确诊或疑似先天性寨卡病毒感染的巴西儿童的围产期特征和长期结果:ZIKAction儿科登记

Isadora Cristina de Siqueira , Breno Lima de Almeida , Maria Lucia Costa Lage , Leticia Serra , Alessandra Carvalho , Maricélia Maia de Lima , Maria de Fatima Neri Góes , Marília De Santa Inês Neri Crispim , Mirela Monteiro da Costa Pereira , Bernardo Gratival Gouvea Costa , Heather Bailey , Thomas Byrne , Carlo Giaquinto , Georgina Fernandes , Elisa Ruiz-Burga , Claire Thorne
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引用次数: 0

摘要

尽管对寨卡病毒(ZIKV)感染的科学知识越来越多,但关于妊娠期寨卡病毒感染和先天性寨卡病毒综合征(CZS)的问题仍然存在。方法ZIKAction儿科登记处是一个记录在子宫内接触ZIKV和/或确诊或疑似cz的儿童的国际登记处。其目的是描述这些儿童的特征(即临床、放射学、神经发育特征),并通过回顾性病例记录审查描述结果、长期后遗症和管理。该分析描述了该登记处巴伊亚分部儿童的孕产妇和围产期特征,根据小头畸形分类评估了他们的神经影像学、眼科、听力和脑电图异常情况,并报告了住院情况。包括2015-2018年出生、2020-2021年在萨尔瓦多三家公共卫生机构注册的儿童。结果129例儿童(女性57%)中,实验室确诊先天性寨卡病毒感染15例(11.6%),疑似cz感染114例(88.4%)。分娩时,正常小头畸形15例(11.6%),中度小头畸形30例(23.3%),重度小头畸形84例(65.1%)。出生头围z评分中位数为-3·51 [IQR, -4·69,-2·73]。随访期间,所有患儿神经影像学异常,脑电图异常占80·3%(94/117),眼科异常占62·2%(77/120),听力障碍占27·4%(34/124)。小头畸形的分型与胎龄、眼科和脑电图异常显著相关。在125名有住院数据的儿童中,52名(41.6%)在最近的随访中住院,中位年龄为15.8[4.0,34.4]个月;感染是主要原因。结论先天性寨卡病毒感染是一种新发疾病,其谱系多样且不完全清楚。持续的长期随访对于了解长期预后和了解未来的健康和教育需求至关重要。
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Perinatal characteristics and longer-term outcomes in Brazilian children with confirmed or suspected congenital Zika infection: ZIKAction Paediatric Registry

Background

Despite growing scientific knowledge of Zika virus (ZIKV) infection, questions remain regarding ZIKV infection in pregnancy and congenital ZIKV syndrome (CZS).

Methods

The ZIKAction Paediatric Registry is an international registry of children with documented ZIKV exposure in utero and/or with confirmed or suspected CZS. Its aim is to characterize these children (i.e., clinical, radiological, neurodevelopmental features) and describe outcomes, longer-term sequelae and management through retrospective case note review. This analysis described the maternal and perinatal characteristics of children in the Registry’s Bahia arm, assessed their neuroimaging, ophthalmic, hearing and electroencephalography abnormalities by microcephaly classification and reported on hospitalisations. Children born in 2015-2018 and enrolled 2020-2021 in three public health facilities in Salvador were included.

Results

Of 129 (57% female) children, 15 (11·6%) had laboratory-confirmed congenital ZIKV infection and 114 (88·4%) suspected CZS. At delivery, 15 (11·6%) were normocephalic, 30 (23·3%) moderately microcephalic, and 84 (65·1%) severely microcephalic. Median birth head circumference z-score was -3·51 [IQR, -4·69,-2·73]. During follow-up, all children had abnormal neuroimaging, 80·3% (94/117) abnormal electroencephalogram, 62·2% (77/120) ophthalmic abnormalities, and 27·4% (34/124) hearing impairment. Microcephaly classification was significantly associated with gestational age, and ophthalmological and electroencephalography abnormalities. Of 125 children with hospitalisation data, 52 (41·6%) had been hospitalised by most recent follow-up, at median age of 15·8 [4·0, 34·4] months; infections were the leading cause.

Conclusion

Congenital ZIKV infection is an emerging disease with a varied and incompletely understood spectrum. Continued long-term follow-up is essential to understand longer-term prognosis and to inform future health and educational needs.

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来源期刊
Dialogues in health
Dialogues in health Public Health and Health Policy
CiteScore
0.70
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0.00%
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审稿时长
134 days
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