Should patients prescribed long-term low-dose aspirin receive proton pump inhibitors? A systematic review and meta-analysis

被引:19
作者
Tran-Duy, A. [1 ,2 ]
Vanmolkot, F. H. [3 ]
Joore, M. A. [1 ]
Hoes, A. W. [2 ]
Stehouwer, C. D. A. [3 ,4 ]
机构
[1] Maastricht Univ, Med Ctr, Dept Clin Epidemiol & Med Technol Assessment, NL-6202 AZ Maastricht, Netherlands
[2] Univ Med Ctr Utrecht, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands
[3] Maastricht Univ, Med Ctr, Dept Internal Med, NL-6202 AZ Maastricht, Netherlands
[4] Maastricht UMC, CARIM Sch Cardiovasc Dis, Maastricht, Netherlands
关键词
HELICOBACTER-PYLORI INFECTION; UPPER GASTROINTESTINAL COMPLICATIONS; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; ATHEROSCLEROTIC VASCULAR-DISEASE; GASTRODUODENAL MUCOSAL INJURY; AMERICAN-HEART-ASSOCIATION; PEPTIC-ULCER; CARDIOVASCULAR-DISEASE; ACETYLSALICYLIC-ACID; SECONDARY PREVENTION;
D O I
10.1111/ijcp.12634
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Several clinical guidelines recommend the use of proton pump inhibitors (PPIs) in patients taking low-dose aspirin but report no or limited supporting data. We conducted a systematic review and meta-analysis to examine the effects of co-administration of PPIs in patients taking low-dose aspirin on the risks of adverse gastrointestinal (GI) and cardiovascular (CV) events, and on patient adherence to aspirin. Methods: We searched PUBMED, EMBASE and Cochrane Central Register of Controlled Trials databases for relevant articles published through November 2013. We included randomised controlled trials (RCTs) and observational studies in patients taking low-dose aspirin with and without PPIs. Risk of bias was assessed using the Cochrane Collaboration's tool (for RCTs) and the Newcastle-Ottawa Scale (for observational studies). Pooled risk ratios (RRs) were computed using a random-effects model. Results: We included 13 studies, of which 12 (2 RCTs and 10 observational studies) reported on GI events, and one (cohort study) on both GI bleeding and CV events. No study reported on adherence to aspirin. Co-administration of PPIs in patients receiving low-dose aspirin was associated with risk reductions of 73% (RR 0.27, 95% CI 0.17-0.42) and 50% (RR 0.50, 95% CI 0.32-0.80) in the occurrence of peptic ulcer and GI bleeding respectively. There was evidence of bias in publications reporting on the GI events. Conclusions: The practice of co-prescribing PPIs in patients taking lowdose aspirin is supported by some data, but the evidence is rather weak. It currently remains unclear whether the benefits of co-administration of PPIs in users of low-dose aspirin outweigh their potential harms.
引用
收藏
页码:1088 / 1111
页数:24
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