首页> 外文期刊>International Journal of Population Data Science >Data-driven drug safety signal detection methods in pharmacovigilance using electronic primary care records: A population based study
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Data-driven drug safety signal detection methods in pharmacovigilance using electronic primary care records: A population based study

机译:电子基层医疗记录的药物警戒中数据驱动的药物安全信号检测方法:一项基于人群的研究

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ABSTRACT ObjectivesThough an effective drug to treat heart failure and heart rhythm abnormalities, digoxin has side effects, such as confusion. Adverse drug events (ADEs) are major public health issues, but signal detection of ADEs is challenging for healthcare professionals. The objectives of this study is to evaluate if data-driven techniques can be used to detect ADEs, specifically examine the best method to detect the known event of confusion in patients prescribed digoxin from electronic primary care records and generate evidence for unknown ADEs. ApproachIn this study, we analysed 195,454 patients from a general practitioner (GP) database Wales, UK held in the SAIL (Secured Anonymised Information Linkage) databank with 51,920 patients prescribed digoxin and the rest acted as controls. All diagnostic events within 1 year after taking digoxin were considered. We used different data-driven analytic techniques - the proportional reporting ratio (PRR), the reporting odds ratio (ROR), the information component (IC), and the Yule’s Q (YULE) to detect signal of a statistical association between digoxin and associated adverse events. ResultsThe YULE detected the highest number of 544 signals, the IC the lowest number of 117 signals, and they commonly identified 83 same signals. All ROR based signals were included in the YULE based signals. It detected that 8.09 people per 10,000 who took digoxin suffered from the side effect of confusion including acute confusional state of cerebrovascular origin and others. All 4 methods can detect the confusion event with the values of IC =5.35 (standard deviation =0.312), PRR=1407.2 (95% confidence interval=[993.72, 1992.71]), ROR== 2813.39 (95% confidence interval=[1692.443, 4676.776]), and YULE=0.99 (95% confidence interval=[0.9992892, , 0.9992895]) respectively. Also some unknown signals, such as “carcinoma in situ of rectum”, were identified by the 4 methods. One common signal detected which was not clearly mentioned in clinical guideline is “digoxin poisoning” with the values of IC =1.87 (standard deviation =0.0946), PRR=214.71 (95% confidence interval=[68.75, 670.56]), ROR=215.67(95% confidence interval=[69.05, 673.63]), and YULE=0.99 (95% confidence interval=[0.9907,0.9908]) respectively. This finding is consistent with the previous study that digoxin can sometimes have toxic effects, particularly at high blood concentrations, because it normally takes a long time to be broken down by the body. ConclusionData-driven analytic methods are a valuable aid to signal detection of ADEs from large electronic health records for drug safety monitoring. This study finds the methods can detect known ADE and so could potentially be used to detect unknown ADE.
机译:摘要目的尽管地高辛是治疗心力衰竭和心律异常的有效药物,但它具有副作用,例如精神错乱。不良药物事件(ADEs)是主要的公共卫生问题,但对ADEs的信号检测对于医疗保健专业人员而言是一项挑战。这项研究的目的是评估是否可以使用数据驱动技术来检测ADE,特别是检查从电子基层医疗记录开出地高辛的患者中检测已知混淆事件的最佳方法,并生成未知ADE的证据。方法在本研究中,我们分析了SAIL(安全匿名信息链接)数据库中来自英国威尔士的全科医生(GP)数据库中的195,454位患者,其中有51,920位处方了地高辛的患者,其余患者作为对照。考虑服用地高辛后1年内的所有诊断事件。我们使用了不同的数据驱动分析技术-比例报告率(PRR),报告比值比(ROR),信息成分(IC)和Yule's Q(YULE)来检测地高辛与相关药物之间的统计关联信号不良事件。结果YULE检测到544个信号的最高数量,IC检测到117个信号的最低数量,他们通常识别出83个相同的信号。所有基于ROR的信号都包含在基于YULE的信号中。它检测到每10,000名服用地高辛的人中有8.09人患有混淆的副作用,包括脑血管来源的急性混淆状态等。这4种方法均可检测到IC = 5.35(标准偏差= 0.312),PRR = 1407.2(95%置信区间= [993.72,1992.71]),ROR == 2813.39(95%置信区间= [1692.443] ,4676.776])和YULE = 0.99(95%置信区间= [0.9992892,,0.9992895])。通过这4种方法还可以识别出一些未知信号,例如“直肠原位癌”。临床指南中未明确提及的一种常见信号是“地高辛中毒”,IC值为1.87(标准差= 0.0946),PRR = 214.71(95%置信区间= [68.75,670.56]),ROR = 215.67 (95%置信区间= [0.9907,0.9908])(95%置信区间= [69.05,673.63])和YULE = 0.99。这一发现与以前的研究一致,即地高辛有时会产生毒性作用,特别是在高血药浓度下,因为地高辛通常需要很长时间才能被人体分解。结论数据驱动的分析方法为从大型电子健康记录进行ADEs信号检测提供了宝贵的帮助,可用于药物安全性监测。这项研究发现这些方法可以检测已知的ADE,因此有可能被用于检测未知的ADE。

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