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Pharm 14

front 1

A cardiac pacemaker current opens when the membrane becomes more negative near the end of repolarization. Which channel behavior best describes the If current?

A. Outward K+ channel opens
B. Inward Na+ channel opens
C. Inward Ca2+ channel closes
D. Outward Cl− channel opens

back 1

B. Inward Na+ channel opens

front 2

Increased extracellular potassium most commonly causes which effect on pacemaker cells?

A. Speeds automatic firing
B. Stops or slows firing
C. Increases triggered activity
D. Prolongs refractory recovery

back 2

B. Stops or slows firing

front 3

A hospitalized patient on aggressive diuresis develops palpitations and frequent premature beats. Which electrolyte change most facilitates ectopic pacemakers?

A. Hypermagnesemia
B. Hypercalcemia
C. Hypokalemia
D. Hyponatremia

back 3

C. Hypokalemia

front 4

Which electrophysiologic profile is most consistent with hyperkalemia?

A. Longer AP, faster conduction
B. Longer AP, faster pacemaker
C. Shorter AP, slower conduction
D. Shorter AP, faster pacemaker

back 4

C. Shorter AP, slower conduction

front 5

Which pattern is most characteristic of hypokalemia in cardiac tissue?

A. Prolonged AP, more arrhythmias
B. Shortened AP, less automaticity
C. Slower rate, less ectopy
D. Faster conduction, shorter ERP

back 5

A. Prolonged AP, more arrhythmias

front 6

A patient receives a β-blocker for sinus tachycardia. Which part of the pacemaker action potential is primarily reduced?

A. Phase 0 upstroke
B. Phase 1 notch
C. Phase 3 repolarization
D. Phase 4 slope

back 6

D. Phase 4 slope

front 7

Increased vagal discharge slows SA-node firing not only by flattening phase 4, but also by:

A. Shortening atrial refractory period
B. Making diastolic potential more negative
C. Increasing phase 0 amplitude
D. Blocking ventricular calcium channels

back 7

B. Making diastolic potential more negative

front 8

Which change most directly accelerates pacemaker discharge?

A. Decreased phase 4 slope
B. Increased phase 4 slope
C. Shortened phase 0
D. Prolonged plateau duration

back 8

B. Increased phase 4 slope

front 9

Which condition would be expected to accelerate pacemaker discharge by steepening phase 4?

A. β-adrenergic stimulation
B. Vagal stimulation
C. Severe hyperkalemia
D. Class II blockade

back 9

A. β-adrenergic stimulation

front 10

A patient with congenital long-QT syndrome has a pause-dependent polymorphic ventricular arrhythmia. Which triggered activity is most likely?

A. DAD during phase 4
B. EAD during phase 3
C. Reentry during phase 0
D. Automaticity during phase 1

back 10

B. EAD during phase 3

front 11

Early afterdepolarizations are classically worsened by which rhythm condition?

A. Fast heart rates
B. Irregular AV block
C. Slow heart rates
D. Ventricular pacing

back 11

C. Slow heart rates

front 12

A patient with digitalis excess develops triggered ventricular beats that worsen with tachycardia. Which mechanism best explains this arrhythmia?

A. EAD in phase 3
B. DAD in phase 4
C. Reentry in AV node
D. Block in bundle branch

back 12

B. DAD in phase 4

front 13

Delayed afterdepolarizations are most strongly linked to which intracellular abnormality?

A. Reduced intracellular sodium
B. Increased intracellular calcium
C. Reduced intracellular potassium
D. Increased intracellular chloride

back 13

B. Increased intracellular calcium

front 14

A patient with myocardial ischemia develops tachy-triggered ectopy consistent with delayed afterdepolarizations. Which additional setting is classically associated with the same mechanism?

A. Long-QT bradycardia
B. Catecholamine excess
C. Complete AV block
D. Severe hypothermia

back 14

B. Catecholamine excess

front 15

A patient with partial AV block due to excessive parasympathetic tone improves after a muscarinic antagonist. Which drug was most likely given?

A. Adenosine
B. Atropine
C. Verapamil
D. Propranolol

back 15

B. Atropine

front 16

An electrophysiologist describes an arrhythmia in which a single impulse repeatedly reenters previously activated myocardium. What is this mechanism also called?

