Cheer Susan M, Bang Lynne M, Keating Gillian M
Adis International Limited, Auckland, New Zealand.
CNS Drugs. 2004;18(11):747-54; discussion 755-6. doi: 10.2165/00023210-200418110-00004.
Ropinirole is a non-ergoline dopamine agonist that exhibits a high affinity for D(2) and D(3) receptors but little or no affinity for D(1)-like and non-dopaminergic receptors. Symptoms of restless legs syndrome (RLS) [measured using the International Restless Legs scale and Clinical Global Impression-Global Improvement Scale scores] significantly improved with ropinirole compared with placebo in large, randomised, double-blind trials. Ropinirole reduced periodic leg movements and improved sleep efficiency relative to baseline and placebo in several trials (two of which were randomised, double-blind and relatively large) in patients with RLS. Ropinirole was generally well tolerated in patients with RLS; adverse events were generally mild to moderate in nature and consistent with those expected of dopamine agonists. Few patients receiving ropinirole withdrew from therapy because of adverse events, the most predominant of which were nausea and headache.
罗匹尼罗是一种非麦角林类多巴胺激动剂,对D(2)和D(3)受体具有高亲和力,但对D(1)样和非多巴胺能受体几乎没有或没有亲和力。在大型随机双盲试验中,与安慰剂相比,使用罗匹尼罗治疗时,不安腿综合征(RLS)的症状[使用国际不安腿量表和临床总体印象-总体改善量表评分进行测量]有显著改善。在多项试验(其中两项为随机、双盲且规模相对较大的试验)中,与基线和安慰剂相比,罗匹尼罗可减少RLS患者的周期性腿部运动并提高睡眠效率。RLS患者对罗匹尼罗的耐受性总体良好;不良事件一般性质为轻度至中度,且与多巴胺激动剂预期的不良事件一致。很少有接受罗匹尼罗治疗的患者因不良事件而退出治疗,其中最主要的不良事件是恶心和头痛。