From the The INCLEN Trust International, New Delhi, India.
Department of Community Medicine, Government Medical College, Thiruvananthapuram, Kerala, India.
Pediatr Infect Dis J. 2020 May;39(5):389-396. doi: 10.1097/INF.0000000000002594.
Safety of pentavalent (DTwP-HBV-Hib) vaccine has been a public concern in India and other countries. This study attempted to document the association of serious adverse events following immunization (AEFI, including hospitalizations and deaths of all causes) with the 3 doses of pentavalent and oral poliovirus (OPV) vaccines.
A cohort of 30,688 infants in 2 south Indian districts were enrolled and followed-up between October 2014 and May 2016, following their first vaccination with DTwP-HBV-Hib and OPV at public health facilities. During weekly follow-ups, by telephone or home visits, the serious AEFIs (hospitalizations and deaths) occurring any time after each vaccination until 4 weeks after third dose were documented. The incidence risk ratios (IRRs) of serious AEFIs in the first (days 0-6) and fourth weeks (days 21-27) after the vaccine doses were compared using the poisson regression analysis.
Of the 30,688 infants enrolled, 30,208 received their third doses of vaccines. During the 4-week periods following each vaccination, there were 365 hospitalizations and 17 deaths. Adjusted incidence risk ratio of 3 doses combined for post-vaccination serious AEFIs during the first week compared with fourth week was 0.8 [95% confidence interval: 0.6-1.0].
There was no increased risk of a serious AEFIs during the first week after any of the 3 doses of pentavalent and OPV vaccination compared with the fourth week. In the absence of any temporal clustering, mortality and hospitalization rates observed in vaccinated infants probably reflects the natural occurrence of such events.
五价疫苗(DTwP-HBV-Hib)在印度和其他国家的安全性一直是公众关注的问题。本研究试图记录五价疫苗和口服脊髓灰质炎(OPV)疫苗接种后严重不良事件(AEFI,包括所有原因的住院和死亡)与 3 剂接种的关联。
2014 年 10 月至 2016 年 5 月期间,在南印度的 2 个地区招募了 30688 名婴儿,在公共卫生机构接种 DTwP-HBV-Hib 和 OPV 后进行了随访。在每周的随访中,通过电话或家访,记录每次接种后任何时间至第 3 剂后 4 周内发生的严重 AEFI(住院和死亡)。使用泊松回归分析比较疫苗接种后第 1 天(第 0-6 天)和第 4 周(第 21-27 天)严重 AEFI 的发病率风险比(IRR)。
在 30688 名入组的婴儿中,30208 名婴儿接受了第 3 剂疫苗。在每次接种后的 4 周内,有 365 名婴儿住院,17 名婴儿死亡。与第 4 周相比,第 1 周接种 3 剂疫苗后严重 AEFI 的调整后发病率风险比为 0.8(95%置信区间:0.6-1.0)。
与第 4 周相比,在接种 3 剂五价疫苗和 OPV 疫苗后的第 1 周,AEFI 没有增加的风险。在没有任何时间聚集的情况下,接种婴儿中观察到的死亡率和住院率可能反映了此类事件的自然发生。