University of Michigan, Ann Arbor, MI.
J Oncol Pract. 2018 Jun;14(6):e368-e374. doi: 10.1200/JOP.18.00086. Epub 2018 May 22.
Patients with cancer are an especially vulnerable population to potential drug-drug interactions (DDIs). This makes it important to adequately screen them for DDIs. The objective of this study was to compare the abilities of nine DDI screening tools to detect clinically relevant interactions with oral oncolytics.
Subscription-based tools (ie, PEPID, Micromedex, Lexicomp, Facts & Comparisons) and free tools (ie, Epocrates Free, Medscape, Drugs.com, RxList, WebMD) were compared for their abilities to detect clinically relevant DDIs for 145 drug pairs including an oral oncology agent. Clinical relevance was determined by a pharmacist using Stockley's Drug Interactions. Descriptive statistics were calculated for each tool, including sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV), and then compared grouped by free or subscription-based tools for the secondary analysis and analyzed via generalized estimating equations.
For individual metrics, PPV had overall higher values (0.88 to 0.97) relative to the low values included for sensitivity (0.65 to 0.96), specificity (0.53 to 0.93) and NPV (0.38 to 0.83). The top-performing subscription and free tools, Lexicomp and Drugs.com, had no statistically significant differences in performance. Overall, subscription tools had a significantly higher sensitivity (0.85 ± 0.017 v 0.78 ± 0.017; P = .0082) and NPV (0.57 ± 0.039 v 0.48 ± 0.032; P = .031) than free tools. No differences were observed between the specificity and PPV.
Due to the low performance of some tools for sensitivity, specificity, and NPV, individual performance should be examined and prioritized on the basis of the intended use when selecting a DDI tool. If a strong-performing subscription-based tool is unavailable, a strong-performing free option, like Drugs.com, is available.
癌症患者是潜在药物-药物相互作用(DDI)的高危人群。因此,充分筛选他们的 DDI 非常重要。本研究的目的是比较九种 DDI 筛选工具检测口服肿瘤药物相关临床相关相互作用的能力。
基于订阅的工具(即 PEPID、Micromedex、Lexicomp、Facts & Comparisons)和免费工具(即 Epocrates Free、Medscape、Drugs.com、RxList、WebMD)被比较,以检测包括一种口服肿瘤药物在内的 145 对药物的临床相关 DDI。临床相关性由药剂师使用 Stockley 的药物相互作用来确定。为每个工具计算了描述性统计数据,包括敏感性、特异性、阳性预测值(PPV)和阴性预测值(NPV),然后按免费或订阅工具分组进行二次分析,并通过广义估计方程进行分析。
对于个体指标,PPV 的总体值(0.88 至 0.97)高于敏感性(0.65 至 0.96)、特异性(0.53 至 0.93)和 NPV(0.38 至 0.83)的低值。表现最好的订阅和免费工具 Lexicomp 和 Drugs.com 在性能上没有统计学上的显著差异。总体而言,订阅工具的敏感性(0.85 ± 0.017 比 0.78 ± 0.017;P =.0082)和 NPV(0.57 ± 0.039 比 0.48 ± 0.032;P =.031)显著高于免费工具。特异性和 PPV 之间没有差异。
由于一些工具的敏感性、特异性和 NPV 性能较低,在选择 DDI 工具时,应根据预期用途检查和优先考虑个体性能。如果没有功能强大的订阅工具,那么功能强大的免费工具(如 Drugs.com)也可用。