Wang Jin, Chi Chih-Lin, St Peter Wendy L, Carlson Angie, Loth Matt, Pradhan Prajwal Mani, Liang Yue, Chen Wei-Yu, Lenskaia Tatiana, Robinson Jennifer G, Adam Terrence J
Institute for Health Informatics, University of Minnesota, Minneapolis, MN, USA.
OptumLabs Visiting Fellow, Cambridge, MA, USA.
AMIA Jt Summits Transl Sci Proc. 2020 May 30;2020:664-673. eCollection 2020.
Simvastatin is a commonly used medication for lipid management and cardiovascular disease, however, the risk of adverse events (AEs) with its use increases via drug-drug interaction (DDI) exposures. Patients were extracted if initially diagnosed with cardiovascular disease and newly initiated simvastatin therapy. The cohort was divided into a DDI-exposed group and a non-DDI exposed group. The DDI-exposed group was further divided into gemfibrozil, clarithromycin, and erythromycin exposure groups. The outcome was defined as a composite of predefined AEs. Our results show that the simvastatin-DDI group had a higher illness burden with longer simvastatin exposure time and more medical care follow-up compared with the simvastatin-non-DDI exposed group. AEs occurred more frequently in subjects exposed to interacting drugs with a higher risk for clarithromycin and erythromycin exposed subjects than for gemfibrozil subjects.
辛伐他汀是一种常用于血脂管理和心血管疾病治疗的药物,然而,其使用过程中因药物相互作用(DDI)暴露而导致不良事件(AE)的风险会增加。纳入最初诊断为心血管疾病并新开始辛伐他汀治疗的患者。该队列被分为DDI暴露组和非DDI暴露组。DDI暴露组进一步分为吉非贝齐、克拉霉素和红霉素暴露组。结局定义为预定义不良事件的综合指标。我们的结果表明,与非DDI暴露的辛伐他汀组相比,辛伐他汀-DDI组的疾病负担更高,辛伐他汀暴露时间更长,医疗随访更多。与吉非贝齐组相比,暴露于相互作用药物的受试者中不良事件更频繁发生,克拉霉素和红霉素暴露受试者的风险更高。