Gruber D, Trottenberg T, Kivi A, Schoenecker T, Kopp U A, Hoffmann K T, Schneider G-H, Kühn A A, Kupsch A
Department of Neurology, Charité, University Medicine Berlin, Campus Virchow, Berlin, Germany.
Neurology. 2009 Jul 7;73(1):53-8. doi: 10.1212/WNL.0b013e3181aaea01.
High-frequency stimulation of the globus pallidus internus (GPi) is a highly effective therapy in primary dystonia. Recent reports have also demonstrated almost immediate improvement of motor symptoms in patients with tardive dystonia after pallidal deep brain stimulation (DBS). Here, we show the long-term effect of continuous bilateral GPi DBS in tardive dystonia on motor function, quality of life (QoL), and mood.
Nine consecutive patients undergoing DBS for tardive dystonia were assessed during continuous DBS at 3 time points: 1 week, 3 to 6 months, and last follow-up at the mean of 41 (range 18-80) months after surgery using established and validated movement disorder and neuropsychological scales. Clinical assessment was performed by a neurologist not blinded to the stimulation settings.
One week and 3 to 6 months after pallidal DBS, Burke-Fahn-Marsden Dystonia Rating Scale (BFMDRS) motor scores were ameliorated by 56.4 +/- 26.7% and 74.1 +/- 15.8%, BFMDRS disability scores by 62.5 +/- 21.0% and 88.9 +/- 10.3%, and Abnormal Involuntary Movement Scale (AIMS) scores by 52.3 +/- 24.1% and 69.5 +/- 27.6%, respectively. At last follow-up, this improvement compared with the presurgical assessment was maintained as reflected by a reduction of BFMDRS motor scores by 83.0 +/- 12.2%, BFMDRS disability scores by 67.7 +/- 28.0%, and AIMS scores by 78.7 +/- 19.9%. QoL improved significantly in physical components, and there was a significant improvement in affective state. Furthermore, cognitive functions remained unchanged compared with presurgical status in the long-term follow-up. No permanent adverse effects were observed.
Pallidal deep brain stimulation is a safe and effective long-term treatment in patients with medically refractory tardive dystonia.
苍白球内侧部(GPi)高频刺激是原发性肌张力障碍的一种高效治疗方法。近期报告还显示,迟发性肌张力障碍患者在接受苍白球深部脑刺激(DBS)后,运动症状几乎立即得到改善。在此,我们展示了双侧GPi持续DBS治疗迟发性肌张力障碍对运动功能、生活质量(QoL)和情绪的长期影响。
对9例连续接受DBS治疗迟发性肌张力障碍的患者,在持续DBS期间的3个时间点进行评估:术后1周、3至6个月,以及最后一次随访,平均随访时间为术后41(范围18 - 80)个月,使用已确立并经过验证的运动障碍和神经心理学量表。临床评估由一名不了解刺激设置的神经科医生进行。
苍白球DBS术后1周和3至6个月,伯克 - 法恩 - 马斯登肌张力障碍评定量表(BFMDRS)运动评分分别改善了56.4±26.7%和74.1±15.8%,BFMDRS残疾评分分别改善了62.5±21.0%和88.9±10.3%,异常不自主运动量表(AIMS)评分分别改善了52.3±24.1%和69.5±27.6%。在最后一次随访时,与术前评估相比,这种改善得以维持,表现为BFMDRS运动评分降低83.0±12.2%,BFMDRS残疾评分降低67.7±28.0%,AIMS评分降低78.7±19.9%。生活质量在身体方面显著改善,情感状态也有显著改善。此外,在长期随访中,认知功能与术前状态相比保持不变。未观察到永久性不良反应。
苍白球深部脑刺激是药物难治性迟发性肌张力障碍患者安全有效的长期治疗方法。