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先天性寨卡综合征患儿的 2 年随访:临床模式的演变。

Two-year follow-up of children with congenital Zika syndrome: the evolution of clinical patterns.

机构信息

School of Medicine, Universidade Federal Fluminense, Niteroi, Rio de Janeiro, Brazil.

出版信息

Eur J Pediatr. 2022 Mar;181(3):991-999. doi: 10.1007/s00431-021-04280-z. Epub 2021 Oct 18.

Abstract

The aim of the study was to describe neurological manifestations in children with congenital Zika syndrome (CZS) in the first 2 years of age. In this prospective observational study, children with CZS treated at a university hospital received a neurological assessment and were evaluated using two neurodevelopmental scales (the Denver II test and the assessment of gross motor development of the World Health Organization) by a pediatric neurologist on admission to the study and at 4, 8, 12, 18, and 24 months of age. The data collected were stored in Microsoft Excel version 14.6.3. Thirty-eight children (27 males and 11 females; a median age of 4.3 months (interquartile range (IQR): 1.6-11.4)) with CZS were evaluated. Irritability was present in 50% and 27% of the children at 8 months and 24 months, respectively. Axial hypertonia was highly prevalent at 4 months (77%), with a decrease to 50% at 24 months. At all ages, spastic tetraparesis was the most common motor abnormality (> 80%). Twenty-seven (71%) participants were diagnosed with epilepsy, and the median age at seizure onset was 6 months (IQR: 3.5-8). The most frequent types of seizures were focal seizures and spasms, with spasms being the most frequent in the first year of life (52%) and focal crises being the most frequent in the second year of life (50%).Conclusion: This study allowed observation of neurological abnormalities over time, the evolution of epileptic manifestations, and recognition of new patterns of clinical neurological abnormalities, helping clinicians to recognize CZS earlier, minimizing the impact of new outbreaks. What is Known: • Clinical patterns of SZC patients at pre-established ages or date of data collection • More frequent studies with data collection of clinical-radiological features of patient's over his first year of life What is New: • Comprehensive clinical neurological progression data regarding CZS in the first 2 years of life, recognizing patterns • Hypothesis including a new CZS spectrum with milder clinical-radiological features.

摘要

本研究旨在描述 2 岁以下先天性寨卡综合征(CZS)患儿的神经表现。在这项前瞻性观察研究中,在大学医院接受治疗的 CZS 患儿在入组时和 4、8、12、18 和 24 月龄时由儿科神经科医生进行神经评估,并使用两种神经发育量表(丹佛发展筛查测验和世界卫生组织粗大运动发育评估)进行评估。收集的数据存储在 Microsoft Excel 版本 14.6.3 中。共评估了 38 名 CZS 患儿(27 名男性,11 名女性;中位数年龄为 4.3 个月(四分位距(IQR):1.6-11.4))。8 个月和 24 个月时,分别有 50%和 27%的患儿出现烦躁不安。4 个月时,轴向强直高度普遍(77%),24 个月时降至 50%。在所有年龄,痉挛性四肢瘫是最常见的运动异常(>80%)。27 名(71%)患儿诊断为癫痫,癫痫发作的中位年龄为 6 个月(IQR:3.5-8)。最常见的发作类型是局灶性发作和痉挛,痉挛在生命的第一年最常见(52%),局灶性危象在生命的第二年最常见(50%)。结论:本研究观察了神经异常随时间的演变、癫痫表现的演变以及新的临床神经异常模式的认识,有助于临床医生更早地识别 CZS,最大限度地减少新疫情的影响。已知:•在既定年龄或数据收集日期,SZC 患者的临床模式•更频繁地进行研究,收集患者生命第一年的临床-影像学特征数据新发现:•在生命的前 2 年,对 CZS 进行全面的临床神经进展数据观察,识别模式•提出了一个新的 CZS 谱,具有更轻微的临床-影像学特征的假说。

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