首页> 外文期刊>Pharmacoepidemiology and drug safety >Non-aspirin NSAIDs, cyclooxygenase-2 inhibitors and risk for cardiovascular events-stroke, acute myocardial infarction, and death from coronary heart disease.
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Non-aspirin NSAIDs, cyclooxygenase-2 inhibitors and risk for cardiovascular events-stroke, acute myocardial infarction, and death from coronary heart disease.

机译:非阿司匹林NSAIDS,环氧氧酶-2抑制剂和心血管事件 - 中风的风险,急性心肌梗死和冠心病死亡。

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PURPOSE: To determine if certain non-steroidal anti-inflammatory drugs (NSAIDs) are associated with increased risk of cardiovascular events: acute myocardial infarction (AMI), stroke, and death from coronary heart disease (CHD). METHODS: We conducted a retrospective cohort study of Tennessee Medicaid enrollees aged 35-94 years between 1 January 1999 and 31 December 2005. Eligible persons were non-institutionalized, had continuous enrollment, and had no serious illness prior to cohort entry. Exposure to celecoxib, rofecoxib, valdecoxib, ibuprofen, naproxen, diclofenac, and indomethacin was studied. The outcome was hospitalization for AMI, stroke, or death from CHD among those with and without a history of cardiovascular disease (CVD). Adjusted hazard ratios (aHR) and 95% confidence intervals (95% CI) are reported. RESULTS: There were 610 001 persons in the final cohort and 14% had a baseline history of CVD. In those without CVD (N = 525 249) there were 1 566 678 person-years of follow-up and 12 184 events. In this group, non-users had 7.90 events/1000 person-years. Events/1000 person-years were 10.41 for current use of celecoxib (aHR 1.00, 95% CI 0.89-1.13), 10.91 for rofecoxib (aHR 1.21, 95% CI 1.07-1.37), 12.46 for valdecoxib (aHR 1.30 95% CI 1.04-1.61), and 13.25 for indomethacin (aHR 1.36, 95% CI 1.11-1.66) compared to non-users. Among patients with a past history of CVD (N = 84 752) there were 397 977 person-years of follow-up and 10 248 events. Non-users had 28.30 events/1000 person-years. Among those with CVD, rofecoxib use was associated with increased event rate (30.28 events/1000 person-years [aHR 1.21, 95% CI 1.08-1.37]) and naproxen was associated with a decreased event rate (22.66 events/1000 person-years [aHR 0.88, 95% CI 0.79-0.99]). Among new users, the results were similar except risk among naproxen users was no longer different than non-users. CONCLUSIONS: We found an increased risk of cardiovascular events among all and new current users of rofecoxib, valdecoxib, and indomethacin in patients with no history of CVD. Among patients with CVD, all and new current rofecoxib use was associated with an increased risk of a cardiovascular event.
机译:目的:确定某些非甾体抗炎药(NSAIDs)是否与心血管事件的风险增加有关:冠心病(CHD)的急性心肌梗死(AMI),中风和死亡。方法:我们在1999年1月1日至2005年12月3日期间,进行了田纳西医疗报告的田纳西州注册登记册。符合条件的人是非制度化的,持续入学,并且在队列中没有严重疾病。研究了Celecoxib,Rofecoxib,Valdecoxib,布洛芬,萘普生,双氯芬和吲哚美辛。结果为AMI,中风或死亡的住院治疗,在没有心血管疾病(CVD)的那些中的CHD中。报告调整后的危险比(AHR)和95%置信区间(95%CI)。结果:最终队列中有610 001人,14%有CVD的基线历史。在没有CVD的那些(n = 525 249)中,有1 566 678人的后续行动和12个事件。在本集团中,非用户有7.90个事件/ 1000人年。事件/ 1000人 - 年为10.41,用于电流使用Celecoxib(AHR 1.00,95%CI 0.89-1.13),10.91用于ROFecoxib(AHR 1.21,95%CI 1.07-1.37),12.46 for Valdecoxib(AHR 1.30 95%CI 1.04与非用户相比,Indomethacin(AHR 1.36,95%CI 1.11-1.66),13.25。在过去历史的患者中,CVD(n = 84 752),有397 977人的后续时间和10个248个活动。非用户有28.30个活动/ 1000人 - 年。在CVD的那些中,ROFecoxib使用与增加的事件率相关联(30.28次事件/ 1000人 - 年[AHR 1.21,95%CI 1.08-1.37])和萘普森与活动率下降有关(22.66个事件/ 1000人 - 年[AHR 0.88,95%CI 0.79-0.99])。在新用户中,结果类似于萘普生用户之间的风险与非用户不再不同。结论:在没有CVD历史的患者中,我们发现所有和新的rofecoxib,valdecoxib和吲哚美辛的心血管事件的风险增加。在CVD的患者中,所有和新的目前的ROFecoxib使用与心血管事件的风险增加有关。

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