左旋多巴加入脑卒中康复:ESTREL随机临床试验。

JAMA Pub Date : 2025-09-22 DOI:10.1001/jama.2025.15185
Stefan T Engelter,Josefin E Kaufmann,Annaelle Zietz,Andreas R Luft,Alexandros Polymeris,Valerian L Altersberger,Karin Wiesner,Martina Wiegert,Jeremia P O Held,Yannik Rottenberger,Anne Schwarz,Friedrich Medlin,Ettore A Accolla,Sandrine Foucras,Georg Kägi,Gian Marco De Marchis,Svetlana Politz,Matthias Greulich,Alexander A Tarnutzer,Rolf Sturzenegger,Mira Katan,Urs Fischer,Krassen Nedeltchev,Janine Schär,Katrien Van Den Keybus Deglon,Pierre-André Rapin,Alexander Salerno,David J Seiffge,Elias Auer,Julian Lippert,Leo H Bonati,Corina Schuster-Amft,Szabina Gäumann,Joelle N Chabwine,Andrea Humm,J Carsten Möller,Raoul Schweinfurther,Bartosz Bujan,Piotr Jedrysiak,Peter S Sandor,Roman Gonzenbach,Veit Mylius,Dietmar Lutz,Carmen Lienert,Nils Peters,Patrik Michel,René M Müri,Sabine Schädelin,Lars G Hemkens,Gary A Ford,Philippe A Lyrer,Henrik Gensicke,Christopher Traenka,
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Levodopa is used in stroke rehabilitation despite mixed evidence for its effectiveness.\r\n\r\nObjective\r\nTo determine whether levodopa compared with placebo, administered in addition to standardized rehabilitation based on active task-oriented training, is associated with enhanced motor recovery in patients with acute stroke.\r\n\r\nDesign, Setting, and Participants\r\nA double-blind, placebo-controlled randomized clinical trial at 13 stroke units and centers and 11 collaborating rehabilitation centers in Switzerland. Between June 14, 2019 (first patient, first visit), and August 27, 2024 (last patient, last visit), 610 patients with acute ischemic or hemorrhagic stroke with clinically meaningful hemiparesis (ie, a total score of ≥3 points on the following National Institutes of Health Stroke Scale items: motor arm, motor leg, or limb ataxia) were randomized 1:1 to receive levodopa or placebo. Statistical analyses were conducted from November 2024 to August 2025.\r\n\r\nIntervention\r\nPatients received levodopa/carbidopa (100 mg/25 mg; n = 307) or placebo (n = 303) 3 times daily for 39 days, alongside standardized rehabilitation therapy based on active task-oriented training.\r\n\r\nMain Outcomes and Measures\r\nThe primary outcome was the adjusted mean between-group difference in the Fugl-Meyer Assessment (FMA) total score (range, 0-100 points; fewer points indicate worse motor function; 6-point difference considered patient-relevant) at 3 months.\r\n\r\nResults\r\nAmong the 610 participants (median [IQR] age, 73 [64-82] years; 252 [41.3%] female; median baseline FMA total score, 34 [14-54]), 28 participants died by 3 months, leaving 582 (95.4%) participants eligible for the primary analysis. At 3 months, the median (IQR) FMA total score was 68 (42-85) points in the levodopa group and 64 (44-83) points in the placebo group. The mean difference in the FMA total score between the levodopa and placebo groups was -0.90 points (95% CI, -3.78 to 1.98; P = .54). There were 126 serious adverse events in the levodopa group and 129 in the placebo group; the most common was infection (levodopa, n = 55; placebo, n = 44).\r\n\r\nConclusions and Relevance\r\nIn this randomized clinical trial, among patients receiving inpatient rehabilitation for acute stroke, levodopa added to standardized rehabilitation did not significantly improve motor function at 3 months compared with placebo plus standardized rehabilitation. 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引用次数: 0

