
Urge incontinence: Mechanism: Treatment:
Results from detrusor hyperactivity and is characterized by a sudden urge to urinate that may come at any time, not just increased intraabdominal pressure. Oxybutynin.
293
Cancer-related anorexia/cachexia syndrome: Treatment: What does not work:
Progesterone analogs (megestrol acetate and medroxyprogesterone acetate), and corticosteroids have been shown to increase appetite and weight gain in patients. Cannabinoids show no effect.
294
Friedreich Ataxia: Genetics
Autosomal recessive condition characterized by an excessive number of trinucleotide repeat sequences, resulting in a tocpherol transfer protein.
295
Lupus anticoagulant, an antiphospholipid antibody, is pro-thrombotic immunoglobulin that causes:
A spuriously (not genuine) prolonged partial thromboplastin time in vitro.
296
PVCs are common in patients post-myocardial infarction: Treatment:
Recognized by their widened QRS (>120 msec), bizarre morphology, and compensatory pause. Worse prognosis but no treatment unless symptomatic then Beta blocker.
297
Diastolic and continuous murmurs as well as loud systolic murmurs revealed on cardiac auscultation should:
Be investigated using transthoracic doppler echocardiography. Midsystolic soft murmurs in asymptomatic young patient require no further work up.
298
Cor pulmonale: Define: Signs include: What is seen on right heart catheterization:
Impaired function of the right ventricle due to pulmonary hypertension that usually occurs due to chronic lung disease. Signs: Elevated JVP, right ventricle heart sound, tricuspid regurgitation murmur, pulsatile liver, LEE, ascites. Right heart catheterisation shows elevated pulmonary artery systolic pressure (>25 mmHg).
299
Hypothyroid myopathy:
With an unexplained elevation in serum creatine kinase concentration and myopathy. Presents with fatigue, myalgias, proximal muscle weakness, sluggish ankle reflexes. Check TSH and free T4.
300
Most likely diagnosis of an asymptomatic, immunocompetent adult patient with a non-healing, isolated ulcer in the vermillion zone of the lower lip and a significant history of sun exposure:
Squamous cell carcinoma: Biopsy shows invasive cords of squamous cells with keratin pearls.
301
Unilateral foot drop is characterized by: Common causes:
A “steppage” gait, exaggerated hip and knee flexion while walking. Common causes include L5 radiculopathy and compression peroneal neuropathy. L5 radiculopathy may also have weak foot inversion and plantar flexion.
302
Symmetric growth restriction:
Usually caused by fetal anomalies, abnormal fetal karyotype, and early MATERNAL VIRAL INFECTION. CMV most common and most women have no apparent symptoms.
303
Asymmetric growth restriction:
Generally appears later in the pregnancy and is caused by maternal vascular disease, including hypertension, diabetes, and smoking.
304
Thrombotic thrombocytopenic purpura-hemolytic uremic syndrome (TTP-HUS): Blood smear: Treatment:
Unexplained hemolytic anemia and thrombocytopenia in a patient with renal failure and neurologic symptoms. Presence of fragmented cells in the peripheral smear suggest microangiopathic hemolytic anemia (MAHA). Plasmapheresis. (ADAMTS-13)
305
Radioiodine therapy most common side effect:
Hypothyroidism is most common duh. Increased ophthalmopathy is second at 10%. corticosteroids before and after help.
306
Thyroid-stimulating hormone-secreting pituitary adenoma is characterized:
Central hyperthyroidism with elevated TSH (or inappropriately normal), T3, and T4. Patients have goiter due to TSH effects on tissue growth. VISUAL DISTURBANCES and HA from tumor growth.
307
Chronic gastrointestinal blood loss is the most common cause:
Iron-deficiency anemia in an adult male or a postmenopausal woman. Test for occult blood in the stool.
308
Osteoarthritis drug of choice for pain:
Acetaminophen because of proven efficacy and a favorable side effect profile.
309
Patient with abdominal pain, microcytic anemia, positive fecal occult blood, and hepatomegaly with a hard edge on the liver palpation:
Typical features of gastrointestinal malignancy, like colon cancer, metastatic to the liver. Liver metastases manifests as right upper quadrant pain, mildly elevated liver enzymes, and firm hepatomegaly. Diagnose with CT abdomen.
310
Rheumatoid arthritis predisposes to:
Amyloidosis. you see renal involvement with nephrotic syndrome. Stain with Congo red and demonstrates apple-green birefringence under polarised light.
311
Chronic GERD and Barrett's esophagus are at risk for:
Adenocarcinoma of the esophagus.
312
Beck-Wiedemann syndrome: Genetics: Characteristics: What
Dysregulation of imprinted gene expression in chromosome 11p15. Characterized by macrosomia, umbilical hernia/omphalocele, hemihyperplasia (asymmetric larger arm/leg), and hypoglycemia. Children must closely monitored for development of Wilms tumor or hepatoblastoma. GET ABDOMINAL ULTRASOUND.
313
What type of glomerular disease is found in African American, obesity, heroin use, and HIV:
Focal segmental glomerulosclerosis (FSGS).
314
Most common causes of nephrotic syndrome:
Focal segmental glomerulosclerosis (FSGS) and membranous nephropathy.
315
Patients with decreased fetal movement should undergo antenatal fetal testing starting with:
Nonstress test (NST), followed by a contraction stress test (CST) or biophysical profile if the NST is nonreactive. A CST can be performed if there is no contraindications to labor.
316
Umbilical artery doppler velocity: What is it used for:
Evaluation of umbilical artery flow in fetal intrauterine growth restriction only.
317
Biophysical profile: What are the five criteria:
Amniotic fluid level; Fetal breathing movement; Fetal movement; Fetal tone; Fetal heart rate. You get 2 points for each for total of 10. Abnormal 0, 2, and 4. Equivocal: 6 points.
318
A normal contraction stress test indicates that: When should you repeat antepartum test:
Fetal compromise is unlikely. The chance of fetal death within 1 week of a normal test is rare, so antepartum testing may be repeated 1 week later.
319
Patient is a 28 weeks gestation with preterm labor and rupture of the membrane. US shows bilateral renal agenesis in fetus: What do you do next:
Labor should be allowed to proceed in patients where the fetus has been diagnosed with severe congenital anomaly incompatible with life.
320
Patients with Wolff-Parkinson-White syndrome (WPW): Describe arrhythmia: Treatment unstable vs stable:
An accessory pathway conducts depolarization directly from the atria to the ventricles with traversing the AV node. Hemodynamically unstable require immediate electrocardioversion: Hemodynamically stable patients PROCAINAMIDE (preferred) or ibutilide.
321
In WPW what agents are not used:
Adenosine, beta blockers, calcium channel blockers and digoxin. These agents may promote conduction across the accessory pathway and lead to degeneration of AF to VF.
322
CHF vs COPD exacerbation: what are the blood gas differences:
ABG CHF: hypoxia, HYPOCAPNIA, and respiratory alkalosis; example pH 7.46, pO2 73 mmHG, ((pCO2 31 mmHg)). ABG COPD: hypoxia, HYPERCAPNIA, and respiratory acidosis: example pH 7.39, pO2 80 mmHg ((pCO2 50 mmHg)).
323
CHF vs COPD exacerbation: What are differences on auscultation:
CHF: Bibasilar crackles. COPD: Widespread bilateral wheezes.
324
Specific test for CHF:
B-type natriuretic peptide (BNP) or pulmonary capillary wedge pressure.
325
Common bacterial pathogens cystic fibrosis: Gram-negative rod:
Pseudomonas aeruginosa. Most common cause pneumonia in adolescent and adults.
326
Common bacterial pathogens cystic fibrosis: Gram-negative coccobacilli:
Nontypeable Haemophilus influenzae
327
Common bacterial pathogens cystic fibrosis: Gram-positive cocci in chains:
Streptococcus pneumoniae. Most common cause of pneumonia in all patients.
328
Common bacterial pathogens cystic fibrosis: Gram-positive cocci in clusters:
Staphylococcus aureus. Most common cause in infants and young children with CF
329
Patients with Neisseria meningitidis can have:
Petechial rash. Almost 75% have a petechial rash that is prominent on the axilla, wrists, flanks, and ankles.
330
Group B Streptococcus (Streptococcus agalactiae): Rash describe:
DOES NOT HAVE A RASH.
331
Elderly patient with hip fracture after syncopal episode: Workup:
Surgery can be delayed up to 72 hours. Elderly patient with syncopal episode should get ECG, cardiac markers and chest- x-ray. If pulmonary edema and pleural effusion you need Echo.
332
Hypokalemia combined with computed tomography scan showing 3-cm adrenal mass suggests: Lab findings: Causes:
Primary hyperaldosteronism Conn’s disease). Low renin and elevated aldosterone and serum bicarbonate. Causes hypertension, mild hypernatremia, hypokalemia, and metabolic alkalosis.
333
Patients who undergo central venous catheterization need:
Portable chest x-ray to confirm proper placement of the catheter tip and absence of complications beofre administering drugs or other agents through the catheter.
334
Ischemic cardiac pain can sometimes be mistaken for: What test:
Epigastric pain, especially in the setting of symptoms that worsened with exertion. An exercise stress test without imaging if the baseline ECG is normal. Stress test positive then Coronary angiography (gold standard for Dx CAD).
335
Effects of maneuvers on hypertrophic cardiomyopathy: What increases murmur intensity: Why:
Valsalva (straining phase), Abrupt standing (from sitting or supine position), Nitroglycerin. Physiologic effect: Decrease in preload.
336
Effects of maneuvers on hypertrophic cardiomyopathy: What decreases murmur intensity: Why:
1. Sustained hand grip 2. Squatting (from standing position) 3. Passive leg raise Physiologic effect: 1. Increase Afterload 2. Increase Afterload & Preload 3. Increase Preload
337
Trigeminal neuralgia: Symptoms: Treatment:
Severe, unbearable pain in face that is knife like, comes in paroxysms, and occurs 10-20 times a day and last a few seconds. Carbamazepine (Prolonged use causes aplastic anemia, get routine CBCs).
338
Intravenous drug user with bacterial endocarditis with acute embolic stroke: Treatment:
MRI of brain. TEE of heart. Blood cultures and intravenous antibiotic therapy. Then watch. No need for antiplatelet therapy (aspirin) that you normally give in acute ischemic stroke due to atherosclerotic thrombosis or embolism. Medullary thyroid cancer (MTC): Presentation: Hard nodule, elevated calcitonin, malignant cells.
339
Multiple Endocrine Neoplasia (MEN) Type I:
Primary hyper((parathyroid)) Entero((pancreatic)) tumors: ((Pituitary)) tumors:
340
Multiple Endocrine Neoplasia (MEN) Type 2A:
Medullary ((thyroid)) cancer (MTC) ((Pheochromocytoma)): ((Parathyroid)) hyperplasia:
341
Multiple Endocrine Neoplasia (MEN) Type 2B:
Medullary ((thyroid)) cancer (MTC) ((Pheochromocytoma)): Other: mucosal & interstitial neuromas, ((marfanoid habitus)) Kyphoscoliosis and lordosis.
342
MEN 2 A & B genetics:
Autosomal dominant mutations involving RET proto-oncogene located on chromosome 10.
343
A nail puncture wound in an adult resulting in osteomyelitis is most likely due:
Pseudomonas aeruginosa
344
Acute cocaine toxicity with myocardial ischemia: Signs/symptoms: Treatment:
Psychomotor agitation, dilated pupils, atrophic nasal mucosa, hypertension, ECG changes. Treatment supplemental oxygen and intravenous benzodiazepines.
345
Duodenal hematomas most commonly occur following direct trauma: Treatment:
Treatment is conservatively with nasogastric suction and parenteral nutrition. Most hematomas spontaneously resolve in 1-2 weeks. Pain is from gastric secretions being blocked.
346
COPD medications beta agonist:
Albuterol: bronchodilator
347
COPD medications anticholinergic:
ipratropium and tiotropium: bronchodilator:
348
Unilateral subacute hip pain in a male child coupled with progressive antalgic gait, thigh muscle atrophy, decreased range of motion and collapse if the ipsilateral femoral head on x-ray:
Idiopathic avascular necrosis of the femoral capital epiphysis (Legg-Calve-Perthes disease)
349
D-transposition of the great vessels (TGV) is the most common: Presentation:
Congenital cyanotic heart disease in the neonatal period. Presents in the first few hours of life with cyanosis and a single loud second heart sound, and a narrow mediastinum “egg on a string” x-ray. Treat prostaglandins keep PDA open.
350
A solitary pulmonary nodule is defined as a lesion:
351
Assessment of malignancy risk for solitary pulmonary nodule: High Risk:
Nodule size (cm) ≥2.0; Age(yr) >60; Smoking status Current; Smoking cessation (yr)
352
Chagas disease: Cause: Endemic area: Presentation: Treatment:
A chronic protozoal disease caused by Trypanosoma cruzi. Latin America. Pedal edema, JVD, S3, and cardiomegaly. Because infection causes megaesophagus, megacolon, and/or cardiac dysfunction. Tx: Benznidazole
353
Pheochromocytoma treatment:
Do not give beta blockers without alpha blockers. A beta blocker alone may cause increases in blood pressure due to unopposed alpha- receptors. Remember alpha-1 causes vasoconstriction of peripheral vessels.
354
Pressors such as norepinephrine can cause:
Ischemia of the distal fingers and toes secondary to vasospasm. Diagnosis is suggested by symmetric duskiness and coolness of all the finger tips. Norepinephrine has alpha-1 agonist properties which cause vasoconstriction. This phenomenon can occur in intestines and kidneys.
355
Pulmonary compliance is measured by: Formula:
The plateau pressure is the measured during an inspiratory hold maneuver Formula: Plateau pressure = elastic pressure + PEEP
356
Peak airway pressure is measured by: Formula
Useful in mechanically ventilated patients. Peak airway pressure (the maximum pressure measured as the tidal volume is being delivered) equals the sum of the resistance pressure (flow x resistance) and the plateau pressure. Formula: Peak airway pressure = resistive pressure + plateau pressure
357
Positive end expiratory pressure(PEEP) is calculated using:
end-expiratory hold maneuver
358
Adult respiratory distress syndrome (ARDS) on mechanical ventilation: First step in management:
Decrease the FiO2 to relatively non-toxic values
359
Pellagra triad:
(3Ds): Diarrhea, Dermatitis, and Dementia, and if untreated Death. Due to niacin deficiency seen in corn based diets in Asia, Africa, and China.
360
Patients with massive pulmonary embolism usually present with: Effects on heart function:
Signs of low arterial perfusion (hypotension, syncope), and acute dyspnea, pleuritic chest pain, and tachycardia. Thrombus increases pulmonary vascular resistance and right ventricular pressure, causing ventricular hypokinesis and dilation, decreased preload, and hypotension.
361
Cardinal symptoms in acute exacerbation of COPD: Treatment:
Increased dyspnea, cough, and sputum production. If patient has 2 of these give antibiotics. Moderate to severe COPD exacerbation or those requiring ventilation also receive antibiotics.
362
The risk factors for a polyp to progressing into malignancy are from highest malignancy chance:
Villous adenoma, sessile adenoma, and size >2.5 cm.
363
During an acute phase myocardial infarction what heart sound can be heard:
An abnormal fourth heart sound (atrial gallop) due to left ventricular stiffening and dysfunction induced by myocardial ischemia.
364
Chronic obstructive pulmonary disease (COPD): What are the two types and what is the difference in DLCO:
Diffusing capacity of the lung (DLCO( is decreased in emphysema and normal in bronchitis.
365
DLCO can be decreased in:
interstitial lung disease. Sarcoidosis, Asbestosis.
366
Infectious cavernous sinus thrombosis (CST): Mechanism: Signs/symptoms:
Because the facial/ophthalmic venous system is valveless, uncontrolled infection of the skin sinuses, and orbit can spread to the cavernous sinus. Red flag symptoms include severe headache; bilateral periorbital edema; and cranial nerve II, IV, V, and VI deficits. May see papilledema with ICH.
367
Indications for a renal & bladder ultrasound in children: Treatment:
Infants and children age
368
Ruptured ovarian cyst: Presentation: Pelvic ultrasound findings: Treatment:
Presentation: Acute onset of severe unilateral pelvic pain immediately after strenuous activity or sexual intercourse. Pelvic ultrasound can confirm the diagnosis by showing free fluid in the pelvis. Uncomplicated analgesics, Complicated surgery.
369
Tight blood glucose control in patients with diabetes decreases the risk of:
Microvascular complications (retinopathy, nephropathy), but increases risk of hypoglycemia. No change in all cause mortality.
370
Turners syndrome patients have ovarian dysgenesis which leads to:
Low estrogen levels and inability to mestate. The poor ovarian function because FSH levels to be high due to lack of negative feedback. LH is also elevated for the same reason.
371
Anemia of chronic disease is a disorder of: Characterized by:
Iron utilization that most commonly occurs in the setting of chronic inflammation. Normocytic anemia with decreased serum iron, decreased total-iron binding capacity: decreased iron saturation, and normal/elevated ferritin.
372
Membranoproliferative glomerulonephritis, type 2, is a unique glomerulopathy:
That is caused by persistent activation of the alternative complement pathway. Leaves dense intramembranous deposits that stain for C3.
373
Drug induced interstitial nephritis is usually caused by: Presentation:
Cephalosporins, penicillins, sulfonamides, NSAIDs, rifampin, phenytoin, and allopurinol. Patient present with arthralgias, rash, renal failure, and the urinalysis will show eosinophiluria.
374
Patient with androgen producing adrenal tumors: What is elevated specifically:
Dehydroepiandrosterone-sulphate
375
Any male adolescent who presents with epistaxis, a localized mass, and a bony erosion on the back of the nose has:
An angiofibroma until proven otherwise.
376
Cardiac amyloidosis should be suspected in patients with:
Unexplained congestive heart failure (predominantly diastolic dysfunction), echocardiography findings of increased ventricular wall thickness with normal ventricular cavity dimensions (especially in the absence of hypertension, and low voltage on ECG.
377
Metabolic alkalosis defined as:
pH >7.45 and serum bicarbonate level > 24 mEq/L
378
Main causes for saline- responsive Metabolic Alkalosis:
Vomiting/ nasogastric aspiration; Prior diuretic use; Current diuretic use.
379
Main causes of non-saline-responsive Metabolic Alkalosis:
Excess mineralocorticoids activity ( Primary aldosteronism, cushing's disease, ectopic ACTH production); Barter & Gitleman syndrome.
380
Evaluation of bilious emesis in the neonate: Abdominal x-ray findings: Free air, hematemesis, unstable vital signs: Next step:
Surgery
381
Evaluation of bilious emesis in the neonate: Abdominal x-ray findings: Dilated loops of bowel: Next step: Possible diagnosis:
Contrast enema; If microcolon then diagnosis Meconium ileus; If rectosigmoid transition zone, then Hirschsprung disease.
382
Evaluation of bilious emesis in the neonate: Abdominal x-ray findings: NG tube in misplaced duodenum: Next step: Diagnosis:
Upper GI series; If ligament of treitz on right side of abdomen, then malrotation. (Volvulus)
383
Evaluation of bilious emesis in the neonate: Abdominal x-ray findings: Double bubble sign: Next step: diagnosis:
Duodenal atresia
384
Tamoxifen: Mechanism: Used to treat: Increases the risk of what cancer:
Estrogen antagonist on breast tissue, agonist on endometrium, and decreases risk of osteoporosis. Treatment and prevention of breast cancer. Increases the risk of endometrial cancer. Overall mortality benefit.
385
Bell’s Palsy: Lesions in the CNS occurring above the facial nucleus will:
Typically cause a contralateral lower facial weakness that spares the forehead.
386
Bell’s Palsy: Forehead muscle sparing is suggestive of an:
Intracranial lesion and would warrant brain imaging to evaluate ischemia or tumors.
387
Invasive aspergillosis occurs in: Chest x-ray shows:
Immunocompromised patients, who may present with fever, cough, dyspnea, or hemoptysis. Chest x-ray may show a cavitary lesion, and CT scan shows pulmonary nodules with a halo sign or lesions with an air crescent.
388
Neuroleptic malignant syndrome (NMS): Define: Characterize: Treatment:
Associated with medications that block dopamine transmission such as high potency, typical antipsychotics like haloperidol. Clinical features fever, rigidity, mental status changes, and autonomic instability. Treatment stop drug, control hyperthermia, and maintenance of electrolyte balance. Dantrolene for skeletal muscle relaxation.
389
Premenstrual syndrome (PMS) & premenstrual dysphoric disorder (PMDD): First line treatment:
Selective serotonin reuptake inhibitors (SSRIs) such as fluoxetine.
390
Situational syncope typical scenario would include: Mechanism:
A middle age or older male, who loses his consciousness immediately after urination, or a man who loses his consciousness during coughing fits. Mechanism includes autonomic dysregulation.
391
Patient has an episode of massive hemoptysis: Defined: Treatment:
Defined as > 600mL of expectorated blood over 24-hour period or a bleeding rate >100 mL/hour. Greatest danger is aspyxiation due to airway flooding. Patient placed with bleeding lung in the dependent position (lateral position). Bronchoscopy.
