U World Flashcards

(38 cards)

1
Q

Aortic valve replacement indications:

A
  1. Symptomatic (SAD) - syncope, angina, dyspnea
  2. Severe AS in pts undergoing CABG or other valvular surgery
  3. A symptomatic pts with severe AS and either poor LV systolic fx, LV hypertrophy >15mm, valve area
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2
Q

Phase 1a ventricular arrhythmias

A

within 10 mins of coronary occlusion; acute ischemia causes heterogeneity in conduction, delayed conduction increases the chance of re-entry.

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3
Q

Phase 1b ventricular arrhythmias

A

10-60 mins after MI; due to abnormal automaticity

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4
Q

Mitral regurgitation

A

seen in dilated and ischemic cardiomyopathy; holosystolic murmur at apex with radiation to the axilla

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5
Q

Causes of outflow obstruction in hypertrophic cardiomyopathy

A
  1. Bulging of the interventricular septum

2. systolic anterior motion (SAM) of mitral valve leaflets

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6
Q

Bronchiectasis appearance on CT and potential complication

A

tubular airways with thickened walls; hemoptysis

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7
Q

Treatment for infective endocarditis due to strep mutans

A

IV antibiotics (aqueous pencillin G or IV ceftriaxone) for 4 wks

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8
Q

Myasthenia gravis (paraneoplastic syndrome) involved site and clinical features:

A

acetylcholine receptor in postsynaptic membrane; fluctuating muscle weakness - ocular (ptosis and diplopia), bulbar (dysphagia, dysarthria) and facial, neck, and limb muscles

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9
Q

Lambert-Eaton syndrome (paraneoplastic syndrome) involved site and clinical features:

A

presynaptic membrane voltage-gated calcium channels; proximal muscle weakness, autonomic dysfunction (dry mouth), cranial nerve involvement (ptosis), diminished or absent DTRs

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10
Q

Dermatomyositis/polymyositis (paraneoplatic syndrome) involved sites and clinical features:

A

muscle fiber injury; symmetrical and proximal muscle weakness, interstitial lung disease, Raynaud’s, and esophageal dysmotility, polyarthritis, skin findings (Gottron’s papules and heliotrope rash)

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11
Q

Female athlete triad

A
  1. decreased caloric intake
  2. oligo-amenorrhea
  3. osteoporosis
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12
Q

Morton’s neuroma

A

pain btwn the 3rd and 4th toes on the plantar surface w/ clicking sensation (Mulder’s sign)

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13
Q

Tarsal tunnel syndrome

A

compression of the tibial nerve that causes numbness, burning, and aching of the distal plantar surface of the foot and toes

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14
Q

Isolated systolic hypertension (ISH)

A

decreased compliance of the arteries with age that causes isolated systolic pressure increase and widened pulse pressure; treat with thiazides, CCBs, or ACE inhbitor

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15
Q

Pulmonary HTN

A

pulmonary artery pressure >25 mm at rest or >30 mm w/ exercise

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16
Q

Causes of pulmonary HTN

A
  1. Disorders of the respiratory system, hypoxemia
  2. Pulmonary venous HTN (LV disease, mitral valve disease, pulmonary veno-occlusive disease)
  3. chronic thromboembolic disease
  4. Pulmonary arterial HTN (primary or associated with vasculopathy)
  5. Pulmonary capillary hemangiomatosis
17
Q

Modified Wells criteria for pretest probability of PE

A
  • Clinical signs of DVT (+3)
  • Alternate diagnosis less likely (+3)
  • Previous PE or DVT (+1.5)
  • HR >100 (+1.5)
  • Recent surgery or immobilization (+1.5)
  • Hemoptysis (+1)
  • Cancer (+1)

Total score: > or = to 4, PE likely

18
Q

Cardiac index

A

CO/body surface area

19
Q

Normal hemodynamic measurements

A

Right atrial pressure (preload) - 4mmHg
Pulmonary capillary wedge pressure (preload) - 9mmHg
Cardiac index (pump function) - 2.8 to 4.2 L/min/m2
Systemic vascular resistance (after load) - 1150 dynes*sec/cm5
Mixed venous oxygen saturation - 60-80%

