Developmental outcomes following vaccine-proximate febrile seizures in children

被引:6
|
作者
Deng, Lucy [1 ,4 ]
Wood, Nicholas [1 ,4 ]
Macartney, Kristine [1 ,4 ]
Gold, Michael [5 ]
Crawford, Nigel [6 ,7 ]
Buttery, Jim [7 ,8 ]
Richmond, Peter [9 ,10 ]
Barton, Belinda [2 ,3 ,4 ]
机构
[1] Childrens Hosp Westmead, Natl Ctr Immunisat Res & Surveillance, Westmead, NSW, Australia
[2] Childrens Hosp Westmead, Childrens Hosp Educ Res Inst, Westmead, NSW, Australia
[3] Childrens Hosp Westmead, Kids Neurosci Ctr, Westmead, NSW, Australia
[4] Univ Sydney, Childrens Hosp Westmead, Sch Clin, Sydney, NSW, Australia
[5] Univ Adelaide, Discipline Paediat, Sch Med, Womens & Childrens Hosp, Adelaide, SA, Australia
[6] Univ Melbourne, Dept Paediat, Royal Childrens Hosp, Melbourne, Vic, Australia
[7] Murdoch Childrens Res Inst, Parkville, Vic, Australia
[8] Monash Univ, Monash Childrens Hosp, Dept Paediat, Infect & Immun,Monash Ctr Hlth Care Res & Impleme, Clayton, Vic, Australia
[9] Telethon Kids Inst, Wesfarmers Ctr Vaccines & Infect Dis, Perth, Australia
[10] Univ Western Australia, Sch Paediat & Child Hlth, Perth, WA, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
SOCIOECONOMIC-STATUS; SENSITIVE PERIODS; INFLUENZA VACCINE; RISK; CONVULSIONS; IMMUNIZATION; PERTUSSIS; MEASLES; SURVEILLANCE; GUIDELINES;
D O I
10.1212/WNL.0000000000009876
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To compare the developmental and behavioral outcomes of children experiencing an initial vaccine-proximate (VP) febrile seizure (FS) to those having a non-VP-FS (NVP-FS) and controls who have not had a seizure. Methods In this prospective multicenter cohort study, children with their first FS before 30 months of age between May 2013 and April 2016 were recruited from 4 Australian pediatric hospitals and classified as having VP-FS or NVP-FS. Similar-aged children with no seizure history were recruited as controls. The Bayley Scales of Infant and Toddler Development, Third Edition (Bayley-III) was administered to participants with FS 12 to 24 months after their initial FS and to controls 12 to 42 months of age at the time of assessment. The primary outcome was the Bayley-III cognitive score. Children's preacademic skills were assessed with the Woodcock-Johnson Tests of Achievement, Third Edition, and their behavior and executive functioning were obtained from parent questionnaires. Results There was no significant difference in cognitive function between children with VP-FS (n = 62), those with NVP-FS (n = 70), and controls (n = 90) (F-2,F-219= 2.645,p= 0.07). There were no differences between the groups for all other measures and no increased risk of borderline/significant impairment or behavior in the clinical range in children with VP-FS compared to those with NVP-FS or controls. Conclusion VP-FS was not associated with an increased risk of developmental or behavioral problems in young children compared to children with NVP-FS or controls. Parents and providers should be reassured by the absence of adverse effects of VP-FS on the development of children.
引用
收藏
页码:E226 / E238
页数:13
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