摘要

多巴增强多巴胺能信号传导,可能刺激神经可塑性,这可能潜在地促进中风后的运动恢复。左旋多巴用于中风康复,尽管其有效性证据不一。目的确定左旋多巴与安慰剂相比,在积极任务导向训练的基础上进行标准化康复治疗,是否与急性脑卒中患者的运动恢复增强有关。设计、环境和参与者:一项双盲、安慰剂对照的随机临床试验,在瑞士的13个卒中单位和中心以及11个合作康复中心进行。在2019年6月14日(第一例患者,第一次就诊)至2024年8月27日(最后一例患者,最后一次就诊)期间,610例急性缺血性或出血性卒中伴临床意义偏瘫患者(即,在美国国立卫生研究院卒中量表中:运动臂、运动腿或肢体共济失调的总分≥3分)被1:1随机分配接受左旋多巴或安慰剂治疗。统计分析时间为2024年11月至2025年8月。干预:患者接受左旋多巴/卡比多巴(100mg / 25mg; n = 307)或安慰剂(n = 303)治疗,每日3次,持续39天,同时进行基于主动任务导向训练的标准化康复治疗。主要结果和测量主要结果是3个月时Fugl-Meyer评估(FMA)总分(范围0-100分;越少表示运动功能越差;6分的差异被认为与患者相关)的调整平均组间差异。结果在610名参与者中(中位[IQR]年龄73[64-82]岁,女性252[41.3%],基线FMA总分中位34[14-54]),28名参与者在3个月内死亡,582名(95.4%)参与者符合初步分析。3个月时,左旋多巴组的中位(IQR) FMA总分为68(42-85)分,安慰剂组为64(44-83)分。左旋多巴组和安慰剂组FMA总分的平均差异为-0.90分(95% CI, -3.78 ~ 1.98; P = 0.54)。左旋多巴组严重不良事件126例,安慰剂组129例;最常见的是感染(左旋多巴,55例;安慰剂,44例)。结论和相关性在这项随机临床试验中,在接受急性卒中住院康复的患者中,左旋多巴加标准化康复与安慰剂加标准化康复相比,在3个月时没有显著改善运动功能。这些结果不支持使用左旋多巴作为辅助康复治疗来增强急性中风后的运动恢复。临床试验注册号:NCT03735901。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Levodopa Added to Stroke Rehabilitation: The ESTREL Randomized Clinical Trial.
Importance Levodopa enhances dopaminergic signaling and may stimulate neuroplasticity, which could potentially enhance motor recovery after stroke. Levodopa is used in stroke rehabilitation despite mixed evidence for its effectiveness. Objective To determine whether levodopa compared with placebo, administered in addition to standardized rehabilitation based on active task-oriented training, is associated with enhanced motor recovery in patients with acute stroke. Design, Setting, and Participants A double-blind, placebo-controlled randomized clinical trial at 13 stroke units and centers and 11 collaborating rehabilitation centers in Switzerland. Between June 14, 2019 (first patient, first visit), and August 27, 2024 (last patient, last visit), 610 patients with acute ischemic or hemorrhagic stroke with clinically meaningful hemiparesis (ie, a total score of ≥3 points on the following National Institutes of Health Stroke Scale items: motor arm, motor leg, or limb ataxia) were randomized 1:1 to receive levodopa or placebo. Statistical analyses were conducted from November 2024 to August 2025. Intervention Patients received levodopa/carbidopa (100 mg/25 mg; n = 307) or placebo (n = 303) 3 times daily for 39 days, alongside standardized rehabilitation therapy based on active task-oriented training. Main Outcomes and Measures The primary outcome was the adjusted mean between-group difference in the Fugl-Meyer Assessment (FMA) total score (range, 0-100 points; fewer points indicate worse motor function; 6-point difference considered patient-relevant) at 3 months. Results Among the 610 participants (median [IQR] age, 73 [64-82] years; 252 [41.3%] female; median baseline FMA total score, 34 [14-54]), 28 participants died by 3 months, leaving 582 (95.4%) participants eligible for the primary analysis. At 3 months, the median (IQR) FMA total score was 68 (42-85) points in the levodopa group and 64 (44-83) points in the placebo group. The mean difference in the FMA total score between the levodopa and placebo groups was -0.90 points (95% CI, -3.78 to 1.98; P = .54). There were 126 serious adverse events in the levodopa group and 129 in the placebo group; the most common was infection (levodopa, n = 55; placebo, n = 44). Conclusions and Relevance In this randomized clinical trial, among patients receiving inpatient rehabilitation for acute stroke, levodopa added to standardized rehabilitation did not significantly improve motor function at 3 months compared with placebo plus standardized rehabilitation. These results do not support the use of levodopa as an adjunct to rehabilitation therapy for enhancing motor recovery after acute stroke. Trial Registration ClinicalTrials.gov Identifier: NCT03735901.
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