脑瘫儿童视力损伤的自然史。

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Jessica Galli, Erika Loi, Stefano Calza, Serena Micheletti, Anna Molinaro, Alessandra Franzoni, Andrea Rossi, Francesco Semeraro, Lotfi B Merabet, Elisa Fazzi
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引用次数: 0

摘要

目的:纵向评估脑性瘫痪(CP)儿童脑性视力障碍(CVI)的自然史,并确定哪些早期视觉体征或症状与学龄期认知性视觉障碍(CVD)有关:51名患有CP和CVI的儿童在三个时间点接受了眼科、眼球运动和基本视觉功能评估:T0(6-35 个月)、T1(3-5 岁)和 T2(≥6 岁)。我们还在 T2 阶段进行了认知视觉评估。使用广义估计方程(二元)和累积联系模型(序数)拟合的逻辑回归对相关结果进行建模:结果:除眼底异常外,眼科缺陷随着时间的推移趋于稳定(T1-T0,p = 0.01;T2-T1,p = 0.02;T2-T0,p 解释:虽然所有患儿在每个时间点都被确诊为 CVI,但随着时间的推移,一些视觉体征和症状有所改善;在某些病例中,这些体征和症状在 T1 和 T2 期完全恢复。这些结果表明,在发育过程中,与 CP 相关的 CVI 具有 "永久性",但并非 "一成不变"。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Natural history of cerebral visual impairment in children with cerebral palsy.

Aim: To longitudinally evaluate the natural history of cerebral visual impairment (CVI) in children with cerebral palsy (CP) and identify which early visual signs or symptoms are associated with cognitive visual disorders (CVDs) at school age.

Method: Fifty-one individuals with CP and CVI underwent an ophthalmological, oculomotor, and basic visual function evaluation at three time points: T0 (6-35 months old); T1 (3-5 years old); and T2 (≥6 years old). We also performed a cognitive visual evaluation at T2. Logistic regression fitted using a generalized estimation equation (binary) and cumulative link models (ordinal) were used to model the outcomes of interest.

Results: Ophthalmological deficits were stable over time, except for ocular fundus abnormalities (T1-T0, p = 0.01; T2-T1, p = 0.02; T2-T0, p < 0.01) and strabismus, whose frequency increased with age (T2-T0, p= 0.02 with T2-T0, p = 0.05). Conversely, fixation (T1-T0, T2-T0, p < 0.01), smooth pursuit (T2-T1, T2-T0, p < 0.01), saccades (T1-T0, T2-T1, T2-T0, p < 0.01), as well as visual acuity, contrast sensitivity, and visual field (T1-T0, T2-T0, p < 0.01) all improved over time. Early oculomotor dysfunction was associated with CVD at T2.

Interpretation: Although a diagnosis of CVI was confirmed in all children at each time point, several visual signs and symptoms improved over time; in some cases, they reached complete recovery at T1 and T2. These results emphasize the 'permanent' but 'not unchanging' nature of the CVI associated with CP during development.

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来源期刊
CiteScore
7.80
自引率
13.20%
发文量
338
审稿时长
3-6 weeks
期刊介绍: Wiley-Blackwell is pleased to publish Developmental Medicine & Child Neurology (DMCN), a Mac Keith Press publication and official journal of the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) and the British Paediatric Neurology Association (BPNA). For over 50 years, DMCN has defined the field of paediatric neurology and neurodisability and is one of the world’s leading journals in the whole field of paediatrics. DMCN disseminates a range of information worldwide to improve the lives of disabled children and their families. The high quality of published articles is maintained by expert review, including independent statistical assessment, before acceptance.
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