392
Raloxifene first line agent for: Increases the risk of:
Prevention of osteoporosis, and it decreases breast cancer risk. It increase the risk of thromboembolism. Generally women should not get pregnant after rubella vaccination: How long: Recommended waiting time is 28 days, but if women inadvertently get pregnant shortly after vaccination for rubella, they can be reassured that here is little risk to the fetus and they can proceed with ((routine prenatal care)).
393
Digoxin is a cardiac glycoside with adverse effects that include:
Nausea, vomiting, diarrhea, vision changes, and arrhythmias. Get a drug level.
394
Key differences in primary hyperparathyroidism (PHPT) and chronic kidney disease (Secondary hyperparathyroidism:
PTH levels are usually much higher in secondary than primary. In addition, serum calcium levels are low to normal in secondary hyperparathyroidism. Serum phosphorous may be low or normal in PHPT were it tends to be high in kidney disease.
395
Post bone marrow transplant (BMT) with fever, dyspnea, abdominal pain, and diarrhea. Chest x-ray shows multifocal, diffuse infiltrates or CT with parenchymal opacifications or multiple nodules:
CMV pneumonitis after BMT is about 45 days, also manifests as upper and lower gastrointestinal ulcers. Diagnosis with bronchoalveolar lavage.
396
Patients with intrauterine fetal demise who develop coagulation abnormalities:
Should be induced without delay. Especially with low platelets. Remember fibrinogen levels are high in pregnancy therefore anything in the low normal can be an early sign of disseminated intravascular coagulation (DIC).
397
What is the most important direct role of hCG in pregnancy:
Maintenance of the corpus luteum.
398
Progesterone is the hormone responsible for:
Preparing the endometrium for implantation of a fertilized ovum.
399
What inhibits uterine contractions:
Progesterone
400
What causes induction of prolactin production by the pituitary during pregnancy:
Estrogen
401
Human chorionic gonadotropin (hCG) is a hormone secreted by:
Syncytiotrophoblast
402
Whipple’s disease classical biopsy findings: Presentation: Pathogen:
PAS positive material in the lamina propria of the small intestines. Arthralgias, ((weight loss)), fever, ((diarrhea)), and abdominal pain. Tropheryma whippeli.
403
Myotonic muscular dystrophy: Genetics: Presentation:
Autosomal dominant expansion CTG chromosome 19q 13.3. Onset 12-30. Patient with facial weakness, handgrip myotonia, dysphagia. ((Arrhythmias, cataracts, balding, and testicular atrophy/infertility)). Remember Duchenne and Becker have earlier age of onset without underlined.
404
Opioid intoxication presents with:
((Miosis)), depressed mental status, decreased respiratory rate, decreased bowel sounds, ((hypotension)), and ((bradycardia)).
405
Neonatal sepsis treatment after complete blood count and CSF cultures:
Administering systemic antibiotics ampicillin plus gentamicin.
406
Most common cause of sepsis in neonatal period:
GBS and E. coli. Term infants more likely GBS. Preterm is E. coli.
407
Difference in treatment of infant botulism compared to foodborne botulism:
Infant borne: Ingestion of C. botulinum ((spores)) from environmental. Tx: ((Human)) derived botulinum immune ((globulin.)) Foodborne botulism: Ingestion of ((preformed)) C. botulinum ((toxin)). Tx: ((Equine))-derived botulinum ((antitoxin)).
408
Patient presents with septic shock and developed AST and ALT elevation one day later: Labs:
Presentation most consistent with ((ischemic hepatic injury)), or ((shock liver)). Hallmark of ischemic hepatopathy is a rapid and massive increase in the transaminases with modest accompanying elevation in total bilirubin and alkaline phosphatase. If patient survives liver enzymes return to normal in a few weeks.
409
Sinus pauses on monitor, prolonged PR interval or QRS duration: Differential diagnosis:
Sick sinus syndrome, ((bradyarrhythmias)), atrioventricular block; Can be ((intermittent)).
410
Intraventricular conduction delay refers to:
Prolonged QRS duration.
411
Torsades de Pointes is due to:
Polymorphic ventricular tachycardia in the setting of prolonged QT interval. Long QTc interval
412
When looking at multiple endocrine neoplasia in a patient with HA and HT: If eye exam is normal:
Get plasma free metanephrine or 24-hour urine metanephrines.
413
Papillary thyroid cancer (PTC): Characterized: Prognosis:
Most common thyroid cancer. Characterized by a slow infiltrative local spread affecting other parts of thyroid gland and regional lymph nodes. Prognosis good. nonencapsulated
414
Follicular thyroid cancer: Histopathology:
Demonstration of invasion of the capsule and blood vessels is required to differentiate follicular cancers from follicular adenomas. Early hematogenous spread to the lungs, brain, and bone.
415
Medullary cancer of the thyroid can secrete:
Calcitonin
416
Presence of Hurthle cells on biopsy of thyroid gland:
Can be seen in both follicular and papillary cancers. Hurthle cell carcinoma is a variant of follicular cell carcinoma.
417
Vitiligo: What is it: What is it associated with:
Vitiligo is an autoimmune condition characterized by areas of depigmentation lacking melanocytes. Vitiligo is sometimes associated with other autoimmune conditions such as pernicious anemia, autoimmune thyroid disease, type I diabetes mellitus, primary adrenal insufficiency, hypopituitarism, and alopecia areata.
418
In a case-control study, if the outcome is uncommon in the population:
The odds ration (OR) is a close approximation of the relative risk (RR) (“rare disease assumption”).
419
Thalamic hemorrhage may present with:
Contralateral hemiparesis and sensory loss. Typically associated with nonreactive miotic pupils and eyes that deviate TOWARD the side of hemiparesis.
420
Basal ganglia hemorrhage may present with:
Contralateral hemiparesis and sensory loss. Homonymous hemianopsia, and Gaze palsy.
421
Pons hemorrhage may present with:
Deep coma & total paralysis within minutes, PINPOINT reactive pupils.
422
Ethylene glycol poisoning key findings:
Calcium oxalate crystals (rectangular, envelope-shaped crystals) are seen in urine. Common in antifreeze.
423
Methyl alcohol poisoning key findings:
Can cause visual changes (“snowfield vision”) and pancreatitis.
424
Trichinellosis typically presents with:
``` Gastrointestinal complaints (abdominal pain, nausea, vomiting) followed by the characteristic triad of periorbital edema, myositis, and eosinophilia (hallmark of the disease). Other clinical findings include fever, subungual splinter hemorrhages or retinal hemorrhages. ```
425
Patients with febrile neutropenia and no obvious focus of infection given normal x-ray and urinalysis:
Severe neutropenia seen in chemo patients should get blood cultures followed by monotherapy with an antipseudomonal beta-lactam agent (cefepime, meropenem, piperacillin-tazobactam) provides both gram-negative & gram-positive coverage.
426
Acute lymphoblastic leukemia is predominantly seen in: Presents with: Labs show:
Seen in children from ages 2-10. Varying degrees of anemia, neutropenia, and thrombocytopenia. Blast cells have condensed nuclear chromatin, small nucleoli and scant agranular cytoplasm. Histochemical staining strongly positive periodic acid Schiff (PAS). Deoxynucleotidyltransferase (TdT) is positive 95% time. 25% lymphoblasts bone marrow diagnostic.
427
Features for ischemic reperfusion syndrome: Mechanism: Diagnosis:
A form of compartment syndrome (CS). Post-ischemic CS is due to interstitial edema and possibly intracellular swelling following tissue ischemia and subsequent reperfusion such as after and embolectomy. Compartment pressure > 300 mmHg.
428
Initial stabilization of acute ST-elevation MI: Initial drugs given:
Aspirin, Clopidogrel, Nitrates (sublingual), beta blocker (unless hypotension, bradycardia, CHF, heart block), High dose statin, anticoagulation (depends on planned revascularization).
429
Initial stabilization of acute ST-elevation MI: Drug given if patient has persistent pain, hypertension, or heart failure:
Intravenous nitroglycerin (not if hypotension, right ventricular infarct, or severe aortic stenosis occurs)
430
Initial stabilization of acute ST-elevation MI: Drug given persistent pain:
Intravenous morphine
431
Initial stabilization of acute ST-elevation MI: Drug given for unstable sinus bradycardia:
Intravenous atropine Initial stabilization of acute ST-elevation MI: Drug given pulmonary edema: Intravenous furosemide (not if patient is hypotensive or hypovolemic)
432
Osteosarcoma X-ray findings: Epidemiology:
Spiculated “sunburst” pattern and periosteal elevation known as the Codman triangle. Most common primary bone tume affecting children and young adults.
433
Ewing sarcoma X-ray findings:
An osteolytic lesion with a periosteal reaction that produces layers of reactive bone, giving the classic “onion skin” appearance. Second most common primary bone tumor.
434
Osteoid osteoma X-ray findings: Features:
Sclerotic, cortical lesion on imaging with a central nidus of lucency. It typically causes pain that is worse at night and unrealted to activity. Pain is quickly relieved by NSAIDs.
435
Dermatitis herpetiformis (DH) presents with: Associated with: Treatment:
Erythematous papules, vesicles, and bullae that occur bilaterally, symmetrically, and in grouped “herpetiform” arrangement on the extensor surfaces elbows, knees, upper back, and buttocks. Associated with gluten-sensitive entropathy (celiac disease). Tx: Dapsone
436
Choriocarcinoma Lab:
Increased beta-hCG
437
Teratomas Lab:
Elevations in serum concentration AFP or beta-HCG can appear, due to coexistence of other germ cell tumor components.
438
Seminomas Lab:
Serum tumor markers are usually normal, although beta-hCG maybe somewhat elevated if they contain synctiotrophoblastic giant cells.
439
Yolk sac tumor (endodermal sinus tumor) Lab:
Germ cell tumor accompanied by an increase in serum AFP.
440
Trauma if FAST exam is inconclusive or is positive:
Inconclusive: diagnostic peritoneal lavage (DPL). Positive: Laparotomy.
441
Evaluation of secondary amenorrhea with a negative β-hCG: What are the next labs ordered:
Check prolactin, TSH, FSH
442
Evaluation of secondary amenorrhea with a negative β-hCG, but increased prolactin: What test:
Brain MRI
443
Evaluation of secondary amenorrhea with a negative β-hCG, but increased TSH:
Diagnosis hypothyroidism
444
Evaluation of secondary amenorrhea with a negative β-hCG, but increases FSH:
Premature ovarian failure
445
Secondary amenorrhea defined as:
Absence of menses for ≥3 cycles or ≥6 months in women who menstruated previously.
446
Aortic valve endocarditis and intravenous drug abuse are associated with an increased risk of:
Periannular extension of endocarditis.
447
Serum Sickness like reaction is most commonly caused by: Presentation: Treatment:
Caused by β-lactams, and sulfa drugs. Symptoms arise 1-2 weeks after exposure and include fever, urticarial rash, polyarthralgia, and lymphadenopathy. Remove offending agent.
448
Congestive heart failure due to left ventricular systolic dysfunction is characterized by:
Decreased cardiac output/index, increased systemic vascular resistance (SVR), and an increase in left ventricular end-diastolic volume (LVEDV).
449
Carcinoid syndrome clinical manifestations: Tests:
Skin: flushing, telangiectasia, cyanosis; GI: diarrhea, cramping; Cardiac: valvular lesions (right>left); Pulmonary: bronchospasms; Niacin deficiency (dermatitis, diarrhea, dementia). Diagnosis 24-hour urine 5-hydroxyindoleacetic acid. CT/MRI to localize tumor. OctreoScan to detect metastasis.
450
Cell-free fetal DNA testing is a noninvasive and highly sensitive and specific screening test for:
fetal aneuploidy and can be ordered at ≥10 weeks gestation.
451
Abnormal cell-free fetal DNA testing results can be confirmed by:
Chorionic villus sampling at 10-12 weeks or amniocentesis at 15-20 weeks.
452
First trimester combined test:
Pregnancy- associated plasma protein, β-hCG, nuchal translucency.
453
Second trimester quadruple screen:
Maternal serum ɑ-fetoprotein, estriol, β-hCG, inhibin A.
454
Most common organ origins of osteolytic metastasis:
most common in cancers that have spread to bone from the lung, thyroid, kidney, and colon.
455
Most common organ origins of osteoblastic metastasis:
It is more frequently seen in spread of prostate, bladder, and stomach cancer.
456
What is the purpose of diagnostic or prognostic exercise testing? (stress testing)
To localize ischemia or assess viability to recommend exercise
457
small cell carcinoma causes what syndrome
SIADH
458
diverticulitis, what test do you use?
CT scan of abdomen
459
What is the strongest risk factor for future pre-term birth?
Prior PTB is the strongest risk factor for future PTB, and recurrences often occur at the same gestational age
460
For Addisons' crisis/ adrenal insufficiency - what test?
ACTH stimulation test
461
Test to distinguish cushing's disease and cushion's syndrome and primary pituitary insufficiency
Dexamethasone suppression test.
462
Vaccines needed by HIV patients
1. The Flu Vaccine 2. Pneumococcal vaccine 3. Diphtheria, tetanus, and pertussis vaccines 4. HPV vaccine 5. Hep B vaccine
463
HIV patients who need the meningococcus vaccine have these risk factors:
* Live in a city that has had a meningitis outbreak (such as New York City) * Travel to a city that has had a meningitis outbreak * Have or will have close contact with other men who have sex with men from a city that has had a meningitis outbreak
464
When is a HIDA scan done?
When the ultrasound is inconclusive, because it deals with the gall bladder, no need in patient who already has cholecystectomy.
465
HIV patients who need the Hep A vaccine have these risk factors:
* People who use intravenous (IV) drugs * Men who have sex with men * People who already have other forms of liver disease * People with a bleeding disorder called hemophilia * People who travel to certain parts of the world
466
HIV patients can get these live vaccines if their CD4+T cell counts are above 200
Varicella and Zoster vaccines
467
Most common sites of ulnar nerve entrapment
at the elbow, followed by the wrist
468
Pulmonary embolism, treatment
heparin therapy
469
Cubital tunnel syndrome, where is the nerve compression located?
Cubital tunnel syndrome is used to describe ulnar nerve impingement along the cubital tunnel at the medial edge of the elbow. It is the most common location of nerve impingement in the elbow area
470
Guyon's canal syndrome, where is the nerve compression located?
Guyon's canal syndrome, or ulnar tunnel syndrome, refers to nerve compression affecting the ulnar nerve as it passes through an anatomical space in the wrist called Guyon's canal
471
Rh isoimmunization, mother is O-Rh (-) , what happens to an O-Rh(+) newborn?
Rh(+) factors from newborn leaks into mothers bloodstream, causes anti IgG Rh antibodies.
472
Diabetic neuropathy - what type of urinary symptoms can they have.
Intermittent urinary incontinence, overflow incontinence by an acontractyle bladder (think detrusor muscle - lack of innervation)
473
In patients with neurofibromatosis type 1, what type of hypertension is seen in these patients?
Essential hypertension, from renal vascular lesions, most commonly in the renal vasculature.
474
What is the most common peroxisomal disorder?
Adrenoleukodystrophy (ALD)
475
What is the Adrenoleukodystrophy (ALD) Genetics?
Adrenoleukodystrophy (ALD) is an X-linked disorder
476
What is the pathogenesis of Adrenoleukodystrophy (ALD)?
Mutations may prevent normal transport of very long chain fatty acids (VLCFAs) into peroxisomes, thereby preventing beta-oxidation and breakdown of VLCFAs. Accumulation of abnormal VLCFAs in CNS, Leydig cells of the testes, and the adrenal cortex
477
Children and adolescents with hypertension. What percentile do you treat?
blood pressure greater than the 95th percentile for age, height, weight.
478
Cardiac auscultation - aortic area - systolic ejection murmur. What's the diagnosis?
Aortic stenosis
479
Cardiac auscultation - pulmonic area - systolic ejection murmur. What's the diagnosis?
Pulmonic stenosis, flow murmur, ASD (atrial septal defect)
480
Cardiac auscultation - pulmonic area - systolic ejection click. What's the diagnosis?
Pulmonic stenosis
481
Cardiac auscultation - left sternal border area - systolic ejection murmur. What's the diagnosis?
Hypertrophic cardiomyopathy
482
Cardiac auscultation - left sternal border area - early diastolic murmur. What's the diagnosis?
Aortic regurgitation, pulmonic regurgitation
483
Cardiac auscultation - mitral area - holostolic murmur. What's the diagnosis?
mitral regurgitation
484
Cardiac auscultation - mitral area - mid/late systolic click. What's the diagnosis?
mitral valve prolapse
485
Cardiac auscultation - mitral area - mid/late diastolic murmur. What's the diagnosis?
mitral stenosis
486
Cardiac auscultation - tricuspid area - holosystolic murmur. What's the diagnosis?
tricuspid regurgitation, ventral septal defect
487
Cardiac auscultation - mitral area - mid/late diastolic murmur. What's the diagnosis?
tricuspid stenosis, ASD (atrial septal defect)
488
Increased blood flow in what areas of the heart cause ASD murmurs?
ASD murmurs caused by increased blood flow across pulmonic valve and tricuspid valve
489
Neurologic complications of endocarditis with replacement valve?
Embolic stroke, brain abscess or cerebritis, meningitis, acute encephalopathy, meningoencephalitis.
490
Indications for gastric bypass surgery in an adult.
Adults with a body mass index (BMI) ≥40 kg/m2 without comorbid illness or a BMI 35.0 to 39.9 kg/m2 with at least one serious comorbidity, such as type 2 diabetes or hypertension, are candidates for a bariatric surgical procedure. Adults with BMI between 30.0 to 34.9 kg/m2 and either difficult to control type 2 diabetes mellitus or metabolic syndrome should be considered as candidates
491
Signs suggesting radial nerve damage with humeral fracture.
Wrist drop, loss of thumb abduction
492
What is Tinel's sign?
Tapping over the median nerve at the wrist elicits tingling in the median nerve distribution.
493
What are the 6 P's of compartment syndrome:
Pain, pallor paresthesias, poikilothermic, paralysis, pulselessness
494
Carpal tunnel syndrome - What nerve is affected and where? - Hx/PE - Dx
- Entrapment of the median nerve at the wrist. - Presents w/ aching over the thenar area of the hand and proximal forearm (maybe shoulder). - parasthesia/numbness in median nerve distribution - Symptoms worsen at night - Phalen's maneuver and Tinel's sign are (+)
495
In the hand, the median nerve supplies motor innervation to which muscles?
1st and 2nd lumbrical muscles and the muscles of the thenar eminence.
496
In the hand, the median nerve innervates the skin where?
The median nerve innervates the skin of the palmar side of the thumb, the index and middle finger and half the ring finger.
497
Injury of the median nerve above the elbow is caused by a supracondylar fracture - what are the motor and sensory deficits?
Loss of pronation of forearm, weakness in flexion of the hand at the wrist, loss of flexion of radial half of digits and thumb, loss of abduction and opposition of thumb. Presence of an ape hand deformity when the hand is at rest, due to an hyperextension of index finger and thumb, and an adducted thumb. Presence of benediction sign when attempting to form a fist, due to loss of flexion of radial half of digits. Sensory deficit: Loss of sensation in lateral 3 1⁄2 digits including their nail beds, and the thenar area.
498
What are common mechanisms of injury of the ulnar nerve at the elbow?
Cubital tunnel syndrome, fracture of the medial epicondyle
499
What are the clinical features caused by injury of the ulnar nerve at the elbow?
Ulnar lesions at the elbow typically present with numbness and tingling in the fourth and fifth digits, medial elbow pain, nocturnal numbness and paresthesia, and worsening of symptoms with elbow and/or repeated wrist flexion
500
What are the sensory deficits caused by injury of the ulnar nerve at the elbow?
Sensory deficit: Loss of sensation or paresthesiae in ulnar half of the palm and dorsum of hand, and the medial 1½ digits on both palmar and dorsal aspects of the hand
501
What are the sensory deficits caused by injury of the ulnar nerve at the wrist?
Loss of sensation or paresthesia in ulnar half of the palm, and the medial 1½ digits on the palmar aspect of the hand. The dorsal aspect of the hand is unaffected.
502
What are the motor deficits caused by injury of the ulnar nerve at the wrist?
Loss of flexion of ulnar half of digits, or the 4th and 5th digits, loss of ability to cross the digits of the hand. Presence of a claw hand deformity when the hand is at rest.
