Centre for Rheumatology Research, Landspitali University Hospital, Reykjavik, Iceland.
Eur J Clin Pharmacol. 2010 Jun;66(6):619-25. doi: 10.1007/s00228-010-0789-2. Epub 2010 Feb 16.
To examine the risk of thromboembolic cardiovascular events in users of coxibs and NSAIDs in a nationwide cohort.
Data were synchronised from three nationwide databases, the Icelandic Medicines Registry (IMR), The Icelandic National Patient Registry (INPR) and the Registry for Causes of Death at Statistics Iceland (RCD), for prescriptions for NSAIDs or coxibs with respect to hospitalisation for unstable angina pectoris, myocardial infarction and cerebral infarction over a 3-year period. The Cox proportional hazards model and Poisson regression were used to analyse the data.
A total of 108,700 individuals received prescriptions for NSAIDs or coxibs (ATC code M01A), of whom 78,539 received one drug only (163,406 person-years). Among those receiving only one drug 426 individuals were discharged from hospital with endpoint diagnoses. In comparison to diclofenac, the incidence ratios, adjusted for age and gender, were significantly higher for cerebral infarction (2.13; 95% CI 1.54-2.97; P < 0.001), for myocardial infarction (1.77; 95% CI 1.34-2.32; P < 0.001) and for unstable angina pectoris (1.52; 95% CI 1.01-2.30; P = 0.047) for patients who used rofecoxib. For naproxen users, the incidence ratio was 1.46 for myocardial infarction (95% CI 1.03-2.07; P = 0.03), but was reduced in ibuprofen users (0.63; 95% CI 0.40-1.00; P = 0.05). The youngest users of rofecoxib (< or =39 years) had the highest hazard ratio (HR) for cardiovascular events (8.34; P < 0.001), while those > or =60 years had a lower but still significantly elevated HR (1.35; P = 0.001).
This Icelandic nationwide registry-based study amounting to 163,406 patient-years showed increased risk of cardiovascular events, i.e. cerebral infarction, myocardial infarction and unstable angina pectoris, among rofecoxib and naproxen users in comparison to diclofenac users. The added risk was most pronounced in young adults using rofecoxib.
在一个全国性队列中,研究 COXIB 和 NSAIDs 使用者发生血栓栓塞性心血管事件的风险。
从冰岛药品登记处(IMR)、冰岛国家患者登记处(INPR)和冰岛死因登记处(RCD)这三个全国性数据库中同步数据,观察 3 年内 COXIB 和 NSAIDs 处方与不稳定型心绞痛、心肌梗死和脑梗死住院之间的关系。采用 Cox 比例风险模型和泊松回归分析数据。
共 108700 人接受 NSAIDs 或 COXIB(ATC 代码 M01A)治疗,其中 78539 人仅接受一种药物治疗(163406 人年)。在仅接受一种药物治疗的人群中,有 426 人因终点诊断出院。与双氯芬酸相比,罗非昔布使用者脑梗死(2.13;95%CI 1.54-2.97;P<0.001)、心肌梗死(1.77;95%CI 1.34-2.32;P<0.001)和不稳定型心绞痛(1.52;95%CI 1.01-2.30;P=0.047)的发病率比值校正年龄和性别后明显更高。对于萘普生使用者,心肌梗死的发病率比值为 1.46(95%CI 1.03-2.07;P=0.03),但布洛芬使用者的发病率比值降低(0.63;95%CI 0.40-1.00;P=0.05)。年龄最小的罗非昔布使用者(<39 岁)心血管事件的危险比(HR)最高(8.34;P<0.001),而年龄较大的患者(>60 岁)的 HR 虽有所降低,但仍显著升高(1.35;P=0.001)。
这项基于冰岛全国性登记处的研究共纳入 163406 人年,结果显示与双氯芬酸使用者相比,罗非昔布和萘普生使用者发生心血管事件(即脑梗死、心肌梗死和不稳定型心绞痛)的风险增加。在使用罗非昔布的年轻成年人中,这种风险增加最为显著。