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C-C5-01: Drug Safety Data Mining with a Tree-Based Scan Statistic

机译:C-C5-01:具有基于树的扫描统计信息的药物安全性数据挖掘

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Background/AimsActive post-marketing drug safety surveillance has traditionally focused on predefined drug-adverse event (AE) pairs. However, evaluating predefined pairs does not illuminate unsuspected potential AEs. Drug safety data mining is a surveillance approach that formally evaluates the relationship between medications and a very large number of AEs. We used varying specifications of the tree-based scan statistic data mining method (TreeScan) to search for adverse events among clozapine drug users. MethodsElectronic health records from three HMO Research Network health plans were assessed. We used TreeScan to evaluate a hierarchical clinical classification to identify signals of excess risk during prevalent drug exposure as compared to unexposed time. The test statistic - a Poisson based log likelihood ratio - is adjusted for multiple testing inherent in the many potential AEs evaluated. Four alternate specifications were incorporated: ramp-up periods of 180 and 400 days and outcome definitions using inpatient plus outpatient diagnoses and inpatient diagnoses only. For each drug and specification, we calculated expected and observed counts for each level of the hierarchical tree, adjusting for age, sex, and health plan. ResultsWe identified 242,000 to 580,000 exposed clozapine days and 150 to 345 exposed outcomes across the different specifications. Both ramp-up periods found 17 unique statistical signals using inpatient plus outpatient diagnoses. Of those, several represent confounding by indication (three signals in mental health, two for injury and poisoning) and others are known AEs (e.g., convulsions, hypotension, GI system). Limiting outcomes to the inpatient setting reduced the number of signals to 14 (180-day ramp-up) and 10 (400-day ramp-up). Overall, the inpatient-only AE signals were in the same clinical systems, with some exceptions. The inpatient specification signaled for circulatory events and diseases of the heart, but hypotension was no longer found. Genitourinary AEs signaled using inpatient plus outpatient diagnoses but were not identified using inpatient diagnoses only. ConclusionsData mining using electronic health records is an important complement to other post-marketing drug safety research. Once specifications are finalized, TreeScan will be applied to assess the safety of over 100 oral outpatient medications.
机译:背景/目标积极的售后药品安全监视传统上将重点放在预定义的药品不良事件(AE)对上。但是,评估预定义的对并不会说明未预料到的潜在AE。药物安全数据挖掘是一种监视方法,可以正式评估药物与大量AE之间的关系。我们使用了基于树的扫描统计数据挖掘方法(TreeScan)的各种规范来搜索氯氮平吸毒者中的不良事件。方法评估来自三个HMO Research Network健康计划的电子健康记录。我们使用TreeScan评估了分级的临床分类,以识别与未暴露的时间相比,在普遍的药物暴露期间过度风险的信号。测试统计量-基于Poisson的对数似然比-已针对许多潜在潜在AE进行的固有多次测试进行了调整。纳入了四个替代规范:180天和400天的加速期以及仅使用住院患者加门诊诊断和住院诊断的结果定义。对于每种药物和规格,我们计算了层次树的每个级别的预期和观察到的计数,并根据年龄,性别和健康计划进行了调整。结果我们确定了不同规格的氯氮平暴露天数为242,000至580,000天,暴露结果为150至345天。通过住院和门诊诊断,两个加速期都发现了17个独特的统计信号。在这些中,一些表示通过指示混杂(精神健康中的三个信号,两个关于伤害和中毒的信号),而其他已知的AE(例如惊厥,低血压,胃肠道系统)。将结果限制在住院环境中可以将信号数量减少到14(180天加速)和10(400天加速)。总体而言,仅住院患者的AE信号在相同的临床系统中,但有一些例外。住院规范说明了心脏的循环事件和疾病,但不再发现低血压。泌尿生殖道AEs是通过住院加门诊诊断来发出信号的,但不能仅通过住院诊断来识别。结论使用电子健康记录进行数据挖掘是对其他上市后药物安全性研究的重要补充。一旦确定了规格,TreeScan将用于评估100多种口服门诊药物的安全性。

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