503
What are common mechanisms of ulnar nerve damage at the wrist?
penetrating wound or Guyon canal cyst
504
What are the major abnormalities of the heart muscle in these cardiomyopathies: dilated, hypertrophic, restrictive
Dilated - impaired contractility Hypertrophic - impaired relaxation Restrictive - impaired elasticity
505
For dilated cardiomyopathy, explain if it increases or decreases: - Left ventricular cavity size (end diastole) - Left ventricular cavity size (end systole) - Ejection fraction (EF) - Wall thickness
For dilated cardiomyopathy: - ↑↑ Left ventricular cavity size (end diastole) - ↑↑ Left ventricular cavity size (end systole) - ↓↓ Ejection fraction (EF) - ↓, variable Wall thickness
506
For hypertrophic cardiomyopathy, explain if it increases or decreases: - Left ventricular cavity size (end diastole) - Left ventricular cavity size (end systole) - Ejection fraction (EF) - Wall thickness
For hypertrophic cardiomyopathy: - ↓ Left ventricular cavity size (end diastole) - ↓↓ Left ventricular cavity size (end systole) - ↑ or ↔ Ejection fraction (EF) - ↑↑ Wall thickness
507
For restrictive cardiomyopathy, explain if it increases or decreases: - Left ventricular cavity size (end diastole) - Left ventricular cavity size (end systole) - Ejection fraction (EF) - Wall thickness
For dilated cardiomyopathy: - ↑ Left ventricular cavity size (end diastole) - ↑ Left ventricular cavity size (end systole) - ↓ or ↔ Ejection fraction (EF) - ↑, variable Wall thickness
508
What does an S3 gallop signify is happening to the blood volume and blood flow in the heart? What disease is this associated with?
An S3 gallop signifies the end of rapid ventricular filling in the setting of fluid overload and is associated with dilated cardiomyopathy.
509
How do you diagnose dilated cardiomyopathy?
Echocardiography
510
What does the chest x-ray show in dilated cardiomyopathy?
■ CXR shows an enlarged, balloon-like heart and pulmonary congestion.
511
What is the treatment for dilated cardiomyopathy?
■ Address the underlying etiology (e.g., stop all alcohol use, treat endocrine disorders). ■ Treat symptoms of CHF with diuretics, and prevent disease progression with ACEIs, β-blockers, and aldosterone antagonists. Consider anticoagulation to ↓ thrombus risk only if AF or an intraventricular thrombus is present. Digoxin is a second-line agent; avoid CCBs in CHF. ■ Consider an ICD if EF
512
What is the pathophysiology of hypertrophic cardiomyopathy?
LVH results in impaired left ventricular relaxation and filling (diastolic dysfunction). Hypertrophy frequently involves the interventricular septum, leading to left ventricular outflow tract obstruction and impaired ejection of blood.
513
What is the most common cause of sudden death in young, healthy athletes in the United States?
The congenital form of hypertrophic cardiomyopathy, hypertrophic obstructive cardiomyopathy (HOCM).
514
What is the genetics of hypertrophic obstructive cardiomyopathy (HOCM)?
It is inherited as an autosomal-dominant trait in 50% of HOCM patients.
515
What does an S4 gallop signify?
A stiff, noncompliant ventricle
516
↑ “atrial kick” is associated with which cardiomyopathy?
hypertrophic cardiomyopathy.
517
Spherocytosis tests:
eosin-5 maleimide test (flow cytometry) with acid glycerol lysis test
518
Causes of postoperative fever ( the 5 Ws):
Wind (lungs): Pulmonary embolism; Pneumonia; Aspiration; Wound: Surgical site infection Water: Urinary tract infection (UTI) Walk: Deep venous thrombosis Wonder drugs/products: Drug fever; Blood products; Intravenous lines.
519
Immunologic blood transfusion reactions: Febrile nonhemolytic
(most common reaction): Fever and chills; Within 1-6 hours of transfusion; Caused by cytokine accumulation during blood storage.
520
Immunologic blood transfusion reactions: Acute hemolytic: Presents with: Mechanism:
Fever, flank pain, hemoglobinuria, renal failure and DIC; Within 1 hour of transfusion. Positive direct Coombs test, pink plasma; Caused by ABO incompatibility.
521
Immunologic blood transfusion reactions: Delayed Hemolytic: Mechanism:
Mild fever and hemolytic anemia; Within 2-10 days after transfusion; Positive direct Coombs test, positive antibody screen; Caused by anamnestic antibody response.
522
Immunologic blood transfusion reactions: Anaohacltic: Presentaion: Mechanism:
Rapid onset of shock, angioedema/urticaria and respiratory distress; Within a few seconds to minutes of transfusion; Caused by recipient anti-IgA antibodies
523
Immunologic blood transfusion reactions: Urticarial/allergic: Presentation; Mechanism
Urticaria, flushing, angioedema and pruritus; Within 2-3 hours of transfusion; Caused by recipient IgE antibodies and mast cell activation.
524
Immunologic blood transfusion reactions: Transfusion-related acute lung injury: Presentation: Mechanism:
Respiratory distress and signs of noncardiogenic pulmonary edema; Within 6 hours of transfusion; Caused by donor anti-leukocyte antibodies.
525
Define Mean:
Mathematical average
526
Define median:
splits an ordered dataset in half.
527
Define mode:
The most frequently observed value.
528
Three way to diagnose syphilis:
Nontreponemal serological tests (VDRL, RPR) are used for screening test, and treponemal serologic tests (FTA-ABS) are used to confirm. Darkfield microscopy is also an effective method for diagnosing, but requires equipment. Darkfield is used because serologic testing has a high false negative rate.
529
Polymyositis: Distinguishing features: Laboratory/Diagnosis:
Symmetrical proximal muscle weakness; Increasing difficulty climbing stairs, getting up from a chair, carrying heavy groceries; Less prominent hip/shoulder involvement; Labs: Elevated muscle enzymes (creatine kinase, aldolase, lactate dehydrogenase, aspartate aminotransferase), possible autoantibodies, EMG abnormal.
530
Polymyalgia rheumatica: Distinguishing features: Laboratory/Diagnosis:
Age usually >50. Aching and morning stiffness>pain in shoulders, hips, neck, torso. Synovitis, bursitis, decreased range of motion. No significant tenderness. Possible systemic symptoms; Clinical diagnosis. Significantly elevated ESR. Symptoms improve with corticosteroids.
531
Hematological complications Infectious mononucleosis (IM): Mechanism:
Can cause autoimmune hemolytic anemia and thrombocytopenia, which is due to cross reactivity of the EBV-induced antibodyeas against RBCs and platelets. These antibodies are IgM cold agglutinin antibodies lead to compliment mediated RBC destruction (Coombs +). Onset 2-3 weeks.
532
What causes similar symptoms of angina pectoris, but is caused by vasospasm of coronary vessels?
Prinzmetal’s (variant) angina
533
Prinzmetal’s (variant) angina: Etiology, epi, ECG, cardiac enzymes
Prinzmetal’s (variant) angina mimics angina pectoris but is caused by vasospasm of coronary vessels. It classically affects young women at rest in the early morning and is associated with ST-segment elevation in the absence of cardiac enzyme elevation.
534
What is the classic triad of angina?
substernal chest pain that is provoked by exertion and relieved by rest or nitrates.
535
What drugs have been shown to have a mortality benefit in the treatment of angina?
Only ASA and β-blockers
536
What patient groups may have atypical, clinically silent MIs?
Women, diabetics, the elderly, and post–heart transplant patients
537
How do you treat acute symptoms of coronary artery disease (CAD)?
ASA, O2 and/or IV nitroglycerin, and IV mor- phine, and consider IV β-blockers.
538
How do you treat chronic symptoms of coronary artery disease (CAD)?
nitrates, ASA, and β-blockers; CCBs are second-line agents for symptomatic control only
539
Define acute coronary syndromes.
A spectrum of clinical syndromes caused by plaque disruption or vasospasm that leads to acute myocardial ischemia.
540
Define unstable angina.
chest pain that is new onset, is accelerating (i.e., occurs with less exertion, lasts longer, or is less responsive to medications), or occurs at rest; it is distinguished from stable angina by patient history.
541
Unstable angina signals the presence of possible ___________ based upon plaque instability.
impending infarction
542
Non-ST-Elevation Myocardial Infarction (NSTEMI) indicates ___________ marked by elevations in ____ , ____ or ___
NSTEMI indicates myocardial necrosis marked by elevations in troponin I, troponin T, or CK-MB
543
If chest pain is new onset, accelerating, or occurring at rest then it is called _________
unstable angina
544
Acute treatment of Unstable Angina/Non-ST-Elevation Myocardial Infarction (NSTEMI) is the same as that for stable angina. What is it?
Clopidogrel, unfractionated heparin or enoxaparin, and glycoprotein IIb/IIIa inhibitors (e.g., eptifibatide, tirofiban, abciximab) should also be considered.
545
How do you treat patients with chest pain refractory to medical therapy, a TIMI score of ≥ 3, a troponin elevation, or ST changes > 1 mm?
Give Heparin and scheduled for angiography and possible revascularization (percutaneous coronary intervention [PCI] or CABG).
546
TIMI Risk Score for Unstable Angina/NSTEMI (0-7 points possible). 4 points possible for history, 3 points for presentation. What are the criteria?
1. Age ≥ 65 years = 1 2. ≥ 3 CAD risk factors (family history, DM, tobacco, hypertension, ↑ cholesterol) = 1 3. Known CAD (stenosis > 50%) = 1 4. ASA use in past seven days = 1 5. Severe angina (≥ 2 episodes within 24 hours) = 1 6. ST deviation ≥ 0.5 mm 7. + cardiac marker
547
Higher-risk patients (risk score ≥ 3) benefit more from what drugs and test?
Enoxaparin (vs. unfractionated heparin), glycoprotein IIb/IIIa inhibitors, and early angiography.
548
Define ST-Elevation Myocardial Infarction (STEMI).
ST-segment elevations and cardiac enzyme release 2° to prolonged cardiac ischemia and necrosis.
549
Hx / PE findings in patient with ST-Elevation Myocardial Infarction (STEMI).
■ Presents with acute-onset substernal chest pain, commonly described as a pressure or tightness that can radiate to the left arm, neck, or jaw. ■ Associated symptoms may include diaphoresis, shortness of breath, light- headedness, anxiety, nausea/vomiting, and syncope. ■ Physical exam may reveal arrhythmias, new mitral regurgitation (ruptured papillary muscle), hypotension (cardiogenic shock), and evidence of new CHF (rales, peripheral edema, S3 gallop).
550
How to diagnose ST-Elevation Myocardial Infarction (STEMI)? Name key ECG findings only.
ECG: Look for ST-segment elevations or new LBBB. ST-segment depressions in leads V1–V2 can also be reciprocal change indicating infarction in the posterior wall.
551
Describe which leads the ST-segment abnormalities are seen in ST-Elevation Myocardial Infarction (STEMI) consistent with an inferior MI.
ST-segment elevation in leads II, III, and aVF is consistent with an inferior MI involving the RCA/PDA and LCA.
552
Describe which leads the ST-segment abnormalities are seen in ST-Elevation Myocardial Infarction (STEMI) consistent with an anterior MI.
ST-segment elevation in leads V1–V4 usually indicates an anterior MI involving the LAD and diagonal branches
553
Describe which leads the ST-segment abnormalities are seen in ST-Elevation Myocardial Infarction (STEMI) consistent with an lateral MI.
ST-segment elevation in leads I, aVL, and V5–V6 points to a lateral MI involving the LCA.
554
Describe which leads the ST-segment abnormalities are seen in ST-Elevation Myocardial Infarction (STEMI) consistent with an posterior wall MI.
ST-segment depression in leads V1–V2 can be “reciprocal change” indicative of an acute infarct in the posterior wall.
555
Treatment of ST-Elevation Myocardial Infarction (STEMI). Name 6 key medications.
ASA, β-blockers, clopidogrel, morphine, nitrates, and O2.
556
Drug treatment of ST-Elevation Myocardial Infarction (STEMI) if patient is in heart failure or in cariogenic shock.
Do not give β-blockers; instead, give ACEIs, provided that the patient is not hypotensive.
557
Treatment of ST-Elevation Myocardial Infarction (STEMI). Name surgical procedure(s).
Emergent angiography and PCI should be performed
558
Name other causes of ST-segment elevation besides ST-Elevation Myocardial Infarction (STEMI).
Acute pericarditis, LVH, LBBB, and a normal variant (e.g., “early repolarization”).
559
What part of the heart is this MI occurring? In this patient with acute chest pain, the ECG demonstrated acute ST-segment elevation in leads II, III, and aVF with reciprocal ST-segment depression and T-wave flattening in leads I, aVL, and V4–V6.
Inferior wall MI.
560
What part of the heart is this MI occurring? This patient presented with acute chest pain. The ECG showed acute ST-segment elevation in leads aVL and V1–V6, and hyperacute T waves.
Anterior wall MI.
561
Treatment of STEMI: If the patient presents within three hours, PCI cannot be performed within 90 minutes, and there are no contraindications to thrombolysis (e.g., a his- tory of hemorrhagic stroke or recent ischemic stroke, severe heart failure, or cardiogenic shock), how do you treat?
Thrombolysis with tPA, reteplase, or streptokinase should be performed instead of PCI.
562
Treatment of STEMI: In the setting of three-vessel disease, left main coronary artery disease, discrete lesions not amenable to PCI, or diffuse disease with good target vessels, how do you treat?
PCI should be attempted immediately for the lesion thought to be responsible for STEMI; the patient is a candidate for CABG afterward.
563
What is the long-term treatment of STEMI patient?
Long-term treatment includes ASA, ACEIs, β-blockers, high-dose statins, and clopidogrel (if PCI was performed). Modify risk factors with dietary changes, exercise, and tobacco cessation.
564
What is the most common complication and cause of death following acute MI?
Arrhythmia
565
What is Dressler's syndrome? Etiology, epidemiology, S&S, labs?
Dressler’s syndrome, an autoimmune process occurring 2–10 weeks post- MI, presents with fever, pericarditis, pleural effusion, leukocytosis, and ↑ ESR.
566
Besides arrhythmia, what are less common complications of STEMI?
Reinfarction, left ventricular wall rupture, VSD, pericarditis, papillary muscle rupture (with mitral regurgitation), left ventricular aneurysm or pseudoaneurysm, and mural thrombi.
567
``` Fill in the timeline of common post-MI complications: ■ First day: ■ 2–4 days: ■ 5–10 days: ■ Weeks to months: ```
A timeline of common post-MI complications: ■ First day: Heart failure (treat with nitroglycerin and diuretics). ■ 2–4 days: Arrhythmia, pericarditis (diffuse ST elevation with PR depression). ■ 5–10 days: Left ventricular wall rupture (acute pericardial tamponade causing electrical alternans, pulseless electrical activity), papillary muscle rupture (severe mitral regurgitation). ■ Weeks to months: Ventricular aneurysm (CHF, arrhythmia, persistent ST elevation, mitral regurgitation, thrombus formation).
568
Total cholesterol > 200 mg/dL, LDL > 130 mg/dL, triglycerides > 500 mg/ dL, and HDL
CAD
569
Name etiologies for hypercholesterolemia, and therefore, CAD.
Etiologies include obesity, DM, alcoholism, hypothyroidism, nephrotic syndrome, hepatic disease, Cushing’s disease, OCP use, high-dose diuretic use, and familial hypercholesterolemia.
570
HISTORY/PE for hypercholesterolemia / CAD.
■ Most patients have no specific signs or symptoms. ■ Patients with extremely high triglyceride or LDL levels may have xanthomas (eruptive nodules in the skin over the tendons), xanthelasmas (yellow fatty deposits in the skin around the eyes), and lipemia retinalis (creamy appearance of retinal vessels).
571
How do you diagnose hypercholesterolemia / CAD?
■ Conduct a fasting lipid profile for patients > 20 years of age and repeat ev- ery five years or sooner if elevated. ■ Total serum cholesterol > 200 mg/dL on two different occasions is diagnos- tic of hypercholesterolemia.
572
Describe the mg/dL of LDL and HDL to qualify as dyslipidemia.
Dyslipidemia: ■ LDL > 130 mg/dL or ■ HDL
573
ATP III Guidelines for Risk Stratification of Hypercholesterolemia: What are the mg/dL LDL goals for each category of risk factors: - CAD or CAD risk equivalents - 2+ risk factors - 0-1 risk factor
- CAD or CAD risk equivalents:
574
ATP III Guidelines for Risk Stratification of Hypercholesterolemia: What are the mg/dL LDL that a patient would start lifestyle modification for each category of risk factors: - CAD or CAD risk equivalents - 2+ risk factors - 0-1 risk factor
- CAD or CAD risk equivalents: > 100 mg/dL - 2+ risk factors: > 130 mg/dL - 0-1 risk factor: > 160 mg/dL
575
ATP III Guidelines for Risk Stratification of Hypercholesterolemia: What are the mg/dL LDL at which you would consider drug therapy for each category of risk factors: - CAD or CAD risk equivalents - 2+ risk factors - 0-1 risk factor
- CAD or CAD risk equivalents: > 130 mg/dL - 2+ risk factors: > 160 mg/dL - 0-1 risk factor: > 190 mg/dL
576
What are CAD risk equivalents, according to the ATP III Guidelines for Risk Stratification of Hypercholesterolemia?
symptomatic carotid artery disease, peripheral arterial disease, abdominal aortic aneurysm, diabetes.
577
What are the risk factors according to the ATP III Guidelines for Risk Stratification of Hypercholesterolemia? What is a "negative" risk factor?
Cigarette smoking, hypertension, low HDL ( 45 years; women > 55 years). An HDL > 60 mg/dL counts as a “negative” risk factor and removes one risk factor from the total score.
578
If your total serum cholesterol is
LDL > 130 mg/dL or HDL
579
What is the diagnostic threshold in mg/dL of LDL and HDL for dyslipidemia?
LDL > 130 mg/dL or HDL
580
What is the first intervention in a hyperlipidemia patient with no known atherosclerotic disease?
The first intervention should be a 12-week trial of diet and exercise in a patient with no known atherosclerotic vascular disease.
581
What is the BP goal in uncomplicated hypertension?
582
What is the BP goal for diabetics or patients with renal disease?
583
Define hypertension.
Defined as a systolic BP > 140 mmHg and/or a diastolic BP > 90 based on three measurements separated in time
584
Hematological complications of Infectious mononucleosis (IM): Mechanism:
Can cause autoimmune hemolytic anemia and thrombocytopenia, which is due to cross reactivity of the EBV-induced antibodies against RBCs and platelets. These antibodies are IgM cold agglutinin antibodies lead to compliment mediated RBC destruction (Coombs +). Onset 2-3 weeks.
585
Downs syndrome cardiac abnormalities in order of most often seen:
1 Complete atrioventricular canal 2 Ventricular septal defect 3 Atrial septal defect
586
Nocardiosis: Microbiology: Epidemiology: Clinical Features: Treatment:
Gram-positive rod (beaded or branching), partially acid-fast, aerobic. Found in soil. Most common in immune compromised or elderly patients.Inhalation of aerosolized saprophytes or traumatic inoculation skin. Pneumonia like TB, Neural tropism (brain abscess), cutaneous involvement. Tx: TMP-SMX.
587
Differentiate Rotator cuff tear, Adhesive capsulitis, and Rotator cuff tendonitis based on injection of joint with lidocaine:
In the case of isolated rotator cuff tendonitis, any pain and limitation of motion is resolved by injection. Does do this for the other two.
588
Lynch syndrome II of the Hereditary Nonpolyposis Colorectal Cancer (HNPCC): What cancer are th more prone to get: What is difference between Lynch syndrome I:
Lynch syndrome II is distinctly associated with a high risk of extracolonic tumors, the most common of which is endometrial carcinoma.
589
Cauda equina syndrome:
Radicular pain, asymmetric motor weakness, hyporeflexia/areflexia. Late bladder/bowel dysfunction. A sensory level at the umbilicus excludes this.
590
Conus medullaris syndrome:
Sudden onset severe back pain, symmetrical motor weakness, hyperreflexia. Early onset bladder/bowel dysfunction.
591
Gastric adenocarcinoma staging process:
Initial endoscopy/biopsy positive for adenocarcinoma; Ct abdomen and pelvis; Limited stage = surgical resection. Advanced stage = Chemotherapy, palliative.
592
Community-acquired pneumonia (CAP): Risk assessment:
CURB-65 (1 point each): 2 or more inpatient Tx. score ≥ 4 ICU. Confusion Uremia (BUN > 20 mg/dL) Tachpnea (Respirations > 30/min) Hypotension 65 Community-acquired pneumonia (CAP): Treatment: Outpatient, Inpatient, ICU Outpatient Healthy: Macrolide or Doxycycline Outpatient Comorbid: Fluoroquinolones or beta-lactam + macrolide Inpatient: Fluoroquinolones (levofloxacin, moxifloxacin) or beta-lactam + macrolide ICU: Beta-lactam + macrolide (IV) or Fluoroquinolones + beta-lactam
593
Atrial fibrillation is most commonly caused by ectopic foci within:
Pulmonary veins
594
The most common cause of atrial flutter is a reentrant circuit around:
The tricuspid annulus
595
Slurred upsloping R waves:
Delta waves are characteristic of WPW syndrome.
596
Tumor lysis syndrome is characterized by labs:
Calcium decreased; Phosphate increased; Potassium increased; Uric acid increased; Tx: Allopurinol: Most common tumors lymphomas (Burkitt’s) and leukemias (ALL).
597
Malignant otitis externa (MOE) is a serious infection of the ear seen in: Most common organism:
Elderly patients with poorly controlled diabetes. Pseudomonas aeruginosa.
