Ward Katherine N, Bryant Naomi J, Andrews Nick J, Bowley Jennifer S, Ohrling Anu, Verity Christopher M, Ross Euan M, Miller Elizabeth
Centre for Virology (UCL Campus), Division of Infection and Immunity, Royal Free and University College Medical School, Windeyer Institute of Medical Sciences, 46 Cleveland St, London W1T 4JF, United Kingdom.
Pediatrics. 2007 Aug;120(2):314-21. doi: 10.1542/peds.2006-3743.
We sought to investigate the risk of serious neurologic disease after immunization in early childhood.
The results of a 3-year prospective study of children (2-35 months old) in Britain and Ireland with encephalitis and/or severe illness with convulsions and fever were linked to each child's vaccine history. Cases were reported via the British Paediatric Surveillance Unit's network. The self-controlled case-series method was used to investigate associations between immunization and acute potential adverse events. The risk periods investigated were 0 to 3 and 0 to 7 days post-diphtheria, tetanus, whole cell pertussis, Haemophilus influenzae type b or meningococcal C conjugate vaccine and 6 to 11 and 15 to 35 days post-measles, mumps, rubella vaccine.
A total of 157 disease episodes from 155 children met the analytical case definition. There were 11 cases of herpes simplex encephalitis and 23 cases of primary human herpesvirus 6 and/or 7 infection. There was no evidence of a raised relative incidence of serious neurologic disease in any of the specified risk periods with the exception of a raised relative incidence of 5.68 in the 6-11 days after measles, mumps, rubella vaccine. Based on this relative incidence, between 3 and 6 of the 6 cases in this period were estimated to be attributable to the vaccine with a best estimate of 5. The 6 cases all had fever with convulsions lasting >30 minutes; in all but 1, there was complete recovery by discharge from hospital. Of the 5 patients who recovered, 1 had a concurrent primary human herpesvirus 6 infection and one a primary human herpesvirus 7.
Six to 11 days after measles, mumps, rubella vaccine there is an increased risk of fever and convulsions lasting >30 minutes. All 6 of the episodes temporally related to immunization met the criteria for complex febrile convulsions. The estimated attributable risk of serious neurological disease was similar to that previously found for measles vaccine.
我们试图调查幼儿期免疫接种后发生严重神经系统疾病的风险。
对英国和爱尔兰2至35个月大患脑炎和/或伴有惊厥和发热的重症疾病儿童进行的一项为期3年的前瞻性研究结果与每个儿童的疫苗接种史相关联。病例通过英国儿科监测单位的网络报告。采用自控病例系列法调查免疫接种与急性潜在不良事件之间的关联。所调查的风险期为白喉、破伤风、全细胞百日咳、b型流感嗜血杆菌或脑膜炎球菌C结合疫苗接种后0至3天和0至7天,以及麻疹、腮腺炎、风疹疫苗接种后6至11天和15至35天。
155名儿童的157次疾病发作符合分析病例定义。有11例单纯疱疹性脑炎和23例原发性人疱疹病毒6型和/或7型感染。除麻疹、腮腺炎、风疹疫苗接种后6至11天相对发病率升高5.68外,在任何指定风险期均无严重神经系统疾病相对发病率升高的证据。基于这一相对发病率,估计该时期6例病例中有3至6例可归因于疫苗,最佳估计数为5例。这6例病例均有发热伴惊厥持续>30分钟;除1例外,所有病例出院时均完全康复。在康复的5例患者中,1例同时感染原发性人疱疹病毒6型,1例感染原发性人疱疹病毒7型。
麻疹、腮腺炎、风疹疫苗接种后6至11天,发热和惊厥持续>30分钟的风险增加。与免疫接种在时间上相关的所有6次发作均符合复杂性热性惊厥的标准。严重神经系统疾病的估计归因风险与先前麻疹疫苗的发现相似。