A. Triggered activity
B. Circus movement
C. Phase-4 automaticity
D. Exit block

back 16

B. Circus movement

front 17

A young adult has paroxysmal tachycardia due to an accessory AV pathway connecting atria and ventricles outside the AV node. Which syndrome is most likely?

A. Lown-Ganong-Levine
B. Mobitz type I
C. Wolff-Parkinson-White
D. Brugada syndrome

back 17

C. Wolff-Parkinson-White

front 18

In Wolff-Parkinson-White syndrome, the accessory bypass tract is called the:

A. Bundle of His
B. Bundle of Kent
C. Bachmann bundle
D. Moderator band

back 18

B. Bundle of Kent

front 19

For a reentry circuit to sustain itself, the conduction time around the loop must be:

A. Shorter than the ERP
B. Equal to the ERP
C. Longer than the ERP
D. Independent of the ERP

back 19

C. Longer than the ERP

front 20

Why does reentry fail when conduction time around a circuit is too short?

A. Tissue remains superexcitable
B. Tissue is still refractory
C. Calcium stores are depleted
D. Sodium channels are upregulated

back 20

B. Tissue is still refractory

front 21

A patient has a macroreentrant tachycardia. One antiarrhythmic strategy is to make the returning impulse encounter tissue that still cannot be re-excited. This is best accomplished by:

A. Shortening refractory period
B. Increasing refractory period
C. Increasing phase 4 slope
D. Accelerating AV conduction

back 21

B. Increasing refractory period

front 22

In a patient with a reentry-mediated arrhythmia, a drug abolishes the circuit by delaying impulse travel until previously activated tissue becomes unexcitable. Which effect best explains this?

A. Further slowing conduction
B. Faster sinus discharge
C. Shorter action potential
D. Enhanced ectopic automaticity

back 22

A. Further slowing conduction

front 23

Antiarrhythmic drugs generally suppress the automaticity of which pacemaker source more than the SA node?

A. AV nodal tissue
B. Purkinje reserve rhythm
C. Ectopic pacemakers
D. Atrial myocardium

back 23

C. Ectopic pacemakers

front 24

Antiarrhythmic drugs typically alter conduction, excitability, and refractoriness more strongly in which tissue?

A. Normally polarized tissue
B. Depolarized tissue
C. Fibrotic valves
D. Pericardial tissue

back 24

B. Depolarized tissue

front 25

A sodium-channel blocker is most effective during rapid tachycardia because it preferentially binds channels in which states?

A. Resting and closed
B. Activated and inactivated
C. Resting and refractory
D. Closed and repolarized

back 25

B. Activated and inactivated

front 26

Useful channel-blocking antiarrhythmics bind poorly or not at all to which channel state?

A. Activated
B. Inactivated
C. Resting
D. Open-refractory

back 26

C. Resting

front 27

A ventricular tachyarrhythmia slows after administration of a drug whose effect becomes stronger the more often channels cycle through opening and inactivation. This property is called:

A. Reverse dependence
B. State dependence
C. Chemical antagonism
D. Noncompetitive blockade

back 27

B. State dependence

front 28

A drug blocks diseased myocardium particularly well when the resting potential is lost and many channels remain unavailable even at rest. Which state predominates in that tissue?

A. Resting channels
B. Closed channels
C. Inactivated channels
D. Dephosphorylated channels

back 28

C. Inactivated channels

front 29

In cells with abnormal automaticity, antiarrhythmic drugs most commonly reduce spontaneous firing by reducing the slope of which phase?

A. Phase 0
B. Phase 2
C. Phase 3
D. Phase 4

back 29

D. Phase 4

front 30

In abnormal automatic foci, reduction of phase-4 slope is most often achieved by blocking which ions’ channels?

A. K+ or Cl−
B. Na+ or Ca2+
C. Mg2+ or K+
D. Cl− or Ca2+

back 30

B. Na+ or Ca2+

front 31

As antiarrhythmics flatten phase 4 in abnormal automatic cells, the resting membrane potential tends to move closer to the equilibrium potential of:

A. Sodium
B. Calcium
C. Potassium
D. Chloride

back 31

C. Potassium

front 32

Which Vaughan-Williams class acts primarily by sodium-channel blockade?

