澳大利亚左旋多巴的使用情况:对药品福利计划 10% 数据的分析

IF 2.1 Q3 CLINICAL NEUROLOGY
Andrew Evans, Benjamin J Waterhouse
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引用次数: 0

摘要

背景 左旋多巴仍是治疗帕金森病的主要药物,但随着时间的推移,患者会出现运动波动和左旋多巴诱发的运动障碍,需要使用附加疗法来控制新出现的症状。然而,迄今为止,澳大利亚或其他国家尚未就左旋多巴的剂量应达到何种程度才应考虑使用附加疗法达成明确共识。研究目的 研究澳大利亚帕金森病患者的治疗模式,尤其关注首次加用左旋多巴时的剂量。方法 这是一项回顾性、观察性、非干预性研究,研究对象是澳大利亚人类服务部药品福利计划(PBS)10%样本中的帕金森病患者。研究人员从 2007 年 1 月 1 日至 2021 年 12 月 31 日的 12 个月处方中提取了患者的所有报销处方(包括普通处方和优惠处方)、处方医生类型和项目代码等数据,这些处方中至少有三张左旋多巴的 PBS 报销处方。结果 共纳入 154 850 名患者,其中 42 330 人(27%)在此期间开始接受附加疗法。在接受附加疗法之前的 12 个月中,左旋多巴的剂量从 100 毫克/天到 1000 毫克/天不等。大多数患者的附加疗法处方由神经科医生开具,约 40% 的患者在首次开始附加疗法前的左旋多巴剂量为 600 毫克/天或以上。结论 在澳大利亚,很大一部分患者接受的左旋多巴单药治疗剂量被认为偏高,其中许多患者可能会从在治疗方案中添加附加疗法中获益。数据可能来自第三方,且未公开。支持本研究结果的数据可从澳大利亚服务机构获得。本研究在获得许可的情况下使用这些数据。经澳大利亚服务机构外部请求评估委员会许可,可在以下网站获取数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Levodopa use in Australia: an analysis of Pharmaceutical Benefits Scheme 10% data
Background Levodopa remains the mainstay of treatment of Parkinson’s disease, however, over time motor fluctuations and levodopa-induced dyskinesia develop, requiring add-on therapies to control emerging symptoms. To date, however, there is no clear consensus in Australia, or elsewhere, at which dose of levodopa that add-on therapies should be considered. Objectives The purpose of this study was to examine the treatment patterns of patients with Parkinson’s disease in Australia, with particular focus on levodopa doses at the time of first add-on. Methods This was a retrospective, observational, non-interventional study of patients with Parkinson’s disease within the Australian Department of Human Services Pharmaceutical Benefits Scheme (PBS) 10% sample. Data on all reimbursed prescriptions (both general and concession), prescriber type and item code were extracted for patients who were dispensed at least three PBS reimbursed prescriptions for levodopa in the previous 12 months prescription from 1 January 2007 to 31 December 2021. Results 154 850 unique patients were included, of whom 42 330 (27%) commenced add-on therapy during the period. In the 12 months prior to add-on therapy, levodopa doses ranged from 100 mg/day to 1000 mg/day. The majority of patients were prescribed add-on therapy by a neurologist and approximately 40% of patients were prescribed levodopa doses of 600 mg/day or more prior to the first add-on therapy being initiated. Conclusions A large proportion of patients in Australia are managed with levodopa monotherapy doses that are considered high and many of these patients may benefit from the addition of add-on therapy to their regimen. Data may be obtained from a third party and are not publicly available. The data that support the findings of this study are available from Services Australia. Restrictions apply to the availability of these data, which were used under license for this study. Data are available at with the permission of Services Australia’s External Request Evaluation Committee.
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来源期刊
BMJ Neurology Open
BMJ Neurology Open Medicine-Neurology (clinical)
CiteScore
3.20
自引率
3.70%
发文量
46
审稿时长
13 weeks
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