A型肉毒毒素治疗脑瘫后上肢功能:6例2年随访。

Heli Sätilä, Anne Kotamäki, Matti Koivikko, Ilona Autti-Rämö
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引用次数: 29

摘要

本研究的目的是在2年的随访期间调查肉毒毒素A (BTXA)治疗对上肢损伤和功能的影响。采用前瞻性纵向研究设计,在干预前后进行评估,纳入6例脑瘫患者(3男3女),研究开始时年龄为3岁4个月至11岁11个月。观察指标为痉挛(改良Ashworth, MAS)、主动和被动活动范围(ROM)、握感(捏、键握、三指握、窄柱握、宽柱握、笔握、对角握);把握,释放;双手功能、精细运动功能(墨尔本单侧上肢功能评估)、运动模式(上肢医师评定量表,ULPRS)、功能技能和自我护理能力(儿科残疾评估量表,PEDI)、上肢使用(House分类)和美容外观。在每次治疗后的基线、1个月、3个月和6个月由相同的检查人员重复评估,然后每6个月进行一次,直到24个月。1名受试者在研究开始时共接受4次注射(0、6、12和18个月),1次注射2次(0和12个月),4次注射1次。研究期间对2名受试者进行了上肢手术,其中1名在研究结束2个月后进行了手术。所有儿童都受益于BTXA治疗,肌肉张力降低,主动和被动ROM增加。到6个月时,痉挛恢复,但有4名儿童被动,特别是主动ROM保持比基线时更好。在握力、手工任务或墨尔本评估得分方面没有发现明显的变化。运动模式的改变(ULPRS)在两个孩子中维持了3个月,在4个孩子中维持了3个月以上,从而延伸到肉毒杆菌毒素a的药物作用之外。在2年期间,除了一个孩子外,所有孩子在PEDI功能技能和照顾者辅助量表得分方面都有改善。House分类显示,在BTXA治疗后1个月和3个月,分别有1个孩子和1个孩子有1级改善,3个月后有1个孩子有3级改善。每次治疗后,父母报告所有儿童在1个月时的外观至少有一级改善,其中4名儿童至少维持到6个月。在研究期间进行手术的两名受试者中,观察到手术后主动和被动ROM有明显改善,House分类有两个等级的改善。在这个有限的系列中,肉毒毒素治疗后肌肉张力的降低并没有转化为患手更好的抓握或精细运动功能的质量(墨尔本评估),但似乎对上肢运动模式(ULPRS)、上肢使用(House分类)和美容外观有积极影响。评估脑瘫儿童的上肢功能需要多种措施。
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Upper limb function after botulinum toxin A treatment in cerebral palsy: two years follow-up of six cases.

The objective of this study was to investigate the effects of botulinum toxin A (BTXA) treatment on impairment and function of the upper limb during a 2-year follow-up period. A prospective longitudinal study design with assessments before and after intervention was utilized, involving six patients with cerebral palsy (three boys and three girls) aged 3 years 4 months to 11 years 11 months at commencement of study. The outcome measures were spasticity (modified Ashworth, MAS), active and passive range of movement (ROM), grips (pinch, key grip, 3-finger grip, narrow cylinder grip, wide cylinder grip, pen grip and diagonal grip; grasping, releasing; pronation-supination), bimanual functions, fine motor functions (Melbourne Assessment of Unilateral Upper Limb Function), movement pattern (Upper Limb Physician's Rating Scale, ULPRS), functional skills and self-care capability (Paediatric Evaluation of Disability Inventory, PEDI), upper extremity use (House Classification) and cosmetic appearance. The assessments were repeated by the same examiners at baseline and at 1, 3 and 6 months after each BTXA treatment and then every 6 months until 24 months. One subject received a total of four injections (at 0, 6, 12 and 18 months), one two injections (at 0 and 12 months) and four one injection at the beginning of the study period. Upper extremity surgery was performed on two subjects during the study and one was operated on 2 months after completion of the study. All children benefited from the BTXA treatment in terms of reduction in muscle tone and increase in active and passive ROM. By 6 months, spasticity returned, but in four children passive and especially active ROM remained better than at baseline. No significant changes in grips, bimanual tasks or Melbourne Assessment scores were detected. The change in movement pattern (ULPRS) was maintained for 3 months in two children and beyond this in four, thus extending beyond the pharmacologic effects of botulinum toxin A. All but one child showed improvement in PEDI functional skill and caregiver assistance scale scores during the 2-year period. The House classification showed a one-grade improvement in one child at 1 month and in one child at 3 months and a three-grade improvement in one child at 3 months after BTXA treatment. After each treatment, the parents reported at least a one-grade improvement in cosmetic appearance in all children at 1 month and in four children maintained at least until 6 months. In two subjects operated during the study period, a distinct improvement in active and passive ROM and a two-grade improvement in the House classification were observed after the operation. In this limited series, the reduction in muscle tone after BTXA treatment did not translate into better gripping or quality of fine motor functions (Melbourne Assessment) of the affected hand, but seemed to have a positive effect on upper limb movement pattern (ULPRS), upper extremity use (House Classification) and cosmetic appearance. Assessment of upper limb function in a child with cerebral palsy demands a variety of measures.

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Musculoskeletal Conditions Neuromuscular Conditions Hypertonia Rheumatologic Conditions Acquired Brain Injury
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