Dyspnea and Cough (Tyler) DSA + Johnson Dyspnea Flashcards

1
Q

What is a cinical finding in chronic cough indicative of asthma?

A

episodic wheezing

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2
Q

What are alarm sx of cough?

A

fever

productive cough

progressive dyspnea

persistent wheezing

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3
Q

What are the most common sx of wegener’s

A

upper respiratory in 90% of pts

lower respiratory in 60%

renal involvement in 75%

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4
Q

What complication are wegener’s pts at high risk for?

A

venous thrombotic events

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5
Q

What lab tests are positive in wegener’s

A

>90% of ppl have positive c-ANCA/antiproteinase-3

10-25% have p-ANCA

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6
Q

What is the tx plan for Wegener’s?

A

induction of remission: prednisone + cyclophosphamide or rituximab w/ steroids

maintaining remission: azithioprine or methotrexate or rituximab

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7
Q

What is rituximab?

risks?

A

b-cell depleting Ab approved for tx of wegeners and microscopic polyangitis

both this and cyclophosphamide incr risk of infection

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8
Q

WHich drug used for treating wegeners should not be used in pts with kidney disfunction?

A

methotrexate

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9
Q

Prophylaxis for what infection should be done w/ cyclophosphamid tx?

A

pneumocystis jirovecii

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10
Q

What systems are mainly affected in churg-strauss?

A

small and medium vessels

skin and lung most common

can be heart, GI and peripheral nerves also

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11
Q

What are the clinical findings in Churg-Strauss?

A

marked peripheral eosinophilia

chest XR = transient opacities to pulmonary nodules

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12
Q

What is the treatment plan for Churg-Strauss?

A

corticosteroid taper over 3-6 mos and cyclophosphamide until complete remission

replace cyclophosphamide w/ methotrexate or azathioprine for maintenance

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13
Q

What are the 2 most frequently affected organs in sarcoidosis?

A

lung

liver

(followed by eyes, bone, skin, hear, and parotid gland)

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14
Q

What are 3 dangerous complications of myocardial sarcoidosis?

A

restrictive cardiomyopathy

cardiac dysrhythmias

conduction disturbances

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15
Q

What CBC measurement is elevated in sarcoidosis?

A

sed rate

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16
Q

What is the significance of elevated ACE levels in sarcoidosis?

A

commonly elevated, but neither sensitive nor specific enough to be of diagnostic value

17
Q

What are the radiograph stages of sarcoidosis?

A

I: hilar adenopathy alone

II: hilar adenopathy w/ parenchymal involvement

III: parenchymal involvement alone

IV: advanced fibrotic changes principally in upper lobes

18
Q

What is the general Tx of sarcoidosis?

A

corticosteriods

methotrexate, azathioprine, cyclosporine, or anti-TNF therapy with infliximab (used in steroid-intolerant pts or steroid-refractory dz)

19
Q

What is usually the most common sx of IPF?

A

progressive dyspnea

20
Q

What are the 2 FDA approved drugs for the use of IPF?

A

pirfenidone: antifibrotic w/out known MOA; tid and monitor LFTs
nintedanib: tyrosine kinase inh taken bid; diarrhea is major side efect

21
Q

What are the ACC/AHA stages of HF

A

A: at risk for HF, no structural Dz, no sx

B: structural heart disease, no sx

C: Structural dz + sx

D: refractory HF, needs biventricular pacemaker, LVAD, transplant; 1 yr mortality 50-60%

22
Q

What are the NYHA functional classifications of HF?

A

1: no limitation of phys activity, asymptomatic
2: slight limitation of PE, exertional sx, no sx at rest
3: marked limitations, less than ordinary activity causes sx, no sx at rest
4: unable to do PE w/out sx; SYMPTOMATIC AT REST

23
Q

What defines systolic HF?

A

EF < 40%, decr vent emptying so decr SV

S3 gallop

sx associated w/ hypoperfusion

24
Q

What characterizes diastolic HF?

A

normal EF

stiff ventricles, resistance to vent filling

SOB, DOE, pulmonary edema

25
What characterizes high output HF?
EF reduced, but high CO hyperthyroidism, pregnancy, anemia, beriberi, paget's dz
26
What characterizes low output HF?
seen in ischemic heart dz, HTN dilated cardiomyopathy, valvular and pericardial dz
27
What common drugs should be avoided in HF?
NSAIDS inh COX 1 and 2 --\> inh prostaglandin syn --\> renal vasoconstriction --\> makes fluid overload worse
28
How do DIP and RB-ILD differ on CT?
DIP: **peripheral or diffuse** ground-glass opacities, **reticular** markings, sometimes small cysts RB-ILD: bronchial wall **thickening**, **centrilobular** nodules, **patchy** ground-glass opacities
29
In what lobes does IPF predominate?
lower lobes | (rarely upper)
30
What does IPF look like on CT?
subpleural ground glass opacities + reticular patterns (rare to see ground glass w/out reticular - usually leads to alt dx) predominant to lower lobes