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Machine learning liver-injuring drug interactions with non-steroidal anti-inflammatory drugs (NSAIDs) from a retrospective electronic health record (EHR) cohort

机译:机器学习肝脏损伤药物与非甾体抗炎药物(NSAIDs)的药物相互作用,从回顾性电子健康记录(EHR)队列

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Drug-drug interactions account for up to 30% of adverse drug reactions. Increasing prevalence of electronic health records (EHRs) offers a unique opportunity to build machine learning algorithms to identify drug-drug interactions that drive adverse events. In this study, we investigated hospitalizations’ data to study drug interactions with non-steroidal anti-inflammatory drugs (NSAIDS) that result in drug-induced liver injury (DILI). We propose a logistic regression based machine learning algorithm that unearths several known interactions from an EHR dataset of about 400,000 hospitalization. Our proposed modeling framework is successful in detecting 87.5% of the positive controls, which are defined by drugs known to interact with diclofenac causing an increased risk of DILI, and correctly ranks aggregate risk of DILI for eight commonly prescribed NSAIDs. We found that our modeling framework is particularly successful in inferring associations of drug-drug interactions from relatively small EHR datasets. Furthermore, we have identified a novel and potentially hepatotoxic interaction that might occur during concomitant use of meloxicam and esomeprazole, which are commonly prescribed together to allay NSAID-induced gastrointestinal (GI) bleeding. Empirically, we validate our approach against prior methods for signal detection on EHR datasets, in which our proposed approach outperforms all the compared methods across most metrics, such as area under the receiver operating characteristic curve (AUROC) and area under the precision-recall curve (AUPRC).
机译:药物 - 药物相互作用占多达30%的不良药物反应。增加电子健康记录(EHRS)的流行提供了一个独特的机会,可以建立机器学习算法,以识别驱动不良事件的药物药物相互作用。在这项研究中,我们研究了住院的数据,以研究导致药物诱导的肝损伤(DiRi)的非甾体抗炎药物(NSAID)的药物相互作用。我们提出了一种基于逻辑回归的机器学习算法,可以从ehr数据集中获知几个已知的相互作用,约40万住院。我们所提出的建模框架成功地检测87.5%的阳性对照,这些阳性对照是由已知的药物定义,该药物与双氯芬酸相互作用,导致帝力的风险增加,并正确地排名八个普通规定的NSAID的总体风险。我们发现,我们的建模框架在从相对较小的EHR数据集中推断出药物 - 药物相互作用的关联。此外,我们已经确定了在伴随美洛昔康和eSomeprazole期间可能发生的新颖和潜在的肝毒性相互作用,其通常在一起以与之共同的胃肠道(Gi)出血。经验上,我们验证了我们对EHR数据集上的先前信号检测方法的方法,其中我们所提出的方法优于大多数度量的所有比较方法,例如在精密召回曲线下的接收器操作特征曲线(AUROC)和区域下的区域。 (AUPRC)。

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