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用于扭转性肌张力障碍的脑深部电刺激术

Deep brain stimulation for torsion dystonia.

作者信息

Alterman R L, Snyder B J

机构信息

Department of Neurosurgery, Mount Sinai School of Medicine, New York, New York 10029, USA.

出版信息

Acta Neurochir Suppl. 2007;97(Pt 2):191-9. doi: 10.1007/978-3-211-33081-4_21.

Abstract

Deep brain stimulation (DBS) at the globus pallidus pars internus (GPi) is an effective treatment for some patients with medically refractory torsion dystonia. In this chapter we review the classification and treatment of torsion dystonia including the current indications for DBS surgery. Details of the DBS procedure and programming of the DBS devices are discussed. Pallidal DBS is most effective in patients with primary generalized dystonia. Children and adolescents possessing the DYT1 gene mutation may respond best of all. Patients with cervical dystonia may also improve with pallidal DBS but definitive clinical evidence is lacking. As a group, patients with secondary dystonias respond less well to DBS than do patients with primary dystonia; however, patients with dystonia secondary to anoxic brain injury who have grossly intact basal ganglia anatomy, and patients with tardive dystonia may represent secondary dystonia subtypes for whom pallidal DBS is a viable option.

摘要

苍白球内侧部(GPi)的深部脑刺激(DBS)对一些药物难治性扭转痉挛患者是一种有效的治疗方法。在本章中,我们回顾了扭转痉挛的分类和治疗,包括目前DBS手术的适应症。讨论了DBS手术的细节和DBS设备的程控。苍白球DBS对原发性全身性肌张力障碍患者最有效。携带DYT1基因突变的儿童和青少年可能反应最佳。颈部肌张力障碍患者接受苍白球DBS也可能改善,但缺乏确凿的临床证据。总体而言,继发性肌张力障碍患者对DBS的反应不如原发性肌张力障碍患者;然而,基底节解剖结构基本完整的缺氧性脑损伤继发肌张力障碍患者以及迟发性肌张力障碍患者可能是苍白球DBS可行的继发性肌张力障碍亚型。

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