Institute of Immunization and Prevention, Zhejiang Center for Disease Control and Prevention, Hangzhou, China.
Hum Vaccin Immunother. 2022 Dec 31;18(1):2021711. doi: 10.1080/21645515.2021.2021711. Epub 2022 Feb 2.
The aim of this study is to describe the reporting rate of adverse events following immunization (AEFI) with pentavalent vaccine: diphtheria-pertussis-tetanus-poliomyelitis-Haemophilus influenzae type b (DPT-IPV/Hib), and to determine whether the reporting rate of AEFI following DPT-IPV/Hib was higher than the average level of the other vaccines.
Review and describe the AEFI reported to national adverse event following immunization surveillance system (NAEFISS) in Zhejiang province from 2015 to 2020. Reporting rates of AEFI were calculated by age, city, severity of AEFI, categories of AEFI, and reaction categories. The data mining algorithm used in this study was reporting odds ratio (ROR). A value of ROR‑1.96SE >1 (standard error [SE]) was considered as positive signal.
NAEFISS received 5726 AEFI reports following DTP-IPV/Hib, with a reporting rate of 20.01/10000 doses. Of the reported AEFI, 202 were serious vaccine product-related reactions, including two cases of anaphylactic shock, five cases of Guillain Barre Syndrome (GBS) and two cases of acute disseminated encephalomyelitis. The reporting rate of fever/redness/induration was the highest among all the clinical diagnosis (14.97/10000 doses). The positive signals were obtained for allergic rash (ROR-1.96SE: 1.36), febrile convulsion (ROR-1.96SE: 1.32) and GBS (ROR-1.96SE: 1.16).
The present findings bolstered that the DTP-IPV/Hib administered as the four-dose schedule was generally well tolerated in Chinese infants as we did not identify any new/unexpected safety concern from the NAEFISS during a six-year timespan.
本研究旨在描述五联疫苗(白喉-百日咳-破伤风-脊髓灰质炎-流感嗜血杆菌 b 型[DPT-IPV/Hib])接种后不良事件(AEFI)的报告率,并确定 DPT-IPV/Hib 接种后 AEFI 的报告率是否高于其他疫苗的平均水平。
回顾和描述 2015 年至 2020 年期间浙江省国家疫苗不良反应监测系统(NAEFISS)报告的 AEFI。通过年龄、城市、AEFI 严重程度、AEFI 类别和反应类别计算 AEFI 的报告率。本研究中使用的数据挖掘算法是报告比值比(ROR)。ROR-1.96SE>1(标准误差[SE])的值被认为是阳性信号。
NAEFISS 收到 5726 例 DTP-IPV/Hib 接种后 AEFI 报告,报告率为 20.01/10000 剂。在报告的 AEFI 中,有 202 例为严重疫苗相关反应,包括两例过敏性休克、五例吉兰-巴雷综合征(GBS)和两例急性播散性脑脊髓炎。所有临床诊断中,发热/红肿/硬结的报告率最高(14.97/10000 剂)。过敏皮疹(ROR-1.96SE:1.36)、热性惊厥(ROR-1.96SE:1.32)和 GBS(ROR-1.96SE:1.16)获得阳性信号。
在六年的时间内,NAEFISS 未发现任何新的/意外的安全性问题,这支持了在我国婴儿中按四剂方案接种 DPT-IPV/Hib 总体上具有良好的耐受性。