Hoare Brian J, Wallen Margaret A, Imms Christine, Villanueva Elmer, Rawicki Hyam Barry, Carey Leeanne
School of Occupational Therapy, La Trobe University, Victorian Paediatric Rehabilitation Service, Monash Medical Centre, 246 Clayton Road, Clayton, Victoria, Australia, 3086.
Cochrane Database Syst Rev. 2010 Jan 20;2010(1):CD003469. doi: 10.1002/14651858.CD003469.pub4.
Cerebral palsy (CP) is "a group of permanent disorders of the development of movement and posture causing activity limitation(s) that are attributed to non-progressive disturbance that occurred in the developing fetal or infant brain" (Rosenbaum 2007, p.9). The spastic motor type is the most common form of CP. Therapeutic management may include splinting/casting, passive stretching, facilitation of posture/movement, spasticity-reducing medication and surgery. Botulinum toxin-A (BoNT-A) is now used as an adjunct to these techniques in an attempt to reduce spasticity, improve range of movement and function.
To assess the effectiveness of injections of BoNT-A or BoNT-A and occupational therapy in the treatment of the upper limb in children with CP.
We searched the Cochrane Controlled Trials Register/CENTRAL (The Cochrane Library, Issue 3, 2008), MEDLINE (1966 to August Week 1 2008), EMBASE (1980 to 2008 Week 28) and CINAHL (1982 to August Week 1 2008).
All randomised controlled trials (RCTs) comparing BoNT-A injection or BoNT-A injection and occupational therapy in the upper limb(s) with other types of treatment (including no treatment or placebo) in children with CP.
Two authors using standardised forms extracted the data independently. Each trial was assessed for internal validity and rated for quality using the PEDro scale. Data were extracted and entered into RevMan 5.0.15.
Ten trials met the inclusion criteria. PEDro quality ratings ranged from 6/10 to 10/10. Concentration of BoNT-A ranged from 50U/1.0ml to 200U/1.0ml saline with doses of 0.5U to 16U/kg body weight and total doses of 220 to 410 Units (Botox(R)).A combination of BoNT-A and occupational therapy is more effective than occupational therapy alone in reducing impairment, improving activity level outcomes and goal achievement, but not for improving quality of life or perceived self-competence. When compared with placebo or no treatment, there is moderate evidence that BoNT-A alone is not effective.
AUTHORS' CONCLUSIONS: This systematic review found high level evidence supporting the use of BoNT-A as an adjunct to managing the upper limb in children with spastic CP. BoNT-A should not be used in isolation but should be accompanied by planned occupational therapy.Further research is essential to identify children most likely to respond to BoNT-A injections, monitor longitudinal outcomes, determine timing and effect of repeated injections and the most effective dosage, dilution and volume schedules. The most effective adjunct therapies including frequency and intensity of delivery also requires investigation.
脑性瘫痪(CP)是“一组运动和姿势发育的永久性障碍,导致活动受限,这归因于胎儿或婴儿发育中的大脑发生的非进行性紊乱”(罗森鲍姆,2007年,第9页)。痉挛型运动障碍是CP最常见的形式。治疗管理可能包括夹板固定/石膏固定、被动拉伸、姿势/运动促进、减轻痉挛的药物治疗和手术。肉毒杆菌毒素A(BoNT-A)现在被用作这些技术的辅助手段,以试图减轻痉挛、改善运动范围和功能。
评估注射BoNT-A或BoNT-A与职业治疗对CP儿童上肢的治疗效果。
我们检索了Cochrane对照试验注册库/CENTRAL(Cochrane图书馆,2008年第3期)、MEDLINE(1966年至2008年8月第1周)、EMBASE(1980年至2008年第28周)和CINAHL(1982年至2008年8月第1周)。
所有比较BoNT-A注射或BoNT-A注射与职业治疗对CP儿童上肢治疗与其他类型治疗(包括不治疗或安慰剂)的随机对照试验(RCT)。
两位作者使用标准化表格独立提取数据。每项试验均评估其内部效度,并使用PEDro量表对质量进行评分。数据被提取并录入RevMan 5.0.15。
10项试验符合纳入标准。PEDro质量评分范围为6/10至10/10。BoNT-A的浓度范围为50U/1.0ml至200U/1.0ml生理盐水,剂量为0.5U至16U/千克体重,总剂量为220至410单位(保妥适)。BoNT-A与职业治疗相结合在减轻损伤、改善活动水平结果和目标达成方面比单独的职业治疗更有效,但在改善生活质量或自我感知能力方面并非如此。与安慰剂或不治疗相比,有中等证据表明单独使用BoNT-A无效。
本系统评价发现了高水平证据支持使用BoNT-A作为治疗痉挛型CP儿童上肢的辅助手段。BoNT-A不应单独使用,而应辅以有计划的职业治疗。进一步的研究对于确定最可能对BoNT-A注射有反应的儿童、监测纵向结果、确定重复注射的时间和效果以及最有效的剂量、稀释度和体积方案至关重要。最有效的辅助治疗方法,包括治疗频率和强度,也需要进行研究。