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肉毒杆菌毒素治疗与致残性局灶性肌张力障碍相关的非典型帕金森病。

Botulinum toxin treatment in atypical parkinsonian disorders associated with disabling focal dystonia.

作者信息

Müller J, Wenning G K, Wissel J, Seppi K, Poewe W

机构信息

Department of Neurology, Innsbruck University Hospital, Austria.

出版信息

J Neurol. 2002 Mar;249(3):300-4. doi: 10.1007/s004150200009.

Abstract

We investigated the efficacy of botulinum toxin A (BtxA) therapy in patients with atypical parkinsonian disorders (APD) exhibiting different types of disabling focal dystonia unresponsive to oral drug therapy. Eight patients with functionally disabling focal dystonia out of a series of 60 consecutive patients with APDs regularly treated at our outpatient movement disorders clinic were included. Patients were diagnosed according to established criteria and had disabling limb dystonia (n=4) or craniocervical dystonia (n=4) unresponsive to oral pharmacological treatment. Localization and dose of BtxA injections was determined individually based on clinical examination as well as EMG in patients with limb dystonia. BtxA reduced dystonic symptoms in all patients; only one developed a transient local side-effect. BtxA was particularly effective in the long-term treatment (up to 50 months) of blepharospasm associated with progressive supranuclear palsy (PSP). BtxA also alleviated PSP-associated retrocollis and orofacial dystonia with lower lip retraction associated with PSP and multiple system atrophy. BtxA treatment of limb dystonia in corticobasal degeneration (CBD) temporarily improved hand and arm function in early-disease stages while treatment in advanced stages reduced pain, facilitated hygiene and prevented secondary contractures. Limb dystonia was also alleviated by BtxA therapy in one patient with neuronal multisystem degeneration of undetermined cause. The results suggest that BtxA therapy may represent an effective means of alleviating disabling focal dystonia in different APDs. Particularly in early stage APD with disabling limb dystonia local BtxA injections may result in functional improvement.

摘要

我们研究了A型肉毒毒素(BtxA)疗法对非典型帕金森病(APD)患者的疗效,这些患者表现出不同类型的致残性局灶性肌张力障碍,对口服药物治疗无反应。我们纳入了在我们门诊运动障碍诊所定期接受治疗的60例连续APD患者中8例有功能致残性局灶性肌张力障碍的患者。患者根据既定标准进行诊断,患有对口服药物治疗无反应的致残性肢体肌张力障碍(n = 4)或颅颈肌张力障碍(n = 4)。对于肢体肌张力障碍患者,根据临床检查以及肌电图单独确定BtxA注射的部位和剂量。BtxA减轻了所有患者的肌张力障碍症状;只有1例出现短暂的局部副作用。BtxA在与进行性核上性麻痹(PSP)相关的眼睑痉挛的长期治疗(长达50个月)中特别有效。BtxA还缓解了PSP相关的颈后倾以及与PSP和多系统萎缩相关的口面部肌张力障碍伴下唇回缩。在皮质基底节变性(CBD)中,BtxA治疗肢体肌张力障碍在疾病早期暂时改善了手和手臂功能,而在晚期治疗则减轻了疼痛,便于护理并预防了继发性挛缩。BtxA疗法还缓解了1例病因不明的神经元多系统变性患者的肢体肌张力障碍。结果表明,BtxA疗法可能是减轻不同APD中致残性局灶性肌张力障碍的有效手段。特别是在患有致残性肢体肌张力障碍的早期APD中,局部注射BtxA可能会导致功能改善。

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