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首页> 外文期刊>Clinical rehabilitation >A randomized controlled trial studying efficacy and tolerance of a knee-ankle-foot orthosis used to prevent equinus in children with spastic cerebral palsy
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A randomized controlled trial studying efficacy and tolerance of a knee-ankle-foot orthosis used to prevent equinus in children with spastic cerebral palsy

机译:一项随机对照试验,研究用于预防痉挛性脑瘫患儿马nu的膝踝足矫形器的疗效和耐受性

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Objective: To examine whether using a knee-ankle-foot orthosis helps maintain ankle-foot dorsiflexion range of motion over time.Design: A multicentre randomized controlled trial.Setting: Two hospitals and one rehabilitation centre in the Netherlands and the USA.Subjects: Children (4-16 years old) with spastic cerebral palsy who were able to walk.Intervention: Use of a knee-ankle-foot orthosis, equipped with an Ultraflex? ankle power unit, for at least 6 hours every other night for one year.Main measures: Primary outcome measure: ankle-foot dorsiflexion range of motion. Secondary outcome measures: ankle-foot and knee angle in gait and gross motor function. Wearing time was also measured. Measurements were taken at baseline and at 3, 6, 9 and 12 months.Results: 28 children (experimental group: n=15, control group: n=13) participated in the study. 11 participants (experimental: n=4, control: n=7) did not complete all five measurements, as they needed additional treatment. No significant difference was found in the decrease of ankle-foot dorsiflexion range of motion between the experimental and control groups (difference: -1.05°, 95% confidence interval: -4.71° - 2.61°). In addition, secondary outcome measures did not show differences between groups. Despite good motivation, knee-ankle-foot orthosis wearing time was limited to a mean±SD of 3.2±1.9 hours per prescribed night due to discomfort.Conclusions: Knee-ankle-foot orthosis with dynamic ankle and fixed knee are poorly tolerated and are not beneficial in preventing a reduction in ankle-foot dorsiflexion range of motion in children with spastic cerebral palsy, at least with limited use.
机译:目的:研究使用膝-踝-脚矫形器是否有助于维持踝脚背屈运动的范围设计:一项多中心随机对照试验背景:荷兰和美国的两家医院和一个康复中心能够行走的痉挛性脑瘫儿童(4-16岁)。干预措施:膝关节,踝足矫形器的使用以及Ultraflex?踝关节动力装置,一年至少隔一夜保持6个小时。主要措施:主要预后措施:踝足背屈运动范围。次要结局指标:步态和大运动功能的脚踝和膝盖角度。还测量了佩戴时间。在基线,3、6、9和12个月进行测量。结果:28名儿童(实验组:n = 15,对照组:n = 13)参加了研究。 11名参与者(实验性:n = 4,对照组:n = 7)未完成所有五次测量,因为他们需要其他治疗。实验组和对照组之间的踝足背屈运动范围的减少没有显着差异(差异:-1.05°,95%置信区间:-4.71°-2.61°)。此外,次要结局指标未显示两组之间的差异。尽管动机良好,但由于不适,膝-踝-足矫形器的佩戴时间被限制为每处方每晚平均±SD 3.2±1.9小时。结论:动态踝关节和固定膝的膝-踝-足矫形器耐受性差且至少在有限的使用范围内,对预防痉挛性脑瘫患儿脚踝背屈运动范围的减少无益。

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