Hemodynamic Disorder Lecture 3 Flashcards

1
Q

Why is infective endocarditis so important?

A

it is 100% fatal if unDx and unTx and 20% fatal id Dx and Tx appropriately

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2
Q

Right sided infective endocarditis embolus always goes to ____

A

lung

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3
Q

myocardial abscess

A

forms when infective embolus goes to CA

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4
Q

What is a normal QT interval corrected for HE, QTc?

A

<440 miliseconds ***

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5
Q

What are causes of long QT

A

ischemic heart disease
low K, Ca, or Mg
channelopathy
many other things

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6
Q

What is the risk of early afterdepolairzations (aka long QT)

A

ventricular tachycardia

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7
Q

What is the risk of ventricualr tachycardia?

What is the preventative treatment for ventricular tachycardia?

A

sudden death

defibrillator

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8
Q

loss of fucntion in repolarizing outward K channel, I-KS

A

LQT1 (prolongation of phase 2)

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9
Q

inactivating mutation in Na channel

A

LQT3 (prolong phase 3)

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10
Q

loss of fucntion in repolarizing outward K channel, I-KR

A

LQT2

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11
Q

the type of polymorphic ventricular tachycardia typical of congenital LQT syndromes is called

A

torsades de pointes

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12
Q

What is life saving preventative Tx for torsades de pointes

A

defibrillator

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13
Q

group of channelopathies causing shorted cardiac myocyte APs –> ventricular tachycardia –> sudden death

A

brugada syndrome

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14
Q

brugada syndrome is most common in what age/race/gender

A

young asian males

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15
Q

persistently elevation of ST segments (>2 mm) descending with an upward convexity to an inverted T wave in leads V1-V3
(AT REST)

A

brugada pattern

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16
Q

Tx of brugada syndrome

A

defibrillator

17
Q

mutations in ryanodine receptor

A

catecholaminergic

polymorphic ventricular tachycardia

18
Q

What triggers arrhythmias?

A

high intracell Ca causing delayed afterpolarizations

19
Q

Life saving-preventative treatment for arrythmias

A

Beta blockade or defibrillator

20
Q

how many babies, children, and young adults die of cahnnelopathies each year

A

4,000

21
Q

recognizing EKG signs of a _______ could save the life of a young person

A

channelopathy

22
Q

Gross: pale mottled flabby dilated heart

A

viral myocarditis

23
Q

pale septum

A

viral myocarditis

24
Q

muations in genese encofding desomsomal proteins or myocyte adhesion; probably with a 2nd hit

A

RT ventricular cardiomyopahty

25
Q

What does right ventricular cardiomyopathy cause?

A

re-entrant ventricular tachycardia

26
Q

disease possibly assc with enteric viral infection of the right heart

A

Rt ventricualr cardiomyopathy

27
Q

fatty replacement of myocytes frequently with lyphocytic inflitationd and later fibrous scarring

A

Rt ventricular cardiomyopathy

28
Q

notch in terminal part of QRS is called ____ and can be a manifestation of ____

A

epsilon wave

Rt ventricular cardiomyopathy

29
Q

life saving preventative treatment Rt ventricualr cardiomyopathy

A

defibrillator

30
Q

describe the cardiac AP in the left ventricle, what channels are open and what/where ions move

A

phase 4 (-90): I-K1 moves K+ out of cells
Phase 0 (+10mV): I-Na moves Na+ into cells
Phase 1: I-to1,2 moves K+ out and Cl- out
phase 2: I-Ca-L and I-KS move Ca in and K+ out (at equal rates)
phase 3: I-KS, KR, K1 move K+ out (back to -90mV)

31
Q

ST segment convex to top

A

Type 1 ECG brugada sign

32
Q

ST segment downward straight

A

Type 1 ECG brugada sign

33
Q

ventricular tachycardia or ventricular fibrillation during emotional or physical stress from a mutation in SR Ca release channel

A

familial catecholaminergic

polymorphic ventricular tachycardia

34
Q

Microscopic: multifocal inflammation, intersitial, usually mononuclear and is assc with myocyte injury and necrosis

*predominant cells are lymphocytes and macrophages

A

viral myocarditis