Uppsala Monitoring Centre, Uppsala, Sweden.
Pharmacoepidemiol Drug Saf. 2020 Aug;29(8):951-957. doi: 10.1002/pds.5022. Epub 2020 May 12.
Statistical screening of Vigibase, the global database of individual case safety reports, highlighted an association between the MedDRA Preferred Term (PT) "colitis" and nintedanib. Nintedanib is a protein kinase inhibitor authorized in accelerated regulatory procedures for the treatment of idiopathic pulmonary fibrosis (IPF). The aim of this report is to describe the integration of two types of real-world evidence, spontaneous reports of adverse drug reactions (ADR), and observational health data (OHD) in the assessment of a post-authorization safety signal of ischemic colitis.
Assessment of the statistical signal of "nintedanib - colitis" was undertaken using data from VigiBase, OHD from the Observational Heath Data Sciences and Informatics (OHDSI) collaborative, published literature, and openly available regulatory documents. Evidence synthesis was performed to support Bradford Hill criteria in causality assessment.
Evidence for strength of association, specificity, consistency, and analogy was found upon review of the case series. OHD was used to calculate incidence rates of colitis in new users of nintedanib across multiple populations, supportive of consistency, and further evidence for strength of association. Literature review identified support for biological plausibility and analogy. Signal assessment was supplemented with characterization of real-world users and exploration of potential risk factors using OHD.
An integrated approach using two forms of real-world data, spontaneous reports of ADRs and data from observational databases allowed a comprehensive and efficient signal assessment of nintedanib and colitis. Further exploration of the complementary use of real-time OHD in signal assessment could inform more efficient approaches to current signal management practices.
对全球个体病例安全报告数据库 Vigibase 进行统计筛选,突出了 MedDRA 首选术语(PT)“结肠炎”与尼达尼布之间的关联。尼达尼布是一种蛋白激酶抑制剂,在加速监管程序中获得授权,用于治疗特发性肺纤维化(IPF)。本报告的目的是描述两种类型的真实世界证据(药物不良反应自发报告和观察性健康数据)在评估缺血性结肠炎的上市后安全性信号中的整合。
使用 Vigibase 数据、Observational Heath Data Sciences and Informatics(OHDSI)合作的观察性健康数据、已发表的文献和公开的监管文件,评估“尼达尼布-结肠炎”的统计信号。证据综合用于支持因果关系评估中的布拉德福·希尔标准。
在对病例系列的审查中发现了关联强度、特异性、一致性和类推的证据。观察性健康数据用于计算尼达尼布新使用者在多个人群中的结肠炎发生率,支持一致性,并进一步支持关联强度的证据。文献综述为生物学合理性和类推提供了支持。信号评估还补充了使用观察性健康数据对真实世界使用者进行特征描述和探索潜在风险因素。
使用两种形式的真实世界数据(药物不良反应自发报告和观察性数据库数据)的综合方法,允许对尼达尼布和结肠炎进行全面和有效的信号评估。进一步探索实时观察性健康数据在信号评估中的互补使用,可以为当前信号管理实践提供更有效的方法。