Cardio Flashcards

1
Q

QT prolongation: Drugs that increase duration of ventricular action potential

A

Type 1A anti-arrhythmics: quinidine, TCA, procainamide, disopyramide, phenothiazines

Type III: amiodarone and sotalol

Other causes of prolonged QT
-IC bleed (SAH)
-Systemic hypothermia
-Hypocalcemia (ST portion)

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2
Q

Causes QT shortening

A

Hypercalcemia
Digital glycosides

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3
Q

Electrical alternans with sinus tachycardia

A

Cardiac tamponade

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4
Q

What tachyarrhythmia has an accelerated phase 4 depolarization ?

A

Idiopathic VT and AT

If absent / decelerated phase 4 repolarization: sinus node dysfunction

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5
Q

Infection that can cause AV block typically at the level of the AV node with narrow junctional escape rhythm >40beats/min

A

Lyme carditis (Borrekia burgdorferi)

  • improves after 1 week of antibiotic therapy
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6
Q

Which AV conduction block is Permanent Pacing is required

A

Mobitz type 2 AV block, high grade AV block, or 3rd degree AV Block that is not reversible or physiologic

OR symptomatic AV block

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7
Q

Adjunctive pharmacologic treatment useful in AV block.

A

Atropine 0.5 to 2mg IV OR
isopretwrenol 1-4ug/min IV

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8
Q

Normal PR interval

A

120-200ms

QRS: <-= 100ms

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9
Q

Mechanisms of Pathologic tachycardia

A
  • reentrant reentrant arrhythmias dependent on AV nodal conduction
  • large reentry circuits within atrial tissue (atrial flutter)
  • focal atrial tachycardia that can be due to automaticity
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10
Q

Postural orthostatic tachycardia syndrome (POTS)

A

Sinus rate increased by 30bpm or >120bpm within 10 min of standing without hypotension

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11
Q

Reversal agent of Dabigatran

A

Idarucizumab

Factor X- inhibitors (Rivaroxaban, Apixaban Endoxaban): Andexanet alfa

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12
Q

CHA2DS2VASc and what is the score to start anticoagulation

A

CHF 1
Hypertension 1
Age >75 2
DM 1
STROKE/TIA, embolus 2
Vascular disease 1
Age 65-75 1
Sex female

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13
Q

HAS-BLED

A

HTN: 1
abnormal renal and liver function; 1 each
Bleeding disthesis 1
labile INR ( in warfarin)1
Age >65 1
Drug/ alcohol 1 each

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14
Q

Cardia imaging that can additionally detect area of ventricular scar

A

cardiac MRI with Gd contrast

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15
Q

Class 1 anti arrhythmic drugs and the MOA

A

Na channel blocker, blocks Na
1C- flecainamide and propefenone
1A- qunidine, procainamide, disopyrimid and TCA
1B- lidocaine, mexilitine

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16
Q

Class 2 anti arrhythmic drugs and the MOA

A

Beta blockers
Blocks the phase 4 depolarization by suppressing AV/SA nodal activity

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17
Q

Class 3 anti arrhythmic drugs and the MOA

A

K channel blocker: prolonged phase 3 repolarization

Amiodarone
Ibutalide
Doferilide
Sotalol

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18
Q

Class 4 anti arrhythmic drugs and the MOA

A

CCB: decreases slope of phase 0,3,4
Prolonged repolarization via AV node.

Non dihydropyridine CCB: Diltiazem and Verapamil

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19
Q

PVC / NSVT with ACS for ICD indication

A
  1. > 40days after the AMI: LVEF <30% OR LVEF <35% symptomatic HF (FC II or III)
  2. > 5days after AMI: decrease LVEF + non sustained VT + inducible sustained VT or VF on EP test
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20
Q

PVCs and NSVT associated with depressed ventricular function and HF, indication for ICD

A

LVEF <35% NYHA II and III HF (decreased 5-year mortality from 36 to 29%)

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21
Q

Tachyarrhythmia that always indicates structural abnormality or focus of automaticity

A

Sustained monomorphic VT

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22
Q

Arrhythmias with repolarization abnormalities and genetic arrhythmias syndrome

A

Acquired long QT: Torsades de pointes
Congenital long QT syndrome: LQTS 1,2,3
short QT syndrome: QTc <0.36s

23
Q

What is Brugada syndrome

A

ST segment elevation > 0.2mV + coved ST segment + negative T wave in more than one anterior precordial lead (V1-V3) + episode of syncope or cardiac arrest due to polymorphic VT in the absence of structural disease

24
Q

Definition of electrical storm or VT storm

A

3 or more VT or VF episodes in 24 hours

25
Q

Medical treatment of Brugada syndrome with frequent VTs

A

Quinidine and catheter ablation

26
Q

High-output heart failure

A

B eri beri (vitamin B deficiency)
A nemia
T hyrotoxicosis
A rteriovenous shunt

M yeloproliferative disorder
O besity
C hronic lung disease
C irrosis

27
Q

Early radiologic signs of acute HF

A

-upper zone venous distribution
-thickening of interlobular septa

28
Q

Indication of Cardiac resynchronization therapy in Hf

A

-NYHA III and IV HFrEF on optimal medical management with mod to severe residual symptoms
-minimally symptomatic pt with QRS >149ms + LBBB

29
Q

SCD in HF: appropriate candidates for ICD

A
  • NYHA II or III with LVEF <35% regardless of etiology
  • post MI on optimal medical management but with residual LVEF =/< 30% even if asymptomatic
    -symptomatic HF not caused by CAD <60yo
30
Q

Which arrhythmia/s have a mechanism of Reentry?

