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加巴喷丁对痉挛的控制效果:一项定量研究。

Effectiveness of gabapentin in controlling spasticity: a quantitative study.

作者信息

Priebe M M, Sherwood A M, Graves D E, Mueller M, Olson W H

机构信息

Department of Physical Medicine and Rehabilitation, Baylor College of Medicine, Houston, Texas, USA.

出版信息

Spinal Cord. 1997 Mar;35(3):171-5. doi: 10.1038/sj.sc.3100366.

Abstract

The purpose of this investigation was to study the effectiveness of gabapentin in controlling spasticity in persons with spinal cord injury (SCI) using a surface EMG-based quantitative assessment technique called the brain motor control assessment (BMCA). Six men from a Veterans Affairs Medical Center with spasticity due to traumatic SCI were studied as part of a multi-center, placebo-controlled, cross-over, clinical trial of gabapentin. Spasticity was evaluated using multi-channel surface EMG recordings of muscles in the lower extremities, abdomen and low back before and during treatment with oral gabapentin or placebo. Gabapentin or placebo was given orally in doses 400 mg three times daily for 48 h. Following a 10 day wash-out period subjects were crossed-over to receive the medication not received the first time. This was followed by an elective open-label extension. Group results during the controlled trial did not reach statistical significance at the dosage used. One subject demonstrated a dramatic improvement in spasticity that was apparent both clinically and with the BMCA. Other subjects demonstrated modest improvements which were seen in the BMCA but not recognized clinically. During the open label extension, the four subjects who participated experienced important clinical improvements with higher doses (to 3600 mg/day). These improvements were often in components of spasticity in which the BMCA had detected subclinical changes during the cross-over trial. A seventh subject was studied using the BMCA at doses of 1200 mg T.I.D. gabapentin, off gabapentin and 800 mg T.I.D. gabapentin and demonstrated quantitatively a dose-related effect with higher doses of gabapentin which matched clinical observations. Gabapentin at doses of 400 mg T.I.D. may be effective in controlling some features of spasticity in persons with SCI. Higher doses provide greater control of spasticity, and controlled studies using higher doses are needed to evaluate gabapentin's efficacy.

摘要

本研究的目的是使用一种名为脑运动控制评估(BMCA)的基于表面肌电图的定量评估技术,研究加巴喷丁在控制脊髓损伤(SCI)患者痉挛方面的有效性。作为加巴喷丁多中心、安慰剂对照、交叉临床试验的一部分,对来自退伍军人事务医疗中心的6名因创伤性SCI而出现痉挛的男性进行了研究。在口服加巴喷丁或安慰剂治疗前和治疗期间,使用多通道表面肌电图记录下肢、腹部和下背部肌肉的情况来评估痉挛。加巴喷丁或安慰剂以每日三次、每次400毫克的剂量口服,持续48小时。经过10天的洗脱期后,受试者交叉接受第一次未服用的药物。随后进行了选择性开放标签扩展研究。在对照试验期间,所用剂量的组结果未达到统计学显著性。一名受试者的痉挛症状在临床和BMCA评估中均有显著改善。其他受试者有适度改善,在BMCA评估中可见,但临床未识别。在开放标签扩展研究期间,参与的4名受试者在更高剂量(至3600毫克/天)下有重要的临床改善。这些改善通常出现在痉挛的某些方面,而在交叉试验期间BMCA已检测到这些方面存在亚临床变化。对第七名受试者在加巴喷丁剂量为每日三次、每次1200毫克、停用加巴喷丁以及每日三次、每次800毫克加巴喷丁的情况下使用BMCA进行研究,结果定量显示加巴喷丁剂量越高,效果越明显,这与临床观察结果相符。每日三次、每次400毫克剂量的加巴喷丁可能对控制SCI患者痉挛的某些特征有效。更高剂量能更好地控制痉挛,需要使用更高剂量进行对照研究以评估加巴喷丁的疗效。

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