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非甾体抗炎药与中风风险增加相关:一项全国性病例交叉研究。

Increased risk of stroke associated with nonsteroidal anti-inflammatory drugs: a nationwide case-crossover study.

机构信息

George Institute for International Health, Royal Prince Alfred Hospital and University of Sydney, Sydney, Australia.

出版信息

Stroke. 2010 Sep;41(9):1884-90. doi: 10.1161/STROKEAHA.110.585828. Epub 2010 Jul 29.

Abstract

BACKGROUND AND PURPOSE

Limited studies assessed cerebrovascular safety of individual nonsteroidal anti-inflammatory drugs (NSAIDs). We evaluated the risk of ischemic and hemorrhagic stroke associated with short-term use of selective and nonselective NSAIDs in a Chinese population with a high incidence of stroke.

METHODS

A retrospective case-crossover study was conducted by analyzing the Taiwan National Health Insurance Database. We identified all ischemic and hemorrhagic stroke patients in 2006, aged >or=20 years, based on International Classification of Diseases, 9th Revision, Clinical Modification diagnosis codes from inpatient claims and defined the index date as the date of hospitalization. For each patient, we defined case period as 1 to 30 days before the index date and control period as 91 to 120 days before the index date. A pharmacy prescription database was searched for NSAID use during the case and control periods. We calculated adjusted ORs and their 95% CIs with a conditional logistic regression model.

RESULTS

A total of 28 424 patients with ischemic stroke and 9456 patients with hemorrhagic stroke were included. For ischemic stroke, a modest increased risk was evident for all oral NSAIDs with adjusted ORs (95% CI) ranging from 1.20 (1.00 to 1.44) for celecoxib to 1.90 (1.39 to 2.60) for ketorolac. For hemorrhagic stroke, oral ketorolac was associated with a significantly higher risk with OR of 2.69 (1.56 to 4.66). Significantly increased risk was found for parenteral NSAIDs, in particular ketorolac, with an OR of 3.92 (3.25 to 4.72) for ischemic stroke and 5.98 (4.40 to 8.13) for hemorrhagic stroke.

CONCLUSIONS

Use of selective and nonselective NSAIDs was associated with an increased risk of both ischemic and hemorrhagic stroke, strikingly high for parenteral ketorolac.

摘要

背景与目的

有限的研究评估了单一非甾体抗炎药(NSAIDs)的脑血管安全性。我们评估了在卒中高发的中国人群中,短期使用选择性和非选择性 NSAIDs 与缺血性卒中和出血性卒中的相关性风险。

方法

通过分析台湾全民健康保险数据库,我们进行了一项回顾性病例交叉研究。我们基于国际疾病分类第 9 版临床修订版的住院记录诊断代码,确定了所有 2006 年年龄≥20 岁的缺血性卒中和出血性卒中患者,并将索引日期定义为住院日期。对于每位患者,我们将病例期定义为索引日期前 1 至 30 天,对照期定义为索引日期前 91 至 120 天。我们在病例期和对照期内检索了 NSAID 的用药记录。我们使用条件逻辑回归模型计算了调整后的比值比(OR)及其 95%置信区间(CI)。

结果

共纳入了 28424 例缺血性卒中和 9456 例出血性卒中患者。对于缺血性卒中,所有口服 NSAIDs 的风险均有适度增加,调整后的 OR(95%CI)范围为塞来昔布的 1.20(1.00 至 1.44)至酮咯酸的 1.90(1.39 至 2.60)。对于出血性卒中,口服酮咯酸的风险显著升高,OR 为 2.69(1.56 至 4.66)。对于注射用 NSAIDs,尤其是酮咯酸,缺血性卒中和出血性卒中的风险均显著增加,OR 分别为 3.92(3.25 至 4.72)和 5.98(4.40 至 8.13)。

结论

选择性和非选择性 NSAIDs 的使用与缺血性卒中和出血性卒中的风险增加相关,尤其是注射用酮咯酸的风险显著增加。

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