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Systematic review with meta‐analysis: risk of adverse cardiovascular events with proton pump inhibitors independent of clopidogrel

机译:具有Meta分析的系统审查:与氯吡格雷无关的质子泵抑制剂不良心血管事件的风险

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Summary Background Clopidogrel's anti‐platelet effects may be attenuated by a pharmacokinetic interaction with co‐prescribed proton pump inhibitors, which inhibit oxidative pathways that convert clopidogrel into its active metabolites. Despite this, the impact of PPI s on cardiovascular risk in the absence of clopidogrel is not well defined. Aim To report on a systematic review and meta‐analysis of the association between PPI s and cardiovascular risk, independent of clopidogrel. Methods The databases of MEDLINE , EMBASE , Cochrane Central Register of Controlled Trials, Scopus, Web of Science, and ClinicalTrials.gov were systematically searched in October 2017. The primary outcome was association between PPI monotherapy and any adverse cardiovascular event. The secondary outcome was association between proton pump inhibitor monotherapy and acute myocardial infarction. Studies were excluded if they reported or did not adjust for concomitant anti‐platelet therapy or involved participants aged less than 18?years. Results A total of 22 studies were included in the systematic review. Data from 16 studies were included in the meta‐analysis (involving 447?408 participants). Of these, eight were randomised controlled trials, seven were observational studies and one was a retrospective analysis of a randomised controlled trial. An increased risk of any adverse cardiovascular event with PPI monotherapy was observed using pooled data from observational studies (risk ratio 1.25, 95% CI 1.11‐1.42, I 2 81%, P ??0.001), but not from randomised controlled trials (risk ratio 0.89, 95% CI 0.34‐2.33, I 2 0%, P ?=?0.85). Conclusion There is no clear evidence of an association between PPI monotherapy and increased cardiovascular risk.
机译:发明内容背景氯吡格雷的抗血小板效应可以通过与共规则的质子泵抑制剂的药代动力学相互作用抑制,其抑制将氯吡格雷转化为其活性代谢物的氧化途径。尽管如此,PPI S在没有氯吡格雷的情况下对心血管风险的影响并不明确。旨在报告PPI S和心血管风险之间的关联的系统评价和荟萃分析,与氯吡格雷无关。方法在2017年10月系统地检测了Medline,Embase,Cochrane中央登记册,Scopus,Scip,Sciens和Clinicaltrials.gov的数据库。主要结果是PPI单药治疗与任何不良心血管事件之间的关联。次要结果是质子泵抑制剂单药治疗和急性心肌梗死之间的关联。如果他们报告或未调整伴随的抗血小板治疗或涉及少于18岁的参与者,则排除研究。结果在系统审查中共有22项研究。来自16项研究的数据包括在META分析中(涉及447个?408名参与者)。其中,八项是随机对照试验,七项是观察性研究,一个是对随机对照试验的回顾性分析。使用来自观察性研究的汇集数据(风险比1.25,95%CI 1.11-1.42,I 2 81%,P≤11.<0.001),观察到具有PPI单疗法的任何不良心血管事件的风险增加的风险增加(风险比0.89,95%CI 0.34-2.33,I 2 0%,P?= 0.85)。结论PPI单药治疗与心血管风险增加的关联没有明确的证据。

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    Department of Epidemiology and Preventive MedicineMonash UniversityMelbourne Australia;

    Department of Epidemiology and Preventive MedicineMonash UniversityMelbourne Australia;

    Department of Epidemiology and Preventive MedicineMonash UniversityMelbourne Australia;

    Department of Epidemiology and Preventive MedicineMonash UniversityMelbourne Australia;

    Department of GastroenterologyAlfred HealthMelbourne Australia;

    Department of Epidemiology and Preventive MedicineMonash UniversityMelbourne Australia;

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  • 正文语种 eng
  • 中图分类 药理学;
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