Analysis on surveillance results of adverse events following immunization in Ningbo City
10.19485/j.cnki.issn2096-5087.2018.03.014
- VernacularTitle:宁波市疑似预防接种异常反应监测结果分析
- Author:
Shao-Ying ZHOU
1
;
Rui MA
Author Information
1. 宁波市疾病预防控制中心免疫预防所
- Keywords:
Adverse events following immunization;
Vaccine;
Immunization planning
- From:
Journal of Preventive Medicine
2018;30(3):274-277
- CountryChina
- Language:Chinese
-
Abstract:
Objective To analyze the occurrence characteristics of adverse events following immunization (AEFI) in Ningbo and to provide the basis for evaluating the safety of vaccine. Methods The AEFI case data from 2009 to 2016 were collected by the Chinese Adverse Events Following Immunization Information Management System and the Chinese Immunization Planning Information Management System. The descriptive analysis was used for AEFI reporting time, demographic characteristics, classification, outcome and vaccine distribution. Results From 2009 to 2016, 5036 AEFI cases were reported. The average incidence rate was 18.36 per 100000. The most of the cases were reported from May to August, which accounted for 44.18％. The most of cases were occurred in the infant group (≤ 1 year old), which accounted for 66.30％. The highest incidence rate was occurred in the age group of 6 years, which was 47.87 per 100000. Among 5036 cases of AEFI, 4946 cases were vaccine reaction, accounting for 98.21％. The most of symptoms were fever, swelling and indurations, accounting for 84.69％. There were 4523 cases (89.81％) of AEFI occurred within two day after vaccination. The incidence rate of Non national immunization program vaccine (19.59 per 100000) was higher than that of national immunization program vaccine (17.89 per 100000) (P<0.05) . Except 151 unknown, 96.86％ (4878/5036) cases were improved and recovered. Three cases of sequelae were all coincidence event. Among the 4 cases of death, in addition to 1 case of systemic disseminated BCG infection, 3 of the other cases were coincidental event. Conclusion AEFI cases occurred mainly in the infant group and occurred within two day after vaccination. In general, the safety of vaccines was satisfied.
