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厄瓜多尔先天性寨卡病毒感染婴儿的长期结局:一项回顾性纵向研究。

Long-Term Outcomes of Infants with Congenital Zika Virus Infection in Ecuador: A Retrospective Longitudinal Study.

机构信息

Pediatric Infectious Disease Department, La Paz University Hospital, Madrid, Spain.

Pediatric Neurology Department, Francisco Icaza Bustamante Children's Hospital, Guayaquil, Ecuador.

出版信息

J Trop Pediatr. 2021 Jul 2;67(3). doi: 10.1093/tropej/fmaa066.

Abstract

BACKGROUND

Few congenital Zika syndrome (CZS) cases have been notified in Ecuador and, to our knowledge, there are no significant published studies dealing with their clinical evolution. We present a detailed clinical characterization of 21 children with congenital Zika virus (ZIKV) infection born in Ecuador who were followed up until September 2019.

METHODS

We did a retrospective longitudinal study of children attended by the infectious disease specialists of Francisco Icaza Bustamante Children's Hospital (Guayaquil) due to congenital ZIKV infection suspicion. The inclusion criteria consisted of laboratory confirmed diagnosis of congenital ZIKV infection.

RESULTS

Sixteen of these 21 cases of congenital ZIKV infection showed clinical, neuroimaging and laboratory findings strongly suggestive of CZS and 5 children showed laboratory findings compatible with congenital ZIKV infection without congenital manifestations associated to CZS. All children with CZS showed neurodevelopmental delay, spasticity and hyperreflexia during follow-up, whereas the majority of them (14/15) experienced recurrent epileptic seizures and dysphagia (12/13). Two CZS cases died during follow-up. Visual evoked potential and hearing screening with acoustically evoked auditory brainstem response were abnormal in 50% and 37.5% of CZS cases, respectively. Congenital ZIKV infection without findings consistent with CZS at birth was not clinically relevant at 23 months of age in the five cases of our cohort.

CONCLUSIONS

Severe neurodevelopmental delay, severe microcephaly, epileptic seizures and dysphagia were present at 2 years of age in most CZS cases of our cohort.

摘要

背景

厄瓜多尔已通报少数先天性寨卡综合征 (CZS) 病例,据我们所知,尚无针对其临床演变的重大已发表研究。我们报告了 21 例在厄瓜多尔出生的先天性寨卡病毒 (ZIKV) 感染患儿的详细临床特征,这些患儿在 2019 年 9 月前接受了随访。

方法

我们对因疑似先天性 ZIKV 感染而由弗朗西斯科·伊卡萨·巴斯塔曼特儿童医院(瓜亚基尔)传染病专家诊治的儿童进行了回顾性纵向研究。纳入标准为实验室确诊的先天性 ZIKV 感染。

结果

21 例先天性 ZIKV 感染中有 16 例存在强烈提示 CZS 的临床、神经影像学和实验室发现,5 例存在与 CZS 相关的先天性表现无关的实验室发现提示先天性 ZIKV 感染。所有 CZS 患儿在随访期间均表现出神经发育迟缓、痉挛和反射亢进,其中大多数(14/15)出现复发性癫痫发作和吞咽困难(12/13)。2 例 CZS 患儿在随访期间死亡。50%的 CZS 患儿的视觉诱发电位和听力筛查伴声诱发脑干反应异常,37.5%的 CZS 患儿听觉诱发电位异常。在我们的队列中,5 例出生时无 CZS 发现的先天性 ZIKV 感染在 23 个月时无临床意义。

结论

在我们的队列中,大多数 CZS 患儿在 2 岁时存在严重的神经发育迟缓、严重小头畸形、癫痫发作和吞咽困难。

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