Why the study?
Does morphine coadministration influence the pharmacokinetics and pharmacodynamics of aspirin in healthy volunteers?
Does morphine coadministration influence the pharmacokinetics and pharmacodynamics of aspirin in healthy volunteers?
Unlike its known interaction with P2Y12 inhibitors, morphine coadministration has a negligible effect on aspirin-induced platelet inhibition, suggesting concurrent use does not compromise aspirin efficacy in acute coronary syndromes.
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Does not compromise aspirin efficacy in ACS; contrasts known P2Y12 interactions and extends opioid-antiplatelet data.
Aspirin is a cornerstone in the antiplatelet therapy for acute coronary syndromes. Coadministration of morphine may potentially influence the intestinal absorption, pharmacokinetics, and pharmacodynamics, as seen with P2Y₁₂ inhibitors. In this trial, healthy volunteers were randomized to receive morphine (5 mg, i.v. bolus injection) at one of seven different time points before, after, or with aspirin (162 mg, p.o.) in a double-blind, placebo-controlled fashion. After a 14-day washout, subjects received placebo instead of morphine. Pharmacokinetics were determined by liquid chromatography, and aspirin’s effects were measured by platelet function tests (whole-blood platelet aggregation: multiplate, platelet plug formation: PFA-100). Morphine increased the total acetylsalicylic acid exposure by 20% compared with placebo when given simultaneously with aspirin, whereas Cmax and tmax were not altered. Morphine had no significant effect on aspirin-induced platelet inhibition. In contrast to coadministration with P2Y₁₂ inhibitors, morphine appears to have negligible interaction with aspirin.
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Bartko et al. (2018) studied this question.
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