598
Malignant otitis externa (MOE): Most common fungal cause:
Aspergillus.
599
Behcet’s syndrome: Etiology: Epidemiology: Characteristics:
Multisystemic inflammatory condition seen commonly in Turkish, Asian, and Middle Eastern populations. Characterised by recurrent oral and genital ulcers, skin lesions (erythema nodosum), eye lesions including anterior/posterior uveitis.
600
Most accurate way to determine estimated gestational age (EGA):
Ultrasound dating with fetal crown-rump measurement in the first trimester. 2nd and third not as accurate.
601
Women who miss screening (unknown GBS status) should be treated in labor if: Treatment:
They are in labor
602
Physicians should have a high index of suspicion for physical/sexual abuse in children with:
Sudden behavioral problems, families with unstable economic backgrounds, or parents with a history of drug/alcohol abuse.
603
Transient proteinuria is the most common cause of isolated proteinuria in children and should be evaluated:
With repeat urine dipsticks on two separate occasions to R/O persistent proteinuria, which requires more work up.
604
Idiopathic pulmonary fibrosis (IPF): Mechanism: Pulmonary function test findings:
Excessive collagen deposition in extracellular matrix around alveoli; Leads to decreased lung volume (low total lung capacity, functional residual capacity, and residual volume) with preserved or increased forced expiratory volume in 1 second/forced vital capacity. Impaired gas exchange resulting in reduced diffusion capacity of carbon monoxide and increased alveolar-arterial gradient.
605
Elevated serum protein with normal albumin (gamma gap) suggests disorders such as:
``` Multiple myeloma (MM), amyloidosis, Waldenstrom's macroglobulinemia, and monoclonal gammopathy of undetermined significance (MGUS). ```
606
Multiple myeloma vs monoclonal gammopathy of undetermined significance (MGUS): Differentiate:
MGUS patients usually have
607
Although MGUS patients are asymptomatic, they require:
Metastatic skeletal bone survey
608
Chronic lymphocytic leukemia(CLL): Staging system and how it relates to prognosis:
``` Stage 0 = Lymphocytosis only = Good Stage I = Lymphocytosis + adenopathy = Fair Stage II = Splenomegaly = Fair Stage III = Anemia = Intermediate Stage IV = Thrombocytopenia = Poor ```
609
Chronic lymphocytic leukemia (CLL): Typical pathology report:
“smudge cells” = leukocytes that have undergone partial breakdown during preparation of a stained smear or tissue section, because of their greater fragility.
610
The best markers indicating resolution of DKA are the:
Serum anion gap and beta-hydroxybutyrate levels.
611
1° (Essential) Hypertension: Etiology, epidemiology, risk factors
Hypertension with no identifiable cause. Represents 95% of cases of hyperten- sion. Risk factors include a family history of hypertension or heart disease, a high-sodium diet, smoking, obesity, race (blacks > whites), and advanced age.
612
1° (Essential) Hypertension: History, S&S, Physical exam
■ Hypertension is asymptomatic until complications develop. ■ Patients should be evaluated for end-organ damage to the brain (stroke, dementia), eye (cotton-wool exudates, hemorrhage), heart (LVH), and kid- ney (proteinuria, chronic kidney disease). Renal bruits may signify renal artery stenosis as the cause of hypertension.
613
1° (Essential) Hypertension: diagnosis
■ Conduct cardiovascular, neurologic, ophthalmologic, and abdominal ex- ams. ■ Obtain a UA, BUN/creatinine, CBC, and electrolytes to assess the extent of end-organ damage.
614
``` In the JNC-7 Classification and Management of Hypertension, define systolic and/or diastolic BP: Normal = Prehypertension = Stage 1 hypertension = Stage 2 hypertension = ```
Normal =
615
``` In the JNC-7 Classification and Management of Hypertension, describe drug therapy w/out comorbidities: Normal = Prehypertension = Stage 1 hypertension = Stage 2 hypertension = ```
Normal = none Prehypertension = none Stage 1 hypertension = Thiazide diuretics for most patients; ACEIs, ARBs, β-blockers, CCBs, or a combination may be considered. Stage 2 hypertension = Two-drug combination for most patients (usually a thiazide diuretic plus an ACEI, an ARB, a β-blocker, or a CCB).
616
Treatment protocol for hypertension.
■ Rule out 2° causes of hypertension, particularly in younger patients. ■ Begin with lifestyle modifications (e.g., weight loss, smoking cessation, salt reduction). Weight loss is the single most effective lifestyle modification. The BP goal in otherwise healthy patients is
617
Define secondary hypertension.
Hypertension 2° to an identifiable organic cause
618
5 causes of 2° hypertension – CHAPS
``` Cushing's syndrome Hyperaldosteronism (Conn's syndrome) Aortic coarctation Pheochromocytoma Stenosis of renal arteries ```
619
Define Hypertensive Crises.
A spectrum of clinical presentations in which elevated BPs lead to end-organ damage.
620
History / PE findings of Hypertensive Crises:
Presents with end-organ damage revealed by chest pain (ischemia or MI), back pain (aortic dissection), or changes in mental status (hypertensive en- cephalopathy).
621
Hypertensive crises are diagnosed based on:
Hypertensive crises are diagnosed on the basis of the extent of end-organ damage, not BP measurement.
622
Hypertensive urgency Vs. Hypertensive emergency: describe both
■ Hypertensive urgency: Diagnosed on the basis of an elevated BP with only mild to moderate symptoms (headache, chest pain, syncope) and without end-organ damage. ■ Hypertensive emergency: Diagnosed by a significantly elevated BP with signs or symptoms of impending end-organ damage such as ARF, intracranial hemorrhage, papilledema, or ECG changes suggestive of ischemia or pulmonary edema.
623
What is the criteria for a Malignant hypertension diagnosis?
Diagnosed on the basis of progressive renal fail- | ure and/or encephalopathy with papilledema.
624
``` Hypertensive crises: - Hypertensive urgency - Hypertensive emergency - Malignant hypertension Are all diagnosed by PB measurement (True or False) ```
Hypertensive crises are diagnosed on the basis of the extent of end-organ damage, not BP measurement.
625
Drug treatment of 1° Hypertension with heart failure:
Thiazide diuretics, β-blockers, ACEIs, ARBs, aldosterone antagonists.
626
Drug treatment of 1° Hypertension with post-MI:
β-blockers, ACEIs, aldosterone antagonists.
627
Drug treatment of 1° Hypertension with high CVD risk:
Thiazide diuretics, β-blockers, ACEIs, CCBs.
628
Drug treatment of 1° Hypertension with diabetes:
Thiazide diuretics, β-blockers, ACEIs, ARBs, CCBs.
629
Drug treatment of 1° Hypertension with chronic kidney disease:
ACEIs, ARBs
630
Drug treatment of 1° Hypertension with recurrent stroke prevention:
Thiazide diuretics, ACEIs
631
7 Common Causes of 2° Hypertension:
- 1° renal disease - Renal artery stenosis - OCP use - Pheochromocytoma - Conn’s syndrome (hyperaldosteronism) - Cushing’s syndrome - Coarctation of the aorta
632
Description and treatment of renal and drug causes of 2° Hypertension: - 1° renal disease - Renal artery stenosis - Etiologies of RAS are Fibromuscular dysplasia (50 y/o) - OCP use
- 1° renal disease - Often unilateral renal parenchymal disease. - Treat with ACEIs - Renal artery stenosis - Especially common in patients 50 years of age with recent-onset hypertension. - Diagnose with MRA or renal artery Doppler ultrasound. May be treated with angioplasty or stenting. Consider ACEIs if unilateral, not if bilateral. - OCP use - Common in women > 35 years of age, obese women, and those with long-standing use. - Discontinue OCPs
633
How do you treat renal artery stenosis? Why must you be careful w/ prescribing ACEIs?
May be treated with angioplasty or stenting. Consider ACEIs as adjunctive or temporary therapy in unilateral disease. (In bilateral disease, ACEIs can accelerate kidney failure by preferential vasodilation of the efferent arteriole.) Open surgery is a second option if angioplasty is not effective or feasible.
634
Description and treatment of adrenal causes of 2° Hypertension: - Pheochromocytoma - Conn's syndrome (hyperaldosteronism)
- Pheochromocytoma - An adrenal gland tumor that secretes epinephrine and norepinephrine, leading to episodic headache, sweating, and tachycardia - Diagnose with urinary metanephrines and catecholamine levels or plasma metanephrine. Surgical removal of tumor after treatment with both α-blockers and β-blockers. - Conn's syndrome (hyperaldosteronism) - Most often 2° to an aldosterone-producing adrenal adenoma. Causes the triad of hypertension, unexplained hypokalemia, and metabolic alkalosis - Remove tumor
635
Description and treatment of pituitary cause of 2° Hypertension: - Cushing's syndrome
- Cushing's syndrome - Due to an ACTH-producing pituitary tumor, an ectopic ACTH-secreting tumor, or cortisol secretion by an adrenal adenoma or carcinoma. - Remove tumor
636
How do you treat hypertensive urgencies?
Hypertensive urgencies: Can be treated with oral antihypertensives (e.g., β-blockers, clonidine, ACEIs) with the goal of gradually lowering BP over 24–48 hours
637
How do you treat hypertensive emergencies?
Treat with IV medications (labetalol, nitro- prusside, nicardipine) with the goal of lowering mean arterial pressure by no more than 25% over the first two hours to prevent cerebral hypoperfusion or coronary insufficiency.
638
Pericardial disease results from acute or chronic _______ ______ and may lead to _______ ________.
Results from acute or chronic pericardial insults; may lead to pericardial effusion.
639
What antihypertensive drug do you prescribe to patients with Diabetes with proteinuria?
ACEIs or ARBs.
640
What antihypertensive drug do you prescribe to patients with CHF?
β-blockers, ACEIs or ARBs, diuretics (including spironolactone).
641
What antihypertensive drug do you prescribe to patients with Isolated systolic hypertension?
Diuretics are preferred; long-acting dihydropyridines.
642
What antihypertensive drug do you prescribe to patients with MI?
β-blockers without intrinsic sympathomimetic activity; ACEIs.
643
What antihypertensive drug do you prescribe to patients with osteoporosis?
Thiazide diuretics.
644
What antihypertensive drug do you prescribe to patients with BPH?
α1-adrenergic blockers.
645
What causes pericardial disease? What is a major complication of pericardial disease?
Results from acute or chronic pericardial insults; may lead to pericardial effusion.
646
What are 2 ways pericarditis can compromise cardiac output?
Tamponade or constrictive pericarditis
647
What is the most common cause of pericarditis?
Idiopathic
648
What are the 11 known causes of pericarditis?
Viral infection, TB, SLE, uremia, drugs, radiation, injury, acute renal failure and neoplasms. May also occur after MI (either within days after MI or as a delayed phenomenon, i.e., Dressler’s syndrome) or open heart surgery.
649
What are the S&S of pericarditis?
■ May present with pleuritic chest pain, dyspnea, cough, and fever. ■ Chest pain tends to worsen in the supine position and with inspiration.
650
What are the physical exam findings of pericarditis?
■ Exam may reveal a pericardial friction rub, elevated JVP, and pulsus paradoxus (a ↓ in systolic BP > 10 mmHg on inspiration).
651
In pericarditis, what are the firsts tests you order? What do you have to rule out first?
CXR, ECG, and echocardiogram to rule out MI and pneumonia.
652
What are the ECG changes you see in pericarditis?
ECG changes include diffuse ST-segment elevation and PR-segment depressions followed by T-wave inversions
653
What do you see in the echocardiography of a pericarditis patient?
Pericardial thickening or effusion may be evident on echocardiography.
654
Medications that cause idiopathic intracranial hypertension (pseudotumor cerebri):
Growth hormone, tetracyclines (minocycline, doxycycline), and excessive vitamin A (isotretinoin, all-trans-retinoic acid)
655
Influenza onset of symptoms:
Abrupt and often dramatic, URI symptoms are mild, but systemic symptoms are prominent with possible high fever, myalgias, headache.
656
Viral upper respiratory syndrome onset of symptoms:
Slow, stepwise, migratory, or evolving. URI symptoms, rhinorrhea, coryza, sneezing, mild pharyngitis, while systemic symptoms usually mild.
657
Current guidelines for treating all confirmed or suspected influenza:
Within 48 hours of symptoms onset. Neuraminidase inhibitors (oseltamivir, zanamivir).
658
The single most important prognostic consideration in the treatment of patients with breast cancer:
Tumor burden which is based on TMN staging.
659
Suspected pseudotumor cerebri in a young obese female with a headache is suggestive:
Can cause blindness.
660
What is the best test to perform on a patient with suspected diverticulitis:
CT scan is best.
661
Vaccination against hepatitis B decrease:
The incidence of hepatocellular carcinoma.
662
Tachycardia-mediated cardiomyopathy caused by atrial fibrillation with rapid ventricular response can be resored to function by:
Rate and rhythm control.
663
IgA nephropathy is the most common cause of:
Glomerulonephritis in adults:
664
Antipsychotic medication effects (dopamine antagonism) Pathway Mesolimbic:
Effect: Antipsychotic efficacy.
665
Antipsychotic medication effects (dopamine antagonism) Pathway Nigrostriatal:
Effect: Extrapyramidal symptoms: Acute dystonia, akathisia, parkinsonism.
666
Antipsychotic medication effects (dopamine antagonism) Pathway Tuberoinfundibular:
Effect: Hyperprolactinemia.
667
During a subclavian central venous catheter placement, if tension pneumothorax:
Needle thoracostomy.
668
Suspect the following conditions whenever a patient presents with hypokalemic, alkalosis, and normotensive:
Surreptitious vomiting, diuretic abuse, Bartter syndrome, Gitelman syndrome.
669
Patient who presents with equinus varus of the calcaneus and talus, varus of the midfoot, and adduction of the forefoot: Treatment:
Stretching, manipulation, followed by serial casting. This is clubfoot (talipes equinovarus)
670
Erysipelas: Organism: Description:
Streptococcus pyogenes; Fiery red, tender, painful plaque with sharply demarcated edges.
671
Cellulitis (purulent): Organism: Description:
Staphylococcus Aureus; Folliculitis, Furuncle, Carbuncle.
672
Cellulitis (nonpurulent): Organism: Description:
Streptococci; Flat lesion with less demarcation than in erysipelas.
673
Light's Criteria to distinguish transudate from exudate:
Pleural fluid protein/serum protein ratio >0.5 Pleural fluid lactate dehydrogenase (LDH)/serum LDH ratio >0.6 Pleural fluid LDH>⅔ of the upper limit of normal serum LDH
674
Normal pleural fluid findings pH: pH Transudate: pH Exudate: pH Empyema:
pH 7.60 normal pH 7.4-7.55 transudate pH 7.30-7.45 exudate pH
675
What gives a pleural fluid glucose level of
Glucose ratio
676
Bacillary angiomatosis: Describe: Presentation: Treatment:
Bright, red, firm, friable, exophytic nodules in an HIV infected patient. Bacillary angiomatosis is caused by Bartonella, a gram-negative bacillus. Tx: Oral erythromycin.
677
Acute rheumatic fever cause: Treatment:
Group A streptococcus (GAS)/ Streptococcus pyogenes: Causes pharyngitis. Tx: Penicillin.
678
Acute rheumatic fever: Presentation:
Suspected in a child with sore throat, fever, pericarditis, erythema marginatum, arthritis, chorea, and subcutaneous nodules.
679
Gallbladder carcinoma: Epidemiology: Diagnosis: Prognosis:
Often arises in Hispanics and Southwestern Native American females with history of gallstones. Typically diagnosed after cholecystectomy. Highly fatal, but if confined to gallbladder 73-100% cure rate.
680
Cytomegalovirus (CMV) esophagitis: Characterized: Biopsy shows: Treatment:
Focal substernal burning pain and odynophagia. Large linear ulcerations generally shallow in lower esophagus. Presence of intranuclear and intracytoplasmic inclusions on biopsy. Tx: IV ganciclovir. Acyclovir does not work because CMV does not have thymidine kinase enzyme to activate.
681
Herpes simplex virus esophagitis: Characterized: Biopsy shows: Treatment:
Usually multiple, small, and well circumscribed with a round/ovoid “volcano-like” appearance. Cells show ballooning degeneration and eosinophilic intranuclear inclusions. Tx: Acyclovir.
682
Untreated hyperthyroid patients are at risk for:
Rapid bone loss resulting from increased osteoclastic activity in bone cells. Also at risk for cardiac tachyarrhythmias AF.
683
Which type of medication reconciliation intervention is most likely to result in a decrease in adverse drug events and health care utilization:
Pharmacist directed interventions.
684
Neonatal chlamydial eye infection: Treatment: Risk for:
Occurs days 5-14 days. Oral erythromycin. Erythromycin can cause infantile hypertrophic pyloric stenosis.
685
Which class I antiarrhythmics can cause prolongation of QRS or QT interval: Mechanism:
Flecainide and propafenone. They work by blocking sodium channels. In patients with fast heart rates, the drug has less time to dissociate, leading to more channels blocked, which leads to progressive decrease in impulse conduction and widened QRS.
686
Elderly patients with impaired thirst response are predisposed to prerenal azotemia due to:
Intravascular volume depletion and poor renal perfusion (renal arteriolar vasoconstriction).
687
Aphasia syndrome: Broca's area: Spontaneous speech: Comprehension: Repetition: Associated features:
Spontaneous speech: Sparse and nonfluent. Comprehension: Relatively preserved. Repetition: Impaired. Associated: Right hemiparesis. Located in dominant right frontal lobe.
688
Aphasia syndrome: Wernicke's area: Spontaneous speech: Comprehension: Repetition: Associated features:
Spontaneous speech: Fluent and voluminous, but lacks meaning Comprehension: Greatly diminished. Repetition: Impaired. Associated: Right superior visual field defect.
689
Aphasia syndrome: Spontaneous speech: Comprehension: Repetition: Associated features:
Spontaneous speech: Fluent with pneumonic errors. Comprehension:Relatively preserved. Repetition: Very poor. Associated: None.
690
In patients with hyperthyroidism- related tachy systolic atrial fibrillation: Drug choice:
beta blocker such as propranolol
691
Management of atypical squamous cells of undetermined significance (ASC-US) in women age ≥25:
Next is HPV testing. If positive get colposcopy. If negative repeat pap smear and HPV test in 3 years.
692
Management of (ASC-US) 0r LSIL in women age 21-24:
Repeat pap smear at 12 months. If ASC-H or AGC or HSIL get a colposcopy. If negative or ASC-US or LSIL then repeat pap smear at 12 months Must have a negative pap smear X2 to return to normal screening.
693
Preterm labor defined as:
Regular contractions causing cervical dilation and/or effacement at
694
Patients in preterm labor at
A tocolytic agent (calcium channel blocker), magnesium sulfate for neuroprotection, and corticosteroids for acceleration of fetal lung maturity.
695
All women should be screened for at first prenatal visit:
syphilis, HIV, and hepatitis B.
696
In an infant with menigoccoumia, watch out for Waterhouse-Friderichsen syndrome: Characterized:
A sudden vasomotor collapse and skin rash (large purpuric lesions on the flanks) due to hemorrhage. This is due to adrenal hemorrhage.
697
Drug induced type 1 hypersensitivity reactions are immediate in onset and mediated by:
IgE and mast cells/basophils.
698
Mild manifestations of a drug allergy (urticaria and pruritus without systemic symptoms) are usually treated:
With antihistamines and discontinuation of the offending drug. As long as no signs of shock then epinephrine.
699
Infectious mononucleosis (IM): Etiology: Epidemiology: Presentation:
Most commonly caused by the Epstein-Barr virus. Transmitted person to person through saliva typically infecting 15-24 years old. Presentation triad of exudative tonsillitis/pharyngitis, posterior or diffuse cervical lymphadenopathy, and fever. There can be a rash with IM in some patient given ampicillin or amoxicillin.
700
Stridor in infants and children due to vascular ring: Presents: Characteristics:
Presents before age 1 year. Persistent stridor that improves with neck extension. Associated with cardiac abnormalities. Vascular rings, which can encircle both the trachea and esophagus, are caused by abnormal development of the aortic arch.
701
Stridor in infants and children due to Laryngomalacia: Presents: Characteristics:
Stridor most severe at age 4-8 months. Persistent stridor that worsens in supine position and improves in prone position.
702
Stridor in infants and children due to Croup (Laryngotracheobronchitis): Presents: Characteristics:
Most common from age 6 months to 6 years. Associated with “barky” cough, fever, rhinorrhea and congestion.
703
The single most common cause of asymptomatic isolated elevation of alkaline phosphatase in an elderly patient is:
Paget’s disease of bone (osteitis deformans). Usually diagnosed on routine laboratory testing.
704
Known to cause post-viral URI necrotizing pulmonary bronchopneumonia with multiple nodular infiltrates that can cavitate to cause abscesses:
Staphylococcus aureus
705
Polymyalgia rheumatica: Symptoms: Physical findings: Labs: Treatment:
Age >50, bilateral pain and morning stiffness > 1 month, involvement of 2 of the following: neck, shoulders or proximal arms, proximal thigh or hip, constitutional (fever, malaise, weight lose). Physical exam shows decreased active ROM in shoulders, neck and hips. Labs: ESR >40, sometimes >100, elevated CRP, normocytic anemia. Tx: Glucocorticoids (low-dose prednisone).
