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首页> 外文期刊>Sleep >Modafinil for the treatment of daytime sleepiness in Parkinson's disease: a double-blind, randomized, crossover, placebo-controlled polygraphic trial.
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Modafinil for the treatment of daytime sleepiness in Parkinson's disease: a double-blind, randomized, crossover, placebo-controlled polygraphic trial.

机译:莫达非尼用于治疗帕金森氏病的日间嗜睡:一项双盲,随机,交叉,安慰剂对照的多项试验。

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OBJECTIVES: To assess the therapeutic efficacy of modafinil in the treatment of increased daytime sleepiness in patients with Parkinson's disease (PD). DESIGN: Double-blind, randomized, placebo-controlled crossover study with two 2-week treatment blocks, separated by a 2-week washout phase. SETTING: Tertiary Parkinson's disease care center and sleep laboratory at university hospital neurology department. PATIENTS: Fifteen patients with idiopathic PD and daytime sleepiness (Epworth sleepiness score (ESS) 10 or more). INTERVENTIONS: Administration of placebo or modafinil as a single morning dose in a randomized crossover order. The modafinil dose was 100 mg in the first, and 200 mg in the second treatment week. MEASUREMENTS AND RESULTS: At baseline and at the end of each treatment block, sleepiness was evaluated using subjective (perceived sleepiness with the ESS) and objective measures (maintenance of wakefulness test). Twelve patients completed the study (9 male, 3 female; mean age 65.0 +/- 7.6 years, mean disease duration 6.8 +/- 4.1 years). Epworth scores were significantly improved with modafinil (3.42 +/- 3.90) compared to placebo (0.83 +/- 1.99; p = 0.011). Latency to sleep in the maintenance of wakefulness test was not significantly altered by modafinil treatment: 10.9 (3-40)/15.1 (2.5-40) minutes before/after placebo and 12 (2.6-40)/17.8 (4.2-40) minutes before/after modafinil (p = 0.139) [data given as mean +/- standard deviation or median (range)]. CONCLUSIONS: The results of this study suggest that modafinil improves daytime sleepiness in PD patients, at least on a subjective or behavioral level. Modafinil treatment may be considered for EDS in PD patients, in whom otherwise treatable causes of Excessive Daytime Sleepiness (EDS) are absent.
机译:目的:评估莫达非尼治疗帕金森病(PD)患者日间嗜睡的疗效。设计:双盲,随机,安慰剂对照的交叉研究,分为两个2周的治疗阶段,每个治疗阶段间隔2周。地点:大学医院神经科的第三级帕金森氏病护理中心和睡眠实验室。患者:15例特发性PD和白天嗜睡(Epworth嗜睡评分(ESS)为10或更高)的患者。干预:安慰剂或莫达非尼以随机交叉顺序作为单次早晨剂量给药。在第一个治疗周莫达非尼剂量为100 mg,在第二个治疗周为200 mg。测量和结果:在基线和每个治疗阶段结束时,使用主观(通过ESS感知到的困倦)和客观测量(保持觉醒测试)来评估困倦程度。 12名患者完成了研究(男9例,女3例;平均年龄65.0 +/- 7.6岁,平均病程6.8 +/- 4.1年)。与安慰剂组(0.83 +/- 1.99; p = 0.011)相比,莫达非尼(3.42 +/- 3.90)的Epworth评分显着提高。通过莫达非尼治疗,维持清醒测试的睡眠潜伏期没有显着改变:安慰剂治疗前后分别为10.9(3-40)/15.1(2.5-40)分钟和12(2.6-40)/17.8(4.2-40)分钟莫达非尼之前/之后(p = 0.139)[数据以平均值+/-标准偏差或中位数(范围)给出]。结论:该研究结果表明莫达非尼至少在主观或行为水平上改善了PD患者的白天嗜睡。 PD患者可考虑使用莫达非尼治疗EDS,否则就没有可治疗的白天过度嗜睡(EDS)原因。

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