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Cardiac Pharmacology Effects on ECG Flashcards

7 cards from real CET practice questions. Tap to flip, then mark Knew It or Still Learning โ€” missed cards come back until you master them.

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  1. Amiodarone is known to prolong which ECG interval, increasing the risk of Torsades de Pointes?

    Answer: QT interval

    Amiodarone prolongs the QT interval by blocking potassium channels, which can precipitate Torsades de Pointes in susceptible patients.

  2. A patient receiving IV adenosine for SVT shows a brief pause on the ECG strip. What does this pause represent?

    Answer: Transient AV block

    Adenosine transiently blocks AV conduction, producing a brief AV block that terminates re-entrant SVT and appears as a pause on the ECG.

  3. Which beta-blocker ECG effect helps differentiate it from calcium channel blocker toxicity on the ECG?

    Answer: Bradycardia with narrow QRS vs. bradycardia with wide QRS

    Beta-blocker toxicity typically causes bradycardia with a narrow QRS, while calcium channel blocker toxicity may cause bradycardia with a wide QRS and conduction abnormalities.

  4. Sotalol combines beta-blocking and Class III antiarrhythmic properties. Which ECG change is most expected?

    Answer: Prolonged QT interval

    Sotalol's Class III action blocks potassium channels, prolonging repolarization and the QT interval.

  5. A patient on procainamide develops a wide-complex tachycardia on ECG. What drug toxicity phenomenon is most likely?

    Answer: Proarrhythmia with widened QRS

    Procainamide toxicity causes QRS widening due to sodium channel blockade, which can lead to proarrhythmic ventricular tachycardia.

  6. Which ECG finding in a digitalis-toxic patient most urgently requires physician notification?

    Answer: Bidirectional ventricular tachycardia

    Bidirectional ventricular tachycardia is a hallmark of severe digitalis toxicity and is a life-threatening emergency requiring immediate intervention.

  7. Flecainide, a Class IC drug, primarily affects the ECG by:

    Answer: Widening the QRS complex significantly

    Flecainide blocks fast sodium channels, markedly slowing intraventricular conduction and widening the QRS complex.