Development of a System for Postmarketing Population Pharmacokinetic and Pharmacodynamic Studies Using Real-World Data From Electronic Health Records

被引:23
|
作者
Choi, Leena [1 ]
Beck, Cole [1 ]
McNeer, Elizabeth [1 ]
Weeks, Hannah L. [1 ]
Williams, Michael L. [1 ]
James, Nathan T. [1 ]
Niu, Xinnan [2 ]
Abou-Khalil, Bassel W. [3 ]
Birdwell, Kelly A. [4 ]
Roden, Dan M. [2 ,4 ,5 ]
Stein, C. Michael [4 ,5 ]
Bejan, Cosmin A. [2 ]
Denny, Joshua C. [2 ,4 ]
Van Driest, Sara L. [4 ,6 ]
机构
[1] Vanderbilt Univ, Med Ctr, Dept Biostat, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Med Ctr, Dept Biomed Informat, Nashville, TN USA
[3] Vanderbilt Univ, Dept Neurol, Med Ctr, Nashville, TN USA
[4] Vanderbilt Univ, Med Ctr, Dept Med, Nashville, TN USA
[5] Vanderbilt Univ, Med Ctr, Dept Pharmacol, Nashville, TN 37232 USA
[6] Vanderbilt Univ, Med Ctr, Dept Pediat, Nashville, TN 37232 USA
基金
美国国家卫生研究院;
关键词
PHARMACOLOGY; EXTRACTION; SAMPLES;
D O I
10.1002/cpt.1787
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Postmarketing population pharmacokinetic (PK) and pharmacodynamic (PD) studies can be useful to capture patient characteristics affecting PK or PD in real-world settings. These studies require longitudinally measured dose, outcomes, and covariates in large numbers of patients; however, prospective data collection is cost-prohibitive. Electronic health records (EHRs) can be an excellent source for such data, but there are challenges, including accurate ascertainment of drug dose. We developed a standardized system to prepare datasets from EHRs for population PK/PD studies. Our system handles a variety of tasks involving data extraction from clinical text using a natural language processing algorithm, data processing, and data building. Applying this system, we performed a fentanyl population PK analysis, resulting in comparable parameter estimates to a prior study. This new system makes the EHR data extraction and preparation process more efficient and accurate and provides a powerful tool to facilitate postmarketing population PK/PD studies using information available in EHRs.
引用
收藏
页码:934 / 943
页数:10
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