英国临床实践中的Opicapone:帕金森病患者的有效性、安全性和成本分析

IF 2.3 Q3 CLINICAL NEUROLOGY Neurodegenerative disease management Pub Date : 2022-04-01 Epub Date: 2022-03-21 DOI:10.2217/nmt-2021-0057
Christine Schofield, K Ray Chaudhuri, Camille Carroll, Jagdish C Sharma, Nicola Pavese, Jonathan Evans, Thomas Foltynie, Heinz Reichmann, Laura Zurowska, Patrício Soares-da-Silva, Andrew Lees
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引用次数: 3

摘要

目的:OPTIPARK研究的亚分析旨在确认阿匹卡彭在临床实践中对帕金森病患者和运动波动的有效性和安全性,特别是在英国,并评估阿匹卡彭对治疗成本的影响。方法:患者在左旋多巴的基础上加用阿匹卡彭治疗6个月。在3个月和6个月时评估临床结果和6个月时的治疗费用。结果:大多数患者的一般情况在3个月时改善,在6个月时持续改善。Opicapone在两个时间点改善了运动和非运动症状,总体耐受性良好,总治疗费用减少了3719英镑。结论:在英国的临床实践中,在左旋多巴中加入Opicapone可改善临床效果并降低治疗费用。
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Opicapone in UK clinical practice: effectiveness, safety and cost analysis in patients with Parkinson's disease.

Aim: This subanalysis of the OPTIPARK study aimed to confirm the effectiveness and safety of opicapone in patients with Parkinson's disease and motor fluctuations in clinical practice specifically in the UK and to assess the impact of opicapone on treatment costs. Methods: Patients received opicapone added to levodopa for 6 months. Clinical outcomes were assessed at 3 and 6 months and treatment costs at 6 months. Results: Most patients' general condition improved at 3 months, with sustained improvements reported at 6 months. Opicapone improved motor and non-motor symptoms at both timepoints, was generally well tolerated and reduced total treatment costs by GBP 3719. Conclusion: Opicapone added to levodopa resulted in clinical improvements and reduced treatment costs across UK clinical practice.

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CiteScore
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