Ashworth Nigel L, Peloso Paul M, Muhajarine Nazeem, Stang Maryrose
Division of Physical Medicine and Rehabilitation, University of Alberta, Edmonton, Alberta, Canada.
J Rheumatol. 2004 May;31(5):951-6.
To identify the unbiased differences in all cause mortality among populations using 4 non-steroidal antiinflammatory drugs (NSAID): nabumetone, Arthrotec, diclofenac plus a cytoprotective agent dispensed separately (diclofenac+), and naproxen.
We performed a population based historical cohort study using linked data from several provincial health care databases. Logistic regression was used to produce estimates of the mortality associated with the study drugs unbiased by known confounders. The entire population of the province of Saskatchewan, Canada entitled to drug plan benefits in 1995 was eligible (approximately 91% of 1 million people). Participants were identified if they filled a prescription for one of the 4 study NSAID (18,424 individuals). They were then followed forward in time for 6 months to determine all cause mortality.
Compared to nabumetone, the adjusted odds of death for participants taking Arthrotec was 1.4 (95% confidence interval, CI: 0.9-2.1), for diclofenac+ 2.0 (1.3-3.1), and naproxen 3.0 (1.9-4.6).
The multivariate analysis showed patients taking nabumetone and Arthrotec had significantly lower mortality than those taking other study drugs. Nabumetone had 1/3 to 1/5 the mortality associated with the diclofenac+ and naproxen groups. It appears that inherent gastroprotective strategies in the study NSAID may translate into decreased mortality at the population level.
确定使用4种非甾体抗炎药(NSAID)的人群在全因死亡率方面的无偏差异,这4种药物分别为:萘丁美酮、阿西美辛、双氯芬酸加单独配发的细胞保护剂(双氯芬酸+)和萘普生。
我们利用来自几个省级医疗保健数据库的关联数据进行了一项基于人群的历史性队列研究。采用逻辑回归来估算与研究药物相关的死亡率,该死亡率不受已知混杂因素的影响。加拿大萨斯喀彻温省1995年有权享受药物计划福利的全体人口符合条件(约100万人中的91%)。如果参与者开具了4种研究用NSAID之一的处方,则被确定为研究对象(18424人)。然后对他们进行为期6个月的随访,以确定全因死亡率。
与萘丁美酮相比,服用阿西美辛的参与者调整后的死亡 odds 比为1.4(95%置信区间,CI:0.9 - 2.1),服用双氯芬酸+的为2.0(1.3 - 3.1),服用萘普生的为3.0(1.9 - 4.6)。
多变量分析显示,服用萘丁美酮和阿西美辛的患者死亡率显著低于服用其他研究药物的患者。萘丁美酮的死亡率是双氯芬酸+组和萘普生组的1/3至1/5。研究中的NSAID所固有的胃保护策略似乎可转化为人群水平上死亡率的降低。