强化小儿神经康复治疗核黄疸的个案研究。

Journal of Clinical Movement Disorders Pub Date : 2020-02-03 eCollection Date: 2020-01-01 DOI:10.1186/s40734-020-0084-z
Jessie Mann, Dory A Wallace, Stephanie DeLuca
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引用次数: 0

摘要

背景:核黄疸谱系障碍(KSD)是胆红素长期中毒导致广泛神经损伤的结果。一旦胆红素水平正常化,脑病就会变得静止,然而,损伤的后果可能会产生终身影响。KSD的后遗症包括运动障碍、听觉障碍、牙齿发育不良和潜在的认知障碍。虽然KSD是一种罕见的诊断,特别是在发达国家,但有证据表明,全球发病率可能有所增加(Hansen, Semin Neonatol, 2002:103-9;杨志强,刘志强。中国生物医学工程学报(英文版);2009;卡普兰等等。中华儿科杂志(英文版);2011;Maisels, Early Hum Dev 85:727- 32,2009;Olusanya等等。[j];《儿童研究》,2014;Steffensrud,新生儿护理,Rev 4:191- 200,2004)。关于KSD各种特定后遗症的治疗文献各不相同,但一般来说,改善运动技能的特定治疗努力没有证据基础。以下是一个使用习得疗法的病例报告,一种强化的神经运动干预,以改善KSD继发的一些运动功能缺陷。病例介绍:本病例报告介绍了一名患有KSD的男性儿童的两次强化治疗干预的结果。治疗分别在28个月和34个月进行。这孩子表现出精细和大运动缺陷以及沟通迟缓。每个疗程包括每日治疗,每个工作日4小时,持续3周。采用大运动功能量表(GMFM)和Bayley婴幼儿发育量表(Bayley)两种标准化测量方法对患儿进行治疗前后评估。结论:第一次评估时GMFM为34,第二次评估时GMFM为74(干预1后),第三次评估时GMFM为64,第4次评估时GMFM为104(干预2后)。第3次评估时Bayley为18,第4次评估时Bayley为38(干预2后)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Case study on the use of intensive pediatric neurorehabilitation in the treatment of kernicterus.

Case study on the use of intensive pediatric neurorehabilitation in the treatment of kernicterus.

Case study on the use of intensive pediatric neurorehabilitation in the treatment of kernicterus.

Case study on the use of intensive pediatric neurorehabilitation in the treatment of kernicterus.

Background: Kernicterus Spectrum Disorder (KSD) is the result of prolonged bilirubin toxicity resulting in widespread neurological injury. Once the bilirubin levels are normalized the encephalopathy becomes static, however the consequences of the injury can have life-long effects. The sequelae of KSD include motor impairments, auditory deficits, dental dysplasia, and potentially cognitive impairments. While KSD is a rare diagnosis, particularly in developed countries, there is evidence that there may be a global increase in incidence (Hansen, Semin Neonatol 7:103-9, 2002; Johnson, J Perinatol 29:S25-45, 2009; Kaplan etal. Neonatology 100:354-62, 2011; Maisels, Early Hum Dev 85:727-32, 2009; Olusanya etal., Arch Dis Child 99:1117-21, 2014; Steffensrud, Newborn Infant Nurs Rev 4:191-200, 2004). The literature on the treatment of various specific sequelae of KSD is varied, but in general specific therapeutic efforts to improve motor skills are not evidenced-based. The following is a case report on the use of Acquire therapy, an intensive neuromotor intervention, to ameliorate some of the motor-function deficits secondary to KSD.

Case presentation: This case-report presents the results of two intensive therapeutic intervention sessions in one male child with KSD. Treatments occurred at 28 and 34 months. The child presented with fine and gross motor deficits as well as communication delays. Each session consisted of daily therapy for 4 h each weekday for 3 weeks. The child was assessed before and after treatment with 2 standardized measures, the Gross Motor Function Measure (GMFM) and The Bayley Scales of Infant and Toddler Development (Bayley).

Conclusions: The GMFM at the 1st assessment was 34, 74at the 2nd assessment (after intervention 1), and 64 at the third assessment and 104 at the 4th assessment (after intervention 2). The Bayley at the 3rd assessment was 18, and 38 at the 4th assessment (after intervention 2).

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