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:非阿司匹林非甾体抗炎药,环加氧酶2抑制剂和心血管事件中风,急性心肌梗塞和冠心病死亡的风险。

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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(NSAID)是否与心血管事件风险增加相关:急性心肌梗塞(AMI),中风和冠心病死亡(CHD)。方法:我们对1999年1月1日至2005年12月31日之间年龄在35-94岁之间的田纳西州医疗补助登记者进行了一项回顾性队列研究。符合条件的人没有入狱,连续入组,并且在入组前没有严重疾病。研究了塞来昔布,罗非昔布,伐地昔布,布洛芬,萘普生,双氯芬酸和消炎痛的暴露情况。结果是有和没有心血管病(CVD)史的患者因AMI,中风或CHD死亡而住院治疗。报告了调整后的危险比(aHR)和95%置信区间(95%CI)。结果:最终队列中有610 001人,有14%的人有CVD的基线病史。在没有CVD的患者(N = 525 249)中,有1 566 678人年的随访和12 184例事件。在该组中,非用户有7.90事件/ 1000人年。当前塞来昔布的使用事件/ 1000人年为10.41(aHR 1.00,95%CI 0.89-1.13),rofecoxib(aHR 1.21,95%CI 1.07-1.37)为10.91,valdecoxib(aHR 1.30 95%CI 1.04)为12.46 -1.61)和消炎痛的13.25(aHR 1.36,95%CI 1.11-1.66)。在有CVD既往史的患者(N = 84 752)中,有397 977人年的随访和10 248事件。非用户每1000人年有28.30个事件。在患有CVD的患者中,使用罗非昔布与事件发生率增加(30.28事件/ 1000人年[aHR 1.21,95%CI 1.08-1.37])相关,而萘普生与事件发生率降低有关(22.66事件/ 1000人年[aHR 0.88,95%CI 0.79-0.99]。在新用户中,结果相似,除了萘普生用户之间的风险不再与非用户不同。结论:我们发现在没有CVD史的罗非考昔,伐地昔布和消炎痛的所有和新使用者中,发生心血管事件的风险增加。在患有CVD的患者中,目前使用所有罗非昔布和新的罗非考昔都会增加心血管事件的风险。

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