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非处方非甾体抗炎药与胃肠道出血风险

Over the counter non-steroidal anti-inflammatory drugs and risk of gastrointestinal bleeding.

作者信息

Blot W J, McLaughlin J K

机构信息

International Epidemiology Institute, Rockville, MD 20850, USA.

出版信息

J Epidemiol Biostat. 2000;5(2):137-42.

Abstract

BACKGROUND

Independent analyses of data from a case-control study conducted by the American College of Gastroenterology (ACG) were performed to evaluate and quantify potential risks of gastrointestinal (GI) bleeding associated with use of analgesics at over the counter (OTC) doses.

METHODS

Information on recent (within the past week) use of multiple analgesics, plus data on tobacco, alcohol and other factors, were obtained from 627 patients enrolled in the ACG GI bleeding registry and from 590 procedure-matched controls. Odds ratios (OR) were calculated as the measure of association between GI bleeding and the exposures of interest.

RESULTS

Risk of GI bleeding was increased 2-3 fold among recent users of aspirin, ibuprofen and other nonsteroidal anti-inflammatory drugs (NSAIDs) at OTC doses, with risk increasing in a dose-related manner. In contrast, no excess was found among acetaminophen (paracetamol) users. Alcohol consumption was also a risk factor, with doubled risks of GI bleeding among drinkers.

DISCUSSION

While these study results are not definitive, the findings are consistent with limited other data also reviewed, and suggest the need for further epidemiologic research to clarify the association between use of NSAIDs at OTC levels and risk of GI bleeding, and to determine whether NSAIDs and alcohol may interactively combine to enhance risk.

摘要

背景

对美国胃肠病学会(ACG)进行的一项病例对照研究的数据进行了独立分析,以评估和量化非处方(OTC)剂量使用镇痛药相关的胃肠道(GI)出血的潜在风险。

方法

从627名纳入ACG胃肠道出血登记处的患者和590名手术匹配对照中获取了近期(过去一周内)多种镇痛药使用情况的信息,以及烟草、酒精和其他因素的数据。计算比值比(OR)作为胃肠道出血与感兴趣暴露之间关联的度量。

结果

近期以OTC剂量使用阿司匹林、布洛芬和其他非甾体抗炎药(NSAIDs)的人群中,胃肠道出血风险增加了2至3倍,且风险呈剂量相关增加。相比之下,对乙酰氨基酚(扑热息痛)使用者中未发现过量风险。饮酒也是一个风险因素,饮酒者胃肠道出血风险加倍。

讨论

虽然这些研究结果并不确定,但这些发现与其他有限的已审查数据一致,并表明需要进一步的流行病学研究来阐明OTC水平使用NSAIDs与胃肠道出血风险之间的关联,并确定NSAIDs和酒精是否可能相互作用以增加风险。

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