A. Class I
B. Class II
C. Class III
D. Class IV

back 32

A. Class I

front 33

A patient with atrial arrhythmia receives a Class IA drug. What is the expected effect on action-potential duration?

A. Minimal change
B. Shortening
C. Prolongation
D. Biphasic effect

back 33

C. Prolongation

front 34

Which channel-binding kinetic profile is characteristic of Class IA antiarrhythmics?

A. Rapid dissociation
B. Intermediate dissociation
C. Slow dissociation
D. No measurable dissociation

back 34

B. Intermediate dissociation

front 35

A Class IB antiarrhythmic is chosen for ventricular ectopy. Which combination best describes it?

A. Prolongs AP; slow kinetics
B. Shortens AP; rapid kinetics
C. Minimal AP effect; slow kinetics
D. Prolongs AP; intermediate kinetics

back 35

B. Shortens AP; rapid kinetics

front 36

A Class IC agent is started for a supraventricular arrhythmia. Which property best fits this drug subclass?

A. Shortens AP markedly
B. Prolongs AP markedly
C. Minimal AP effect
D. β-receptor blockade

back 36

C. Minimal AP effect

front 37

Compared with Class IA and IB drugs, Class IC drugs dissociate from sodium channels with:

A. Very rapid kinetics
B. Intermediate kinetics
C. Slow kinetics
D. Zero-order kinetics

back 37

C. Slow kinetics

front 38

A patient’s antiarrhythmic decreases sympathetic influence on the heart rather than primarily blocking sodium channels. Which class is this?

A. Class I
B. Class II
C. Class III
D. Class IV

back 38

B. Class II

front 39

The principal cardiac target reduced by Class II antiarrhythmic drugs is:

A. Muscarinic activity
B. Beta-adrenergic activity
C. Sodium-potassium ATPase
D. Funny-channel current

back 39

B. Beta-adrenergic activity

front 40

A patient with recurrent ventricular tachycardia is started on a Class III antiarrhythmic. What is the core electrophysiologic action of this class?

A. Blocks fast Na+ channels
B. Prolongs action potential duration
C. Blocks cardiac Ca2+ current
D. Reduces beta-adrenergic activity

back 40

B. Prolongs action potential duration

front 41

A drug is classified as Class III because it blocks which current?

A. IK1 inward rectifier K+
B. Funny Na+ current
C. L-type skeletal Ca2+ current
D. Rapid delayed rectifier K+

back 41

D. Rapid delayed rectifier K+

front 42

A supraventricular tachycardia is treated with a Class IV agent. What is the primary mechanism?

A. Beta-receptor antagonism
B. Na/K ATPase inhibition
C. Cardiac Ca2+ current blockade
D. Delayed rectifier K+ blockade

back 42

C. Cardiac Ca2+ current blockade

front 43

A drug slows conduction most strongly in tissues whose phase 0 upstroke depends on calcium entry. Which structures are most affected?

A. Atria and ventricles
B. His bundle and Purkinje
C. AV node and SA node
D. Ventricles and papillary muscle

back 43

C. AV node and SA node

Calcium-dependent upstroke tissues include the AV and SA nodes.

front 44

Which antiarrhythmic displays properties spanning all four Vaughan-Williams classes?

A. Procainamide
B. Amiodarone
C. Lidocaine
D. Disopyramide

back 44

B. Amiodarone

front 45

A patient becomes hypotensive shortly after receiving procainamide. This is partly due to which additional pharmacologic property?

A. Ganglion blockade
B. Beta-2 antagonism
C. Muscarinic agonism
D. Direct nitric oxide release

back 45

A. Ganglion blockade

front 46

Procainamide lowers peripheral vascular resistance primarily by causing:

A. Increased vagal outflow
B. Coronary vasospasm
C. Renal vasoconstriction
D. Decreased sympathetic ganglionic tone

back 46

D. Decreased sympathetic ganglionic tone

front 47

A Class IA antiarrhythmic slows the phase-0 upstroke in ventricular myocardium. Which ECG change is most expected with procainamide?

