Fan Chunxiang, Li Keli, Zhang Lina, Li Yuan, Song Yifan, Li Yan, Ren Minrui, Rodewald Lance E, Yin Zundong
National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), National Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China.
China CDC Wkly. 2024 Dec 13;6(50):1313-1318. doi: 10.46234/ccdcw2024.261.
Domestic Sabin-strain inactivated poliovirus vaccine (sIPV) was approved for use in China in 2015 and introduced into the national immunization schedule in a sequential schedule with oral poliovirus vaccine (OPV) in May 2016. However, a comprehensive analysis describing the characteristics, occurrences, and incidences of adverse events following immunization (AEFI) with sIPV in China is lacking.
Data on sIPV doses administered and AEFI reported from 2015 to 2022 were obtained from the Chinese National Immunization Information System (CNIIS). Descriptive epidemiological methods and statistics were used to analyze and describe the characteristics, occurrences, and incidences of AEFI following sIPV in China from 2015 to 2022.
From 2015 to 2022, over 110,000,000 sIPV doses were administered, and 46,748 sIPV AEFIs were reported, resulting in an AEFI reporting rate of 42.44/100,000. Most AEFIs (46,333, 99.11%) were non-serious. Causality assessment determined 46,061 (98.53%) AEFIs were vaccine product-related reactions, including 44,001 (94.12%) common and 2,060 (4.41%) rare vaccine reactions. Among common vaccine reactions, reporting rates for fever >38.5 °C, local redness and swelling ≥2.6 cm, and local induration ≥2.6 cm were 12.02/100,000, 5.13/100,000, and 1.67/100,000, respectively. Among rare vaccine reactions, reporting rates for anaphylactic rash, thrombocytopenic purpura, and febrile convulsion were 1.56/100,000, 0.09/100,000, and 0.03/100,000, respectively.
Most reported sIPV AEFIs were non-serious, and the reporting rate of rare vaccine reactions has been very low since sIPV was approved for use in China. As sIPV remains in use in China, surveillance of AEFIs associated with this vaccine needs to be maintained.
国产Sabin株脊髓灰质炎灭活疫苗(sIPV)于2015年在中国获批使用,并于2016年5月按照序贯程序与口服脊髓灰质炎疫苗(OPV)一起纳入国家免疫规划。然而,目前缺乏对中国sIPV免疫后不良反应(AEFI)的特征、发生情况和发病率的综合分析。
从中国国家免疫规划信息系统(CNIIS)获取2015年至2022年期间sIPV接种剂量和报告的AEFI数据。采用描述性流行病学方法和统计学方法,对2015年至2022年中国sIPV免疫后AEFI的特征、发生情况和发病率进行分析和描述。
2015年至2022年期间,共接种超过1.1亿剂sIPV,报告46748例sIPV AEFI,AEFI报告率为42.44/10万。大多数AEFI(46333例,99.11%)为非严重不良反应。因果关系评估确定46061例(98.53%)AEFI为疫苗产品相关反应,包括44001例(94.12%)常见和2060例(4.41%)罕见疫苗反应。在常见疫苗反应中,体温>38.5℃、局部红肿≥2.6 cm和局部硬结≥2.6 cm的报告率分别为12.02/10万、5.1 /10万和1.67/10万。在罕见疫苗反应中,过敏性皮疹、血小板减少性紫癜和热性惊厥的报告率分别为1.56/10万、0.09/10万和0.03/1万。
大多数报告的sIPV AEFI为非严重不良反应,自sIPV在中国获批使用以来,罕见疫苗反应的报告率一直很低。由于sIPV仍在中国使用,需要持续监测与该疫苗相关的AEFI。