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对中国扩大免疫规划引入的萨宾株脊髓灰质炎灭活疫苗(sIPV)接种后不良事件的监测以及与中国江苏省野生株脊髓灰质炎灭活疫苗(wIPV)接种后不良事件的比较。

Surveillance of adverse events following the introduction of inactivated poliovirus vaccine made from Sabin strains (sIPV) to the Chinese EPI and a comparison with adverse events following inactivated poliovirus vaccine made from wild strains (wIPV) in Jiangsu, China.

作者信息

Kang Guodong, Tang Fenyang, Wang Zhiguo, Hu Ran, Yu Jing, Gao Jun

机构信息

Department of Expanded Program on Immunization, Jiangsu Provincial Center for Disease Control and Prevention, Nanjing, China.

出版信息

Hum Vaccin Immunother. 2021 Aug 3;17(8):2568-2574. doi: 10.1080/21645515.2021.1898306. Epub 2021 Mar 29.

DOI:10.1080/21645515.2021.1898306
PMID:33780310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8475579/
Abstract

One dose of inactivated poliovirus vaccine (IPV) was introduced into the Chinese Expanded Program on Immunization (EPI) in 2016. IPV made from Sabin strains (sIPV) was newly licensed in China and its safety has been concerned. This study aimed to evaluate the safety of sIPV and provide a comparison with conventional IPV made from wild strains (wIPV). We collected all IPV-related AEFI reports in Jiangsu from the Chinese National Adverse Events Following Immunization Information System (CNAEFIS) for 2016-2019. We obtained the administered doses of IPV from the Jiangsu provincial Electronic Immunization Registries System (JSEIRS). The AEFI reporting rates per 100,000 doses of vaccine administered were compared for sIPV and wIPV. A total of 699 sIPV and 908 wIPV AEFI cases were collected by CNAEFIS in Jiangsu during 2016-2019. The overall AEFI reporting rates were 53.02 per 100,000 doses and 41.25 per 100,000 doses for sIPV and wIPV, respectively ( < .001). For both sIPV and wIPV, the AEFIs were mainly classified as common adverse reactions. The reporting rate of common adverse reactions was higher for sIPV than for wIPV ( < .001). The most frequently reported symptoms/signs were fever, persistent crying, injection site erythema/swelling, rash, and injection site induration. Only 1.14% of sIPV-associated and 2.31% of wIPV-associated AEFI cases were diagnosed as serious. No difference in reporting rate was observed for serious AEFIs ( = .272). sIPV has a favorable safety profile, although it exhibits a slightly higher reporting rate of common adverse reactions than wIPV.

摘要

2016年,一剂灭活脊髓灰质炎疫苗(IPV)被纳入中国扩大免疫规划(EPI)。由萨宾株制成的IPV(sIPV)在中国新获得许可,其安全性受到关注。本研究旨在评估sIPV的安全性,并与野生株制成的传统IPV(wIPV)进行比较。我们从中国国家免疫接种后不良事件信息系统(CNAEFIS)收集了2016 - 2019年江苏省所有与IPV相关的疑似预防接种异常反应(AEFI)报告。我们从江苏省电子免疫登记系统(JSEIRS)获取了IPV的接种剂量。比较了sIPV和wIPV每10万剂疫苗接种的AEFI报告率。2016 - 2019年期间,CNAEFIS在江苏省共收集到699例sIPV和908例wIPV的AEFI病例。sIPV和wIPV的总体AEFI报告率分别为每10万剂53.02例和41.25例(<0.001)。对于sIPV和wIPV,AEFI主要分类为常见不良反应。sIPV常见不良反应的报告率高于wIPV(<0.001)。最常报告的症状/体征是发热、持续性哭闹、注射部位红斑/肿胀、皮疹和注射部位硬结。只有1.14%的sIPV相关AEFI病例和2.31%的wIPV相关AEFI病例被诊断为严重病例。严重AEFI的报告率未观察到差异(P = 0.272)。sIPV具有良好的安全性,尽管其常见不良反应的报告率略高于wIPV。

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