Shamliyan Tatyana A, Middleton Maria, Borst Clarissa
Evidence-Based Medicine Center, Quality Assurance, Elsevier, Philadelphia, Pennsylvania.
Evidence-Based Medicine Center, Elsevier, Philadelphia, Pennsylvania.
Clin Ther. 2017 Feb;39(2):404-427.e36. doi: 10.1016/j.clinthera.2017.01.011. Epub 2017 Feb 9.
We performed a systematic review of patient-centered outcomes after the concomitant use of proton pump inhibitors (PPIs) and other drugs.
We searched 4 databases in July 2016 to find studies that reported mortality and morbidity after the concomitant use of PPIs and other drugs. We conducted direct meta-analyses using a random-effects model and graded the quality of evidence according to the Grading of Recommendations Assessment, Development and Evaluation working group approach.
We included data from 17 systematic reviews and meta-analyses, 16 randomized controlled trials, and 16 observational studies that examined the concomitant use of PPIs with medications from 10 drug classes. Low-quality evidence suggests that the use of PPIs is associated with greater morbidity when administered with antiplatelet drugs, bisphosphonates, antibiotics, anticoagulants, metformin, mycophenolate mofetil, or nelfinavir. Concomitant PPIs reduce drug-induced gastrointestinal bleeding and are associated with greater docetaxel and cisplatin response rates in patients with metastatic breast cancer. For demonstrated statistically significant relative risks and benefits from concomitant PPIs, the magnitudes of the effects are small, with <100 attributable events per 1000 patients treated, and the effects are inconsistent among specific drugs. Among individual PPIs, the concomitant use of pantoprazole or esomeprazole, but not omeprazole or lansoprazole, is associated with an increased risk for all-cause mortality, nonfatal myocardial infarction, or stroke. Clopidogrel is associated with a greater risk for myocardial infarction compared with prasugrel. Conflicting results between randomized controlled trials and observational studies and high risk for bias in the body of evidence lessened our confidence in the results.
Available evidence suggests a greater risk for adverse patient outcomes after the concomitant use of PPIs and medications from 9 drug classes and warns against inappropriate drug combinations.
我们对质子泵抑制剂(PPI)与其他药物联合使用后的以患者为中心的结局进行了系统评价。
2016年7月,我们检索了4个数据库,以查找报告PPI与其他药物联合使用后死亡率和发病率的研究。我们使用随机效应模型进行直接荟萃分析,并根据推荐分级评估、制定和评价工作组的方法对证据质量进行分级。
我们纳入了17项系统评价和荟萃分析、16项随机对照试验以及16项观察性研究的数据,这些研究考察了PPI与10类药物的联合使用情况。低质量证据表明,PPI与抗血小板药物、双膦酸盐、抗生素、抗凝剂、二甲双胍、霉酚酸酯或奈非那韦联合使用时,发病风险更高。PPI联合使用可减少药物引起的胃肠道出血,并与转移性乳腺癌患者更高的多西他赛和顺铂反应率相关。对于PPI联合使用已证明具有统计学显著意义的相对风险和益处,其效应大小较小,每1000例接受治疗的患者中可归因事件少于100例,且在特定药物之间效应不一致。在个别PPI中,泮托拉唑或埃索美拉唑联合使用,但奥美拉唑或兰索拉唑联合使用则不然,与全因死亡率、非致命性心肌梗死或中风风险增加相关。与普拉格雷相比,氯吡格雷发生心肌梗死的风险更高。随机对照试验和观察性研究之间的结果相互矛盾,且证据主体存在高偏倚风险,这降低了我们对结果的信心。
现有证据表明,PPI与9类药物联合使用后患者出现不良结局的风险更高,并警告不要进行不适当的药物联合。