Challenges in detecting and predicting adverse drug events via distributed analysis of electronic health record data from German university hospitals.

IF 7.7
PLOS digital health Pub Date : 2025-06-26 eCollection Date: 2025-06-01 DOI:10.1371/journal.pdig.0000892
Anna Maria Wermund, Torsten Thalheim, André Medek, Florian Schmidt, Thomas Peschel, Alexander Strübing, Daniel Neumann, André Scherag, Markus Loeffler, Miriam Kesselmeier, Ulrich Jaehde
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Abstract

The Medical Informatics Initiative Germany (MII) aims to facilitate the interoperability and exchange of electronic health record data from all German university hospitals. The MII use case "POLyphamacy, drug interActions and Risks" (POLAR_MI) was designed to retrospectively detect medication-related risks in adult inpatients. As part of POLAR_MI, we aimed to build predictive models for specific adverse events. Here, using the two adverse events gastrointestinal bleeding and drug-related hypoglycaemia as examples, we present our initial investigation to determine whether these adverse events and their associations with potential risk factors can be detected. We applied a two-step distributed analysis approach to electronic health record data from 2018 to 2021. This approach consisted of a local statistical data analysis at ten participating centres, followed by a mixed-effects meta-analysis. For each adverse event, two multivariable logistic regression models were constructed: (1) including only demographics, diagnoses and medications, and (2) extended by laboratory values. As numerically stable estimations of both models were not possible at each centre, we constructed different centre subgroups for meta-analyses. We received prevalence estimates of around 1.2% for GI bleeding and around 3.0% for drug-related hypoglycaemia. Although unavailability of laboratory values was a common reason hindering model estimation, multivariable regression models were obtained for both adverse events from several centres. Regarding our original intention to build predictive models, the median area under the receiver operating characteristic curve was above 0.70 for all multivariable regression models, indicating feasibility. In conclusion, plausible estimates for prevalence and regression modelling odds ratios were received when using a distributed analysis approach on inpatient treatment data from diverse German university hospitals. Our results suggest that the development of predictive models in a distributed setting is possible if the research question is adapted to the infrastructure and the available data.

通过对德国大学医院电子健康记录数据的分布式分析来检测和预测药物不良事件的挑战。
德国医学信息学倡议(MII)旨在促进来自德国所有大学医院的电子健康记录数据的互操作性和交换。MII用例“多药、药物相互作用和风险”(POLAR_MI)旨在回顾性检测成年住院患者的药物相关风险。作为POLAR_MI的一部分,我们旨在建立特定不良事件的预测模型。在这里,以胃肠道出血和药物相关性低血糖这两种不良事件为例,我们提出了我们的初步调查,以确定这些不良事件及其与潜在危险因素的关联是否可以被检测到。我们对2018年至2021年的电子健康记录数据采用了两步分布式分析方法。该方法包括对10个参与研究的中心进行本地统计数据分析,然后进行混合效应荟萃分析。对于每个不良事件,构建了两个多变量logistic回归模型:(1)仅包括人口统计学,诊断和药物;(2)扩展到实验室值。由于不可能在每个中心对两个模型进行数值稳定估计,我们构建了不同的中心亚组进行meta分析。我们得到的患病率估计为胃肠道出血约为1.2%,药物相关性低血糖约为3.0%。虽然无法获得实验室数据是阻碍模型估计的常见原因,但从几个中心获得了两种不良事件的多变量回归模型。对于我们建立预测模型的初衷,所有多变量回归模型的受试者工作特征曲线下的中位数面积都在0.70以上,说明了可行性。总之,当使用分布式分析方法对来自不同德国大学医院的住院患者治疗数据进行分析时,得到了患病率和回归模型比值比的合理估计。我们的研究结果表明,如果研究问题适应基础设施和可用数据,在分布式设置中开发预测模型是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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