Hansen Richard A, Song Liping, Moore Charity G, Gilsenan Alicia W, Kim Mimi M, Calloway Michael O, Murray Michael D
Division of Pharmaceutical Outcomes and Policy, Center for Pharmaceutical Outcomes and Policy, School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina 27599-7360, USA.
Pharmacotherapy. 2009 Mar;29(3):255-62. doi: 10.1592/phco.29.3.255.
To compare the effects of ropinirole with those of placebo on sleep, as evaluated by specific domains of the Medical Outcomes Study (MOS) sleep scale, as well as the Clinical Global Impression-Improvement (CGI-I) scale, in patients with restless legs syndrome (RLS).
Meta-analysis of six randomized, double-blind, placebo-controlled, parallel-group trials conducted in the United States and Europe.
A total of 1679 patients aged 18-79 years with primary moderate-to-severe RLS who received ropinirole (835 patients) or placebo (844 patients).
A systematic review of MEDLINE (January 1980-January 2007) and clinical trial registers was performed to identify placebo-controlled trials of ropinirole that used the 12-item MOS sleep scale to assess sleep in patients with RLS. Individual patient data from both published and nonpublished trials were pooled for meta-analysis. In the eligible studies, immediate-release ropinirole 0.25-6 mg or placebo had been given for at least 12 weeks. In addition, sleep scale summary scores for the domains of sleep quantity, adequacy, disturbance, and daytime somnolence had to have been assessed at baseline and at 12 weeks. Our meta-analysis found that at baseline study patients slept an average of 5.8 hours/night. At the end of 12 weeks, ropinirole-treated patients slept a mean of 2.5 hours/week more and had a 21% greater improvement from baseline in sleep adequacy scores compared with patients receiving placebo. Ropinirole-treated patients also had 14% less sleep disturbance and 8% less daytime somnolence than patients receiving placebo. Clinicians rated 63% of ropinirole-treated patients and 47% of patients receiving placebo as responders based on the CGI-I scale. Mixed effects analysis of covariance was used to estimate treatment effect adjusting for study center as a random effect, as well as the following fixed effects known to affect sleep: baseline sleep characteristics, age, sex, and chronic medical conditions. All differences were statistically significant (p<0.05), even after adjusting for multiple comparisons.
Pooled data from six similarly designed clinical trials provide evidence that ropinirole improves sleep quantity and adequacy, and lessens sleep disturbance and daytime somnolence in patients with primary RLS.
通过医学结局研究(MOS)睡眠量表的特定领域以及临床总体印象改善(CGI-I)量表,比较罗匹尼罗与安慰剂对不安腿综合征(RLS)患者睡眠的影响。
对在美国和欧洲进行的六项随机、双盲、安慰剂对照、平行组试验进行荟萃分析。
共有1679例年龄在18 - 79岁的原发性中度至重度RLS患者,其中835例接受罗匹尼罗治疗,844例接受安慰剂治疗。
对MEDLINE(1980年1月至2007年1月)和临床试验注册库进行系统检索,以确定使用12项MOS睡眠量表评估RLS患者睡眠的罗匹尼罗安慰剂对照试验。将已发表和未发表试验的个体患者数据汇总进行荟萃分析。在符合条件的研究中,速释罗匹尼罗0.25 - 6mg或安慰剂给药至少12周。此外,必须在基线和12周时评估睡眠量表中睡眠量、充足度、干扰和日间嗜睡等领域的总结分数。我们的荟萃分析发现,在基线研究时患者平均每晚睡眠5.8小时。在12周结束时,与接受安慰剂的患者相比,接受罗匹尼罗治疗的患者每周平均多睡2.5小时,睡眠充足度评分从基线的改善幅度高21%。接受罗匹尼罗治疗的患者睡眠干扰也比接受安慰剂的患者少14%,日间嗜睡少8%。根据CGI-I量表,临床医生将63%接受罗匹尼罗治疗的患者和47%接受安慰剂的患者评定为有反应者。采用协方差混合效应分析来估计治疗效果,将研究中心作为随机效应进行调整,并对已知影响睡眠的以下固定效应进行调整:基线睡眠特征、年龄、性别和慢性疾病。即使在进行多重比较调整后,所有差异均具有统计学意义(p<0.05)。
来自六项设计相似的临床试验的汇总数据提供了证据,表明罗匹尼罗可改善原发性RLS患者的睡眠量和充足度,并减轻睡眠干扰和日间嗜睡。