Epidemiology and long-term neurological sequelae of childhood herpes simplex CNS infection

被引:8
作者
Berkhout, Angela [1 ,2 ]
Kapoor, Vishal [1 ,2 ]
Heney, Claire [3 ]
Jones, Cheryl A. [6 ,7 ]
Clark, Julia E. [1 ,2 ]
Britton, Philip N. [6 ,7 ]
Vaska, Vikram L. [2 ,4 ]
Lai, Melissa M. [1 ,5 ]
Nourse, Clare [1 ,2 ]
机构
[1] Univ Queensland, Fac Med, Brisbane, Qld, Australia
[2] Queensland Childrens Hosp, Brisbane, Qld, Australia
[3] Pathol Queensland, Brisbane, Qld, Australia
[4] Mater Pathol, Brisbane, Qld, Australia
[5] Royal Brisbane & Womens Hosp, Brisbane, Qld, Australia
[6] Univ Sydney, Fac Med & Hlth, Sydney Med Sch, Sydney, NSW, Australia
[7] Childrens Hosp Westmead, Sydney Childrens Hosp Network, Sydney, NSW, Australia
关键词
brain; CNS; encephalitis; herpes simplex virus; paediatric; CENTRAL-NERVOUS-SYSTEM; VIRUS TYPE-1; ENCEPHALITIS; CHILDREN; ACYCLOVIR; MANAGEMENT; AUSTRALIA; DISEASE;
D O I
10.1111/jpc.15992
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Aim Herpes simplex CNS infection is a rare but important cause of neurological disability. Long term outcomes after HSV CNS infection in Australia have not yet been fully described. We sought to provide a comprehensive review of HSV CNS infection in children using a retrospective 13-year evaluation of statewide laboratory and clinical records and a parent survey conducted at least one year after the initial infection. Methods All positive PCR HSV 1 and 2 results from cerebrospinal fluid (CSF) or brain tissue were obtained from Queensland pathology providers for children aged 0-16 years between 1 January 2005 and 31 December 2017. Clinical data were obtained from patient records and longer-term outcomes via parent survey at least 1 year after initial infection. Results Forty-three children were identified over the 13-year period, 17 (39.5%) neonates and 26 (60.4%) non-neonates. The annual incidence for HSV CNS infection in Queensland children aged <= 16 years was 0.3/100 000 (95% confidence intervals (CIs): 0.2-0.4) with neonates at highest risk (incidence 2.5/100 000 live births, 95% CI: 1.5-3.9). HSV 1 was the predominant serotype in both neonates and non-neonates (9/17, 52.9% neonates and 19/26, 73.1% non-neonates). Seven (16.3%) children died, five (5/17, 29.4% neonates), directly attributable to HSV CNS infection (all neonates). Twenty-five (58.1%) had neurological morbidity at discharge (9/17 neonates (52.9%) vs. 16/26 (61.5%) non-neonates) and 20/27 (74.1%) reported long-term neurological morbidity at follow-up (5/9 neonates (55.6%) vs. 15/18 non-neonates (83.3%)). Seven children (two neonates and four non-neonates) with long-term neurological sequelae had no neurological morbidity identified at discharge. Conclusion Significant long-term neurologic sequelae were seen in children with HSV CNS infection even in children with no neurological disability identified at discharge from hospital. Careful neurodevelopmental follow-up of all children is recommended.
引用
收藏
页码:1372 / 1378
页数:7
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