Weaver Frances M, Follett Kenneth, Stern Matthew, Hur Kwan, Harris Crystal, Marks William J, Rothlind Johannes, Sagher Oren, Reda Domenic, Moy Claudia S, Pahwa Rajesh, Burchiel Kim, Hogarth Penelope, Lai Eugene C, Duda John E, Holloway Kathryn, Samii Ali, Horn Stacy, Bronstein Jeff, Stoner Gatana, Heemskerk Jill, Huang Grant D
Hines VA Hospital, Center for Management of Complex Chronic Care, Hines, Illinois 60141, USA.
JAMA. 2009 Jan 7;301(1):63-73. doi: 10.1001/jama.2008.929.
Deep brain stimulation is an accepted treatment for advanced Parkinson disease (PD), although there are few randomized trials comparing treatments, and most studies exclude older patients.
To compare 6-month outcomes for patients with PD who received deep brain stimulation or best medical therapy.
DESIGN, SETTING, AND PATIENTS: Randomized controlled trial of patients who received either deep brain stimulation or best medical therapy, stratified by study site and patient age (< 70 years vs > or = 70 years) at 7 Veterans Affairs and 6 university hospitals between May 2002 and October 2005. A total of 255 patients with PD (Hoehn and Yahr stage > or = 2 while not taking medications) were enrolled; 25% were aged 70 years or older. The final 6-month follow-up visit occurred in May 2006.
Bilateral deep brain stimulation of the subthalamic nucleus (n = 60) or globus pallidus (n = 61). Patients receiving best medical therapy (n = 134) were actively managed by movement disorder neurologists.
The primary outcome was time spent in the "on" state (good motor control with unimpeded motor function) without troubling dyskinesia, using motor diaries. Other outcomes included motor function, quality of life, neurocognitive function, and adverse events.
Patients who received deep brain stimulation gained a mean of 4.6 h/d of on time without troubling dyskinesia compared with 0 h/d for patients who received best medical therapy (between group mean difference, 4.5 h/d [95% CI, 3.7-5.4 h/d]; P < .001). Motor function improved significantly (P < .001) with deep brain stimulation vs best medical therapy, such that 71% of deep brain stimulation patients and 32% of best medical therapy patients experienced clinically meaningful motor function improvements (> or = 5 points). Compared with the best medical therapy group, the deep brain stimulation group experienced significant improvements in the summary measure of quality of life and on 7 of 8 PD quality-of-life scores (P < .001). Neurocognitive testing revealed small decrements in some areas of information processing for patients receiving deep brain stimulation vs best medical therapy. At least 1 serious adverse event occurred in 49 deep brain stimulation patients and 15 best medical therapy patients (P < .001), including 39 adverse events related to the surgical procedure and 1 death secondary to cerebral hemorrhage.
In this randomized controlled trial of patients with advanced PD, deep brain stimulation was more effective than best medical therapy in improving on time without troubling dyskinesias, motor function, and quality of life at 6 months, but was associated with an increased risk of serious adverse events.
clinicaltrials.gov Identifier: NCT00056563.
深部脑刺激是晚期帕金森病(PD)的一种公认治疗方法,尽管比较不同治疗方法的随机试验很少,且大多数研究排除了老年患者。
比较接受深部脑刺激或最佳药物治疗的帕金森病患者6个月的治疗效果。
设计、地点和患者:对接受深部脑刺激或最佳药物治疗的患者进行随机对照试验,根据研究地点和患者年龄(<70岁与≥70岁)在7家退伍军人事务医院和6家大学医院进行分层,时间为2002年5月至2005年10月。共纳入255例帕金森病患者(霍恩和雅尔分期≥2期且未服用药物);25%的患者年龄在70岁及以上。最后一次6个月的随访于2006年5月进行。
双侧丘脑底核深部脑刺激(n = 60)或苍白球深部脑刺激(n = 61)。接受最佳药物治疗的患者(n = 134)由运动障碍神经科医生进行积极管理。
主要观察指标是使用运动日记记录的“开”状态(运动控制良好且运动功能不受阻碍)且无烦人的运动障碍的时间。其他观察指标包括运动功能、生活质量、神经认知功能和不良事件。
与接受最佳药物治疗的患者相比,接受深部脑刺激的患者平均每天“开”的时间增加了4.6小时,且无烦人的运动障碍,而接受最佳药物治疗的患者为0小时(组间平均差异为4.5小时/天[95%CI,3.7 - 5.4小时/天];P <.001)。与最佳药物治疗相比,深部脑刺激使运动功能有显著改善(P <.001),71%接受深部脑刺激的患者和32%接受最佳药物治疗的患者经历了具有临床意义的运动功能改善(≥5分)。与最佳药物治疗组相比,深部脑刺激组在生活质量综合测量以及8项帕金森病生活质量评分中的7项上有显著改善(P <.001)。神经认知测试显示,与最佳药物治疗相比,接受深部脑刺激的患者在某些信息处理领域有轻微下降。49例接受深部脑刺激的患者和15例接受最佳药物治疗的患者发生了至少1次严重不良事件(P <.001),包括39例与手术相关的不良事件和1例脑出血继发死亡。
在这项针对晚期帕金森病患者的随机对照试验中,深部脑刺激在改善6个月时的“开”时间、无烦人的运动障碍、运动功能和生活质量方面比最佳药物治疗更有效,但与严重不良事件风险增加相关。
clinicaltrials.gov标识符:NCT00056563