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利用常规电子病历检测儿童药物性血小板减少症信号

Detection of Drug-Induced Thrombocytopenia Signals in Children Using Routine Electronic Medical Records.

作者信息

Nie Xiaolu, Jia Lulu, Peng Xiaoxia, Zhao Houyu, Yu Yuncui, Chen Zhenping, Zhang Liqiang, Cheng Xiaoling, Lyu Yaqi, Cao Wang, Wang Xiaoling, Ni Xin, Zhan Siyan

机构信息

Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, China.

Center for Clinical Epidemiology and Evidence-based Medicine, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

出版信息

Front Pharmacol. 2021 Nov 12;12:756207. doi: 10.3389/fphar.2021.756207. eCollection 2021.

Abstract

Drug-induced thrombocytopenia (DITP) is a severe adverse reaction and a significantly under-recognized clinical problem in children. However, for post-marketing pharmacovigilance purposes, detection of DITP signals is crucial. This study aimed to develop a signal detection model for DITP using the pediatric electronic medical records (EMR) data. This study used the electronic medical records collected at Beijing Children's Hospital between 2009 and 2020. A two-stage modeling method was developed to detect the signal of DITP. In the first stage, we calculated the crude incidence by mining cases of thrombocytopenia to select the potential suspected drugs. In the second stage, we constructed propensity score-matched retrospective cohorts of specific screened drugs from the first stage and estimated the odds ratio (OR) and 95% confidence interval (CI) using conditional logistic regression models. The novelty of the signal was assessed by current evidence. In the study, from a total of 839 drugs, 21 drugs were initially screened as potentially inducing thrombocytopenia. In total, we identified 18 positive DITP associations. Of these, potential DITP risk of nystatin (OR: 1.75, 95% CI: 1.37-2.22) and latamoxef sodium (OR: 1.61, 95% CI: 1.38-1.88) were two new DITP signals in both children and adults. Six associations between thrombocytopenia and drugs including imipenem (OR: 1.69, 95% CI: 1.16-2.45), teicoplanin (OR: 4.75, 95% CI: 3.33-6.78), fusidic acid (OR: 2.81, 95% CI: 2.06-3.86), ceftizoxime sodium (OR: 1.83, 95% CI: 1.36-2.45), ceftazidime (OR: 2.16, 95% CI: 1.58-2.95), and cefepime (OR: 5.06, 95% CI: 3.77-6.78) were considered as new signals in children. This study developed a two-stage algorithm to detect safety signals of DITP and found eighteen positive signals of DITP, including six new signals in a pediatric population. This method is a promising tool for pharmacovigilance based on EMR data.

摘要

药物性血小板减少症(DITP)是一种严重的不良反应,在儿童中是一个未得到充分认识的临床问题。然而,对于上市后药物警戒而言,检测DITP信号至关重要。本研究旨在利用儿科电子病历(EMR)数据开发一种DITP信号检测模型。本研究使用了2009年至2020年在北京儿童医院收集的电子病历。开发了一种两阶段建模方法来检测DITP信号。在第一阶段,我们通过挖掘血小板减少症病例来计算粗发病率,以选择潜在的可疑药物。在第二阶段,我们从第一阶段构建特定筛选药物的倾向评分匹配回顾性队列,并使用条件逻辑回归模型估计比值比(OR)和95%置信区间(CI)。通过现有证据评估信号的新颖性。在该研究中,从总共839种药物中,最初筛选出21种药物可能诱发血小板减少症。我们总共确定了18个DITP阳性关联。其中,制霉菌素(OR:1.75,95%CI:1.37 - 2.22)和拉氧头孢钠(OR:1.61,95%CI:1.38 - 1.88)的潜在DITP风险在儿童和成人中均为两个新的DITP信号。血小板减少症与包括亚胺培南(OR:1.69,95%CI:1.16 - 2.45)、替考拉宁(OR:4.75,95%CI:3.33 - 6.78)、夫西地酸(OR:2.81,95%CI:2.06 - 3.86)、头孢唑肟钠(OR:1.83,95%CI:1.36 - 2.45)、头孢他啶(OR:2.16,95%CI:1.58 - 2.95)和头孢吡肟(OR:5.06,95%CI:3.77 - 6.78)在内的药物之间的六个关联被视为儿童中的新信号。本研究开发了一种两阶段算法来检测DITP的安全信号,并发现了18个DITP阳性信号,包括儿科人群中的六个新信号。该方法是基于EMR数据进行药物警戒的一种有前景的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b939/8633439/bd2c72917e8d/fphar-12-756207-g001.jpg

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