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加巴喷丁与左旋多巴 - 卡比多巴治疗血液透析患者不安腿综合征的随机临床试验

Gabapentin versus levodopa-c for the treatment of restless legs syndrome in hemodialysis patients: a randomized clinical trial.

作者信息

Razazian Nazanin, Azimi Hamid, Heidarnejadian Jafar, Afshari Daryoush, Ghadami Mohammad Rasoul

机构信息

Sleep Disorders Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

Saudi J Kidney Dis Transpl. 2015 Mar;26(2):271-8. doi: 10.4103/1319-2442.152417.

Abstract

To compare the efficacy of gabapentin and levodopa-c (Levodopa/Carbidopa) in reducing restless leg syndrome (RLS) symptoms and sleep problems in hemodialysis patients with RLS in a four-week randomized clinical trial. The diagnosis of RLS was made using the criteria of the International Restless Legs Study Group. Each subject completed three questionnaires: IRLS questionnaire, Pittsburgh Sleep Quality Index and Epworth sleepiness scale. After four weeks of washout period for previous treatments for RLS, subjects were randomly assigned to four weeks of gabapentin (200 mg) or levodopa-c (110 mg). After four weeks of therapy, the questionnaires administered at the outset of the study were re-administered. Both drugs were found effective for the management of RLS. But, the effect of gabapentin was more significant. Gabapentin significantly improved the IRLS total score (change from baseline to post-treatment ≈-17) compared with levodopa-c (change from baseline to post-treatment ≈-13) (P: 0.016). Regarding sleep parameters, levodopa improved sleep quality, sleep latency and sleep duration (P <0.0001). Gabapentin was also effective with respect to sleep parameters (P <0.0001). Our study shows that gabapentin is a safe effective therapy for RLS among hemodialysis patients. This medication may be considered as an alternative or additive treatment to current therapeutic remedies for hemodialysis patients with RLS.

摘要

在一项为期四周的随机临床试验中,比较加巴喷丁和左旋多巴 - 卡比多巴(Levodopa/Carbidopa)对减轻血液透析合并不宁腿综合征(RLS)患者的RLS症状及睡眠问题的疗效。RLS的诊断采用国际不宁腿研究组的标准。每位受试者完成三份问卷:国际不宁腿量表(IRLS)问卷、匹兹堡睡眠质量指数和爱泼华嗜睡量表。在对之前RLS治疗进行四周的洗脱期后,受试者被随机分配接受为期四周的加巴喷丁(200mg)或左旋多巴 - 卡比多巴(110mg)治疗。治疗四周后,重新发放研究开始时使用的问卷。两种药物均被发现对RLS的治疗有效。但是,加巴喷丁的效果更显著。与左旋多巴 - 卡比多巴相比(从基线到治疗后的变化约为 -13),加巴喷丁显著改善了IRLS总分(从基线到治疗后的变化约为 -17)(P:0.016)。关于睡眠参数,左旋多巴改善了睡眠质量、入睡潜伏期和睡眠时间(P <0.0001)。加巴喷丁在睡眠参数方面也有效(P <0.0001)。我们的研究表明,加巴喷丁对血液透析患者的RLS是一种安全有效的治疗方法。这种药物可被视为血液透析合并RLS患者当前治疗方法的替代或辅助治疗。

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