Statistical methods for assessing drug interactions using observational data

被引:1
|
作者
Xu, Qian [1 ,2 ]
Antimisiaris, Demetra [3 ]
Kong, Maiying [1 ]
机构
[1] Univ Louisville, Sch Publ Hlth & Informat Sci, Dept Bioinformat & Biostat, Louisville, KY 40202 USA
[2] Fosun Pharma, Div Biometr & Data Sci, Beijing, Peoples R China
[3] Univ Louisville, Sch Publ Hlth & Informat Sci, Dept Hlth Management & Syst Sci, Louisville, KY 40202 USA
关键词
Drug interaction; generalized propensity score; marginal structural models; multinomial logistic regression; PROPENSITY SCORE; CAUSAL INFERENCE; VARIABLE SELECTION; COMORBIDITIES; DESIGN; MODELS; INDEX;
D O I
10.1080/02664763.2022.2123460
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
With advances in medicine, many drugs and treatments become available. On the one hand, polydrug use (i.e. using more than one drug at a time) has been used to treat patients with multiple morbid conditions, and polydrug use may cause severe side effects. On the other hand, combination treatments have been successfully developed to treat severe diseases such as cancer and chronic diseases. Observational data, such as electronic health record data, may provide useful information for assessing drug interactions. In this article, we propose using marginal structural models to assess the average treatment effect and causal interaction of two drugs by controlling confounding variables. The causal effect and the interaction of two drugs are assessed using the weighted likelihood approach, with weights being the inverse probability of the treatment assigned. Simulation studies were conducted to examine the performance of the proposed method, which showed that the proposed method was able to estimate the causal parameters consistently. Case studies were conducted to examine the joint effect of metformin and glyburide use on reducing the hospital readmission for type 2 diabetic patients, and to examine the joint effect of antecedent statins and opioids use on the immune and inflammatory biomarkers for COVID-19 hospitalized patients.
引用
收藏
页码:298 / 323
页数:26
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