选择性背根切断术对痉挛性脑瘫患儿神经肌肉症状、肌肉形态和运动功能的影响。

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
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Effect of selective dorsal rhizotomy on neuromuscular symptoms, muscle morphology, and motor function in children with spastic cerebral palsy

Effect of selective dorsal rhizotomy on neuromuscular symptoms, muscle morphology, and motor function in children with spastic cerebral palsy

This study looked at changes in neuromuscular symptoms (spasticity, range of motion, strength, selectivity), muscle growth, and motor function (gait and gross motor function) before and 1 year after selective dorsal rhizotomy (SDR) in children with spastic cerebral palsy (SCP). SDR is a permanent tone-reducing modality that is often applied with these children. During the SDR procedure, 25% to 30% of the dorsal rootlets were cut, descending between L1 and S1 (on the spine). Children received an intensive rehabilitation program during the year after the procedure, with the goal to optimize their quality and quantity of movement.

Fifteen children with bilateral SCP, with a median age of 8 years 8 months, participated in the current study. The study group consisted of 11 boys and 4 girls. Eight children were classified in Gross Motor Function Classification System (GMFCS) level II (children walk in most settings and climb stairs holding onto a railing) and seven were in GMFCS level III (children walk using a hand-held mobility device in most indoor settings). The results showed that SDR effectively reduces spasticity, without negatively affecting muscle growth in children with SCP. Moreover, SDR creates potential beneficial circumstances, namely reduced spasticity and improved selectivity and gait, which may potentially facilitate muscle growth.

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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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