Ondo W G, Desaloms J M, Jankovic J, Grossman R G
Department of Neurology, Baylor College of Medicine, Houston, Texas 77030, USA.
Mov Disord. 1998 Jul;13(4):693-8. doi: 10.1002/mds.870130415.
We systematically evaluated the efficacy of both unilateral and bilateral stereotactic pallidotomy in eight patients with generalized dystonia. Six patients had a marked improvement in dystonic movements and motor function; the other two patients also benefited from the procedure but to a lesser extent. The severity of dystonia was assessed before and after surgery by the Burke-Marsden-Fahn Dystonia Scale (BMFDS), the Unified Dystonia Rating Scale (UDRS), and the Activity of Daily Living Scale (ADL). The BMFDS scores decreased by 59.0%, UDRS by 62.5%, and ADL by 47.8% postoperatively. Adverse events were limited to a transient weakness in one patient. We conclude that pallidotomy is a safe and effective treatment in medically refractory cases of generalized dystonia.
我们系统评估了8例全身性肌张力障碍患者接受单侧和双侧立体定向苍白球毁损术的疗效。6例患者的肌张力障碍性运动和运动功能有显著改善;另外2例患者也从该手术中获益,但程度较轻。术前和术后通过伯克-马斯登-法恩肌张力障碍量表(BMFDS)、统一肌张力障碍评定量表(UDRS)和日常生活活动量表(ADL)评估肌张力障碍的严重程度。术后BMFDS评分下降了59.0%,UDRS下降了62.5%,ADL下降了47.8%。不良事件仅限于1例患者出现短暂性无力。我们得出结论,苍白球毁损术在药物难治性全身性肌张力障碍病例中是一种安全有效的治疗方法。