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非甾体抗炎药的心血管安全性:网络荟萃分析。

Cardiovascular safety of non-steroidal anti-inflammatory drugs: network meta-analysis.

机构信息

Institute of Social and Preventive Medicine, University of Bern, Switzerland.

出版信息

BMJ. 2011 Jan 11;342:c7086. doi: 10.1136/bmj.c7086.

DOI:10.1136/bmj.c7086
PMID:21224324
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3019238/
Abstract

OBJECTIVE

To analyse the available evidence on cardiovascular safety of non-steroidal anti-inflammatory drugs.

DESIGN

Network meta-analysis.

DATA SOURCES

Bibliographic databases, conference proceedings, study registers, the Food and Drug Administration website, reference lists of relevant articles, and reports citing relevant articles through the Science Citation Index (last update July 2009). Manufacturers of celecoxib and lumiracoxib provided additional data.

STUDY SELECTION

All large scale randomised controlled trials comparing any non-steroidal anti-inflammatory drug with other non-steroidal anti-inflammatory drugs or placebo. Two investigators independently assessed eligibility.

DATA EXTRACTION

The primary outcome was myocardial infarction. Secondary outcomes included stroke, death from cardiovascular disease, and death from any cause. Two investigators independently extracted data.

DATA SYNTHESIS

31 trials in 116 429 patients with more than 115 000 patient years of follow-up were included. Patients were allocated to naproxen, ibuprofen, diclofenac, celecoxib, etoricoxib, rofecoxib, lumiracoxib, or placebo. Compared with placebo, rofecoxib was associated with the highest risk of myocardial infarction (rate ratio 2.12, 95% credibility interval 1.26 to 3.56), followed by lumiracoxib (2.00, 0.71 to 6.21). Ibuprofen was associated with the highest risk of stroke (3.36, 1.00 to 11.6), followed by diclofenac (2.86, 1.09 to 8.36). Etoricoxib (4.07, 1.23 to 15.7) and diclofenac (3.98, 1.48 to 12.7) were associated with the highest risk of cardiovascular death.

CONCLUSIONS

Although uncertainty remains, little evidence exists to suggest that any of the investigated drugs are safe in cardiovascular terms. Naproxen seemed least harmful. Cardiovascular risk needs to be taken into account when prescribing any non-steroidal anti-inflammatory drug.

摘要

目的

分析非甾体抗炎药心血管安全性的现有证据。

设计

网络荟萃分析。

资料来源

文献数据库、会议录、研究注册处、美国食品和药物管理局网站、相关文章的参考文献列表,以及通过科学引文索引(2009 年 7 月更新)引用相关文章的报告。塞来昔布和罗非考昔的制造商提供了额外的数据。

研究选择

所有比较任何非甾体抗炎药与其他非甾体抗炎药或安慰剂的大规模随机对照试验。两名调查员独立评估纳入标准。

资料提取

主要结局是心肌梗死。次要结局包括卒中、心血管疾病死亡和任何原因死亡。两名调查员独立提取数据。

资料综合

共纳入 31 项试验,涉及 116429 名患者,随访时间超过 115000 患者年。患者被分配至萘普生、布洛芬、双氯芬酸、塞来昔布、依托考昔、罗非考昔、鲁米考昔或安慰剂。与安慰剂相比,罗非考昔与心肌梗死风险最高相关(率比 2.12,95%可信区间 1.26 至 3.56),其次是鲁米考昔(2.00,0.71 至 6.21)。布洛芬与卒中风险最高相关(3.36,1.00 至 11.6),其次是双氯芬酸(2.86,1.09 至 8.36)。依托考昔(4.07,1.23 至 15.7)和双氯芬酸(3.98,1.48 至 12.7)与心血管死亡风险最高相关。

结论

尽管存在不确定性,但几乎没有证据表明所研究的任何药物在心血管方面是安全的。萘普生似乎危害最小。在开具任何非甾体抗炎药时都需要考虑心血管风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/9cb9c1c23e60/tres807735.f4_default.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/59cd9bcab37b/tres807735.f1_default.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/72493a87b9c0/tres807735.f2_default.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/589516970181/tres807735.f3_default.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/9cb9c1c23e60/tres807735.f4_default.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/59cd9bcab37b/tres807735.f1_default.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/72493a87b9c0/tres807735.f2_default.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/589516970181/tres807735.f3_default.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b891/4787723/9cb9c1c23e60/tres807735.f4_default.jpg

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