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鞘内注射巴氯芬治疗多发性硬化相关痉挛:长期随访。

Treatment of spasticity related to multiple sclerosis with intrathecal baclofen: a long-term follow-up.

机构信息

Department of Neurology, Haukeland University Hospital, NO-5021 Bergen, Norway.

出版信息

J Rehabil Med. 2011 May;43(6):511-4. doi: 10.2340/16501977-0811.

Abstract

BACKGROUND

Spasticity is a frequent disabling symptom in patients with multiple sclerosis, which contributes to functional deterioration.

OBJECTIVE

To evaluate the long-term effect of intrathecal baclofen therapy in multiple sclerosis-related spasticity and to evaluate the side-effects of long-term therapy, and the doses of baclofen required.

METHODS

Fourteen patients with multiple sclerosis were followed up clinically for a mean of 62 months (range 19-137 months). Clinical evaluation was made using individual goals, modified Ashworth scale, and Kurtzke Expanded Disability Status Scale.

RESULTS

Spasticity, measured with the modified Ashworth score, decreased in all patients by a mean of 1 point. The score on the Expanded Disability Status Scale improved in 2 cases. Prior to implantation, 10 patients (72%) reported severe pain. After implantation 3 improved and 7 became pain-free. The daily doses needed for treatment were highly individual. The effect of intrathecal baclofen on spasticity lasted observation time. One patient experienced progressive cognitive impairment as a side-effect of baclofen.

CONCLUSION

Intrathecal baclofen is well-tolerated and the effect lasts for up to 12 years. A thorough continuous clinical assessment is required because the differentiation between symptoms of multiple sclerosis progression and side-effects of baclofen may be difficult. Intrathecal baclofen should be considered as an option for long-term treatment of patients with advanced spasticity. Pain control can also be achieved by optimized intrathecal baclofen treatment.

摘要

背景

痉挛是多发性硬化症患者常见的致残症状,会导致功能恶化。

目的

评估鞘内注射巴氯芬治疗多发性硬化相关痉挛的长期疗效,并评估长期治疗的副作用以及所需的巴氯芬剂量。

方法

14 例多发性硬化症患者接受了平均 62 个月(19-137 个月)的临床随访。临床评估采用个体化目标、改良 Ashworth 量表和 Kurtzke 扩展残疾状态量表。

结果

所有患者的痉挛程度(用改良 Ashworth 评分测量)平均降低了 1 分。2 例患者的扩展残疾状态量表评分改善。在植入前,10 名患者(72%)报告有严重疼痛。植入后,3 人疼痛减轻,7 人无痛。治疗所需的每日剂量因人而异。鞘内注射巴氯芬对痉挛的作用持续了观察时间。1 名患者出现了巴氯芬的副作用,认知功能逐渐受损。

结论

鞘内注射巴氯芬耐受性良好,疗效可持续 12 年。由于区分多发性硬化症进展的症状和巴氯芬的副作用可能具有挑战性,因此需要进行彻底的连续临床评估。鞘内注射巴氯芬应被视为治疗晚期痉挛患者的长期治疗选择。通过优化鞘内注射巴氯芬治疗,也可以实现疼痛控制。

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