706
Dialysis patient with low-grade fever, acute watery diarrhea, abdominal pain, and guaiac-positive stool in the setting of prolonged omeprazole use are consistent with:
Likely clostridium difficile colitis. Can be confirmed with a stool assay for toxins A and B. Gastric suppression with PPI and H2 blockers increase risk.
707
Vasovagal syncope is usually a clinical diagnosis and does not need further testing if H and PE point strongly to the diagnosis, but:
Uncertain cases need upright tilt table testing.
708
Infective carditis (IE): Treatment protocol:
Empiric Vancomycin to cover staphylococcus, streptococcus, and enterococcus after getting BC. Then tailor to specific bug.
709
Infective carditis caused by viridans group streptococcus: Treatment:
Intravenous aqueous penicillin G or intravenous ceftriaxone for 4 weeks.
710
In evaluating ascites, a serum-to-ascites albumin gradient (SAAG) is calculated how:
Calculated by subtracting the peritoneal fluid albumin concentration from the serum albumin concentration and is useful to differentiate between portal and non-portal hypertension etiologies. SAAG ≥1.1 g/dL indicates portal hypertension (increased capillary hydrostatic pressure) while a SAAG
711
HELLP syndrome what is the definitive treatment:
Delivery: Vaginal if possible. Cesarian for (maternal hemodynamic instability, nonreassuring fetal status, breech presentation).
712
Cavernous hemangiomas of the brain and viscera are associated with:
Von Hippel-Lindau disease.
713
Spider angiomas are commonly seen during:
Pregnancy, oral contraceptive use, and cirrhosis-related hyperestrogenemia, because spider angiomas are estrogen dependent.
714
Niemann-Pick disease: Pathology: Epidemiology: Onset: Clinical features:
Sphingomyelinase deficiency; Autosomal recessive inheritance, Ashkenazi Jewish heritage; Onset age 2-6 months; Loss of motor milestones, hypotonia, feeding difficulties, “Cherry-red” macula, [HEPATOSPLENOMEGALY], [AREFLEXIA].
715
Tay-Sachs disease: Pathology: Epidemiology: Onset: Clinical features:
β-hexosaminidase A deficiency;Autosomal recessive inheritance, Ashkenazi Jewish heritage; Onset age 2-6 months; Loss of motor milestones, hypotonia, feeding difficulties, “Cherry-red” macula, [HYPERREFLEXIA].
716
Gaucher's disease: Pathology: Clinical features:
Glucocerebrosidase deficiency; Classic features include anemia, thrombocytopenia, and hepatosplenomegaly, and no loss of developmental milestones.
717
Krabbe disease: Pathology: Epidemiology: Onset: Clinical features:
Galactocerebrosidase deficiency; Rare autosomal recessive lysosomal storage disorder; Presents early in infancy; with developmental regression, hypotonia, and areflexia.
718
Hurler syndrome: Pathology: Epidemiology: Onset: Clinical features:
(One of the mucopolysaccharidoses) is a lysosomal storage disease due to lysosomal hydrolase deficiency. It presents at age 6 months-2 years with coarse facial features, inguinal or umbilical hernias, corneal clouding, and hepatosplenomegaly.
719
The kidney compensates for respiratory alkalosis by preferential excreting:
Bicarbonate in the urine. This results in an alkalinized urine (increased urine pH).
720
Number needed to treat (NNT) formula:
``` Absolute risk reduction (ARR) NNT = 1/ARR Example 16.3% incidence clopidogrel + aspirin compared to 12.3% with efrenzia + aspirin ARR = 0.163 - 0.123 = 0.04 NNT = 1/0.04 = 25 ```
721
Indications for oxygen therapy in COPD:
PaO2≤55, SaO2≤88%, hematocrit>55%, or evidence of cor pulmonale.
722
Patient with history of heartburn, significant weight loss, fatigue, smoking has:
Esophageal cancer. Diagnose by barium swallow followed by endoscopy.
723
Esophageal cancer name two types and etiology:
Squamous cell carcinoma: associated with smoking and alcohol consumption. Adenocarcinoma: Barrett's esophagus, a complication of GERD is the main risk factor.
724
Hemoglobin decreased: Normal MCV: Decreased reticulocyte count: Differential:
Leukemia; Aplastic anemia; Infection; Medication side effect.
725
Hemoglobin decreased: Normal MCV: Increased reticulocyte count: Differential:
Hemorrhage; Hemolysis: Intrinsic inherited defects of hemoglobin, RBC membrane, or enzymes. Hemolysis extrinsic: Autoimmune, Paroxysmal nocturnal hemoglobinuria.
726
Hemoglobin decreased: Decreased MCV: Differential:
Iron deficiency; Lead intoxication; Thalassemia; Sideroblastic anemia.
727
Hemoglobin decreased: High MCV: Differential:
B12 deficiency; Folate deficiency. Preventing pneumonia in transplant patients: What drug given prophylaxis: trimethoprim-sulfamethoxazole (TMP-SMX) for Pneumocystis pneumonia (PCP).
728
What vaccines should transplant patient get:
Influenza, pneumococcal, and hepatitis B.
729
Prophylaxis for CMV in transplant patients:
Ganciclovir or valganciclovir.
730
Addison's disease: Most common electrolyte disturbance:
Hyponatremia from mineralocorticoid deficit. You also get hyperkalemia but to a laesser extent.
731
In patient with pancreatic cancer suspicions: What test:
Abdominal ultrasound is the initial imaging performed on patients with jaundice. Great at detecting mass lesions or metastisis.
732
Postoperative monitoring of pancreatic cancer follows:
CA 19-9 level.
733
Any HIV patient with bloody diarrhea and a normal stool examination should have:
Colonoscopy.
734
CMV colitis is characterized by:
Bloody diarrhea with abdominal pain. Colonoscopy shows multiple ulcers and mucosal erosions.
735
CMV biopsy demonstrates:
Large cells containing eosinophilic intranuclear and basophilic intracytoplasmic inclusions.
736
Disseminated MAC infection can cause chronic diarrhea and weight loss, however:
The diarrhea is non-bloody and generally involves the small intestines.
737
Male in his 30s with frequent episodes of substernal squeezing-type chest discomfort that radiates to neck. Not associated with activity or SOB and last for up to 2 hours. No tobacco, ETOH o iliciate drug use. ECG is normal and exercise stress test shows no abnormalities: Diagnosis:
Gastroesophageal reflux disease (GERD) or esophageal motility disorder are common causes of noncardiac chest pain.
738
Child presents with fatigue, peripheral and perioral cyanosis, and a systolic murmur along the left sternal border:
Consistent with tetralogy of fallot (TOF):
739
Tetralogy of fallot (TOF): Name four defects:
Ventricular septal defect; an overriding aorta over the right and left ventricles; right ventricular outflow obstruction, and right ventricular hypertrophy.
740
Tetralogy of fallot (TOF): What occurs with squatting and standing to murmur:
Squatting increases the peripheral systemic vascular resistance (afterload), and decreases the degree of the right to left shunting across the VSD.
741
Pneumococcal polysaccharide vaccine: Mechanism of immunity:
Relatively T-cell independent B-cell response because polysaccharides cannot be presented to T-cells. Moderate levels of intermittent affinity antibodies. Less effective in young and elderly.
742
Pneumococcal polysaccharide vaccine: Advantages:
Increased number of covered strains. Decrease incidence of replacement strains due to lack of mucosal immunity.
743
Pneumococcal conjugate vaccine: Mechanism of immunity:
Polysaccharide-protein conjugate induces T-cell-dependent B-cell response, resulting in improved immunogenicity due to the formation of higher-affinity antibodies and memory cells.
744
Pneumococcal conjugate vaccine: Advantages:
Increase efficacy in elderly and children
745
Pregnant female with SROM and immediately followed by painless, copious vaginal bleeding. Fetal heart rate increases to 180/min and drops to 70/min while patient’s vital signs and abdominal exam remain the same:
Vasa previa: Painless vaginal bleeding that occurs on ROM, fetal deterioration (sinusoidal tracing or bradycardia). Diagnose with antenatal abdominal and transvaginal doppler ultrasound. Offer cesarean delivery.
746
Patient has headaches, a focal neurologic deficit, a solitary ring enhancing lesion on brain CT scan, and a fluid collection in the ethmoid sinus: Patient is immunocompetent:
Most common organism causing this is Viridans streptococcus (Streptococcus intermedius, S. mitis, S. oralis, S. mutans). Spreads from sinusitis.
747
What is an independent predictor of adverse outcomes in CHF:
Hyponatremia. It is caused by increased levels of renin, norepinephrine and antidiuretic hormone. Lead to free water retention.
748
Thyroid exam reveals 2x2 cm left-sided thyroid nodule. Her T3 and T4 are elevated, and TSH is undetectable. Radioactive iodine scan shows uptake only in the left thyroid nodule. Uptake in the rest of the thyroid is markedly reduced. Diagnosis:
Toxic adenoma
749
Thyroid scan in Hashimoto's thyroiditis shows:
Heterogeneous pattern.
750
Thyroid scan graves disease:
Diffusely increased radioactive iodine uptake.
751
Side effect of epidural anesthesia seen during pregnancy:
Hypotension caused by blood redistribution to the lower extremities and venous pooling from sympathetic blockade. Vasodilation and venous pooling.
752
Complication of epidural in pregnancy: Treatment:
Persistent untreated hypotension can lead to decreased placental perfusion and fetal acidosis. Treatment volume expansion with fluids, and place patient on left side to improve venous return.
753
Suspect toxoplasmosis in an AIDS patient with multiple ring-enhancing lesions on CT: Treatment:
Sulfadiazine and pyrimethamine. TMP-SMX is used for prophylaxis.
754
What drug directly blocks the production of renin:
Aliskiren: direct renin inhibitor.
755
Maternal serum ɑ-fetoprotein screening: Elevated with:
Open neural tube defects (anencephaly, open spina bifida); Ventral wall defects (omphalocele, gastroschisis; Multiple gestations. When elevated need careful ultrasound.
756
Maternal serum ɑ-fetoprotein screening: Decreased with:
Aneuploidies: Trisomy 18 and 21.
757
``` After upper abdominal surgery, a combination of factors can cause the vital capacity (VC) and functional residual capacity (FRC) to: Treatment: ```
VC 50% and FRC 30% decrease. Moving from supine to sitting can increase the FRC by 20% to 35%. Increasing the FRC can help prevent postoperative atelectasis.
758
Asplenia RBCs peripheral blood smear:
Howell Jolly bodies.
759
Heinz bodies and bite cells are seen in:
G6PD and Thalassemia.
760
Helmet cells:
Seen in traumatic hemolysis such as DIC, HUS, and ITP.
761
Immunocompromised patient with systemic symptoms, lung nodules, and brain abscess (causing seizures), and the cultures grew gram-positive, partially acid-fast, filamentous, branching rods: Diagnosis: Treatment
Nocardia. TMX-SMX.
762
Primary polydipsia: Defect: Etiology: Clinical Features:
Increase water intake Antipsychotics, anxious, middle age women, central hypothalamic lesion Polyuria and low urine osmolality, Serum Na
763
Central diabetes insipidus: Etiology: Clinical Features:
Decrease ADH release from pituitary Idiopathic, trauma, pituitary surgery, ischemic encephalopathy. Polyuria and low urine osmolality, Serum Na may be >150 mEq/L due to significant thirst impairment.
764
Nephrogenic diabetes insipidus: Etiology: Clinical Features:
ADH resistance in kidney Chronic lithium use, hypercalcemia, heredity (AVPR2 mutation). Polyuria and low urine osmolality, Serum Na 152-150 mEq/L due to intact thirst mechanism
765
Complex partial seizure is characterized by:
Brief (lasting a few minutes) episodes of impaired consciousness, failure to respond to various stimuli during the episodes, staring spell, and automatisms (lip smacking, swallowing, picking movements of the hand), and post ictal confusion.
766
Atypical absence seizures is characterized by:
Brief (lasting a few minutes) episodes of impaired consciousness. Patient may also present with automatisms, but there is no post ictal state. Hyperventilation during EEG causes 3Hz pike.
767
Syphilis treatment for penicillin allergic patient:
Doxycycline X 14 days. In pregnant patient they should undergo desensitization before penicillin.
768
Patient with SOB, tachypnea, and hypoxemia with and S3 on cardiac exam: Treatment:
Most likely left ventricular failure, treat with intravenous diuretics. This is decompensated heart failure.
769
Scleroderma renal crisis peripheral blood smear will show:
schistocytes: fragmented red blood cells.
770
Herpangina: Etiology: Age: Seasonality: Clinical features: Treatment:
Coxsackie A virus; Age 3-10 years; Summer/early fall: Clinical features: fever, pharyngitis, gray vesicles/ulcers on the posterior oropharynx: Treatment: Supportive management.
771
Herpetic gingivostomatitis: Etiology: Age: Seasonality: Clinical features: Treatment:
Herpes simplex virus type 1; Age 6 months-5 years; None; Clinical features: fever, pharyngitis, erythematous gingiva, clusters of small vesicles on anterior oropharynx/lips; Treatment: acyclovir.
772
Fundoscopic findings in central vein occlusion:
Venous dilation and tortuosity due to venous occlusion; Scattered and diffuse hemorrhages due to backup of blood and increased resistance, leading to ischemic damage; “Blood and thunder: appearance due to diffuse hemorrhages; Cotton wool spots, disk swelling. Painless loss of vision.
773
Lateral medullary infarction (Wallenberg syndrome): Etiology: Presentation:
Occurs due to occlusion of the posterior inferior cerebellar or vertebral artery. Patient develops loss of pain and temperature over the ipsilateral face and contralateral body, ipsilateral bulbar muscle weakness, vestibulocerebellar impairment (vertigo, nystagmus), and Horner’s syndrome. Motor function face and body spared.
774
G6PD test during an active episode of hemolysis:
Test may come back as normal, because the most sensitive cells are the first to lys.
775
The hallmark of normal pressure hydrocephalus is the triad:
Gait disturbances, dementia, and urinary incontinence. CT or MRI will show dilated ventricles.
776
The most common site of hypertensive hemorrhage is:
The putamen. The internal capsule that lies adjacent to the putamen is almost always involved, leading to contralateral hemiparesis.
777
Hypertrophic cardiomyopathy first line treatment:
Beta-blocker or a cardiac acting calcium channel blockers such as diltiazem since they promote diastolic relaxation.
778
Complication of bronchiolitis in infants less than 2 months:
Apnea, respiratory failure.
779
Acute appendicitis is a clinical diagnosis based on presentation:
Classic presentation: migratory pain, nausea, vomiting, fever, leukocytosis, McBurney's point tenderness, and Rovsing sign. Should have immediate appendectomy. Only need Ct or ultrasound on atypical presentations.
780
Patient with cirrhosis and hepatic encephalopathy (HE): Treatment:
Supportive care, lowering the serum ammonia. Nonabsorbable disaccharides (lactulose, lactitol). Rifaximin can decrease the number of ammonia producing bacteria in the colon.
781
Parinaud syndrome occurs in most patients with:
Pineal gland masses and presents as limitation of upward gaze, bilateral ptosis, and bilateral retraction. HA, vomiting and obstructive hydrocephalus.
782
Craniopharyngiomas are:
Suprasellar masses that can compress the optic chiasm, resulting in visual field deficits.
783
Aortic regurgitation produces and:
Early diastolic murmur and can be associated with several physical signs caused by a hyperdynamic pulse, including bounding or “water hammer” peripheral pulses.
784
Multiple myeloma common electrolyte disturbance:
Hypercalcemia
785
Patient with ankylosing spondylitis (AS) for 20 years is at risk for:
Vertebral fracture due to rigidity and decreased bone mineralization.
786
Another treatment for essential tremor: Mechanism and complications:
Primidone: anticonvulsant that converts into phenylethylmalonamide and phenobarbital. Primidone can cause acute intermittant porphyria, which manifests as abdominal pain, neurologic, and psychiatric abnormalities.
787
When a wound fails to heal after a prolonged period, biopsies should be obtained to ensure that:
The ulcer has not degenerated into a squamous cell carcinoma. When SCC arise within a burn wound, these ulcers are known as Marjolin's ulcers.
788
Unilateral varicoceles that fail to empty when a patient is recumbent raise suspicion for an underlying:
Mass pathology, such as renal cell carcinoma: Get Ct abdomen.
789
The classic triad of renal cell carcinoma:
Flank pain, hematuria, and a palpable abdominal mass.
790
Bronchiectasis can be identified on:
CT by the presence of dilated bronchi with thickened walls.
791
Potential complication of bronchiectasis:
Hemoptysis
792
Leprosy is a chronic granulomatous disease that primarily affects: Organism: Diagnosis:
The peripheral nerves and skin, and is caused by Mycobacterium leprae. Diagnosis is made by the demonstration of acid-fast bacilli on skin biopsy.
793
Tricuspid regurgitation commonly present in patients with tricuspid endocarditis from IV drug use: Murmur:
Distinguished from other murmurs by augmentation of the intensity of the holosystolic murmur with inspiration.
794
Constrictive pericarditis is caused by: Etiologies US: Etiologies developing countries:
Pericardial scarring and thickening that results in diastolic dysfunction; USA: Viruses, cardiac surgery, chest radiation, and idiopathic; Developing countries such as Africa, India, and China: Tuberculosis.
795
Complications of shoulder dystocia: Prognosis:
Erb-Duchenne palsy: C5, C6, C7; Weakness deltoid and infraspinatus (C5), biceps (C6), and wrist/finger extensors (C7). Fortunately, most infants recover arm function spontaneously within a few months.
796
Cervicofacial actinomycosis most commonly presents: Diagnosis: Treatment:
In the mandibular region as a slow growing, nontender mass with characteristic yellow granular pus (“sulfur granules”). Diagnosis is confirmed by Gram stain (Gram-positive branching bacilli) and culture. Tx: Penicillin.
797
Paget’s Disease of bone (osteitis deformans) is associated with: Labs:
Normal serum calcium and phosphate levels and increased alkaline phosphatase, and urinary hydroxyproline levels.
798
Primary Raynaud’s Phenomenon (RP): Etiology: Clinical presentation: Management:
No underlying cause; Usually women age
799
Secondary Raynaud’s Phenomenon (RP): Etiology: Clinical presentation: Management:
Connective tissue diseases, occlusive vascular conditions, sympathetic drugs, vibrating tools, hyperviscosity syndromes, nicotine; Usually men >40, asymmetric attack, symptoms of underlying disease, tissue injury or digital ulcers, abnormal nailfold capillary examination; Management: CCB for persistent symptoms, aspirin for patients at risk for digital ulceration.
800
Workup for patients with suspected secondary Raynaud's phenomenon (RP):
Complete blood count and metabolic panel Urinalysis Antinuclear antibody (ANA) and rheumatoid factor Erythrocyte sedimentation rate and complement levels (C3 and C4).
801
Patient BP 140/90, examination shows clear lung fields. Her chest x-ray shows prominent pulmonary arteries and an enlarged right heart border. ECG shows right axis deviation. What is the diagnosis:
Pulmonary hypertension: x ray would show enlargement of the pulmonary arteries with rapid tapering of the distal vessels (pruning) and enlargement of the right ventricle.
802
Three things that cause secondary pulmonary hypertension: What differentiates them from primary:
Mitral stenosis; Mitral prolapse; Left ventricular failure. With all three of these you see signs of pulmonary venous congestion.
803
Patients with increased risk for diabetes have the following values:
Fasting blood glucose of 100-125 mg/dL 2-hour OGTT level of 140-199 mg/dL HbA1C 0f 5.7%-6.4%
804
T2DM is diagnosed by one of the following:
Fasting blood glucose ≥126 mg/dL HbA1C ≥6.5% 2-hour OGTT level ≥200 mg/dL Random plasma glucose ≥ 200 mg/dL plus symptoms
805
Turner syndrome most common cardiac anomalies: From most to least:
1. bicuspid aortic valve 2. coarctation of the aorta 3 aortic root dilation
806
Patient with microcytic anemia, disproportionately elevated red blood cell (RBC) count, and peripheral blood smear with hypochromia and poikilocytosis, including target cells: Diagnosis: Treatment:
In asymptomatic patient this is bete-thalassemia minor. No specific therapy is required. Reassurance.
807
The key findings with beta-thalassemia minor:
Asymptomatic, with mild anemia, microcytosis out of proportion to the degree of anemia, hemoglobin >10g/dL
808
Patients with HIV who have subacute-onset of low grade fever, headache, and signs of increased intracranial pressure with normal MRI should be evaluated for:
Cryptococcal meningitis: Diagnosis is established by detection of the cryptococcal antigen or isolation of the organism in cerebrospinal fluid.
809
Progressive multifocal leukoencephalopathy is an:
Opportunistic infection seen in HIV patients caused by the JC virus. It can be detected by polymerase chain reaction testing of CSF. Neuroimaging shows patchy areas of white matter consistent with demyelination.