20
Q

Hypovolemic shock

A

Decreased right atrial pressure, pulmonary capillary wedge pressure, cardiac index, and mixed venous O2 saturation

Increased systemic vascular resistance

21
Q

Cardiogenic shock

A

Increased right atrial pressure, pulmonary capillary wedge pressure, systemic vascular resistance

Decreased cardiac index and mixed venous O2 saturation

22
Q

Septic shock

A

Normal to decreased right atrial pressure and pulmonary capillary wedge pressure

Increased cardiac index and mixed venous O2 saturation

Decreased systemic vascular resistance

23
Q

Avascular necrosis

A

Progressive hip pain w/o restriction of ROM or abnormality of radiographs.
MRI is diagnostic.

24
Q

Ertapenem

A

Doesn’t cover pseudomonas

25
Methotrexate
Inhibits dihydrofolate reductase
26
Nonallergic rhinitis
Nasal congestion, rhinorrhea, sneezing, postnasal drainage w/o specific etiology. - routine allergy testing not necessary prior to empiric therapy. - treat with intranasal antihistamine, intranasal glucocorticoids.
27
Esophageal chest pain
- Prolonged pain lasting more than an hour
28
Medications causing diabetes insipidus
lithium, demeclocycline, foscarnet, cidofovir, and amphotericin
29
Giant cell tumor of bone
- "soap bubble" appearance - Benign tumor of young adults that an lead to pain, swelling, and decreased ROM as well as potential fractures - Located in the epiphyseal region of long bones - Osteoclasts - Treat with surgery.
30
Osteoid osteoma
- sclerotic cortical lesion w/ central lucency | - Pain that's worse at night and relieved by nonsteroidal anti-inflammatory medications.
31
CYP 450 inhibitors
- Increase Warfarin's effect 1. Acetaminophen/NSAIDS 2. Antibiotics/antifungals 3. Amiodarone 4. Cimetidine 5. Cranberry juice, Ginko balboa, vitamin E 6. Omeprazole 7. Thyroid hormone 8. SSRIs
32
CYP 450 Inducers
-Decrease Warfarin's effects 1. Carbamazapine 2. Ginseng 3. Green vegetables 4. oral contraceptives 5. Phenobarbital 6. Rifampin 7. St. john's wart
33
Crystal-induced AKI
Common etiology: 1. acyclovir 2. sulfonamides 3. methotrexate 4. ethylene glycol 5. protease inhibitors - Increase risk with volume depletion and CKD
34
Hereditary telangiectasia (Osler-Weber-Rendu syndrome)
- Autosomal dominant - Diffuse telangiectasias, recurrent epistaxis, and widespread AV malformations (usually in the mucous membranes, skin and GI tract, but also liver, brain and lung) - Pulmonary AVMs can shunt blood from the right to the left side of the heart causing chronic hypoxemia and reactive polycythemia; can also cause massive hemoptysis)
35
Vitamin K deficiency
- Vitamin K is a cofactor in the carboxylation of glutamic acid residues on PT complex proteins - Decreases all PT complex proteins (II, VII, IX, X, proteins C and S) - Increases both PT and PTT - Due to inadequate intake, intestinal malabsorption, or hepatocellular disease.
36
Prophylaxis for splenectomy
daily oral penicillin prophylaxis for 3-5 yrs following splenectomy
37
DVT algorithim
Proximal lower extremity DVT -----> PE w/ hemodynamic instability or massive DVT w/ severe swelling or threatened ischemia -----> if no contraindications to anticoagulation, start thrombolytic therapy. If contraindications exist, consider mechanical thrombectomy, iliac stenting, or surgical thrombectomy - Less severe DVT -----> treat with anticoagulation unless contraindicated in which IVC filter placement is indicated
38
Aquired sideroblastic anemia
- Defective heme synthesis - Often due to pyrodoxine-dependent impairment in early steps of protoporphyrin synthesis - Isoniazid is a pyrodoxine inhibitor. - Dimorphic RBC populations (normocytic and hypochromic) - Increased serum iron and decreased TIBC