Pharmaceutical and clinical implications of proton pump inhibitors with dual antiplatelet therapies: a systematic review

被引:0
|
作者
Jacob J. Gries [1 ]
George Triadafilopoulos [2 ]
Hafeez Ul Hassan Virk [3 ]
Umair Khalid [4 ]
Hani Jneid [5 ]
Yochai Birnbaum [6 ]
Carl J. Lavie [7 ]
Dirk Sibbing [8 ]
Glenn N. Levine [4 ]
Chayakrit Krittanawong [9 ]
机构
[1] Geisinger Medical Center,Department of Internal Medicine
[2] Stanford University School of Medicine,Division of Gastroenterology and Hepatology
[3] University Hospitals Cleveland Medical Center,Harrington Heart & Vascular Institute, Case Western Reserve University
[4] Baylor College of Medicine,Michael E. DeBakey VA Medical Center, Section of Cardiology
[5] University of Texas Medical Branch,Division of Cardiology
[6] Baylor College of Medicine,Section of Cardiology
[7] The University of Queensland School of Medicine,John Ochsner Heart and Vascular Institute, Ochsner Clinical School
[8] Ludwig-Maximilians-University Munich (LMU Munich),University Hospital Munich, Campus Grosshadern
[9] NYU Langone Health,Cardiology Division, NYU School of Medicine
来源
npj Gut and Liver | / 2卷 / 1期
关键词
D O I
10.1038/s44355-024-00012-w
中图分类号
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摘要
Proton pump inhibitors (PPIs) are frequently co-prescribed with dual antiplatelet therapy (DAPT) agents to mitigate the potential of increased gastrointestinal bleeding associated with antiplatelet therapy. Experimental studies have suggested that certain PPIs, such as omeprazole and esomeprazole, may decrease the antiplatelet effects of P2Y12 inhibitors, especially clopidogrel, and, therefore, may potentiate adverse cardiovascular and cerebrovascular events. Data from randomized controlled trials and observational studies have produced mixed results on the clinical implications of this theory. This comprehensive narrative review aims to provide an in-depth analysis of the interactions between PPIs and dual antiplatelet agents, shedding light on their mechanisms and clinical implications and identifying areas for therapeutic optimization. We also address recent advancements in personalized medicine and the potential role of genetic factors in influencing individual responses to PPIs and antiplatelet drugs to optimize treatment outcomes and minimize adverse effects.
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