810
Patient with pronator drift has what type of lesion:
Upper motor neuron lesion. Pronator drift is a relatively sensitive and specific physical exam finding for UMNL. Some stroke patients will demonstrate pronator drift in the absence of other findings.
811
Cerebellar function is assessed by evaluation for:
Dysmetria and rapidly alternating movements. Can Be affected by motor weakness. Cerebellar lesions can produce an upward drift on pronator drift test.
812
A positive PPD test in HIV patient is: What is the treatment:
Skin induration of greater than 5mm in HIV patient. Requires prophylaxis with isoniazid (and pyridoxine) for 9 months. Need chest x-ray too.
813
Patient with congenital heart disease such as DiGeorge syndrome are at greater risk for: Mechanism:
Brain abscesses. Bacteria can spread hematogenously from right to left shunt. They do not get filtered out in the lung capillary bed.
814
Fever, severe headaches (nocturnal or morning), and focal neurologic changes make up the classic triad for:
brain abscesses.
815
The only area of the bladder covered by peritoneum is: What are the consequences:
Dome of the bladder. You can get peritonitis with referred pain to shoulder.
816
What is the most likely part of bladder to rupture during trauma:
Dome of the bladder.
817
Multiple Myeloma are at increased risk for:
Infection due to both a total decrease in functional antibodies and leukopenia that develop as bonemarrow fill with malignant plasma cells.
818
Multiple Myeloma mnemonic:
C-Calcium (hypercalcemia) R-Renal impairment (From IgG antibodies or paraproteins) A-Anemia (from bone marrow being replaced with plasma cells) B-Bone pain (bone pain, lytic lesions fractures)
819
A patient with a new SPN since previous chest- x-ray required:
CT scan
820
Lacunar strokes are due: Typically affect: Risk factors:
Microatheroma and lipohyalinosis in small penetrating arteries of the brain. They often affect the internal capsule and result in pure motor dysfunction. Risk factors Hypertension, hyperlipidemia, smoking and diabetes.
821
Commonly seen renal problem with poorly controlled diabetes:
Type 4 renal tubular acidosis (hyperkalemic renal tubular acidosis) is characterized by non-gap metabolic acidosis, persistent hyperkalemia, and mild-to moderate renal insufficiency.
822
Causes of normal anion gap metabolic acidosis:
``` Diarrhea Fistulas (pancreatic, ileocutaneous); Carbonic anhydrase inhibitors Renal tubular acidosis Ureteral diversion (ileal loop) Iatrogenic ```
823
Patient who is a smoker with elevated calcium, hilar mass on x-ray, anorexia, constipation, increased thirst, and easy fatigability: Diagnosis:
Squamous cell carcinoma of the lung: These tumors can produce parathyroid hormone-related protein (PTHrP). Remember sCa++mous
824
What two conditions can small cell carcinoma of the lung cause:
Small cell lung carcinoma usually causes paraneoplastic syndromes such as ACTH production and SIDH.
825
Acute mediastinitis can occur following cardiac surgery: Presents with: Treatment:
Presents with fever, chest pain, leukocytosis, and mediastinal widening on chest x-ray. Tx: Requires drainage, surgical debridement, and prolonged antibiotic therapy.
826
Acute pain and swelling of the midline sacrococcygeal skin and subcutaneous tissue is most commonly due:
To infection of a pilonidal cyst. Pilonidal cysts are most prevalent in young males especially with larger amounts of body hair.
827
Three things necessary to diagnose DKA:
blood glucose ≥250 mg/dL, pH
828
Antenatal corticosteroids should be administered in pregnant females with:
Preterm premature rupture of membrane (PPROM) before 32 weeks to reduce RDS, necrotizing enterocolitis, neonatal intraventricular hemorrhage, and neonatal death.
829
Indications for GBS prophylaxis when GBS status is unknown:
Delivery at
830
Patients with tetralogy of fallot that are placed in a knee-chest position improves their symptoms how:
Increased systemic vascular resistance.
831
Patient is an avid dancer who presents with 2 weeks of right tibial pain, with normal xray: Diagnosis:
Stress fracture. They are not always seen on x-ray. Tibia is the most common bone to occur. Tx: Rest and healing.
832
Patient with restrictive lung disease and atrial fibrillation with rapid ventricular rate: What drug do you not give:
Amiodarone can cause pulmonary toxicity.
833
Malignant (necrotizing) otitis media externa is caused by: Treatment:
Pseudomonas aeruginosa, Treatment ciprofloxacin.
834
Newborn with cyanosis that is aggravated by feeding and relieved by crying: Diagnosis:
Choanal atresia a congenital nasal malformation is caused by failure of the posterior nasal passage to canalize completely leaving either a bone 90% or membrane 10% obstruction. Failure to move a catheter through nose is suggestive. CT scan.
835
Red flags for other secondary causes of hypogonadotropic hypogonadism in males include: Tests:
Significant headaches, very low testosterone levels (
836
Patient with chest pain, epigastric pain, and air in the mediastinum on chest x-ray:
Consistent with esophageal rupture. Diagnostic study of choice is Gastrografin-contrast esophagography, or CT esophagography.
837
In asymptomatic patients with hypercalcemia what are the steps:
Confirm the hypercalcemia with second reading if still elevated gt PTH level.
838
Acute mitral regurgitation can occur: What happens to pressure:
Due to papillary muscle displacement in patients with acute MI. Leads to excessive volume overload, causing elevated left atrial and ventricular filling pressures and acute pulmonary edema.
839
Ludwig’s angina is an infection of the: Source of infection: Most common cause death:
Submandibular and sublingual glands: Source most commonly an infected tooth 2nd or 3rd molar. Asphyxiation is most common cause death. Olanzapine and clozapine should have what done when taking these medications: BMI measured monthly and a fasting plasma glucose and lipids, BP and waist circumference should be assessed at baseline, 3 months, and then annually. Metabolic syndrome.
840
Patients with resistant hypertension and diffuse atherosclerosis, asymmetric kidney size, recurrent flash pulmonary edema, or elevation in serum creatinine >30% from baseline after starting ACEI or ARB:
Renovascular hypertension. Presence of continuous abdominal bruit.
841
Diastolic decrescendo murmur heard on the right sternal border:
Aortic dissection
842
Aortic dissection what tests:
Get serum creatine incase you have to get chest ct with contrast otherwise you want a TEE.
843
What type of liver finding on biopsy in a patient with Reye syndrome:
Microvesicular fatty infiltrates.
844
Ventricular aneurysm (VA) post MI present with:
Hallmark ECG findings of persistent ST- segment elevation after a recent MI and deep Q waves in the same leads
845
atient with CHF exacerbation being treated with furosemide with improved symptoms, but new onset 6 beats wide complex ventricular tachycardia:
Measure serum electrolytes. Loop diuretics can cause hypokalemia and hypomagnesemia which can cause ventricualar tachycardia, also potentiate digoxin.
846
The strongest influence on long term prognosis following an ST elevation myocardial infarction is the duration:
Of time that passes before coronary blood flow is restored (via PTCA or fibrinolysis).
847
Multiple system atrophy (Shy-Drager syndrome): Characterized: Compilation
1. Parkinsonism 2. Autonomic dysfunction (postural hypotension, abnormal sweating, disturbance of bowel or bladder control, abnormal salivation or lacrimation, impotence, gastroparesis) 3. Widespread neurological signs (cerebellar, pyramidal or lower motor neuron). The accompanying bulbar dysfunction and laryngeal stridor may be fatal.
848
Early defibrillation is the therapy of choice in patients with:
Ventricular fibrillation and pulseless VT.
849
Immediate synchronized cardioversion is used in:
Symptomatic or sustained monomorphic VT (unresponsive to antiarrhythmic) and hemodynamically unstable atrial fibrilation with rapid ventricular response.
850
Pulseless electrical activity or asystole should be managed with:
Uninterrupted CPR along with vasopressor therapy to maintain cerebral and coronary perfusion.
851
Patients with cirrhosis should undergo screening:
Endoscopy to exclude varices, indicate the risk for variceal hemorrhage, and determine strategies (nonselective betablocker) for primary prevention. This is a major cause of morbidity and mortality up to 50% of patients.
852
Cyclosporine side effects:
Nephrotoxicity, hyperkalemia, hypertension, gum hypertrophy, hirsutism, and tremor.
853
Tacrolimus side effects:
Nephrotoxicity, hyperkalemia, hypertension, and tremor
854
The major toxicity of azathioprine:
Dose related diarrhea, leukopenia, and hepatotoxicity.
855
The major toxicity of mycophenolate:
Bone marrow suppression.
856
Central retinal artery occlusion is treated with:
Emergency treated with an ocular massage and high flow oxygen administration.
857
Treatment response is defined:
Occurs when a patient demonstrates significant improvement (with or without remission), generally defined as 50% reduction in baseline of severity.
858
Treatment recovery is defined:
Recovery signifies that the episode is over and presents the option of the patient either discontinuing treatment or continuing maintenance.
859
Cholesterol embolization should be suspected in patients with:
Multisystem involvement with acute or subacute renal failure, typical skin manifestations (livedo reticularis, blue toe syndrome), cerebral or intestinal ischemia, and Hollenhorst plaques after a recent arteriography or cardiac catheterization.
860
Ultrasound of the liver shows a smooth, round big cyst with daughter cysts within it: Diagnosis:
Echinococcosis is a parasitic tapeworm common people who raise sheep. Form hydatid cyst anywhere in the body, but most common liver next is lungs. Most people asymptomatic.
861
Patient with recurrent and migratory superficial thrombophlebitis at unusual sites (arm, chest):
Trousseau’s syndrome is a hypercoagulable disorder. It is usually associated with an occult visceral malignancy such as pancreatic (most common), stomach, lung, or prostate carcinoma. Get CT scan of the abdomen.
862
Meconium ileus is virtually diagnostic for:
cystic fibrosis
863
Slipped capital femoral epiphysis should be promptly treated with:
Surgical pinning of the slipped epiphysis where it lies (in situ) in order to lessen the risk of avascular necrosis of the femoral head and chondrolysis.
864
Patient with blunt abdominal trauma especially children can present with:
Diaphragmatic rupture that does show initially can take months even years. After chest x-ray get ct scan.
865
Lifestyle modification first line intervention for newly diagnosed stage I hypertension. Most effective:
Weight loss in obese patient. Next is DASH diet. Exercise, Dietary sodium decrease. Alcohol intake.
866
The first step in management of a nonreassuring heart rate is to improve fetal oxygenation and uteroplacental blood flow by:
Administering oxygen and changing maternal position. Uterotonic drugs must be discontinued.
867
Dermatomyositis common comorbidity:
Internal malignancies, up to >15% develope these (Most common is ovarian, lung, pancreatic, stomach, or colorectal cancers, or non-hodgkin's lymphoma).
868
Patient with hairy cell leukemia drug of choice:
Cladribine
869
In patients with PaO2 35 to minimize pulmonary complications:
Give corticosteroids.
870
How does systemic sclerosis effect the lower esophagus:
Can cause atrophy and fibrosis of the smooth muscle.
871
Uremic pericarditis: BUN level: Treatment:
BUN >60 mg/dL. Does Not have the normal ECG changes. Dialysis.
872
Which oral diabetes medication can induce weight loss and have a lower hypoglycemic risk:
Glucagon-like peptide-1 (GLP-1) agonist (Exenatide, liraglutide).
873
Aortic stenosis heart murmur describe:
Systolic ejection murmur that radiates to the apex and carotid arteries.
874
Nasopharyngeal carcinoma is associated with what virus:
Epstein-Barr virus (EBV)
875
Paresthesia of the first three and a half digits and occasionally thenar eminence atrophy:
Carpal tunnel syndrome of median nerve.
876
Total T4 and T3 increased with decreased TSH radioactive iodine uptake is decreased:
Thyroiditis, Graves has increased radioactive iodine uptake
877
Levodopa plus carbidopa side effects:
Most common early are hallucinations, dizziness, headache, and agitation. After several years involuntary movements.
878
Cryptosporidium parvum is an important emerging cause of:
Traveler’s diarrhea and should be considered in patients with persistent, watery diarrhea for > 2 weeks.
879
Preventative screening prostate:
PSA should be discussed on a case by case with patient.
880
Bronchiectasis what do you need to make diagnosis:
Chest x-ray is frequently abnormal, but need a CT scan for definitive diagnosis.
881
GBS neonatal screening universal:
35-37 weeks gestation.
882
Three most likely malignant pleural effusions:
Lung carcinoma, breast carcinoma, and lymphoma.
883
In a possible Varicella exposure in an immunocompetent patient who is asymptomatic, and nonimmune should:
Receive post-exposure prophylaxis within 3-5 days exposure. Nearly 70-100% effective in preventing infection when given in 3-5 day.
884
Varicella exposure in an immunocompromised hosts who are asymptomatic and nonimmune should:
Receive varicella zoster immune globulin. The vaccine is a live attenuated virus and is contraindicated in immunocompromised.
885
During the immune clearance phase of HBV, patients need serial measurements:
Both ALT and HBeAg every 3-6 months until they achieve viral clearance.
886
APGAR: What does it stand for how is it scored:
A-Appearance: 0 completely blue/pale; 1 body pink, extremities blue; 2 completely pink P-Pulse: 0 absent; 1 100/min G-Grimace: 0 absent; 1 Grimace/whimper; 2 Cough/sneeze/cry A-Activity/muscle tone: 0 limp; 1 Some flexion; 2 Active/spontaneous R-Respiratory: 0 Absent; 1 Slow, weak cry; 2 Regular, good cry
887
Apgar score of
Further evaluation and resuscitation.
888
Patients with Hodgkin's lymphoma treated with chemotherapy and radiation can have:
Secondary malignancy especially those treated before age 30.
889
Radiation fibrosis occurs most commonly in patients who have received:
Lung field radiation and develop dyspnea, nonproductive cough, and chest pain 4-24 months after therapy.
890
Essential tremor first line and second line medications:
First line Propranolol; Second line primidone and topiramate
891
Cerebral palsy (CP) is a group of clinical syndromes characterized by: Biggest risk factor
Non Progressive motor dysfunction: The three primary subtypes are spastic, dyskinetic, and ataxic. Biggest risk factor is prematurity.
892
In ventricular fibrillation and pulseless ventricular tachycardia: What is of primary importance:
Defibrillation: Time to defibrillation is strongly correlated with survival.
893
INR for Warfarin therapy for VTE, atrial fibrillation, and prosthetic heart valve: Timeframe of use:
VTE and atrial fibrillation: 2.0-3.0 prosthetic heart valve: 2.5-3.5 3 months for reversible risk factor. 6-12 months idiopathic DVT.
894
Lab findings seen in SIADH:
Serum osmolality 100 mOsm/kg (inappropriately elevated) Urine sodium > 40 mEq/L Normal serum creatinine, potassium, and acid-base balance Normal adrenal and thyroid function
895
Treatment SIADH: Asymptomatic or mild symptoms (forgetfulness, unstable gait):
Fluid restriction (2 times serum osmolality
896
Treatment of SIADH: Moderate symptoms (confusion, lethargy):
Hypertonic saline in first 3-4 hours to increase sodium > 120 mEq/L Later treatment same as mild hyponatremia
897
Treatment of SIADH: Severe symptoms: (seizure, inability to communicate and/or coma)
Bolus of hypertonic saline until symptoms resolution | +/- Vasopressin receptor antagonists (conivaptan)
898
Patients with ischemic strokes and negative CT findings for intracranial bleed: Treatment:
Fibrinolytic therapy especially if given in 3-4.5 hours of onset.
899
Paralysis that begins like GBS, but rapidly progresses within hours:
Tick-borne paralysis is characterized by rapidly progressive ascending paralysis (which may be asymmetric). Need to perform a meticulous search for tick because they must feed for 4-7 days and remove it. Most patient spontaneously recover.
900
Recurrent pneumonia in the same anatomic area of the lung as seen on x-ray suggest:
Bronchial obstruction due to an underlying abnormality. You need to get a CT scan to visualize the underlying parenchymal abnormalities. Biopsy via bronchoscopy is next.
901
What two conditions in adults can cause minimal change disease:
NSAIDS and lymphoma (Most common form of nephrotic syndrome in patients with Hodgkin lymphoma).
902
Membranoproliferative glomerulonephritis is associated with:
Hepatitis B and C infections and lipodystrophy.
903
Membranous nephropathy is associated with:
Adenocarcinoma (breast, lung), NSAIDS, Hepatitis B, SLE.
904
Risk factors for endometrial cancer:
Age ≥45, obesity, diabetes, unopposed estrogen exposure, PCOS, early menarche/late menopause.
905
The first priority in evaluating abnormal uterine bleeding (AUB):
Exclude pregnancy with serum beta-hCG. Workup for abnormal uterine bleeding after pregnancy test: First line tests include blood counts, coagulation studies, and TSH. May also include prolactin, FSH, +/- LH, and serum androgens.
906
Patients with persistent symptoms of AUB who have a negative initial work up or risk factors for endometrial cancer require:
Endometrial biopsy
907
Contraindications to radioiodine therapy in Graves patient:
Pregnancy and severe ophthalmopathy.
908
Presbyopia is a common age related eye occurrence due:
Decreased lens elasticity leads to difficulty with near vision.
909
Clinical manifestations of hereditary hemochromatosis:
Hyperpigmentation (bronze diabetes), arthralgia, arthropathy, chondrocalcinosis, elevated hepatic enzymes hepatomegaly (early), cirrhosis (later), and increased risk for HCC, diabetes mellitus, secondary hypogonadism and hypothyroidism, restrictive or dilated cardiomyopathy and conduction abnormalities, increased susceptibility to listeria, vibrio vulnificus, yersinia enterocolitica.
910
Patient with fever, tachycardia, leukocytosis, and metabolic acidosis with small bowel obstruction:
Urgent surgical exploration
911
Medications that block the dopamine (D2) receptor may cause:
Extrapyramidal effects that can resemble Parkinsonism. Think about drug induced parkinsonism from risperidone causing bradykinesia, rigidity, and tremor.
912
Wilson’s disease: Genetics: Characterized: Diagnosis:
``` Rare autosomal recessive; Characterized by abnormal copper deposition in the tissues such as liver, basal ganglia, and cornea. Children tend to present with liver disease while young adults tend to have neuropsychiatric disease. Low ceruloplasmin ( ```
913
Conditions where one may have an increased BUN/creatinine ratio include:
Prerenal failure, gastrointestinal bleeding (secondary to reabsorption of blood from the gastrointestinal tract), and steroid administration.
914
Screening for bladder cancer in patients who are at risk for developing the disease:
Screening for bladder cancer is not recommended.
915
Hyperosmolar hyperglycemic state: What is potassium level:
May look normal on labs but total body potassium is in deficit due to urinary loss caused by glucosuria-induced osmotic diuresis.
916
Friedreich ataxia is the most common type: Presents: Most common cause death:
Spinocerebellar ataxias. Remember the combination of neurologic (ataxia, dysarthria), skeletal (scoliosis, feet deformities), and cardiac (concentric hypertrophic cardiomyopathy) manifestations of the disease. The most common cause of death are cardiomyopathy and respiratory complications.
917
Hepatitis B is a significant risk factor for what renal syndrome in children:
Membranous nephropathy.
918
What agents facilitate stone passage and reduce the need for analgesics:
Alpha-1 receptor blockers such as tamsulosin act on the distal ureter, lowering muscle tone and reducing reflux uteral spasm secondary to stone impaction.
919
Reactive arthritis does not always present with all features: Name features: Treatment:
Urethritis, conjunctivitis, mucocutaneous lesions, enthesitis (site were tendons insert bone), and asymmetric oligoarthritis. Treatment: NSAIDS.
920
OSA has blood gas:
Normal
921
Tension pneumothorax should have:
Immediate thoracostomy.
922
Acute dacryocystitis is characterized by:
The sudden onset of pain and redness in the medial canthus region. Dacryocystitis is an infection of the lacrimal sac common in infants and adults over 40. Staphylococcus aureus and beta hemolytic streptococcus.
923
Hordeolum refers to an:
Abscess located over the upper or lower eyelid.
924
Chalazion is a chronic:
Granulomatous inflammation of the meibomian gland. It appears as a hard painless lid nodule.
925
Neuroleptic Malignant Syndrome (NMS): Treatment:
Dantrolene, bromocriptine, amantadine
926
Sulfasalazine: Used for: Mechanism: Adverse effects:
Antirheumatic drug; TNF and IL-1 suppressor; Hepatotoxicity, stomatitis, hemolytic anemia.
927
Hydroxychloroquine: Used for: Mechanism: Adverse effects:
Antirheumatic drug; TNF and IL-1 suppressor; Retinopathy
928
Methotrexate: Used for: Mechanism: Adverse effects:
Antirheumatic drug; Purine antimetabolite; Hepatotoxicity; Stomatitis, Cytopenia.
929
Leflunomide: Used for: Mechanism: Adverse effects:
Antirheumatic drug; Pyrimidine synthesis inhibitor; Hepatotoxicity, cytopenia.