A. Shortened QT interval
B. Narrowed QRS complex
C. Prolonged QRS duration
D. Shortened PR interval

back 47

C. Prolonged QRS duration

front 48

Procainamide decreases conduction mainly through blockade of:

A. Na+ channels
B. Ca2+ channels
C. If channels
D. KATP channels

back 48

A. Na+ channels

front 49

Procainamide prolongs action potential duration primarily because it also blocks:

A. Chloride channels
B. K+ channels
C. Funny channels
D. T-type Ca2+ channels

back 49

B. K+ channels

front 50

N-acetylprocainamide is best classified as which antiarrhythmic subclass?

A. Class IA
B. Class IB
C. Class IC
D. Class III

back 50

D. Class III

front 51

A patient with renal failure on procainamide develops polymorphic ventricular tachycardia. Accumulation of which metabolite is the likely culprit?

A. Norquinidine
B. Monoethylglycinexylidide
C. Desethylamiodarone
D. N-acetylprocainamide

back 51

D. N-acetylprocainamide

front 52

The ventricular arrhythmia most classically linked to excess NAPA is:

A. Monomorphic VT
B. Torsades de pointes
C. Ventricular flutter
D. Accelerated idioventricular rhythm

back 52

B. Torsades de pointes

front 53

Quinidine most closely resembles which drug in its electrophysiologic actions?

A. Lidocaine
B. Verapamil
C. Procainamide
D. Amiodarone

back 53

C. Procainamide

front 54

Which antiarrhythmic has effects very similar to procainamide and quinidine?

A. Disopyramide
B. Lidocaine
C. Sotalol
D. Diltiazem

back 54

A. Disopyramide

front 55

A patient with atrial flutter is given disopyramide. To avoid dangerous ventricular responses, what should also be added?

A. A drug slowing AV conduction
B. A potassium supplement
C. A direct vasodilator
D. A class IB agent

back 55

A. A drug slowing AV conduction

With atrial flutter/fibrillation, AV nodal slowing should also be provided.

front 56

Disopyramide is most likely to worsen which comorbidity because of its negative cardiac effect?

A. Hypertension
B. Stable angina
C. Heart failure
D. Mitral stenosis

back 56

C. Heart failure

front 57

Dry mouth, urinary retention, constipation, blurred vision, and glaucoma worsening during disopyramide therapy are best explained by:

A. Histamine blockade
B. Atropine-like activity
C. Alpha-1 agonism
D. Nicotinic stimulation

back 57

B. Atropine-like activity

front 58

In the United States, disopyramide is approved only for treatment of:

A. Atrial fibrillation
B. AV nodal reentry
C. Ventricular arrhythmias
D. Sinus tachycardia

back 58

C. Ventricular arrhythmias

front 59

Lidocaine is most accurately described as blocking which channels with rapid kinetics?

A. K+ channels
B. Na+ channels
C. Ca2+ channels
D. If channels

back 59

B. Na+ channels

front 60

Lidocaine preferentially affects which cardiac tissues?

A. SA nodal and atrial
B. Atrial and AV nodal
C. Ventricular and Purkinje
D. AV nodal and His

back 60

C. Ventricular and Purkinje

front 61

An older patient on lidocaine develops paresthesias, tremor, slurred speech, and lightheadedness. These adverse effects are best categorized as:

A. Neurologic
B. Renal
C. Endocrine
D. Hematologic

back 61

A. Neurologic

front 62

After successful cardioversion, which drug is the agent of choice to help prevent recurrent ventricular fibrillation?

A. Procainamide
B. Lidocaine
C. Verapamil
D. Dronedarone

back 62

B. Lidocaine

front 63

A man taking mexiletine reports tremor, lethargy, blurred vision, and intermittent nausea. Which adverse-effect category best fits this drug?

A. Neurologic
B. Hepatic
C. Endocrine
D. Hematologic

back 63

A. Neurologic

front 64

Flecainide most directly blocks which channels?

A. Ca2+ only
B. K+ only
C. Na+ and K+
D. Na+ and Ca2+

back 64

C. Na+ and K+

front 65

Which kinetic property best characterizes flecainide channel unblocking?

