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鞘内注射巴氯芬治疗成人脊髓性痉挛:治疗效果及对住院率的影响。

Intrathecal baclofen therapy for adults with spinal spasticity: therapeutic efficacy and effect on hospital admissions.

作者信息

Nance P, Schryvers O, Schmidt B, Dubo H, Loveridge B, Fewer D

机构信息

Department of Medicine, University of Manitoba, Winnipeg, Canada.

出版信息

Can J Neurol Sci. 1995 Feb;22(1):22-9. doi: 10.1017/s0317167100040452.

Abstract

A prospective trial to demonstrate the efficacy of intrathecal baclofen therapy by implanted pump for adults with spasticity due to spinal cord injury or multiple sclerosis was initiated in our hospital. Of the 140 patients assessed, 7 met the following criteria for inclusion in the study: a modified Ashworth score > 3, a spasm frequency score > 2, and an inadequate response to oral anti-spasticity drugs, (i.e., baclofen, clonidine and cyproheptadine). All patients responded to intrathecal bolus injection of baclofen in the double blind, placebo-controlled screening phase (mean bolus dose = 42.8 micrograms). Programmable Medtronic pumps were implanted in 4 patients while 3 patients received non-programmable Infusaid pumps. Post-implantation, a marked decrease in spasticity occurred with a significant reduction of the Ashworth score (mean = 1.8, p < .005), a reduced spasm score (mean = 0.8, p < .005), and an improved leg swing in the pendulum test. These effects were maintained during a follow-up of 24-41 months (average infusion dose = 218.7 micrograms/day). The gross cost-savings due to reduced hospitalizations related to spasticity was calculated by comparing the cost for the two year period before pump implantation to the same period after treatment for 6 of the 7 patients. The cost of in-hospital implantation as well as the cost of the pumps were deducted from the gross savings. There was a net cost-saving of $153,120. Our findings agree with the reported efficacy and safety of intrathecal baclofen treatment, and illustrate the cost-effectiveness of this treatment.

摘要

我院开展了一项前瞻性试验,以证明植入式泵鞘内注射巴氯芬疗法对因脊髓损伤或多发性硬化症导致痉挛的成人患者的疗效。在评估的140例患者中,7例符合以下纳入研究的标准:改良Ashworth评分>3、痉挛频率评分>2且对口服抗痉挛药物(即巴氯芬、可乐定和赛庚啶)反应不佳。在双盲、安慰剂对照的筛查阶段,所有患者鞘内推注巴氯芬均有反应(平均推注剂量=42.8微克)。4例患者植入了可程控的美敦力泵,3例患者接受了不可程控的英福赛德泵。植入后,痉挛明显减轻,Ashworth评分显著降低(平均=1.8,p<.005),痉挛评分降低(平均=0.8,p<.005),摆锤试验中腿部摆动改善。这些效果在24至41个月的随访期间得以维持(平均输注剂量=218.7微克/天)。通过比较7例患者中6例患者泵植入前两年的费用与治疗后同期的费用,计算出因痉挛相关住院减少而节省的总费用。住院植入费用以及泵的费用从总节省费用中扣除。净节省费用为153,120美元。我们的研究结果与已报道的鞘内注射巴氯芬治疗的疗效和安全性一致,并说明了该治疗的成本效益。

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