Oberle Doris, Pavel Jutta, Keller-Stanislawski Brigitte
Department Safety of Medicinal Products and Medical Devices, Paul-Ehrlich-Institut, Federal Institute for Vaccines and Biomedicines, Langen, Germany.
Pharmacoepidemiol Drug Saf. 2017 Nov;26(11):1321-1327. doi: 10.1002/pds.4292. Epub 2017 Aug 14.
We aimed at investigating whether, in Germany, the number of individual case safety reports (ICSR) of confirmed narcolepsy following Pandemrix® vaccination notified to the Paul-Ehrlich-Institut (PEI, German Federal Institute for Vaccines and Biomedicines) was higher than expected when compared with the prepandemic background incidence rates.
ICSR of narcolepsy after vaccination with Pandemrix® notified to the PEI until September 2016 were reviewed and validated according to the criteria of narcolepsy defined by the Brighton Collaboration (BC). Cases fulfilling the criteria of BC levels of diagnostic certainty 1 to 4a with symptoms onset after vaccination with Pandemrix® were eligible. Adjustment for underreporting was performed with cases of narcolepsy recruited within the scope of the German Narcolepsy Study using capture-recapture methods. An observed versus expected (OvE) analysis was conducted based on adjusted case numbers using risk windows for symptoms onset within 4 and 6 months following vaccination.
By the end of September 2016, a total of 85 ICSR of narcolepsy after vaccination with Pandemrix® had been notified to the PEI 52 of which were eligible. The OvE estimates for the 4 and 6 months risk windows were 3.8 (95% CI: 2.6-5.4) and 2.8 (95% CI: 2.0-3.9), respectively. The number of excess cases was higher in children and adolescents (15-fold and 11.7-fold increased OvE estimate) than in adults (2.1-fold and 1.5-fold increased estimate).
Compared with the prepandemic background incidence rate, the number of incident narcolepsy cases was 3.8-fold and 2.8-fold as high.
我们旨在调查在德国,与大流行前的背景发病率相比,向保罗·埃利希研究所(PEI,德国联邦疫苗和生物制品研究所)通报的接种Pandemrix®疫苗后确诊发作性睡病的个体病例安全报告(ICSR)数量是否高于预期。
对截至2016年9月向PEI通报的接种Pandemrix®疫苗后发作性睡病的ICSR进行审查,并根据布莱顿协作组织(BC)定义的发作性睡病标准进行验证。符合BC诊断确定性1至4a级标准且在接种Pandemrix®疫苗后出现症状的病例符合条件。使用捕获-再捕获方法对德国发作性睡病研究范围内招募的发作性睡病病例进行漏报调整。基于调整后的病例数,使用接种后4个月和6个月内症状发作的风险窗口进行观察与预期(OvE)分析。
截至2016年9月底,PEI共收到85份接种Pandemrix®疫苗后发作性睡病的ICSR,其中52份符合条件。4个月和6个月风险窗口的OvE估计值分别为3.8(95%CI:2.6-5.4)和2.8(95%CI:2.0-3.9)。儿童和青少年中的超额病例数高于成年人(OvE估计值分别增加15倍和11.7倍,而成年人分别增加2.1倍和1.5倍)。
与大流行前的背景发病率相比,发作性睡病的发病病例数分别高出3.8倍和2.8倍。