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Review Question - QID 100615

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QID 100615 (Type "100615" in App Search)
A 50-year-old male is seen in your clinic. Physical examination reveals a resting heart rate of 120. You perform an ECG (the reading from the V5 lead is shown in Figure A). After reviewing the ECG, you decide to start the man on a medication that primarily reduces the rate of depolarization during phase 0 and the latter part of phase 4 in cardiac slow-response tissue. What is the medication?
  • A

Amlodipine

10%

48/489

Ezetimibe

4%

20/489

Adenosine

18%

89/489

Nifedipine

4%

22/489

Verapamil

63%

306/489

  • A

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The drug used to provide rate control for this man's atrial fibrillation is verapamil, based on the mechanism of action described in the question stem.

Verapamil is an L-type calcium channel blocker (CCB) that decreases calcium ion influx occurring during phase 0 and latter part of phase 4 in cardiac slow-response tissue (i.e. SA and AV nodes). CCBs are considered class IV antiarrhythmics; other antiarrhythmic classes include I (affect sodium channels), II (beta blockers), and III (affect potassium channels). Non-dihydropyridine CCBs like verapamil primarily affect cardiac tissue, unlike dihydropyridine CCBs like amlodipine and nifedipine.

Figure A is an EKG strip showing the irregularly irregular ventricular response in atrial fibrillation.

Incorrect Answers:
Answers 1 & 4: Amlodipine and nifedipine are dihydropyridine CCBs that have more of an effect on vascular smooth muscle.
Answer 2: Ezetimibe prevents cholesterol reabsorption at the small intestine brush border.
Answer 3: Adenosine does affect the slow-response cardiac tissue (i.e. AV node), but does so by increasing outward K+ flux, leading to hyperpolarization.

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