...
首页> 外文期刊>BMJ Open >Epidemiological study of severe febrile reactions in young children in Western Australia caused by a 2010 trivalent inactivated influenza vaccine
【24h】

Epidemiological study of severe febrile reactions in young children in Western Australia caused by a 2010 trivalent inactivated influenza vaccine

机译:2010年三价灭活流感疫苗在西澳大利亚州引起的严重发热反应的流行病学研究

获取原文
           

摘要

Background The 2010 influenza vaccination program for children aged 6?months to 4?years in Western Australia (WA) was suspended following reports of severe febrile reactions, including febrile convulsions, following vaccination with trivalent inactivated influenza vaccine (TIV). Methods To investigate the association between severe febrile reactions and TIV, three studies were conducted: (i) rates of febrile convulsions within 72?h of receiving TIV in 2010 were estimated by vaccine formulation and batch; (ii) numbers of children presenting to hospital emergency departments with febrile convulsions from 2008 to 2010 were compared; and (iii) a retrospective cohort study of 360 children was conducted to compare the reactogenicity of available TIV formulations. Findings In 2010, an estimated maximum of 18?816 doses of TIV were administered and 63 febrile convulsions were recorded, giving an estimated rate of 3.3 (95% CI 2.6 to 4.2) per 1000 doses of TIV administered. The odds of a TIV-associated febrile convulsion was highly elevated in 2010 (p0.001) and was associated with the vaccine formulations of one manufacturer—Fluvax and Fluvax Junior (CSL Biotherapies). The risk of both febrile convulsions (p0.0001) and other febrile reactions (p0.0001) was significantly greater for Fluvax formulations compared to the major alternate brand. The risk of febrile events was not associated with prior receipt of TIV or monovalent 2009 H1N1 pandemic vaccine. The biological cause of the febrile reactions is currently unknown. Interpretation One brand of influenza vaccine was responsible for the increase in febrile reactions, including febrile convulsions. Until the biological reason for this is determined and remediation undertaken, childhood influenza vaccination programs should not include Fluvax-type formulations and enhanced surveillance for febrile reactions in children receiving TIV should be undertaken.
机译:背景资料由于三价灭活流感疫苗(TIV)接种后出现了严重的发热反应,包括高热惊厥,西澳大利亚州(WA)的6个月至4岁的儿童2010年流感疫苗接种计划被暂停。方法为了研究严重的发热反应与TIV的关系,进行了三项研究:(i)通过疫苗配方和批次估算2010年接受TIV的72小时内的高热惊厥发生率; (ii)比较了2008年至2010年就诊于医院急诊科时出现高热惊厥的儿童人数; (iii)对360名儿童进行了一项回顾性队列研究,以比较可用的TIV制剂的反应原性。调查结果2010年,估计最多服用18–816剂TIV,并记录了63例高热惊厥,每1000剂TIV服用率估计为3.3(95%CI 2.6至4.2)。与TIV相关的高热惊厥的几率在2010年大大提高(p <0.001),并且与一家生产商Fluuvax和Fluvax Junior(CSL Biotherapies)的疫苗制剂有关。与主要的替代品牌相比,Fluvax制剂出现高热惊厥(p <0.0001)和发生其他高热反应(p <0.0001)的风险明显更高。高热事件的风险与事先接受TIV或单价2009 H1N1大流行疫苗无关。目前尚不清楚发热反应的生物学原因。解释一种品牌的流感疫苗是导致高热反应(包括高热惊厥)增加的原因。在确定其生物学原因并采取补救措施之前,儿童流感疫苗接种计划不应包括Fluvax型制剂,应加强对接受TIV的儿童的发热反应的监测。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号