930
Obesity hypoventilation syndrome causes what metabolic acid/base:
There is respiratory acidosis, so there is a compensatory effort to maintain normal pH, the kidney increase bicarbonate retention and decreases chloride reabsorption.
931
A lesion in the upper thoracic spinal cord results in:
Paraplegia, bladder, and fecal incontinence, and absent sensation from the nipple downwards.
932
A lesion in the lower thoracic spinal cord causes:
Absent sensation from the umbilicus downwards.
933
Postpartum endometritis is most commonly caused by:
Polymicrobial infection composed of gram positive and gram negative organisms, aerobic and anaerobic organisms and occasionally other organisms.
934
Postpartum endometritis: Treatment:
Clindamycin and gentamicin
935
Patient asks “What are the chances that I really do not have breast cancer?”
Negative predictive value: Will vary with the pretest probability of a disease. High probability = low NPV. Low probability = high NPV.
936
Renal tubular acidosis: Type 1: Primary defect: Urine pH: Serum potassium: Cause:
``` Type 1 (distal): Poor hydrogen ion secretion into urine; ≥5.5 pH urine; Potassium low-normal; Causes genetics disorders, medication toxicity, autoimmune (Sjogren's syndrome, rheumatoid arthritis). ```
937
Renal tubular acidosis: Type 2: Primary defect: Urine pH: Serum potassium: Cause:
Type 2 (proximal): Poor bicarbonate resorption;
938
Renal tubular acidosis: Type 4: Primary defect: Urine pH: Serum potassium: Cause:
Type 4: Aldosterone resistance;
939
Streptococcus sanguinis belongs to the viridans group streptococcus which means:
You can get endocarditis from it when you have dental procedure.
940
Why can’t nitrofurantoin be used for complicated cystitis:
Because it does not adequately penetrate renal tissue.
941
Acute pyelonephritis intravenous antibiotics and imaging is indicated if symptoms:
Persist or worsen after 2-3 days.
942
Thyroid storm is often triggered by: Characterized:
Thyroid or non thyroid surgery, infection, iodine contrast, or childbirth. Characterized by tachycardia, hypertension, cardaic arrhythmias, high fever, tremor, altered mentation, and lid lag.
943
Primary therapy for moderate hypothermia:
Active external and internal rewarming, which includes use of heated humidified oxygen and warmed intravenous fluids.
944
Bradycardia associated with hypothermia usually:
Does not require treatment unless it persist with rewarming or if associated with hypotension. Pacemaker cells are refractory to atropine.
945
Patient from Southeast Asia has a chronic cough and hemoptysis with a cavitary lesion on CT imaging:
Fungal ball: Pulmonary aspergillosis. Think this when patient from endemic TB area.
946
Pain with supination or extension of the wrist and point tenderness just distal to the lateral epicondyle:
Lateral epicondylitis (tennis elbow)
947
Rapid onset edema of the face, acral extremities, genitals, trachea, and abdominal organs without urticaria:
Hereditary angioedema is a deficiency or dysfunction in C1 inhibitor, which results in elevated levels of the edema producing factors C2b and bradykinin.
948
Classic triad of normal pressure hydrocephalus (NPH):
Abnormal gait, incontinence, and dementia. Due to decreased CSF absorption.
949
Central cord syndrome: Characterized:
Weakness that is more pronounced in the upper extremities than the lower and accompanied by localized deficits in pain and temperature sensation.
950
Anterior cord syndrome: Characterised:
Bilateral spastic motor paresis distal to the lesion. Usually due to occlusion of anterior spinal artery.
951
Cri-du-chat syndrome is due: Presents:
Due to 5p deletion and presents as microcephaly, hypotonia, short stature, and a cat-like cry.
952
Patient presents with blood at the urethral meatus, a high riding prostate, scrotal hematoma, inability to void despite sensing an urge to void, and a palpably distended bladder.
Posterior urethral injury is associated with pelvic fractures
953
A young woman who presents with a breast lump with no obvious signs of malignancy are present can be:
Asked to return after her menstrual period for reexamination (which may reveal regression of the mass). If decrease in size probably benign. Otherwise proceed with ultrasonography, fine needle aspiration biopsy, and/or excisional biopsy.
954
Mammography is usually not helpful in young women:
Because the density of breast tissue is high in young women.
955
Somnambulism: Define:
Sleepwalking is another non-REM parasomnia. Occurs later in childhood and adolescence.
956
Uveitis pupillary response:
The pupil is constricted with poor light response, in acute angle glaucoma, the pupil is dilated and is nonreactive to light.
957
Open angle glaucoma has a pathologic:
Cupping of the optic disk, persistently elevated intraocular pressure.
958
Eisenmenger syndrome:
Cyanosis and dyspnea secondary to right to left shunting.
959
Pansystolic murmur that is loudest at the left lower sternal border and a diastolic rumble at the apex:
Large ventral septal defects
960
Patient with Northern European ancestry with megaloblastic anemia, atrophic glossitis (shiny tongue), vitiligo, thyroid disease, and neurologic abnormalities (ataxia, loss of position and vibration sense):
Pernicious anemia an autoimmune disease with autoantibodies against gastric intrinsic factor. Results in B12 deficiency.
961
Patient with fever, polyarthralgia, and a pustular rash who works as a commercial sex worker:
Disseminated gonococcal infection: Neisseria gonorrhoeae is the most common sexually transmitted disease causing arthitis. Due to the fastidious growth requirements blood cultures are often negative. Must get nucleic acid amplification testing.
962
Primary hyperparathyroidism: Labs: Treatment:
Hypercalcemia with elevated or inappropriately normal PTH. 24-hour urinary calcium >250 mg. Urine calcium/creatinine >0,02 differentiate from familial hypocalciuric hypercalcemia: Bone mineral density scan for osteopenia/osteoporosis. Sestamibi scan plus ultrasound to locate hyperactive parathyroid tissue prior to surgery.
963
Use the modified Wells score for PE evaluation:
Score +3 points: Clinical signs of DVT; Alternative diagnosis less likely than PE. Score +1.5 points: Previous PE or DT; Heart rate >100; Recent surgery or immobilization. Score +1 points: Hemoptysis; Cancer. Total score for clinical probability ≤4 = PE unlikely Get CT angiogram of chest patient's normal renal function; V/Q scan otherwise >4 = PE likely Start anticoagulation therapy
964
Patient with 6 weeks of periorbital edema, moderate ascites, lower extremity edema, and high urinary protein excretion. Suddenly developed right sided abdominal pain, fever, and gross hematuria:
Renal vein thrombosis (RVT) and other thromboembolism are important complications of nephrotic syndrome because of loss of antithrombin III in the urine.
965
Patient who has cholilithiasis and refuses surgery: Treatment:
Provide patient with ursodeoxycholic acid and advice to avoid fatty foods.
966
Diabetic patient presents with symptoms of anorexia, nausea, vomiting, early satiety, postprandial fullness, and impaired glycemic control:
``` Diabetic gastroparesis (delayed gastric emptying): Treatment Prokinetics metoclopramide, erythromycin, cisapride. Diabetic autonomic neuropathy occurs >50%. ```
967
Thiazide diuretics have some unfavorable metabolic side effects including:
Hyperglycemia, increased LDL cholesterol, and plasma triglycerides. hyponatremia, hypokalemia, and hypercalcemia.
968
Patients with acute pancreatitis can develop hypotension:
Due intravascular volume loss secondary to local and systemic vascular endothelial damage causing vasodilation, increased vascular permeability, and plasma leak into retroperitoneum.
969
Acute lymphoblastic leukemia: Presentation: Diagnosis:
Presents with nonspecific systemic symptoms, bone pain, lymphadenopathy, hepatomegaly, pallor (from anemia), petechia (from thrombocytopenia). Diagnosed with bone marrow biopsy >25% lymphoblasts.
970
Viral (herpes simplex virus) encephalitis: Symptoms: Diagnosis: Treatment:
Fever, altered mental status with confusion and agitation, risk of seizures and coma. Get CSF: Elevated WBC with lymphocytic predominance, normal glucose, and elevated protein. Diagnosed by viral DNA by PCR. Empiric treatment acyclovir.
971
Patient with aortic stenosis (AS): What test do you get before a stress test:
Echocardiogram: Exercise stress test are contraindicated in symptomatic severe AS.
972
Be Careful of the patient on theophylline: TOXICITY:
Theophylline toxicity can manifest as central nervous system stimulation (headache, insomnia, seizure), gastrointestinal disturbance (nausea, vomiting), and cardiac toxicity (arrhythmia). Narrow therapeutic window check levels.
973
Pelvic exam is consistent with a 14 week uterus that is irregular and mobile with prominent posterior mass. Urine pregnancy is negative: Diagnosis:
Uterine leiomyoma
974
Autoimmune hemolytic anemia (AIHA) and hereditary spherocytosis (HS): Differentiate them:
Both can cause extravascular hemolytic anemia. A negative family history and + Coombs test suggest AIHA. A positive family history and negative Coombs test suggest HS. The peripheral blood smear for both may show sperocytes with central pallor.
975
Duchenne muscular dystrophy: Gold standard test for diagnosis:
Genetic testing for dystrophin gene on Xp21.
976
Screening for male active or former smokers aged 65-75:
One-time abdominal ultrasound to evaluate for an abdominal aortic aneurysm.
977
Most common cause of acute bacterial rhinosinusitis:
Streptococcus pneumoniae and nontypable Haemophilus influenzae.
978
Hyperestrogenism in cirrhosis leads to:
Gynecomastia, testicular atrophy, decreased body hair, spider angiomas, and palmar erythema.
979
Patient with elevated conjugated (direct) hyperbilirubinemia along with elevated levels of alkaline phosphatase need:
Abdominal ultrasound to assess hepatic parenchyma and biliary ducts.
980
Porphyria cutanea tarda is a condition that arises from: Presents: Associated with:
Deficiency in uroporphyrinogen decarboxylase, an enzyme in heme synthesis.Presents with painless blisters, increased fragility on the dorsal surfaces of the hands, facial hypertrichosis and hyperpigmentation. Hepatitis C.
981
Mother with Graves with a low birth weight, tachycardia, warm skin irritable neonate: Treatment:
Neonatal thyrotoxicosis caused by transplacental TSH-receptor antibody. Self resolves by 3 months treat with methimazole and beta-blocker.
982
Patient history of normal internal genitalia with ambiguous external genitalia, clitoral hypertrophy, and high FSH/LH with low estrogen is consistent with:
Aromatase deficiency
983
Premature atrial beats are completely:
Benign and neither require workup or treatment.
984
Papillary necrosis presents with:
Massive Hematuria, but episodes are usually mild and resolve spontaneously. Can occur in sickle cell trait.
985
Flattening of both the top and bottom of the flow-volume loop:
A fixed upper airway obstruction will decrease the airflow rate during inspiration and expiration. Laryngeal edema.
986
Patient with burning, localized pain and regional hyperesthesia/allodynia, in the context of recent cancer treatment, has common features: Treatment:
Of herpes zoster (shingles): Treatment: acyclovir, valacyclovir, famciclovir
987
Alzheimer's disease CT and MRI findings:
Diffuse cortical and subcortical atrophy which is disproportionately greater in the temporal and parietal lobes.
988
Immune thrombocytopenia lab findings: Treatment children vs adults:
Isolated thrombocytopenia
989
Most common and serious complication peptic ulcer disease:
Hemorrhage
990
Peripheral blood smear reveals bite cells and red blood cell inclusions seen after crystal violet staining:
Glucose-6 dehydrogenase deficiency
991
Chronic renal failure can cause uremia to occur that has what effect on platelets.
It causes platelet dysfunction. Dialysis usually keeps this from happening, but patients can be treated with desmopressin that exposes factor 8. PT, PTT and TT normal. Only bleeding time prolonged.
992
Zollinger-Ellison syndrome can lead to:
Malabsorption of fat due to pancreatic enzymes inactivated by acid. Can even have jejunal ulcers.
993
Most common pulmonary complication in diffuse systemic sclerosis:
Interstitial fibrosis
994
COPD vs asthma: primary long term treatment:
``` Asthma = inhaled corticosteroid COPD = long acting anticholinergic ```
995
Pseudogout forms from and causes what in joints:
Calcium pyrophosphate crystals that are released from chondrocalcinosis (calcification of articular cartilage) into the joint space. Rhomboid shaped, positively birefringent crystals is diagnostic.
996
Low complement levels, increased rheumatoid factor, increased liver transaminases, with elevated creatinine, proteinuria, and microscopic hematuria with dysmorphic red blood cells:
Cryoglobulinemia is an immune complex disorder (IgM against anti-hepatitis C virus IgG) most commonly due to chronic hepatitis C.
997
Ulcerative colitis is:
p-ANCA positive
998
Severe preeclampsia is characterized by any of the following:
BP ≥160 mmHG systolic or ≥110 mmHG diastolic on 2 occasions ≥4 hours apart during bedrest Thrombocytopenia 1.1 mg/dL or doubling of serum creatinine Elevated transaminases Pulmonary edema New-onset visual or cerebral symptoms Note: Elevated BP in a previously normotensive patient makes diagnosis jump to severe, but not for patients who had high BP before.
999
Deficiency of niacin (vitamin B3): Characterised:
Leads to pellagra, which is characterized by diarrhea, dermatitis (sunburn like rash in sun exposed areas, becomes hyperpigmented), dementia, and if severe, death. Red beefy tongue (glossitis).
1000
Deficiency of riboflavin (vitamin B2): Characterized:
Can lead to cheilosis, glossitis, seborrheic dermatitis (often affecting the genital areas), pharyngitis, and edema and/or erythema of the mouth.
1001
Pyridoxine (vitamin B6) deficiency: Characterised:
Causes irritability, depression, dermatitis, and stomatitis (inflammation of mucosa mouth). Can cause elevated homocysteine concentration which increases risk for venous thromboembolism.
1002
Placenta previa: Risk factors: Clinical features: Diagnosis:
Risk factors: Prior placenta previa, prior cesarean or other uterine surgery, multiparity, advanced age. Clinical features: Painless third trimester bleeding, bleeding with uterine contraction. Diagnosis: Transabdominal followed by transvaginal sonography. NO DIGITAL vaginal examination before US!
1003
Placental abruption: Caused by:Presents with:
Premature placental separation initiated by hemorrhage in the decidua basilis. Vaginal bleeding and abdominal pain are frequent presenting complaints.
1004
Uterine rupture: Presents with: Risk factors:
Sudden onset of intense abdominal pain and vaginal bleeding associated with hyperventilation, agitation, and tachycardia. Although it may occur prior to onset of labor, it is commonly associated with labor, especially in women with a prior cesarean delivery.
1005
Vasa previa: Mechanism: Presentation:
Fetal blood vessels cross the fetal membranes in the lower segment of the uterus between the fetus and the internal cervical os. Presents with painless antepartum hemorrhage, but is associated with rapid deterioration of the fetal heart tracing as the hemorrhage is of fetal origin.
1006
Graves disease during pregnancy: Medications:
First trimester propylthiouracil (PTU), methimazole is a teratogen, but can be used the 2nd, and 3rd trimester. Both cause agranulocytosis.
1007
Trimethoprim (TMP) part of TMP-SMX especially used in HIV patients can cause:
Hyperkalemia, by blocking eNac same mechanism as amiloride. Also blocks creatinine secretion, so may have artificial elevation with no actual kidney damage. Serial monitoring of potassium levels.
1008
Remember when you get a question on athletes using performance enhancing drugs: EPO versus anabolic steroids:
Anabolic steroids can also cause erythrocytosis, so don’t be fooled by high RBCs. EPO does not cause gynecomastia, and anabolic steroids do cause gynecomastia.
1009
What murmurs increase on expiration:
Only left sided murmurs increase on expiration.
1010
An S4 results due to:
The forceful atrial contraction against the thick non-compliant ventricle.
1011
Classic indicators for surgery in patients with aortic stenosis are SAD:
Syncope, Angina, and Dyspnea. The indications for aortic valve replacement are: 1. All symptomatic patients with AS 2. Patients with severe AS undergoing CABG or other valvular surgery 3. Asymptomatic patients with severe AS and either poor LV systolic function, LV hypertrophy >15 mm, valve area
1012
What drugs cause patients to have to increase their levothyroxine dose:
Estrogen (oral increases TBG), tamoxifen, raloxifene, rifampin, phenytoin, carbamazepine, heroin, methadone.
1013
What drugs cause patients to have to decrease their levothyroxine dose:
Androgens, glucocorticoids, anabolic steroids, slow release nicotinic acid.
1014
Non Inflammatory chronic prostatitis: Presents: Labs:
Afebrile and have irritative voiding. UA normal. Expressed prostatic secretions show normal number of leukocytes and culture of the secretions is negative for bacteria.
1015
Chronic bacterial prostatitis: Presents: Labs:
Afebrile and irritative voiding symptoms including frequency, urgency and suprapubic or perineal discomfort. UA normal. Expressed prostatic secretions show leukocyte count greater than 10 WBC/HPF and cultures grow causative pathogens.
1016
Inflammatory chronic prostatitis: Presents: Labs:
Afebrile and irritative voiding symptoms including frequency, urgency and suprapubic or perineal discomfort. UA normal. Expressed prostatic secretions show leukocyte count greater than 10 WBC/HPF and cultures are negative.
1017
Systemic lupus erythematosus (SLE) antibodies:
ANA = sensitive Anti-dsDNA and anti-SM (smooth muscle) = specific Hypocomplementemia (C3 and C4) common
1018
Elevated BNP levels are associated with what heart sound:
S3 which is a soft diastolic sound produced by the tensing of the papillary chordal apparatus when there is rapid influx of blood into the ventricle in early diastole. BNP and S3 are both signs of increased cardiac filling pressure.
1019
Nephrolithiasis prefered imaging:
CT scan of abdomen without contrast.
1020
Bipolar disorder in a first degree relative (parent, sibling, dizygotic twin) raise the likelihood of you having a manic attack:
5-10%, if both parents than 60% chance, if dizygotic twin than 70% chance. General population is only 1%.
1021
Increased gastric residual volume, vomiting, and abdominal distention in a preterm neonate are highly suspicious for necrotizing enterocolitis: Hallmark findings on x-ray:
Include pneumatosis intestinalis (intramural air) or air in the bowel wall and portal vein.
1022
Cat-scratch disease is caused by Bartonella henselae: Treatment:
Oral azithromycin
1023
Patient with large anterior mediastinal mass with elevated levels of β-hCG and AFP, is consistent with:
A nonseminomatous germ cell tumor. Seminomatous only have β-hCG.
1024
Hepatocellular carcinoma can elevated:
AFP
1025
Tuberculosis is a common cause of chronic primary:
``` Adrenal insufficiency (Addison's disease) in endemic areas. Cause aldosterone deficiency and presents with non-anion gap and hyperkalemic and hyponatremic metabolic acidosis. ```
1026
How long do you have to refrain from sports when you infectious mononucleosis:
Avoid contact sports for ≥3 weeks due to the risk of splenic rupture.
1027
Patient with all the signs and symptoms of pregnancy, however, ultrasound reveals a normal endometrial stripe and a negative pregnancy test although home test was positive:
Pseudocyesis: Seen in women with a strong desire to conceive and is a form of conversion disorder.
1028
Main differences between simple renal cyst and malignant renal cyst:
Simple: Thin smooth regular wall, unilocular no septate homogenous content and absence of contrast on CT/MRI Malignant cystic mass: Thick, irregular wall, multilocular, multiple septate, occasional calcification, heterogenous content, and presence of contrast on CT/MRI. Simple just give reassurance.
1029
MEN 2A and 2B genetics:
Autosomal disorder due to germline mutation in RET proto-oncogene in >95%.
1030
Patients placed on high dose glucocorticoids can have:
Glucocorticoid induced myopathy with progressive proximal muscle weakness and atrophy without pain or tenderness. Normal ESR and CK. Most common drug induced myopathy occurs weeks to months.
1031
Patients with diabetes for >10 years develop:
Diabetic microangiopathy, nephropathy, and glomerulosclerosis.
1032
Alanine and lactate are converted into what during gluconeogenesis:
Pyruvate
1033
Meniere's disease: Presentation: Environmental treatment:
Presents with combination of vertigo, ear fullness, tinnitus, and hearing loss. First line therapy consists low salt diet.
1034
Patient with fat necrosis of the breast can be confused with breast cancer:
Can resemble breast cancer, including skin or nipple retraction and calcifications on mammography. Biopsy of the mass will reveal fat globules and foamy macrophages (histiocytes). No treatment is indicated for this self-limited condition.
1035
Patient with severe renal insufficiency GFR
Unfractionated heparin, all others increase bleeding risk due to Xa activity.
1036
Characterize a patient with postoperative cholestasis:
Condition that often develops after a major surgery characterized by hypotension, extensive blood loss into tissues, and massive blood replacement. Alkaline phosphatase is elevated, but ALT and AST are normal to mild elevated. Benign condition.
1037
Schizophrenia: What do you see on neuroimaging:
Enlargement of the cerebral ventricles.
1038
Autism: What do you see on neuroimaging:
Increased total brain volume.
