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首页> 外文期刊>Pharmacoepidemiology and drug safety >Assumptions made when preparing drug exposure data for analysis have an impact on results: A A n unreported step in pharmacoepidemiology studies
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Assumptions made when preparing drug exposure data for analysis have an impact on results: A A n unreported step in pharmacoepidemiology studies

机译:准备分析药物暴露数据时所做的假设对结果产生了影响:药物病变研究中的A N未报告的步骤

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Abstract Purpose Real‐world data for observational research commonly require formatting and cleaning prior to analysis. Data preparation steps are rarely reported adequately and are likely to vary between research groups. Variation in methodology could potentially affect study outcomes. This study aimed to develop a framework to define and document drug data preparation and to examine the impact of different assumptions on results. Methods An algorithm for processing prescription data was developed and tested using data from the Clinical Practice Research Datalink (CPRD). The impact of varying assumptions was examined by estimating the association between 2 exemplar medications (oral hypoglycaemic drugs and glucocorticoids) and cardiovascular events after preparing multiple datasets derived from the same source prescription data. Each dataset was analysed using Cox proportional hazards modelling. Results The algorithm included 10 decision nodes and 54 possible unique assumptions. Over 11?000 possible pathways through the algorithm were identified. In both exemplar studies, similar hazard ratios and standard errors were found for the majority of pathways; however, certain assumptions had a greater influence on results. For example, in the hypoglycaemic analysis, choosing a different variable to define prescription end date altered the hazard ratios (95% confidence intervals) from 1.77 (1.56‐2.00) to 2.83 (1.59‐5.04). Conclusions The framework offers a transparent and efficient way to perform and report drug data preparation steps. Assumptions made during data preparation can impact the results of analyses. Improving transparency regarding drug data preparation would increase the repeatability, reproducibility, and comparability of published results.
机译:摘要目的,用于观察研究的真实数据通常需要在分析之前进行格式化和清洁。数据准备步骤很少报告充分报告,并且可能在研究组之间变化。方法的变化可能会影响研究结果。本研究旨在制定一个框架来定义和记录药物准备和检测不同假设对结果的影响。方法使用临床实践研究DataLink(CPRD)的数据开发并测试了处理处方数据的算法。通过在制备来自相同源处方数据的多个数据集之后估计2个示例药物(口服低血糖药物和糖皮质激素)和心血管事件之间的关联来检查不同假设的影响。使用Cox比例危险建模分析每个数据集。结果算法包括10个决策节点和54个可能的独特假设。识别通过算法超过11 000可能的途径。在两个示例性研究中,对大多数途径发现了类似的危险比和标准误差;然而,某些假设对结果产生了更大的影响。例如,在低血糖分析中,选择不同的变量来定义处方末期日期的危险比(1.56-2.00)到2.83(1.59-5.04)。结论该框架提供了透明和有效的方式来执行和报告药物数据准备步骤。在数据准备期间制作的假设可以影响分析结果。提高药物数据准备的透明度将增加公布结果的可重复性,再现性和可比性。

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