Norén G Niklas, Sundberg Rolf, Bate Andrew, Edwards I Ralph
WHO Collaborating Centre for International Drug Monitoring in Uppsala, Uppsala, Sweden.
Stat Med. 2008 Jul 20;27(16):3057-70. doi: 10.1002/sim.3247.
Interaction between drug substances may yield excessive risk of adverse drug reactions (ADRs) when two drugs are taken in combination. Collections of individual case safety reports (ICSRs) related to suspected ADR incidents in clinical practice have proven to be very useful in post-marketing surveillance for pairwise drug--ADR associations, but have yet to reach their full potential for drug-drug interaction surveillance. In this paper, we implement and evaluate a shrinkage observed-to-expected ratio for exploratory analysis of suspected drug-drug interaction in ICSR data, based on comparison with an additive risk model. We argue that the limited success of previously proposed methods for drug-drug interaction detection based on ICSR data may be due to an underlying assumption that the absence of interaction is equivalent to having multiplicative risk factors. We provide empirical examples of established drug-drug interaction highlighted with our proposed approach that go undetected with logistic regression. A database wide screen for suspected drug-drug interaction in the entire WHO database is carried out to demonstrate the feasibility of the proposed approach. As always in the analysis of ICSRs, the clinical validity of hypotheses raised with the proposed method must be further reviewed and evaluated by subject matter experts.
当两种药物联合使用时,药物之间的相互作用可能会产生过高的药物不良反应(ADR)风险。在临床实践中,与疑似ADR事件相关的个体病例安全报告(ICSR)集合已被证明在上市后监测药物与ADR的两两关联方面非常有用,但在药物相互作用监测方面尚未充分发挥其潜力。在本文中,我们基于与相加风险模型的比较,实施并评估了一种收缩观察与预期比值,用于对ICSR数据中疑似药物相互作用进行探索性分析。我们认为,先前基于ICSR数据提出的药物相互作用检测方法取得的有限成功,可能是由于一个潜在假设,即不存在相互作用等同于具有相乘风险因素。我们提供了用我们提出的方法突出显示的已确定药物相互作用的实证例子,而这些相互作用用逻辑回归无法检测到。在整个世界卫生组织数据库中对疑似药物相互作用进行全数据库筛查,以证明所提出方法的可行性。与ICSR分析中一贯的情况一样,所提出方法提出的假设的临床有效性必须由主题专家进一步审查和评估。