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

机译:密集儿科神经孢子料治疗核心工具的案例研究

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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).? The Author(s). 2020.
机译:背景:Kernicterus谱系障碍(KSD)是胆红素毒性延长的结果,导致普遍的神经损伤。一旦胆红素水平归一化,脑病变得静止,但损伤的后果可以具有终生效效果。 KSD的后遗症包括电机损伤,听觉缺陷,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,特别是发达国家,但有证据表明,可能存在全球发病率增加(汉森,Semin Neonatol 7:103-9,2002; Johnson,J Perinatol 29:S25-45,2009; Kaplan etal。新生儿学100:354-62,2011; Maisels,早期嗡嗡声85:727-32,2009; Olusanya Etal。,Arch Dist 99:1117-21,2014; Steffensrud,新生儿婴儿Nurs Rev 4:191-200 ,2004)。关于治疗KSD各种特异性后遗症的文献,但在一般的特定治疗努力中,提高运动技能的努力不是证明的。以下是关于使用获取治疗,密集的神经系统干预的案例报告,以改善次要的一些电动功能赤字审查:本案报告在一个男性中提出了两个密集的治疗干预课程的结果ksd的孩子。治疗发生在28和34个月。几个月。孩子介绍了良好的和总股票赤字以及通信延误。每次会议由每日4?H每个每日治疗组成3?周。该儿童在治疗之前和之后进行评估,使用2个标准化措施,总机函数措施(GMFM)和拜访婴儿和幼儿开发(Bayley).Conclusions:第一次评估的GMFM为34,74AT第2次评估(干预后1),和第三次评估的64和第4次评估(干预后2)。第3评估的拜访是18岁,第38条评估(干预后2)。作者。 2020。

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