Abstract

Proton pump inhibitors often are prescribed in combination with clopidogrel to decrease risk of gastrointestinal bleeding after acute coronary syndrome. Clopidogrel is a prodrug that has to be metabolized in the liver to generate the active metabolite. Both medications are metabolized largely by the CYP2C19 enzyme; therefore, concerns exist that a drug-drug interaction during concomitant treatment with clopidogrel and a proton pump inhibitor may result in reduction of platelet inhibition. We have reviewed observational and randomized control studies that have evaluated the potential influence of proton pump inhibitors on the platelet inhibitory effect of clopidogrel, along with cardiovascular outcomes. We also have summarized regulatory and academic guidelines for treatment of patients in which concomitant therapy with clopidogrel and proton pump inhibitors may be indicated. Confounding issues, including differential effects of individual proton pump inhibitors on the pharmacodynamics of clopidogrel and variation in clopidogrel metabolism mediated by CYP2C19 gene polymorphisms, also are discussed.

Highlights

  • Clopidogrel is recommended for inhibition of platelet activation and aggregation in patients who are unable to take aspirin or in combination with aspirin in patients with unstable angina or myocardial infarction (MI) or who undergo percutaneous coronary intervention (PCI) [1,2]

  • We have reviewed observational and randomized control studies that have evaluated the potential influence of proton pump inhibitors on the platelet inhibitory effect of clopidogrel, along with cardiovascular outcomes

  • Data from retrospective studies regarding in vitro pharmacodynamic effects of pump inhibitors (PPIs) on clopidogrel are more consistent than data from studies with clinical end points; it is unknown if effects of PPIs on clopidogrel-induced inhibition of platelet activation and aggregation translate to differences in clinical outcomes

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Summary

Introduction

Clopidogrel is recommended for inhibition of platelet activation and aggregation in patients who are unable to take aspirin or in combination with aspirin in patients with unstable angina or myocardial infarction (MI) or who undergo percutaneous coronary intervention (PCI) [1,2]. Addition of a PPI to treatment with aspirin and clopidogrel alone or in combination is recommended for patients with unstable angina or non-ST elevation MI and history of GI bleeding [1]. A case-control study of 2777 patients with upper GI peptic ulcer bleeding and 5532 control subjects without GI bleeding showed that the addition of a PPI to treatment with clopidogrel or ticlopidine was associated with a reduction in bleeding (adjusted relative risk, 0.19; 95% confidence interval [CI], 0.07 - 0.49) compared with clopidogrel or ticlopidine treatment alone [5]. A retrospective cohort study of 347 patients treated with dual antiplatelet therapy showed that the addition of a PPI decreased the risk for a major bleed (defined as a bleed resulting in death, transfusion, or hospitalization) in patients with an additional risk factor for bleeding (p = 0.05) compared with patients not on a PPI [7]

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