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舌下含服阿扑吗啡治疗帕金森病:综述

Sublingual apomorphine in treatment of Parkinson's disease: a review.

作者信息

Hislop Jennifer, Margolesky Jason, Shpiner Danielle S

机构信息

Department of Neurology, University of Miami Miller School of Medicine, Miami, Florida, USA.

出版信息

Int J Neurosci. 2024 May;134(5):474-480. doi: 10.1080/00207454.2022.2115908. Epub 2022 Aug 24.

Abstract

A majority of advanced Parkinson's disease (PD) patients on oral levodopa experience motor fluctuations, including sudden OFF and delayed ON periods. Fast-acting rescue medications are a vital part of the clinician's armamentarium in the treatment of motor fluctuations. Sublingual apomorphine is the first sublingual rescue medication on the market for the treatment of OFF times in PD. Here, we review the development and pharmacology of apomorphine in the treatment of PD as well as the safety and efficacy of sublingual apomorphine established in clinical trials. Finally, we compare sublingual apomorphine to the other rescue medications available and provide our opinion on the use of sublingual apomorphine in clinical practice. Clinical trials have demonstrated that sublingual apomorphine is a safe and effective option in the treatment of motor fluctuations in PD. In a Phase II trial, 100% of patients who achieved a full ON response did so within 30 min and 40% did so within 15 min. The mean duration of effect was 50 min. In a Phase III trial, 77.3% of patients achieved a full ON response. Side effects such as nausea, dizziness and somnolence were common but were generally mild. No patients experienced worsening dyskinesia. Sublingual apomorphine will provide patients with motor fluctuations due to advanced PD another safe and effective option for the treatment of OFF times.

摘要

大多数接受口服左旋多巴治疗的晚期帕金森病(PD)患者会出现运动波动,包括突然的“关”期和延迟的“开”期。速效急救药物是临床医生治疗运动波动的重要手段。舌下含服阿扑吗啡是市场上第一种用于治疗帕金森病“关”期的舌下含服急救药物。在此,我们回顾阿扑吗啡在帕金森病治疗中的研发和药理学,以及临床试验中确立的舌下含服阿扑吗啡的安全性和有效性。最后,我们将舌下含服阿扑吗啡与其他可用的急救药物进行比较,并给出我们对舌下含服阿扑吗啡在临床实践中应用的看法。临床试验表明,舌下含服阿扑吗啡是治疗帕金森病运动波动的一种安全有效的选择。在一项II期试验中,100%达到完全“开”反应的患者在30分钟内实现,40%在15分钟内实现。平均起效持续时间为50分钟。在一项III期试验中,77.3%的患者达到完全“开”反应。恶心、头晕和嗜睡等副作用很常见,但一般较轻。没有患者出现运动障碍恶化。舌下含服阿扑吗啡将为因晚期帕金森病出现运动波动的患者提供另一种治疗“关”期的安全有效选择。

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