Lecture 6 Pulmonary Vascular Disease Flashcards

1
Q

A swan catheter measures what?

A

LA pressure aka pulmonary capillary wedge pressure

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2
Q

Pulmonary arterial hypertension:
elevation of pulm arterial pressure to more than ____ at rest and with a pulmonary capillary wedge pressure less than ____ mm hg

A

25, 15

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3
Q

what generally causes pulmonary arterial hypertension? Who is the classic patient? (according to pathoma)

A
generally idiopathic (IPAH);
young women
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4
Q

IPAH is heritable, due to a inactivating mutation in ____ gene, which normally inhibits ____ proliferation. Other gene mentioned in notes is ____

A

BMPR2;
vascular smooth muscle;
ALK1

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5
Q

what connective tissue disease is associated with PAH?

A

systemic sclerosis (Associated with poor prognosis)

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6
Q

_____ may be the most prevalent cause of PAH worldwide

A

shistosomiasis

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7
Q
clinical findings in PAH:
increased \_\_\_ (heart sound). \_\_\_\_ lift. \_\_\_\_ regurg. late \_\_\_\_.
A

P2 (closing of pulmonic);

parasternal; tricuspid, cyanosis

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8
Q

2 drugs associated with pulm HTN (mentioned in notes/FA)

A

cocaine, anorexigens (also meth)

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9
Q

Give one particularly common example of Pulm HTN due to left heart disease

A

mitral stenosis (or regurg);

ie LV dysfunction, Aortic stenosis

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10
Q

Pulm HTN due to hypoxemia:

disease such as ____ cause hypoxemic _____ of blood vessels, leading to general vaso____ of pulmonary vessels

A

COPD (or sleep apnea, high altitdue);

vasoconstriction, constriction

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11
Q

Recurrent pulmonary _____ can cause pulm HTN due to ____ and decreased cross sectional area of the vascular bed

A

emboli; reorganization (of emboli)

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12
Q

Pulm Aterial HTN pathological changes:
medial ____ due to increased ___ ____;
____ fibrosis;
_____ arteriopathy (High Yield as per pathoma)

A

hypertrophy, smooth muscle;
intimal;
plexiform

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13
Q

what does scleroderma look like on CT (mentioned a few times in class)

A

honeycomb

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14
Q

Path of HTN:
name 2 vasodilators that are decreased;
name a vasoconstrictor that is increased

A

prostacyclin, NO;

endothelin

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15
Q

What should be given first to a patient with PAH?

A

Oxygen

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16
Q

______ syndrome can cause pulmonary HTN secondary to congenital heart defect

A

Eisenmenger’s

17
Q

single classic symptom of Pulm HTN mentioned in pathoma

A

exertional dyspnea;

other symptoms = fatigue, syncope, cough

18
Q

gold standard of diagnosing PAH:

A

right heart catheterization (Swan)

19
Q

heart changes in pulm HTN:

initially _____, then death from decompensated ___ ___

A

RVH; cor pulmonale

20
Q

With RVH, large ___ waves are seen in leads V1 and V2

A

R

21
Q

2 biomarkers of PAH (Associated with survival)

A

BNP; hyponatremia

22
Q

treatment of PAH:
endothelin receptor agonists such as ____.
PDE-5 inhibitors such as ____.
Prostacyclin analogs such as ____

A

bosentan;
sildenafil;
epoprostenol (or iloprost)

23
Q

3 side effects of epoprostenol mentioned in FA:

A

flushing, jaw pain, hypotension

24
Q

Virchow triad associated with developing DVT

A

SHE:

Stasis; hypercoaguability, endothelial damage

25
Q

Pulmonary embolus presents as sudden-onset ____, chest pain, ______, and _____.

A

dyspnea; tachycarida, tachypnea (according to FA)

26
Q

How would you treat a pulmonary embolus causing hemoptysis?

A

blood thinners (mentioned in lecture)

27
Q

What happens to the V/Q ratio in PE?

A

obstruction–>moves ratio towards affinity (because very low Q)

28
Q

prophylaxis/acute management of PE (according to FA)

A

LMWH or unfractionated heparin

29
Q

long term prevention of PE (According to FA)

A

oral anticoagulants such as warfarin

30
Q

CT pulmonary angiography of a patient with PE shows what?

A

filling defects (according to FA)