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本文引用的文献

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Nonsteroidal anti-inflammatory drug use in relation to major upper gastrointestinal bleeding.非甾体抗炎药的使用与上消化道大出血的关系
Clin Pharmacol Ther. 1993 Apr;53(4):485-94. doi: 10.1038/clpt.1993.55.
2
Variation in the risk of peptic ulcer complications with nonsteroidal antiinflammatory drug therapy.非甾体抗炎药治疗中消化性溃疡并发症风险的差异。
Arthritis Rheum. 1993 Jan;36(1):84-90. doi: 10.1002/art.1780360114.
3
Variability in the risk of major gastrointestinal complications from nonaspirin nonsteroidal anti-inflammatory drugs.非阿司匹林类非甾体抗炎药导致严重胃肠道并发症风险的变异性。
Gastroenterology. 1993 Oct;105(4):1078-88. doi: 10.1016/0016-5085(93)90952-9.
4
Risks of bleeding peptic ulcer associated with individual non-steroidal anti-inflammatory drugs.与个别非甾体抗炎药相关的消化性溃疡出血风险。
Lancet. 1994 Apr 30;343(8905):1075-8. doi: 10.1016/s0140-6736(94)90185-6.
5
NSAIDs: time to re-evaluate gut toxicity.非甾体抗炎药:是时候重新评估肠道毒性了。
Lancet. 1994 Apr 30;343(8905):1051-2. doi: 10.1016/s0140-6736(94)90175-9.
6
Risk of upper gastrointestinal bleeding and perforation associated with individual non-steroidal anti-inflammatory drugs.与个体非甾体抗炎药相关的上消化道出血和穿孔风险。
Lancet. 1994 Mar 26;343(8900):769-72. doi: 10.1016/s0140-6736(94)91843-0.
7
Misoprostol reduces serious gastrointestinal complications in patients with rheumatoid arthritis receiving nonsteroidal anti-inflammatory drugs. A randomized, double-blind, placebo-controlled trial.米索前列醇可降低类风湿性关节炎患者接受非甾体抗炎药治疗时严重胃肠道并发症的发生率。一项随机、双盲、安慰剂对照试验。
Ann Intern Med. 1995 Aug 15;123(4):241-9. doi: 10.7326/0003-4819-123-4-199508150-00001.
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The relative gastrointestinal toxicity of the nonsteroidal anti-inflammatory drugs.
Arch Intern Med. 1987 Jun;147(6):1054-9.
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Non-steroidal anti-inflammatory drugs and bleeding peptic ulcer.非甾体抗炎药与出血性消化性溃疡
Lancet. 1986 Mar 1;1(8479):462-4. doi: 10.1016/s0140-6736(86)92927-2.
10
Comparison of an antiinflammatory dose of ibuprofen, an analgesic dose of ibuprofen, and acetaminophen in the treatment of patients with osteoarthritis of the knee.抗炎剂量布洛芬、止痛剂量布洛芬与对乙酰氨基酚治疗膝骨关节炎患者的比较。
N Engl J Med. 1991 Jul 11;325(2):87-91. doi: 10.1056/NEJM199107113250203.

不同非甾体抗炎药导致胃肠道并发症风险的差异:一项协作荟萃分析的结果

Variability in risk of gastrointestinal complications with individual non-steroidal anti-inflammatory drugs: results of a collaborative meta-analysis.

作者信息

Henry D, Lim L L, Garcia Rodriguez L A, Perez Gutthann S, Carson J L, Griffin M, Savage R, Logan R, Moride Y, Hawkey C, Hill S, Fries J T

机构信息

Centre for Clinical Epidemiology and Biostatistics, Faculty of Medicine and Health Sciences, University of Newcastle, New South Wales, Australia.

出版信息

BMJ. 1996 Jun 22;312(7046):1563-6. doi: 10.1136/bmj.312.7046.1563.

DOI:10.1136/bmj.312.7046.1563
PMID:8664664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2351326/
Abstract

OBJECTIVE

To compare the relative risks of serious gastrointestinal complications reported with individual non-steroidal anti-inflammatory drugs.

DESIGN

Systematic review of controlled epidemiological studies that found a relation between use of the drugs and admission to hospital for haemorrhage or perforation.

SETTING

Hospital and community based case-control and cohort studies.

MAIN OUTCOME MEASURES

(a) Estimated relative risks of gastrointestinal complications with use of individual drugs, exposure to ibuprofen being used as reference; (b) a ranking that best summarised the sequence of relative risks observed in the studies.

RESULTS

12 studies met the inclusion criteria. 11 provided comparative data on ibuprofen and other drugs. Ibuprofen ranked lowest or equal lowest for risk in 10 of the 11 studies. Pooled relative risks calculated with exposure to ibuprofen used as reference were all significantly greater than 1.0 (interval of point estimates 1.6 to 9.2). Overall, ibuprofen was associated with the lowest relative risk, followed by diclofenac. Azapropazone, tolmetin, ketoprofen, and piroxicam ranked highest for risk and indomethacin, naproxen, sulindac, and aspirin occupied intermediate positions. Higher doses of ibuprofen were associated with relative risks similar to those with naproxen and indomethacin.

CONCLUSIONS

The low risk of serious gastrointestinal complications with ibuprofen seems to be attributable mainly to the low doses of the drug used in clinical practice. In higher doses ibuprofen is associated with a similar risk to other non-steroidal anti-inflammatory drugs. Use of low risk drugs in low dosage as first line treatment would substantially reduce the morbidity and mortality due to serious gastrointestinal toxicity from these drugs.

摘要

目的

比较各种非甾体抗炎药报告的严重胃肠道并发症的相对风险。

设计

对已发现药物使用与因出血或穿孔入院之间存在关联的对照流行病学研究进行系统评价。

研究背景

基于医院和社区的病例对照研究及队列研究。

主要观察指标

(a)使用各药物时胃肠道并发症的估计相对风险,以布洛芬暴露作为对照;(b)最能概括研究中观察到的相对风险顺序的排名。

结果

12项研究符合纳入标准。11项提供了布洛芬与其他药物的比较数据。在11项研究中的10项里,布洛芬的风险排名最低或并列最低。以布洛芬暴露作为对照计算的合并相对风险均显著大于1.0(点估计区间为1.6至9.2)。总体而言,布洛芬的相对风险最低,其次是双氯芬酸。阿扎丙宗、托美丁、酮洛芬和吡罗昔康的风险排名最高,吲哚美辛、萘普生、舒林酸和阿司匹林处于中间位置。较高剂量的布洛芬与萘普生和吲哚美辛的相对风险相似。

结论

布洛芬严重胃肠道并发症风险低似乎主要归因于临床实践中使用的药物剂量低。高剂量时,布洛芬与其他非甾体抗炎药的风险相似。使用低风险药物的低剂量作为一线治疗将大幅降低这些药物所致严重胃肠道毒性的发病率和死亡率。