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本文引用的文献

1
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.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。
Hum Vaccin Immunother. 2021 Aug 3;17(8):2568-2574. doi: 10.1080/21645515.2021.1898306. Epub 2021 Mar 29.
2
Safety and Immunogenicity of Sabin Strain Inactivated Poliovirus Vaccine Compared With Salk Strain Inactivated Poliovirus Vaccine, in Different Sequential Schedules With Bivalent Oral Poliovirus Vaccine: Randomized Controlled Noninferiority Clinical Trials in China.在中国进行的随机对照非劣效性临床试验:与索尔克株脊髓灰质炎灭活疫苗相比,萨宾株脊髓灰质炎灭活疫苗与二价口服脊髓灰质炎疫苗不同序贯接种程序的安全性和免疫原性。
Open Forum Infect Dis. 2019 Aug 26;6(10):ofz380. doi: 10.1093/ofid/ofz380. eCollection 2019 Oct.
3
Safety and immunogenicity of inactivated poliovirus vaccine made from Sabin strains: A phase II, randomized, dose-finding trial.Sabin 株来源的灭活脊灰病毒疫苗的安全性和免疫原性:一项 II 期、随机、剂量探索试验。
Vaccine. 2018 Oct 29;36(45):6782-6789. doi: 10.1016/j.vaccine.2018.09.023. Epub 2018 Sep 21.
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Polio vaccines: WHO position paper, March 2016-recommendations.脊髓灰质炎疫苗:世界卫生组织立场文件,2016年3月 - 建议
Vaccine. 2017 Mar 1;35(9):1197-1199. doi: 10.1016/j.vaccine.2016.11.017. Epub 2016 Nov 25.

中国2015 - 2022年国产Sabin株脊髓灰质炎灭活疫苗接种后不良事件监测

Surveillance for Adverse Events Following Immunization with Domestic Sabin-Strain Inactivated Poliovirus Vaccine - China, 2015-2022.

作者信息

Fan Chunxiang, Li Keli, Zhang Lina, Li Yuan, Song Yifan, Li Yan, Ren Minrui, Rodewald Lance E, Yin Zundong

机构信息

National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases (NITFID), National Immunization Programme, Chinese Center for Disease Control and Prevention, Beijing, China.

出版信息

China CDC Wkly. 2024 Dec 13;6(50):1313-1318. doi: 10.46234/ccdcw2024.261.

DOI:10.46234/ccdcw2024.261
PMID:39734785
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11673181/
Abstract

INTRODUCTION

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

引言

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。

方法

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。

结果

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。

结论

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。