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左旋多巴缓释制剂(美多芭HBS)治疗帕金森病的夜间及清晨功能障碍

A sustained-release formulation of L-dopa (Madopar HBS) in the treatment of nocturnal and early-morning disabilities in Parkinson's disease.

作者信息

Lees A J

机构信息

National Hospital for Nervous Diseases, London, UK.

出版信息

Eur Neurol. 1987;27 Suppl 1:126-34. doi: 10.1159/000116207.

DOI:10.1159/000116207
PMID:3428306
Abstract

In an open pilot study, 10 patients with Parkinson's disease and nocturnal and/or early-morning disabilities were given Madopar HBS (hydrodynamically balanced system; mean dose 250 mg) shortly before retiring in addition to their usual daytime antiparkinsonian treatment. Eight patients derived worthwhile improvement; the most gratifying responses were seen in the relief of nocturnal bradykinesia, rigidity and tremor. Early-morning symptoms were also improved in 3 out of 5 patients, possibly as a secondary response to an improved nights sleep. Cramps, early-morning dystonia and pain, however, responded poorly. Overall results are sufficiently encouraging to warrant further controlled studies with Madopar HBS in what has been a relatively neglected area of distress for many patients with Parkinson's disease.

摘要

在一项开放性试验研究中,10名患有帕金森病且有夜间和/或清晨功能障碍的患者,除了接受常规的日间抗帕金森病治疗外,在睡前还加用了美多芭HBS(流体动力学平衡系统;平均剂量250毫克)。8名患者有显著改善;最令人满意的反应是夜间运动迟缓、僵硬和震颤得到缓解。5名患者中有3名的清晨症状也有所改善,这可能是夜间睡眠改善的继发反应。然而,痉挛、清晨肌张力障碍和疼痛的反应较差。总体结果足以令人鼓舞,有必要在帕金森病患者这一相对被忽视的痛苦领域,对美多芭HBS进行进一步的对照研究。

相似文献

1
A sustained-release formulation of L-dopa (Madopar HBS) in the treatment of nocturnal and early-morning disabilities in Parkinson's disease.左旋多巴缓释制剂(美多芭HBS)治疗帕金森病的夜间及清晨功能障碍
Eur Neurol. 1987;27 Suppl 1:126-34. doi: 10.1159/000116207.
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Eur Neurol. 1987;27 Suppl 1:93-7.
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Clinical trial of Madopar HBS in parkinsonian patients with fluctuating drug response after long-term levodopa therapy.美多芭HBS治疗长期左旋多巴治疗后药物反应波动的帕金森病患者的临床试验。
Eur Neurol. 1987;27 Suppl 1:114-9. doi: 10.1159/000116205.

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