首页> 外文期刊>The annals of pharmacotherapy >Effect of non-ergot dopamine agonists on health-related quality of life of patients with restless legs syndrome.
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Effect of non-ergot dopamine agonists on health-related quality of life of patients with restless legs syndrome.

机译:非麦角多巴胺激动剂对不安腿综合征患者健康相关生活质量的影响。

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BACKGROUND: Non-ergot dopamine agonists (NEDAs) have become the gold-standard agents for the treatment of restless legs syndrome (RLS). While the efficacy and safety of these drugs have been widely studied, their effect on patients' health-related quality of life (HRQoL) has not been fully elucidated. OBJECTIVE: To better define the usefulness of NEDAs by assessing their impact on HRQoL. METHODS: We performed a meta-analysis of randomized, double-blind, placebo-controlled trials evaluating the use of NEDAs in patients with RLS. A systematic literature search of MEDLINE, EMBASE, and Cochrane CENTRAL was performed from the earliest possible date through July 2008. Trials were included in the analysis if they evaluated NEDAs for the treatment of RLS and reported HRQoL using any RLS disease-specific HRQoL instrument. HRQoL data were pooled and evaluated using an inverse variance weighting approach as standardized mean differences (SMDs) and 95% confidence interval (CI). For trials reporting HRQoL data obtained using the Johns Hopkins RLS-QoL Questionnaire, adjusted mean difference data were pooled to calculate the weighted mean difference (WMD) and 95% CI. RESULTS: Seven trials (N = 1483) met all inclusion criteria. Patients with RLS taking NEDAs had significantly improved overall effect on HRQoL compared with those taking placebo (SMD 0.20; 95% CI 0.10 to 0.30; degree of inconsistency across studies [I(2)] = 0%). When analyzing trials using the Johns Hopkins RLS-QoL questionnaire, the results also showed improvement with NEDAs compared with placebo (WMD 4.72; 95% CI 2.96 to 6.47; I(2) = 0%). Study conclusions were unchanged upon sensitivity analysis. The number of trials for each NEDA was small, limiting the usefulness of between-agent comparisons. CONCLUSIONS: In patients with RLS, use of NEDAs showed improved HRQoL compared with placebo. Since pooled effect sizes observed in this meta-analysis appear to surpass accepted values for minimally important clinical differences, these improvements may be clinically relevant for the average studied patient. However, future studies evaluating long-term treatment of RLS with NEDAs are necessary, as are head-to-head comparative trials and economic assessments.
机译:背景:非麦角多巴胺激动剂(NEDAs)已成为治疗躁动腿综合征(RLS)的金标准药物。尽管已广泛研究了这些药物的功效和安全性,但尚未完全阐明它们对患者健康相关生活质量(HRQoL)的影响。目的:通过评估NEDA对HRQoL的影响,更好地定义其用途。方法:我们进行了一项随机,双盲,安慰剂对照试验的荟萃分析,评估了NELS在RLS患者中的使用。从最早的日期到2008年7月,对MEDLINE,EMBASE和Cochrane CENTRAL进行了系统的文献检索。如果他们评估了NEDA治疗RLS并使用任何RLS疾病特异性HRQoL仪器报告了HRQoL,则该试验包括在分析中。合并HRQoL数据,并使用逆方差加权方法作为标准化均值差(SMD)和95%置信区间(CI)进行评估。对于报告使用Johns Hopkins RLS-QoL问卷获得的HRQoL数据的试验,汇总调整后的均值差数据以计算加权均值差(WMD)和95%CI。结果:七项试验(N = 1483)符合所有纳入标准。与服用安慰剂的患者相比,服用NEDAs的RLS患者对HRQoL的总体效果有显着改善(SMD 0.20; 95%CI 0.10至0.30;研究不一致的程度[I(2)] = 0%)。当使用Johns Hopkins RLS-QoL问卷分析试验时,结果还显示与安慰剂相比,NEDAs有所改善(WMD 4.72; 95%CI 2.96至6.47; I(2)= 0%)。敏感性分析后研究结论未变。每个NEDA的试验次数很少,限制了药物之间比较的有效性。结论:与安慰剂相比,RLS患者使用NEDAs可改善HRQoL。由于在该荟萃分析中观察到的合并效应大小似乎对最小的重要临床差异超过了可接受的值,因此这些改善可能与普通研究患者在临床上相关。但是,未来的研究需要评估NEDAs对RLS的长期治疗,以及有针对性的对比试验和经济评估。

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