1039
OCD:What do you see on neuroimaging:
Abnormalities in Orbitofrontal cortex and striatum
1040
Panic disorder:What do you see on neuroimaging:
Decreased volume of amygdala.
1041
PTSD:What do you see on neuroimaging:
Decreased hippocampal volume.
1042
Caustic ingestion management:
Secure ABC. Decontamination: Remove clothing and visible chemical. X Ray if respiratory symptoms Endoscopy within 24 hours.
1043
Resting state when using carbohydrates, protein, or lipid:
Close to 1.0 carbohydrates. Protein 0.8. Lipids 0.7.
1044
Celiacs disease antibodies: Biopsy:
IgA anti-endosomal and anti tissue transglutaminase antibody. Biopsy shows villous atrophy.
1045
Td or Tdap:
Tdap should be substituted for Td once then Td every 10 years as adult.
1046
Patient with splenectomy vaccines given and when:
Administered ≥14 days before or >14 days after splenectomy.
1047
Dumping syndrome is a common complication:
Postgastrectomy, need to modify diet.
1048
In pregnant patient with appendicitis what do you do:
US with graded compression technique. Non Compression and dilation are diagnostic.
1049
Pregnancy luteoma and theca luteum cysts are:
most common cause of hyperestrogenism in pregnancy Luteoma solid on US. No maternal treatment can cause virilization female fetus.
1050
Causes of crystal induced acute kidney injury:
Acyclovir, sulfonamides, methotrexate, ethylene glycol, protease inhibitors. Cause renal tubular obstruction.
1051
Remember that nephrotic diseases always have a risk factor for:
hypercoagulable: loss of antithrombin III in urine.
1052
In the ovulatory phase of the menstrual cycle, cervical mucus:
Profuse, clear and thin. It will stretch to approximately 6 cm and exhibits ferning on a microscopic slide. pH is 6.5 or greater the most basic of any phase.
1053
Clinical features of paroxysmal nocturnal hemoglobinuria: Labs: Test: Treatment:
Hemolysis leads to fatigue, Cytopenias (impaired hematopoiesis), venous thrombosis (intra abdominal, cerebral veins). Labs show elevated LDH and low haptoglobin (due to hemolysis). Absence of CD55 and CD59. Tx: iron and folate and Eculizumab.
1054
Phenelzine is a monoamine oxidase inhibitor (MAOI): Must avoid what foods: Why:
Foods high in tyramine(aged meats and cheese), as the combination can cause hypertensive crisis.
1055
Patient with BPH what test is best for accessing hydronephrosis when they have elevated creatine:
Renal US.
1056
When patients get massive transfusions and their reflexes become hyperactive: Why:
due to citrate in stored blood products binds up the ionized calcium.
1057
Pregnant patient post epidural difficulty voiding with a post residual void of 600 mL:
Require 24 hour indwelling catheter to decompress the bladder and regain detrusor muscle function. These patients have urinary retention and overflow incontinence.
1058
Pathogenesis of carpal tunnel syndrome:
Deposition of mucopolysaccharides protein complex within the perineurium and endoneurium (accumulation of matrix substance.
1059
Patient with difficulty obtaining therapeutic INR on warfarin and expanding DVT:
Start rivaroxaban (direct factor Xa inhibitor) similar efficacy no labs
1060
Drugs used to decrease frequency of MS:
Beta-interferon and glatiramer acetate
1061
Remember with esophageal perforation xray will show widened mediastinum and moderate left sided pleural effusion. The pleural fluid will contain:
High concentrations of amylase from oral secretions.
1062
Marfan syndrome with early diastolic murmur:
Aortic dissection
1063
Parkinson disease is diagnosed with:
Physical exam showing tremor, rigidity, postural instability, and bradykinesia.
1064
Clinical trial:
Compare outcome of interest
1065
Prospective cohort:
Compare disease incidence.
1066
Retrospective cohort:
Compare disease incidence by reviewing past records.
1067
Case control:
Compare risk factor frequency.
1068
Cross sectional:
Compare disease prevalence.
1069
Primary treatment for a prolactinoma with no visual impairments:
Dopamine agonist (bromocriptine, cabergoline).
1070
Long term analgesic use causes (NSAIDS or aspirin):
Tubulointerstitial nephritis
1071
Patient unable to get pregnant for one year with history of PID, and husband with normal sperm count needs:
Hysterosalpingogram
1072
Maternal thyroid axis during pregnancy:
β-hCG stimulate thyroid hormone (T4) and both increase during first trimester, so TSH go down. There is also an increase in thyroid binding globulin.
1073
Endometrial biopsy showing complex hyperplasia without atypia: Treatment:
Progestin therapy. Hyperplasia with atypia and no plans for pregnancy/fails medical management should have hystersctomy.
1074
Five year old with has several strands of dark, coarse hair across pubis and under both axilla, normal genitalia and no breast buds:
Kid with pubarche has adrenal androgen production (premature adrenarche). Obesity is a risk factor for this. If patient has breast bud (thelarche) then HPG axis.
1075
Well known complication of giant cell or temporal arteritis:
Aortic aneurysm, get serial chest x-ray.
1076
CKD on ACEI with hyperkalemia and is asymptomatic:
Saline hydration with furosemide
1077
Primary hyperaldosteronism renin level:
Undetectable.
1078
Elderly patient in bed for a week gets dizzy on rising out of bed finally:
Orthostatic hypotension
1079
Granulosa cell tumors occur:
In children produce estrogen cause precocious puberty.
1080
Small intestine bacterial overgrowth occurs:
In disease with autonomic or dysmotility. Leads to malabsorption can happen with systemic sclerosis.
1081
Diverticulitis get:
US
1082
Contraindication to the use of succinylcholine for rapid sequence intubation:
Hyperkalemia
1083
Patient in 60’s has dysphagia, coughing, halitosis, and a neck mass:
Zenker (pharyngoesophageal)diverticulum. Has motor disfunction. Barium esophagram Patient with delayed onset prosthetic joint infection >3 months and 3 months Staphylococcus epidermidis
1084
Systemic hypertension is a classic cause of:
Diastolic dysfunction
1085
Primary biliary cirrhosis: Etiology: Treatment:
Autoimmune destruction of the intrahepatic bile ducts and cholestasis. Has elevated IgM and anti-mitochondrial antibodies in the serum. Treatment is ursodeoxycholic slow progression and lengthens transplant free survival time.
1086
Anti-D immune globulin should be given at:
28-32 weeks gestation and again after delivery if the baby is Rh positive.
1087
Ankylosing spondylitis diagnosis:
x-ray
1088
Cardiac auscultation reveals a systolic murmur at the apex that shortens with squatting:
Mitral valve prolapse. Squatting increase venous return.
1089
PCOS has greater risk for what cancer:
Endometrial carcinoma
1090
Ulnar nerve entrapment occurs most commonly at:
The elbow where the ulnar nerve lies at the medial epicondylar groove
1091
D-xylose test of proximal small intestine absorption: If low excretion in urine:
Poor absorption in the small intestine = Celiac sprue.
1092
Agitate elderly person should be treated with:
Haloperidol. Use lorazepam for young people.
1093
Patient with new onset kidney disease who has SLE:
Need a renal biopsy for baseline.
1094
Folate deficiency cause:
Elevated homocysteine.
1095
Cobalamin (B12) deficiency cause:
Elevated homocysteine and methylmalonic acid
1096
Muddy brown granular casts:
Acute tubular necrosis
1097
RBC casts:
Glomerulonephritis
1098
WBC casts:
Interstitial nephritis or pyelonephritis
1099
Fatty cast:
Nephrotic syndrome
1100
Broad and waxy casts:
Chronic renal failure
1101
With threatened abortion after you have ascertained that the fetus is present and alive:
Management reassurance and another US one week later
1102
Clinical presentation with anemia, painless gastrointestinal bleeding, and murmur of aortic stenosis is most consistent with:
Angiodysplasia (arteriovenous malformation) of the gastrointestinal tract seen in patients >60. The bad valve causes disruption of von Willebrand factor leading to more bleeding.
1103
Two NRTI with good placental transfer:
Zidovudine and tenofovir. One should be part of mothers
1104
Within 24 hours of MI all patients should be started on:
ACEI to decrease cardiac remodeling post MI.
1105
Patient with femoral vein DVT on enoxaparin has massive GI bleed and enoxaparin is stopped: Next step:
Placement of a retrievable inferior vena cava filter
1106
Giant cell tumor of the bone: X-ray:Treatment:
An expansible and eccentric osteolytic lesion resembling a soap bubble; Surgery
1107
Etiology ascending versus descending aortic aneurysm:
Ascending due to cystic medial necrosis or connective tissue disorder. Descending due to atherosclerosis.
1108
Diabetic patients age 40-75 should receive:
Statin therapy regardless of baseline lipid levels.
1109
One of the earliest findings of macular degeneration:
Distortion of straight lines that appear wavy.
1110
Patient with UTI and high alkaline urine:
Proteus mirabilis = secrete urease. Can have struvite stones
1111
Ophthalmoscopy reveals loss of fundus details, floating debris and a dark red glow:
Vitreous hemorrhage, most common cause is diabetic retinopathy
1112
Hypercalcemia of malignancy is most commonly caused by:
PTHrP production, breast cancer can produce this and release systemically or through metastasis to bone.
1113
Most common extra-articular manifestation of ankylosing spondylitis:
Anterior uveitis
1114
Urinalysis shows hexagonal crystals and urinary nitroprusside test is positive:
Most likely diagnosis is cystinuria, which is due to amino acid transport abnormality. Stones are radiopaque. Look for positive family history of stones.
1115
Remember heparin induced thrombocytopenia causes patients to be:
Highly thrombogenic for both venous and arterial clots.
1116
Patient with specific phobia such as flying treatment:
Behavioral therapy (exposure, systematic desensitization)
1117
Patient with arm adducted and internally rotated after seizure from eclampsia:
Posterior shoulder dislocation.
1118
One exception to giving vaccines based on chronologic age:
Hepatitis B vaccine, must be ≥2kg (4lb 6oz).
1119
After the diagnosis of a solid testicular mass has been made, (a painless hard mass in testicle + suggestive ultrasound). Management:
The initial management orchiectomy.
1120
Systolic murmur at the lower sternal border, increased with inspiration:
Tricuspid regurgitation
1121
Patient with 6 months of both liquids and food getting stuck in throat, and has epigastric tenderness: Patient with 6 months of both liquids and food getting stuck in throat, and has epigastric tenderness:
Get barium esophagogram followed by possible manometry. Patient initially problem with liquids then solids, most likely obstruction. Patient with both from start most likely motility disorder.
1122
All patients with new onset ascites require:
Paracentesis to determine cause.
1123
Toxic shock syndrome can also be cause from:
Nasal packings from nosebleed, not just tampons.
1124
Initial diagnosis hypertension four tests:
UA Chemistry panel Lipid profile Baseline ECG
1125
Patient with symptoms and signs of adrenal insufficiency: First tests:
``` 250ug cosyntropin (ACTH) stimulation test with cortisol and ACTH levels (GREATER THAN 20 INCREASE IN SERUM CORTISOL IN 30-60 MINUTES RULES OUT ADRENAL INSUFFICIENCY). ```
1126
Most common cause of GI bleeding in an elderly patient:
Diverticulosis: Patient will have painless bleeding. Diverticulitis: Patient will have abdominal pain and infectious symptoms secondary to obstruction of the diverticula. It is uncommon to see bleeding with diverticulitis.
1127
Hemorrhoids very rarely cause:
Massive lower GI bleeding and will usually be detected on rectal exam.
1128
Remember chronic steatorrhea can cause vitamin D:
You need chylomicrons to absorb vitamin D. Low vitamin D causes decreases in both calcium and phosphorous absorption in the intestines. Hypocalcemia, hypophosphatemia, and high PTH.
1129
Bacterial meningitis in children >1 month: Work up: Treatment:
CBC and electrolytes; BC; LP and CSF analysis and cultures. Always give antibiotics before lumbar puncture, but after blood cultures. LP takes long to set up. Ceftriaxone and vancomycin IV. Imaging done before LP in children with coma, focal neurologic findings, and history of neurosurgery.
1130
Why do you not give ceftriaxone to
Ceftriaxone displaces bilirubin from albumin and increases the risk of kernicterus.
1131
Patient with sickle cell disease on OTC, with pleuritic chest pain, tachycardia, tachypnea, normal ECG, and x-ray: Next step:
CT scan of the chest with intravenous contrast.
1132
Dietary recommendations for patient with renal calculi:
1. Decreased dietary protein and oxalate. 2. Decreased sodium intake. 3. Increased fluid intake. 4. Increased dietary calcium
1133
Child with grade I/II systolic ejection murmur left lower sternal border: Heard best when child is lying done and decreases with standing or valsalva:
Still’s murmur: Benin, no work up done. Reassurance.
1134
Maneuvers that decrease venous blood return to the heart (standing, valsalva) typically reduce the intensity of:
Innocent murmurs.
1135
Inflammatory bowel disease has a bimodal distribution with second peak in the 60s: What do you see on biopsy:
Neutrophilic cryptitis seen in both Crohn's and ulcerative colitis.
1136
Patients with cirrhosis can have decreased appetite leading to:
Weight loss. Don’t let this fool you and lead you to think cancer.
1137
Red blood cell distribution width is a measure:
Of the variation in of the range of variation of red blood cell (RBC) volume.
1138
Malignant hypertension is diagnosed with:
Severe hypertension with retinal hemorrhages, exudates, or papilledema.
1139
Hypertensive encephalopathy is diagnosed with:
Severe hypertension with cerebral edema and non-localizing neurologic symptoms and signs.
1140
Patient in his 50s with swelling on his eyelid that comes and goes over the last two years and on examination is a nodular, painless, rubbery lesion on the eyelid: Next step:
Histopathological examination. Patient has a recurrent chalazion, but could be an underlying sebaceous carcinoma.
1141
Tdap is indicated with every:
Pregnancy to protect the infant. This applies to all women including HIV positive.
1142
Patient with RLQ pain and history of recent furunculosis. Abdominal pain shows tenderness to deep palpation without guarding or rebound. Psoas sign is positive and BS present: Next step:
CT of abdomen this is most likely a psoas abscess from resulting hematogenous spread of bacteria from furuncles.
1143
A significant drop in oocyte number occurs:
Ovulatory reserve: takes place during a woman’s fourth decade so that on in 5 women age 35-39 is no longer fertile.
1144
Cutaneous larva migrans: Bug: Presents:
Ancylostoma braziliense; The dog and cat hookworm; Present tropical and subtropical regions USA; Kids sandbox/beaches; Characterized by pruritic, elevated, serpiginous lesions on the skin.
1145
Kids with cystic fibrosis and pneumonia bug and treatment:
Up to age 20 staphylococcus aureus treat with vancomycin first. After 20 pseudomonas is most common treat amikacin, ceftazidime, and ciprofloxacin.
1146
Trachoma presents with:
Follicular conjunctivitis and pannus (neovascularization) formation in the cornea. Treatment topical tetracycline and oral azithromycin.
1147
Transtentorial (Uncal) Herniation: Presents:
Patient presents with blunt head trauma with signs/symptoms of ipsilateral hemiparesis, ipsilateral mydriasis, and strabismus, contralateral hemianopia, and altered mentation. Many times it compresses oculomotor nerve.
1148
Pregnant patient with intense pruritus palms and sole worse at night, no jaundice, no hepatosplenomegaly, elevated bile acids, elevated levels of liver aminotransferases:
Diagnosis of exclusion: Intrahepatic cholestasis of pregnancy (ICP):
1149
Arrest of labor in the first stage is diagnosed when: Treatment:
Dilation is ≥6 cm with ROM and 1 of the following: No cervical change for ≥4 hours despite adequate contractions or No cervical change for ≥6 hours with inadequate contractions. Tx: cesarean
1150
Asbestosis exposure increase the risk for:
Bronchogenic carcinoma number one has pleural plaques. Remember pleural mesothelioma is usually unilateral pleural abnormalities with large effusion.
1151
Patient with post MI day four with new onset chest pain: Most useful lab in this setting:
CK-MB because it returns to baseline in 1-2 days. Troponin T takes 10 days to go down.
1152
Chronic lymphocytic leukemia what is highly characteristic on blood slide:
Smudge cells. Other diagnostic features are marked leukocytosis with predominant lymphocytosis.
1153
The most common causes of digital clubbing:
Lung malignancies and cystic fibrosis
1154
Heparin induced thrombocytopenia gold standard test:
Serotonin release assay.
1155
Patient with HIT immediate first step:
Stop heparin and start direct thrombin inhibitor (argatroban, bivalirudin)
1156
Patient on warfarin taking acetaminophen:
Acetaminophen is CYP450 inhibitor, so increases warfarin effect and causes excessive bleeding. Other drugs that do this NSAIDS, metronidazole, amiodarone, cimetidine, cranberry juice, omeprazole, thyroid hormone, SSRI, ginko bilbo, vitamin E.
1157
Drugs that decrease warfarin's anticoagulation effects:
Carbamazepine, ginseng, green vegetables, oral contraceptives, phenobarbital, rifampin, st. john's wort.
1158
Precocious puberty male with acne normal testicular size, low LH and does not increase after gonadotropin releasing hormone agonist:
Nonclassical congenital adrenal hyperplasia
1159
Massive PE usually causes right atrial pressure:
>10 mmHG and pulmonary artery pressure > 40 mmHg.
1160
Patient with PCOS treatment:
Weight lose and OTC. Metformin for existing DM2
1161
Bacterial meningitis treatment in immunocompromised patient such as post transplant:
vancomycin, plus ampicillin, and plus cefepime or ceftazidime. Steroids given same time. Stopped if culture grows anything besides streptococcus pneumoniae.
1162
The strongest predictor of abdominal aortic aneurysm expansion and rupture are:
Large aneurysm diameter, rapid rate expansion, and current cigarette smoking.
1163
COPD flattening of the diaphragm cause:
Increase work of breathing.
1164
Chronic alcoholic with hypokalemia that want correct:
They have hypomagnesemia give magnesium.
1165
IV drug user with neuro deficits CN intact upgoing plantar reflex:
Get MRI possible spinal cord compression from epidural abscess.
1166
Goodpasture's syndrome: Treatment:
Plasmapheresis
1167
Granulomatosis with polyangiitis (Wegener's): Treatment:
Combination cyclophosphamide and steroids
1168
Most common cause aortic regurgitation in developed countries:
Bicuspid valve.
1169
LActose intolerance is characterized by:
Positive hydrogen breath test, positive stool test for reducing substances, low stool pH and increased stool osmotic gap. No steatorrhea.
1170
Kid with history of intussusception complains of severe abdominal pain intermittent:
Meckel's diverticulum should be suspected as a lead point.
1171
Severe pain with swallowing in an HIV patient off their meds low CD4 count:
Viral esophagitis, HSV or CMV.
1172
Patient with Parkinson's disease with tremor as biggest feature: Treatment:
Trihexyphenidyl (anticholinergic)
1173
Supplemental oxygen in a patient with advanced COPD can worsen hypercapnia due to:
Combination of increased dead space perfusion causing V/Q mismatch, decreased affinity of hemoglobin of CO2, and reduced alveolar ventilation.
1174
Cauda equina syndrome results from:
Compression of spinal nerve roots.
1175
Kid with high initial lead level:
Get venous sample, the finger stick has high false positive results.
1176
Uric acid stones, which are radiolucent, have to be evaluated with:
CT of abdomen.
1177
Fluphenazine adverse effect:
Hypothermia, this can be seen in other antipsychotics
1178
Bipolar with acute agitation should receive:
Second generation antipsychotic first (risperidone). Then titrate the mood stabilizer.
1179
Patients with ankylosing spondylitis can develop: Type of lung disease:
Restrictive disease due to diminished chest wall and spinal mobility.
1180
Patients with carcinoid syndrome can develop vitamin deficiency which vitamin:
Niacin
1181
Carcinoid syndrome: Etiology: Presentation:
Carcinoids are slow growing tumors found in GI tract that secrete histamine, serotonin, and VIP. Liver usually filters these so no symptoms till it metastasis to liver. Presets with episodic flushing, secretory diarrhea, bronchospasm, and cardiac valvular abnormalities.
1182
Hypothyroid levels lipid sodium creatine kinase:
Hyperlipidemia, hyponatremia, elevated creatinine kinase
1183
Patients coming from Mexico with bloody diarrhea, abdominal pain, and mass in liver on CT scan: Treatment:
Entamoeba histolytica: Oral metronidazole
1184
Chikungunya fever: Etiology: Presents:
Mosquito borne viral illness, especially common in Caribbean. Presents with polyarthralgias, lymphopenia, thrombocyopenia and rash.
1185
Tumor found in middle mediastinum:
Bronchogenic cyst
1186
Tumor found in anterior mediastinum:
Thymoma
1187
Tumor found posterior mediastinum:
Neurogenic tumors
1188
Radio opaque stone on CT:
calcium oxalate stone
1189
Most appropriate diagnostic test for acute hepatitis B:
HBsAg and anti- HBc
1190
Most common side effect of erythropoietin:
Worsening of hypertension