A

AVNRT, AVRT
atrial flutter
Scar related VT

31
Q

Which arrhythmia/s have a mechanism of abnormal automaticity?

A

Enhanced (acceleration of phase 4 repolarization): Idiopathic VT, AT

Suppressed (absent or decelerated phase 4 repolarization): sinus node dysfunction

32
Q

Which arrhythmia/s have a mechanism of early after depolarization (EADs phase 2/3)?

A

TdP in long Qt syndrome
PVCs

33
Q

Which arrhythmia/s have a mechanism of delayed afterdepolarization (DADs phase 4)?

A

Reperfusiob PVCs/VT
AT and VT with digitalis toxicity

34
Q

What are the class 1 indication in AV block permanent pacing ?

A

Class 1:
-Complete heart block (acquired); advanced AV block, mobitz type II evidence of infranodal block
-asymptomatic Mobitz type 1 block, with neuromuscular disease associated with progressive conduction tissue disorder

35
Q

What are the class IIa indication in AV block permanent pacing ?

A
  • symptomatic first degree AV block
  • first degree AV block, asymptomatic with Lamin A/C cardiomyopathy
    -symptomatic Mobitz type I block
36
Q

Class I indication for catheter ablation in Symptomatic AF

A

-parox or persistent AF with failed drug therapy
-parox or persistent AF and heart failure with reduced EF

37
Q

Most common genetic cardiovascular disorder and prominent caused if SCR. Before 35

A

HOCM
sudden death can be due to polymorphic VT/VF

38
Q

Most common genetic cardiovascular disorder and prominent caused if SCR. Before 35

A

HOCM
sudden death can be due to polymorphic VT/VF

39
Q

Hemodynamic hallmark of MS

A

Abnormally elevated left Atrioventricular pressure gradient

40
Q

Hallmark of disease progression in MS

A

Inset of atrial fibrillation

41
Q

A soft low pitched rumbling mid to late diastolic murmur seen severe AR

A

Austin flint murmur
“Austin Rint murmur”
AR-AR

42
Q

A high pitched diastolic decrescending blowing murmur along the left sternal border results from dilation of the pulmonary valve ring and occurs in mitral valve disease and severe pulmonary hypertension

A

Graham steell murmur
Seen MVD and PR

43
Q

Mitral commissurotomy indication

A

symptomatic NYHA II - IV, isolated severe MS orifice =< 1 cm2/m2 BSA or < 1.5 cm2 in normal sized adults

44
Q

Hyperplastic disorder affecting medium size and small arteries, predominantly among females

A

Fibromuscular dysplasia

45
Q

Arteries commonly affected in Fibromuscular dysplase

A

More common: Renal and carotid arteries
Less common: iliac, subclavian (most common limb artery affected = iliac arteries)

46
Q

Angiographic finding of Fibromuscular dysplasia

A

String of beads

Tx: PTA, surgical reconstruction

47
Q

Inflammatory occlusive vascular disorder of small and medium sized arteries and veins in the distal upper and lower extremities

A

Thromboangitis Obliterans (Buerger’s disease)

48
Q

Pulseless disease that may involve descending thoracic and abdominal aorta and what is the treatment?

A

Takayasu’s arteritis
Tx: Acute stage: glucocorticoids and immunosuppressives
Critical stenotic artery: surgical bypass or endovascular intervention

49
Q

Pathology of thromboangiitis obliterans on disease progression

A

Initial stage: PMN migration infiltrating walls of the small and medium-sized arteries and veins
Disease progression: PMNs replaced by mononuclear cells, fibroblasts and giant cells
Later stages: Perivascular fibrosis and recanalization

50
Q

Triad of Thromboangiitis obliterans:

A

Claudication of affected extremity, Raynauds phenomenon, migratory superfical vein, thrombophlebitis

51
Q

In Acute limb ischemia, what isbthe most frequent site of thrombosis in situ:

A

Atherosclerotic vessel at site of an atherosclerotic plaque/aneurysm, arterial bypass grafts

52
Q

When to do Amputation in Acute limb ischemia?

A

Done if the limb is not viable, loss of sensation, paralysis and the absence of doppler detected blood flow in both arteries and veins

53
Q

Screening test for Primary Aldosreronism

A

PA/PRA RATIO >30:1 + plasma aldosterone concentration > 555pmol/L (>20ng/dL): 90%

Some antihypertensive medications can affect ratio (must stop drugs 4-6 weeks before test)