Am J Epidemiol. 2013 Nov 1;178(9):1496-504. doi: 10.1093/aje/kwt128. Epub 2013 Sep 7.
In this paper, we propose new methods for analyzing cases of vaccine adverse events spontaneously reported to a surveillance database. The methods use the self-controlled case series approach, extended in several ways with parametric and nonparametric assumptions to account for the specific features of the data (large amount of underreporting and variation of reporting with time since vaccination). This work was motivated by the documented risk of intussusception after RotaShield vaccination (Wyeth-Lederle Vaccines, Radnor, Pennsylvania) and used worldwide spontaneous reports of intussusception occurring after Rotarix vaccination (GlaxoSmithKline Biologics, Research Triangle Park, North Carolina) collected between January 2004 and February 2010. The estimated risk during the 3- to 7-day period after vaccination was approximately 5 times higher after dose 1 of Rotarix than after dose 2, which is similar to published findings on the same topic. We undertook a large simulation study to evaluate the performance of the method in different scenarios, including its robustness to different sample sizes and time-dependent reporting functions. The bias was generally small, the type I error rate was correctly controlled, and the power to detect a risk ratio of 4 was satisfactory, provided that the sample size was over 100. The proposed methods are an effective way to explore and quantify vaccine safety signals from spontaneous reports.
在本文中,我们提出了新的方法来分析主动向监测数据库报告的疫苗不良事件病例。这些方法使用了自对照病例系列方法,并通过参数和非参数假设进行了扩展,以考虑到数据的特定特征(大量漏报和随时间变化的报告)。这项工作的动机是 Rotashield 疫苗接种后出现肠套叠的已知风险(Wyeth-Lederle Vaccines,Radnor,宾夕法尼亚州),并使用了 2004 年 1 月至 2010 年 2 月期间收集的 Rotarix 疫苗接种后发生肠套叠的全球自发报告。接种后 3-7 天期间的估计风险在 Rotarix 的第 1 剂后比第 2 剂高约 5 倍,这与该主题的已发表研究结果相似。我们进行了一项大型模拟研究,以评估该方法在不同情况下的性能,包括对不同样本量和随时间变化的报告函数的稳健性。偏差通常很小,I 型错误率得到正确控制,并且在样本量超过 100 的情况下,检测风险比为 4 的功效令人满意。所提出的方法是从自发报告中探索和量化疫苗安全性信号的有效方法。