Establishing a Validation Framework of Treatment Discontinuation in Claims Data Using Natural Language Processing and Electronic Health Records

IF 5.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY Clinical Pharmacology & Therapeutics Pub Date : 2025-04-08 DOI:10.1002/cpt.3650
Chun-Ting Yang, Kerry Ngan, Dae Hyun Kim, Jie Yang, Jun Liu, Kueiyu Joshua Lin
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Abstract

Measuring medication discontinuation in claims data primarily relies on the gaps between prescription fills, but such definitions are rarely validated. This study aimed to establish a natural language processing (NLP)-based validation framework to evaluate the performance of claims-based discontinuation algorithms for commonly used medications against NLP-based reference standards from electronic health records (EHRs). A total of 36,656 patients receiving antipsychotic medications (APMs), benzodiazepines (BZDs), warfarin, or direct oral anticoagulants (DOACs) were identified from the Mass General Brigham EHRs in 2007–2020. These EHR data were linked with 97,900 Medicare Part D claims. An NLP-aided chart review was applied to determine medication discontinuation from EHR (reference standard). In claims data, discontinuation was defined by having a prescription gap larger than 15–90 days (claims-based algorithms). Sensitivity, specificity, and predictive values of claims-based algorithms against the reference standard were measured. The sensitivity and specificity of 90-day-gap-based algorithms were 0.46 and 0.79 for haloperidol, 0.41 and 0.85 for atypical APMs, 0.47 and 0.75 for BZDs, 0.33 and 0.80 for warfarin, and 0.38 and 0.87 for DOACs, respectively. The corresponding estimates for 15-day-gap-based algorithms were 0.68 and 0.55 for haloperidol, 0.59 and 0.62 for atypical APMs, 0.71 and 0.45 for BZDs, 0.61 and 0.49 for warfarin, and 0.58 and 0.64 for DOACs, respectively. Positive predictive values were primarily affected by medication discontinuation rates and less by gap lengths. The overall accuracy of claims-based discontinuation algorithms differs by medications. This study demonstrates the scalability and utility of the NLP-based validation framework for multiple medications.

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使用自然语言处理和电子健康记录在索赔数据中建立治疗终止的验证框架。
在索赔数据中衡量药物停药主要依赖于处方填充之间的空白,但这样的定义很少得到验证。本研究旨在建立一个基于自然语言处理(NLP)的验证框架,根据电子健康记录(EHRs)中基于NLP的参考标准,评估基于索赔的常用药物停药算法的性能。2007-2020年,共有36,656名接受抗精神病药物(APMs)、苯二氮卓类药物(BZDs)、华法林或直接口服抗凝剂(DOACs)的患者从麻省总医院布莱根电子病历中被确定。这些电子病历数据与97,900份医疗保险D部分索赔有关。应用nlp辅助图表回顾从EHR(参考标准)中确定药物停药。在索赔数据中,停药的定义是处方间隔大于15-90天(基于索赔的算法)。测量了基于索赔的算法相对于参考标准的敏感性、特异性和预测值。基于90天间隙的算法对氟哌啶醇的敏感性和特异性分别为0.46和0.79,对非典型APMs的敏感性和特异性分别为0.41和0.85,对BZDs的敏感性和特异性分别为0.47和0.75,对华法林的敏感性和特异性分别为0.33和0.80,对DOACs的敏感性和特异性分别为0.38和0.87。基于15天间隔的算法的相应估计分别为氟哌啶醇0.68和0.55,非典型APMs 0.59和0.62,BZDs 0.71和0.45,华法林0.61和0.49,DOACs 0.58和0.64。阳性预测值主要受停药率的影响,受间隙长度的影响较小。基于索赔的停药算法的总体准确性因药物而异。本研究证明了基于nlp的多种药物验证框架的可扩展性和实用性。
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来源期刊
CiteScore
12.70
自引率
7.50%
发文量
290
审稿时长
2 months
期刊介绍: Clinical Pharmacology & Therapeutics (CPT) is the authoritative cross-disciplinary journal in experimental and clinical medicine devoted to publishing advances in the nature, action, efficacy, and evaluation of therapeutics. CPT welcomes original Articles in the emerging areas of translational, predictive and personalized medicine; new therapeutic modalities including gene and cell therapies; pharmacogenomics, proteomics and metabolomics; bioinformation and applied systems biology complementing areas of pharmacokinetics and pharmacodynamics, human investigation and clinical trials, pharmacovigilence, pharmacoepidemiology, pharmacometrics, and population pharmacology.
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