BIFAP Research Unit, Division of Pharmacoepidemiology and Pharmacovigilance, Spanish Agency for Medicines and Medical Devices, Madrid, Spain.
Eur J Clin Pharmacol. 2013 Mar;69(3):691-701. doi: 10.1007/s00228-012-1386-3. Epub 2012 Sep 6.
To test the ability a new Spanish primary care research database (BIFAP) to capture the association between upper gastrointestinal bleeding (UGIB) and NSAIDs and other drugs and compare the results with previous studies.
We performed a nested case-control study in persons aged 40-90 years old included in the period 2001-2005. Potential cases were selected through a computer search followed by an individual blinded review. Controls matched for age, sex and calendar year were randomly selected. The exposure window was defined as 0-30 days before the index date. Adjusted odds ratios were obtained through unconditional logistic regression models.
In a study cohort of 669,115 subjects (1,576,442 person-years) we retrieved 1,193 valid incident cases. Increased risks were found with current use of NSAIDs (RR = 1.72; 95 %CI: 1.41-2.09), metamizole (1.52; 1.09-2.13), low-dose aspirin (1.74; 1.37-2.21), other antiplatelet drugs (1.73; 1.27-2.36), and oral anticoagulants (2.00; 1.44-2.77). We did not find an increased risk with current use of oral corticosteroids (1.11; 0.66-1.86), SSRIs (1.05; 0.77-1.42), or paracetamol (1.00; 0.82-1.23). Acid-suppressing drugs reduced the risk among users of NSAIDs (0.58; 0.39-0.85), particularly in users with antecedents of peptic ulcer (0.16; 0.05-0.58). We detected a decreasing time-trend in the relative risk and the population attributable proportion associated with NSAIDs over the study period.
The increased risk of UGIB associated with NSAIDs was lower than previously reported, which could partly be explained by methodological differences, but a decreasing burden over time of this drug safety problem is suggested. BIFAP has shown to be a valuable tool for pharmacoepidemiological research.
检验新的西班牙初级保健研究数据库(BIFAP)捕捉上消化道出血(UGIB)与 NSAIDs 和其他药物之间关联的能力,并与既往研究进行比较。
我们在 2001-2005 年期间纳入年龄 40-90 岁的人群中进行了一项嵌套病例对照研究。通过计算机检索选择潜在病例,然后进行个体盲法审查。按照年龄、性别和日历年份匹配随机选择对照。暴露窗口定义为索引日期前 0-30 天。通过非条件逻辑回归模型获得调整后的比值比。
在一项包含 669115 名受试者(1576442 人年)的研究队列中,我们检索到 1193 例有效首发病例。当前使用 NSAIDs(RR=1.72;95%CI:1.41-2.09)、甲灭酸(1.52;1.09-2.13)、小剂量阿司匹林(1.74;1.37-2.21)、其他抗血小板药物(1.73;1.27-2.36)和口服抗凝剂(2.00;1.44-2.77)与风险增加相关。我们未发现当前使用口服皮质类固醇(1.11;0.66-1.86)、SSRIs(1.05;0.77-1.42)或扑热息痛(1.00;0.82-1.23)与风险增加相关。抑酸药物降低了 NSAIDs 使用者的风险(0.58;0.39-0.85),特别是在有消化性溃疡病史的患者中(0.16;0.05-0.58)。我们发现,在研究期间,与 NSAIDs 相关的 UGIB 的相对风险和人群归因比例呈下降趋势。
与 NSAIDs 相关的 UGIB 风险增加低于既往报道,这部分可以用方法学差异来解释,但提示该药物安全性问题的负担呈时间递减趋势。BIFAP 已被证明是药物流行病学研究的一种有价值的工具。