A. Rapid kinetics
B. Slow kinetics
C. Intermediate kinetics
D. Biphasic kinetics

back 65

B. Slow kinetics

front 66

Flecainide is most appropriately used in patients with:

A. Healthy hearts, supraventricular arrhythmias
B. Prior MI, ventricular ectopy
C. Damaged hearts, ventricular tachycardia
D. Heart failure, atrial flutter

back 66

A. Healthy hearts, supraventricular arrhythmias

front 67

Which electrophysiologic effect is expected with flecainide?

A. QT prolongation
B. AP prolongation
C. Marked ERP shortening
D. No QT prolongation

back 67

D. No QT prolongation

front 68

A patient with prior myocardial infarction and preexisting ventricular ectopy is given flecainide. What is the major concern?

A. Severe bradycardia only
B. Coronary vasospasm
C. Arrhythmia exacerbation
D. AV block reversal

back 68

C. Arrhythmia exacerbation

front 69

In addition to its approved main use, flecainide is noted to be very effective at suppressing:

A. Atrial standstill
B. Premature ventricular contractions
C. Torsades de pointes
D. Junctional escape beats

back 69

B. Premature ventricular contractions

front 70

Propafenone is used primarily for which group of arrhythmias?

A. Ventricular arrhythmias
B. Digitalis arrhythmias
C. Ischemic automaticity
D. Supraventricular arrhythmias

back 70

D. Supraventricular arrhythmias

front 71

Which additional property does propafenone possess?

A. Weak beta blockade
B. Strong alpha blockade
C. Muscarinic agonism
D. Nitrate-like dilation

back 71

A. Weak beta blockade

front 72

Which statement about propafenone is correct?

A. Markedly prolongs QT
B. Greatly prolongs AP
C. Does not prolong AP
D. Shortens SA recovery

back 72

C. Does not prolong AP

front 73

A class III antiarrhythmic prolongs repolarization more at slow heart rates than at fast heart rates. This phenomenon is called:

A. State dependence
B. Reverse-use dependence
C. Tachyphylaxis
D. Phase trapping

back 73

B. Reverse-use dependence

front 74

Reverse-use dependence with most class III agents is clinically dangerous because it can promote:

A. Torsades de pointes
B. Ventricular standstill
C. Sinus arrest only
D. WPW conduction block

back 74

A. Torsades de pointes

front 75

Most class III antiarrhythmic drugs characteristically prolong the:

A. PR interval
B. QRS interval
C. ST segment
D. QT interval

back 75

D. QT interval

front 76

Which drug is an amiodarone analogue lacking iodine and used for atrial flutter or atrial fibrillation?

A. Sotalol
B. Procainamide
C. Dronedarone
D. Mexiletine

back 76

C. Dronedarone

front 77

Which class III drug does not show reverse-use dependence and instead prolongs action potentials relatively uniformly across heart rates?

A. Dronedarone
B. Amiodarone
C. Sotalol
D. Quinidine

back 77

B. Amiodarone

front 78

Shortly after IV antiarrhythmic therapy, a patient develops notable peripheral vasodilation. Which drug most likely caused this?

A. Flecainide
B. Propafenone
C. Verapamil
D. Amiodarone

back 78

D. Amiodarone

front 79

Amiodarone is primarily metabolized by which CYP enzyme?

A. CYP2D6
B. CYP3A4
C. CYP2C19
D. CYP1A2

back 79

B. CYP3A4

front 80

A patient taking amiodarone starts cimetidine. What is the expected effect on amiodarone levels?

A. Levels decrease
B. No change
C. Levels increase
D. Clearance doubles

back 80

C. Levels increase

front 81

A patient on amiodarone begins rifampin. What is the expected pharmacokinetic effect?

A. Levels increase
B. Protein binding rises
C. Half-life doubles
D. Levels decrease

back 81

D. Levels decrease

front 82

Dronedarone acts on calcium, sodium, and potassium channels and also has what additional action?

A. Alpha blockade
B. Beta blockade
C. Muscarinic blockade
D. Adenosine agonism

back 82

B. Beta blockade

front 83

Dronedarone should not be coadministered with which drug group?

A. Thiazides
B. Statins
C. Sulfonylureas
D. Azoles

back 83

D. Azoles

front 84

A wide-complex ventricular tachycardia is misdiagnosed as supraventricular tachycardia in the emergency department. Which IV drug is the classic dangerous error?

