Antiarrhythmics: adenosine interactions: practice question

A Pharmacology question in the style of the NEET PG paper. Answer it first, then read why the right option is right and why each of the others is wrong.

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Pharmacology · Antiarrhythmics: adenosine interactions

Sample item

A 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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Questions about this Pharmacology question

What is the answer to this Pharmacology question?

The best answer is 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.

Why is "Avoid adenosine and give intravenous digoxin instead" not the answer?

Digoxin is slower and less effective for abrupt termination, and the interaction can be managed with dose reduction.

Why is "Increase the dose, because dipyridamole upregulates adenosine recepto…" not the answer?

Dipyridamole does not upregulate receptors; it blocks nucleoside uptake.

Why is "Give the usual dose, because dipyridamole acts only on platelets" not the answer?

Dipyridamole potentiates adenosine through nucleoside transport inhibition, not only through platelets.

What concept does this question test?

It tests Antiarrhythmics: adenosine interactions in Pharmacology. 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.

How hard is this question?

We tag it as a multi-step question: it asks you to combine more than one idea. The tag is our own editorial judgement, not an official difficulty rating, so read the reason for every option, not only the answer.

How should I study Antiarrhythmics: adenosine interactions?

Learn drugs as classes, then the exception in each class that an examiner would pick. Then use the flashcards and the other Pharmacology questions on this site to test what stuck.

Is this a real NEET PG question?

No. It is an original practice item (editorial status: sample, version 1). NextPrep does not publish recalled or leaked questions, and independent faculty review of this item has not been completed yet, so confirm important facts in a standard textbook.