Risk Factors for Bleeding and Clinical Ineffectiveness Associated with Clopidogrel Therapy: A Comprehensive Meta-Analysis

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2020-11-17
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American English
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Wiley
Abstract

Although clopidogrel is a frequently used antiplatelet medication to treat and prevent atherothrombotic disease, clinicians must balance its clinical effectiveness with the potential side effect of bleeding. However, many previous studies have evaluated beneficial and adverse factors separately. The objective of our study was to perform a comprehensive meta-analysis of studies of clopidogrel's clinical effectiveness and/or risk of bleeding in order to identify and assess all reported risk factors, thus helping clinicians to balance patient safety with drug efficacy. We analyzed randomized controlled trials (RCTs) of maintenance use in four stages: search for relevant primary articles; abstract and full article screening; quality assessment and data extraction; and synthesis and data analysis. Screening of 7,109 articles yielded 52 RCTs that met the inclusion criteria. Twenty-seven risk factors were identified. "Definite risk factors" were defined as those with aggregated odds ratios (ORs) > 1 and confidence intervals (CIs) > 1 if analyzed in more than one study. Definite risk factors for major bleeding were concomitant aspirin use (OR 2.83, 95% CI 2.04-3.94) and long duration of clopidogrel therapy (> 6 months) (OR 1.74, 95% CI 1.21-2.50). Dual antiplatelet therapy, extended clopidogrel therapy, and high maintenance dose (150 mg/day) of clopidogrel were definite risk factors for any bleeding. Reduced renal function, both mild and severe, was the only definite risk factor for clinical ineffectiveness. These findings can help clinicians predict the risks and effectiveness of clopidogrel use for their patients and be used in clinical decision support tools.

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Nguyen KA, Eadon MT, Yoo R, Milway E, Kenneally A, Fekete K, Oh H, Duong K, Whipple EC, Schleyer TK. Risk Factors for Bleeding and Clinical Ineffectiveness Associated With Clopidogrel Therapy: A Comprehensive Meta-Analysis. Clin Transl Sci. 2020 Nov 17. doi: 10.1111/cts.12926. Epub ahead of print. PMID: 33202084.
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This study was supported by the Lilly Endowment, Inc. Physician Scientist Initiative and by Indiana University Health and the Indiana Clinical and Translational Sciences Institute, funded in part by grant #ULI TR002529 from the National Institutes of Health, National Center for Advancing Translational Sciences, Clinical and Translational Science Award, and The Advances in Medicine (AIM) grant from Cook Medical. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health or Cook Medical. MTE was supported by NIH/NIDDK K08DK107864.
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