A. Lidocaine
B. Procainamide
C. Verapamil
D. Mexiletine

back 84

C. Verapamil

front 85

Giving IV verapamil to true ventricular tachycardia can precipitate:

A. Hyperkalemia
B. Ventricular fibrillation
C. Atrial standstill
D. Sinus tachycardia

back 85

B. Ventricular fibrillation

front 86

Which extracardiac adverse effect is classically associated with verapamil?

A. Constipation
B. Hemolysis
C. Bronchospasm
D. Tinnitus

back 86

A. Constipation

front 87

Which arrhythmia is the major indication for verapamil?

A. Ventricular tachycardia
B. Supraventricular tachycardia
C. Ventricular fibrillation
D. Torsades de pointes

back 87

B. Supraventricular tachycardia

front 88

A hemodynamically stable young adult has paroxysmal SVT and needs rapid conversion to sinus rhythm in the emergency department. Which drug is preferred?

A. Verapamil
B. Lidocaine
C. Procainamide
D. Adenosine

back 88

D. Adenosine

front 89

In normal ventricular myocytes, ranolazine has what net electrophysiologic effect?

A. Prolonged AP and QT
B. Shortened AP and QT
C. Prolonged PR only
D. Shortened QRS only

back 89

A. Prolonged AP and QT

front 90

Which Vaughan-Williams class corresponds to sodium-channel blockade?

A. Class II
B. Class III
C. Class I
D. Class IV

back 90

C. Class I

front 91

Which Vaughan-Williams class is primarily sympatholytic through β-blockade?

A. Class I
B. Class II
C. Class III
D. Class IV

back 91

B. Class II

front 92

Which Vaughan-Williams class works mainly by prolonging repolarization through potassium-channel blockade?

A. Class III
B. Class I
C. Class IV
D. Class II

back 92

A. Class III

front 93

Which Vaughan-Williams class is composed of calcium-channel blockers?

A. Class II
B. Class III
C. Class I
D. Class IV

back 93

D. Class IV

front 94

Procainamide belongs to which antiarrhythmic subclass?

A. Class IB
B. Class IC
C. Class IA
D. Class III

back 94

C. Class IA

front 95

A patient started on procainamide develops widening of ventricular depolarization and delayed repolarization. What ECG changes are expected?

A. Prolonged QRS and QT
B. Short PR and QT
C. Narrow QRS only
D. Shortened QRS and QT

back 95

A. Prolonged QRS and QT

front 96

Besides Class IA activity, procainamide also has actions resembling which class?

A. Class IV
B. Class II
C. Class IC
D. Class III

back 96

D. Class III

front 97

Long-term procainamide therapy can produce a syndrome resembling which disease?

A. Rheumatoid arthritis
B. Scleroderma
C. Lupus
D. Myasthenia gravis

back 97

C. Lupus

front 98

Quinidine belongs to which antiarrhythmic subclass?

A. Class IB
B. Class II
C. Class III
D. Class IA

back 98

D. Class IA

front 99

Toxic quinidine levels most classically prolong which ECG interval?

A. QT
B. PR
C. RR
D. ST

back 99

A. QT

front 100

A patient on quinidine reports headache, dizziness, and tinnitus. This triad most strongly suggests:

A. Digitalis effect
B. Lupus syndrome
C. Cinchonism
D. Antimuscarinic excess

back 100

C. Cinchonism

front 101

Which organ system is especially prone to adverse effects from quinidine?

A. Renal
B. GI
C. Pulmonary
D. Endocrine

back 101

B. GI

front 102

Compared with other Class IA agents, disopyramide is particularly notable for which additional effect?

A. Strong β blockade
B. Marked vasodilation
C. Pronounced antimuscarinic effects
D. Significant adenosine release

back 102

C. Pronounced antimuscarinic effects

front 103

Disopyramide adverse effect?

A. Fecal incontinence
B. Urinary retention
C. Hemoptysis
D. Polyuria

back 103

B. Urinary retention

front 104

Lidocaine belongs to which antiarrhythmic subclass?

A. Class IA
B. Class IC
C. Class III
D. Class IB

back 104

D. Class IB

front 105

Because of extensive first-pass metabolism, lidocaine used as an antiarrhythmic is typically given:

A. Intravenously
B. Sublingually
C. Intramuscularly
D. Orally

back 105

A. Intravenously

front 106

A patient with digoxin toxicity develops ventricular ectopy. Which antiarrhythmic from your material is also used for digitalis-induced arrhythmias?

