Albright A L, Barry M J, Painter M J, Shultz B
Department of Neurosurgery, Children's Hospital of Pittsburgh, Pennsylvania 15213, USA.
J Neurosurg. 1998 Jan;88(1):73-6. doi: 10.3171/jns.1998.88.1.0073.
Generalized dystonia occurs in 15 to 25% of persons with cerebral palsy (CP) and responds poorly to medical and surgical treatments.
After the authors observed a woman whose dystonic CP was dramatically improved by continuous infusion of intrathecal baclofen, they designed this pilot study to evaluate the effect of this treatment on a group of patients with dystonic CP.
The authors assessed the short-term response to intrathecal baclofen infusion in 12 patients with dystonic CP. An intrathecal catheter was inserted percutaneously and connected to an external microinfusion pump. The infusion began at a rate of 100 microg/day and was increased by 50 microg every 12 hours until the dystonia abated, adverse effects occurred, or the dose reached 900 microg/day with no improvement. Two observers, one blinded and one not blinded to the patient's treatment status, viewed videotapes made before and after the infusions and graded the dystonia in eight body regions, using a 5-point scale. Overall and regional scores were compared by using Wilcoxon signed-rank tests.
Dystonia diminished in 10 of 12 patients whose average daily dose of intrathecal baclofen was 575 microg. Overall dystonia scores and scores for the extremities, trunk, and cervical regions were significantly better after infusion (p = 0.003). The two observers' scores were not significantly different. Programmable infusion pumps were subsequently implanted in eight patients for long-term therapy and improvement was sustained in six (p < 0.05). Intrathecal baclofen infusion is a promising treatment option for generalized dystonia associated with CP. The effects of intrathecal baclofen infusion on dystonia can be evaluated by using short-term continuous infusions.
全身性肌张力障碍发生于15%至25%的脑瘫(CP)患者中,对药物和手术治疗反应不佳。
作者观察到一名患有肌张力障碍型脑瘫的女性通过鞘内持续输注巴氯芬后病情显著改善,之后设计了这项初步研究,以评估该治疗方法对一组肌张力障碍型脑瘫患者的效果。
作者评估了12例肌张力障碍型脑瘫患者对鞘内输注巴氯芬的短期反应。经皮插入鞘内导管并连接至外部微量输注泵。输注以100微克/天的速率开始,每12小时增加50微克,直至肌张力障碍减轻、出现不良反应,或剂量达到900微克/天且无改善。两名观察者,一名对患者的治疗状态不知情,一名知情,观看输注前后拍摄的录像带,并使用5分制对八个身体部位的肌张力障碍进行评分。使用Wilcoxon符号秩检验比较总体和区域评分。
12例患者中有10例肌张力障碍减轻,其鞘内巴氯芬的平均日剂量为575微克。输注后总体肌张力障碍评分以及四肢、躯干和颈部区域的评分显著改善(p = 0.003)。两名观察者的评分无显著差异。随后为8例患者植入了可编程输注泵进行长期治疗,其中6例病情持续改善(p < 0.05)。鞘内输注巴氯芬是治疗与脑瘫相关的全身性肌张力障碍的一种有前景的治疗选择。鞘内输注巴氯芬对肌张力障碍的影响可通过短期持续输注来评估。