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评估不宁腿综合征的疼痛感觉症状:两项临床试验的经验。

Evaluation of painful sensory symptoms in restless legs syndrome: experience from two clinical trials.

机构信息

Interdisciplinary Pain Center, University Medical Center, Breisacher Strasse 64, 79106 Freiburg, Germany.

出版信息

Sleep Med. 2011 Feb;12(2):186-9. doi: 10.1016/j.sleep.2010.11.007. Epub 2011 Jan 21.

Abstract

BACKGROUND

Although "uncomfortable and unpleasant" limb sensations are a core symptom of restless legs syndrome (RLS), change in sensory symptomatology is usually not evaluated as a treatment outcome.

METHODS

In two double-blind trials, patients with idiopathic RLS (n=357 in trial 615 and 398 in trial 604) were randomized to placebo or pramipexole (optimized at 0.125, 0.25, 0.50, or 0.75 mg/day). For entry, trial 604 also required at least moderate mood disturbance. In both trials, 12-week change in RLS-related limb pain was assessed using a 100-mm visual analogue scale (VAS).

RESULTS

At baseline, approximately 75% of patients had limb-pain scores >30. Treatment with pramipexole yielded significant score reduction as early as day 5. At week 12, median score reduction for pramipexole relative to placebo was -33.5 vs. -11.0 (p<0.0001) in trial 615 and -31.0 vs. -11.0 (p<0.0001) in trial 604.

CONCLUSIONS

Painful sensations may be more frequent in RLS than has previously been appreciated, and their amelioration may be a facet of pramipexole's benefit even in patients with concurrent mood disturbance. Limb pain assessment, e.g., by a VAS, is a useful measure of change in RLS symptom severity.

摘要

背景

尽管“不适和不愉快”的肢体感觉是不安腿综合征(RLS)的核心症状,但感觉症状的变化通常不作为治疗结果进行评估。

方法

在两项双盲试验中,特发性 RLS 患者(试验 615 中 357 例,试验 604 中 398 例)被随机分配至安慰剂或普拉克索组(优化剂量分别为 0.125、0.25、0.50 或 0.75mg/天)。对于入组,试验 604 还要求至少有中度情绪障碍。在两项试验中,均使用 100mm 视觉模拟量表(VAS)评估 RLS 相关肢体疼痛的 12 周变化。

结果

在基线时,约 75%的患者肢体疼痛评分>30。普拉克索治疗可在第 5 天即可观察到评分显著降低。在第 12 周,普拉克索相对于安慰剂的评分中位数降低幅度在试验 615 中为-33.5,而在试验 604 中为-31.0(p<0.0001)。

结论

与之前的认识相比,RLS 患者可能更常出现疼痛感觉,即使在伴有情绪障碍的患者中,其改善也可能是普拉克索获益的一个方面。肢体疼痛评估,例如通过 VAS,是 RLS 症状严重程度变化的有用衡量标准。

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