A. Lidocaine
B. Sotalol
C. Esmolol
D. Dronedarone

back 106

A. Lidocaine

front 107

Mexiletine belongs to which Vaughan-Williams subclass?

A. Class IA
B. Class II
C. Class IB
D. Class IC

back 107

C. Class IB

front 108

Flecainide belongs to which antiarrhythmic subclass?

A. Class IA
B. Class IB
C. Class III
D. Class IC

back 108

D. Class IC

front 109

Propafenone belongs to which antiarrhythmic subclass?

A. Class IV
B. Class IC
C. Class IB
D. Class IA

back 109

B. Class IC

front 110

Which additional pharmacologic property does propafenone possess?

A. Alpha-blocking activity
B. Muscarinic agonism
C. Beta-blocking activity
D. Nitrate-like vasodilation

back 110

C. Beta-blocking activity

front 111

Which short-acting β-blocker is specifically used as an antiarrhythmic?

A. Propranolol
B. Carvedilol
C. Sotalol
D. Esmolol

back 111

D. Esmolol

front 112

Which β-blocker also has partial Class III antiarrhythmic activity?

A. Nebivolol
B. Sotalol
C. Metoprolol
D. Atenolol

back 112

B. Sotalol

front 113

Sotalol predisposes patients to which arrhythmia?

A. Sinus arrest
B. Junctional tachycardia
C. Torsades de pointes
D. Ventricular standstill

back 113

C. Torsades de pointes

front 114

Amiodarone is classified primarily as which antiarrhythmic class?

A. Class III
B. Class II
C. Class IA
D. Class IV

back 114

A. Class III

front 115

Which channel/current is classically blocked by amiodarone?

A. If current
B. IKr
C. INa
D. ICaL

back 115

B. IKr

front 116

Amiodarone interferes with metabolism of which hormone pathway?

A. T3 to T4
B. TSH to TRH
C. T4 to T3
D. T4 to rT3

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C. T4 to T3

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A patient on amiodarone also takes warfarin, digoxin, and a statin. Why is close monitoring needed?

A. Amiodarone induces CYP3A4
B. Amiodarone blocks renal secretion
C. Amiodarone inhibits P450 enzymes
D. Amiodarone lowers protein binding

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C. Amiodarone inhibits P450 enzymes

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Which Class III drug resembles amiodarone structurally but lacks its effect on thyroid hormone metabolism?

A. Ibutilide
B. Dronedarone
C. Dofetilide
D. Procainamide

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B. Dronedarone

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Which major toxicity is especially emphasized for dronedarone?

A. Nephrotoxicity
B. Ototoxicity
C. Hepatotoxicity
D. Retinopathy

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C. Hepatotoxicity

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Dofetilide and ibutilide specifically block which current?

A. INa
B. ICaL
C. IK1
D. IKr

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D. IKr

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Verapamil and diltiazem belong to which antiarrhythmic class?

A. Class III
B. Class I
C. Class IV
D. Class II

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C. Class IV

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A patient overdoses on verapamil. Which toxic effect is most expected?

A. AV block, severe depression
B. QT shortening, hypertension
C. Reflex tachycardia, tremor
D. Ventricular fibrillation, tremor

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A. AV block, severe depression

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Which nucleoside is both a prominent vasodilator and an antiarrhythmic, and is the drug of choice for SVT?

A. Adenosine
B. Atropine
C. Ivabradine
D. Verapamil

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A. Adenosine

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What is the mechanism of action of ivabradine?

A. Blocks AV nodal calcium current
B. Blocks IKr in ventricles
C. Blocks If in SA node
D. Inhibits Na/K ATPase

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C. Blocks If in SA node

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A patient with digitalis-induced arrhythmias needs adjunctive ion therapy. Which is preferred?

A. Calcium
B. Sodium
C. Potassium
D. Magnesium

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D. Magnesium

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Which antiarrhythmic from your list can be used to treat Wolff-Parkinson-White syndrome?

A. Verapamil
B. Procainamide
C. Diltiazem
D. Ivabradine

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B. Procainamide