Woo Peter Y M, Chan Danny T M, Zhu X L, Yeung Jonas H M, Chan Anne Y Y, Au Angie C W, Cheng K M, Lau K Y, Wing Y K, Mok Vincent C T, Poon W S
Movement Disorder Group, Division of Neurosurgery, Department of Surgery and Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong.
Department of General Adult Psychiatry, Castle Peak Hospital, Hong Kong.
Hong Kong Med J. 2014 Oct;20(5):455-9. doi: 10.12809/hkmj134082.
Tardive dystonia is an iatrogenic complication of dopamine receptor antagonist medication such as first-generation antipsychotics. It occurs in up to 2% of patients and only 10% recover after stopping medication. Deep brain stimulation for primary dystonia has proven to be effective and its application for secondary dystonias is gaining acceptance. We report our experience in treating three ethnic Chinese schizophrenia patients with severe medically refractory tardive dystonia by globus pallidus internus deep brain stimulation. Preoperatively, all required assistance with essential activities of daily living and two were bed-bound. The mean Burke-Fahn-Marsden Dystonia Rating Scale score was 61 (range, 44-80) and mean Global Dystonia Rating Scale score was 47 (range, 40-52). No procedure-related complications were encountered. By 3 months all could return to unassisted living and walk with support with a mean of 77% and 66% improvement in the Burke-Fahn-Marsden Dystonia Rating Scale and Global Dystonia Rating Scale scores, respectively. Quality-of-life assessment performed for two patients using the EuroQol-5 dimensions visual analogue scale showed a mean improvement of 86% at 3 months. On clinical follow-up, the effect was well maintained for a period of 3 to 10 years. Pallidal deep brain stimulation is a safe and highly effective form of symptomatic treatment for patients with medically refractory tardive dystonia.
迟发性肌张力障碍是多巴胺受体拮抗剂药物(如第一代抗精神病药物)的医源性并发症。其发生率高达2%,停药后仅有10%的患者恢复。深部脑刺激治疗原发性肌张力障碍已被证明有效,其在继发性肌张力障碍中的应用也逐渐得到认可。我们报告了通过内侧苍白球深部脑刺激治疗3例患有严重药物难治性迟发性肌张力障碍的华裔精神分裂症患者的经验。术前,所有患者在日常生活基本活动中均需要协助,其中2例卧床不起。伯克-法恩-马斯登肌张力障碍评定量表平均评分为61分(范围44 - 80分),全球肌张力障碍评定量表平均评分为47分(范围40 - 52分)。未出现与手术相关的并发症。到3个月时,所有患者均可在无协助下生活,并在支撑下行走,伯克-法恩-马斯登肌张力障碍评定量表和全球肌张力障碍评定量表评分分别平均改善了77%和66%。使用欧洲五维健康量表视觉模拟量表对2例患者进行的生活质量评估显示,3个月时平均改善了86%。在临床随访中,这种效果在3至10年的时间内得到了良好维持。苍白球深部脑刺激是治疗药物难治性迟发性肌张力障碍患者的一种安全且高效的对症治疗方式。