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先天性寨卡综合征患儿的粗大运动功能

Gross Motor Function in Children with Congenital Zika Syndrome.

作者信息

Takahasi Eliana Harumi Morioka, Alves Maria Teresa Seabra Soares de Britto, Ribeiro Marizélia Rodrigues Costa, Souza Valéria Ferreira Pereira, Simões Vanda Maria Ferreira, Borges Marcella Costa Ribeiro, Amaral Gláucio Andrade, Gomes Lillian Nunes, Khouri Ricardo, da Silva Sousa Patricia, Silva Antônio Augusto Moura da

机构信息

Sarah Network of Neurorehabilitation Hospitals, São Luís, Maranhão, Brazil.

Public Health Department, Federal University of Maranhão, São Luís, Maranhão, Brazil.

出版信息

Neuropediatrics. 2021 Feb;52(1):34-43. doi: 10.1055/s-0040-1718919. Epub 2020 Oct 27.

Abstract

BACKGROUND

Little information on gross motor function of congenital Zika syndrome (CZS) children is available.

OBJECTIVES

To evaluate gross motor function in CZS children aged up to 3 years, and its associated factors and changes in a minimum interval of 6 months.

METHODS

One hundred children with CZS and cerebral palsy (36 with confirmed and 64 with presumed CZS) were evaluated with the Gross Motor Function Classification System (GMFCS) and Gross Motor Function Measure (GMFM-88/GMFM-66). Forty-six were reevaluated. Wilcoxon tests, Wilcoxon tests for paired samples, percentile scores, and score changes were performed.

RESULTS

Clinical and socioeconomic characteristics (except maternal age), GMFM scores and GMFCS classification of confirmed and probable cases, which were analyzed together, were similar. The mean age was 25.6 months (±5.5); the median GMFM-88 score was 8.0 (5.4-10.8); and the median GMFM-66 score was 20.5 (14.8-23.1); 89% were classified as GMFCS level V. Low economic class, microcephaly at birth, epilepsy, and brain parenchymal volume loss were associated with low GMFM-66 scores. The median GMFM-66 percentile score was 40 (20-55). On the second assessment, the GMFM-66 scores in two GMFCS level I children and one GMFCS level IV child improved significantly. In one GMFCS level III child, one GMFCS level IV child, and the group of GMFCS level V children, no significant changes were observed.

CONCLUSIONS

Almost all CZS children had severe cerebral palsy; in the third year of life, most presented no improvement in gross motor function and were likely approaching their maximal gross motor function potential.

摘要

背景

关于先天性寨卡综合征(CZS)患儿粗大运动功能的信息较少。

目的

评估3岁及以下CZS患儿的粗大运动功能,及其相关因素,并在至少6个月的最短间隔内观察其变化。

方法

采用粗大运动功能分类系统(GMFCS)和粗大运动功能测量量表(GMFM-88/GMFM-66)对100例CZS合并脑性瘫痪患儿(36例确诊CZS,64例疑似CZS)进行评估。46例患儿进行了重新评估。进行了威尔科克森检验、配对样本威尔科克森检验、百分位数评分和评分变化分析。

结果

确诊和疑似病例的临床和社会经济特征(母亲年龄除外)、GMFM评分和GMFCS分类相似。平均年龄为25.6个月(±5.5);GMFM-88评分中位数为8.0(5.4-10.8);GMFM-66评分中位数为20.5(14.8-23.1);89%被分类为GMFCS V级。低经济阶层、出生时小头畸形、癫痫和脑实质体积减少与低GMFM-66评分相关。GMFM-66百分位数评分中位数为40(20-55)。在第二次评估中,2例GMFCS I级患儿和1例GMFCS IV级患儿的GMFM-66评分显著改善。1例GMFCS III级患儿、1例GMFCS IV级患儿和GMFCS V级患儿组未观察到显著变化。

结论

几乎所有CZS患儿都患有严重脑性瘫痪;在生命的第三年,大多数患儿的粗大运动功能没有改善,可能已接近其最大粗大运动功能潜力。

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