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Pharmacology · Antiarrhythmics: adenosine interactions
Sample itemA 40-year-old woman with paroxysmal supraventricular tachycardia has been taking dipyridamole for secondary stroke prevention. Adenosine is planned to terminate an attack. Which adjustment is appropriate?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
A. Reduce the initial dose, because dipyridamole blocks adenosine reuptake and prolongs its action
Adenosine has a half-life of seconds because it is taken up into red cells and endothelium by nucleoside transporters. Dipyridamole blocks this uptake, which potentiates and prolongs adenosine, so a much smaller dose is used to avoid prolonged asystole. Methylxanthines such as theophylline and caffeine have the opposite effect by antagonising adenosine receptors.
Option by option
A. Reduce the initial dose, because dipyridamole blocks adenosine reuptake and prolongs its action (correct)
Correct. Blocked reuptake extends the action of adenosine, so a lower dose is safer.
B. Avoid adenosine and give intravenous digoxin instead
Digoxin is slower and less effective for abrupt termination, and the interaction can be managed with dose reduction.
C. Increase the dose, because dipyridamole upregulates adenosine receptors
Dipyridamole does not upregulate receptors; it blocks nucleoside uptake.
D. Give the usual dose, because dipyridamole acts only on platelets
Dipyridamole potentiates adenosine through nucleoside transport inhibition, not only through platelets.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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