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国际帕金森病和运动障碍学会循证医学综述:帕金森病运动症状治疗的最新进展。

International Parkinson and movement disorder society evidence-based medicine review: Update on treatments for the motor symptoms of Parkinson's disease.

机构信息

Edmund J. Safra Program, Movement Disorder Clinic, Toronto Western Hospital, Toronto, Ontario, Canada.

University of Toronto Department of Medicine, Toronto, Ontario, Canada.

出版信息

Mov Disord. 2018 Aug;33(8):1248-1266. doi: 10.1002/mds.27372. Epub 2018 Mar 23.

Abstract

OBJECTIVE

The objective of this review was to update evidence-based medicine recommendations for treating motor symptoms of Parkinson's disease (PD).

BACKGROUND

The Movement Disorder Society Evidence-Based Medicine Committee recommendations for treatments of PD were first published in 2002 and updated in 2011, and we continued the review to December 31, 2016.

METHODS

Level I studies of interventions for motor symptoms were reviewed. Criteria for inclusion and quality scoring were as previously reported. Five clinical indications were considered, and conclusions regarding the implications for clinical practice are reported.

RESULTS

A total of 143 new studies qualified. There are no clinically useful interventions to prevent/delay disease progression. For monotherapy of early PD, nonergot dopamine agonists, oral levodopa preparations, selegiline, and rasagiline are clinically useful. For adjunct therapy in early/stable PD, nonergot dopamine agonists, rasagiline, and zonisamide are clinically useful. For adjunct therapy in optimized PD for general or specific motor symptoms including gait, rivastigmine is possibly useful and physiotherapy is clinically useful; exercise-based movement strategy training and formalized patterned exercises are possibly useful. There are no new studies and no changes in the conclusions for the prevention/delay of motor complications. For treating motor fluctuations, most nonergot dopamine agonists, pergolide, levodopa ER, levodopa intestinal infusion, entacapone, opicapone, rasagiline, zonisamide, safinamide, and bilateral STN and GPi DBS are clinically useful. For dyskinesia, amantadine, clozapine, and bilateral STN DBS and GPi DBS are clinically useful.

CONCLUSIONS

The options for treating PD symptoms continues to expand. These recommendations allow the treating physician to determine which intervention to recommend to an individual patient. © 2018 International Parkinson and Movement Disorder Society.

摘要

目的

本综述旨在更新基于循证医学的帕金森病(PD)运动症状治疗推荐意见。

背景

运动障碍协会循证医学委员会于 2002 年首次发表了 PD 治疗推荐意见,并于 2011 年进行了更新,我们继续进行了审查,截至 2016 年 12 月 31 日。

方法

对运动症状干预措施的 I 级研究进行了回顾。纳入标准和质量评分标准如前所述。考虑了 5 种临床适应证,并报告了对临床实践的影响的结论。

结果

共有 143 项新研究符合条件。目前尚无预防/延缓疾病进展的有效干预措施。对于早期 PD 的单药治疗,非麦角类多巴胺激动剂、口服左旋多巴制剂、司来吉兰和雷沙吉兰具有临床意义。对于早期/稳定期 PD 的辅助治疗,非麦角类多巴胺激动剂、雷沙吉兰和唑尼沙胺具有临床意义。对于优化的 PD 患者的辅助治疗,对于一般或特定运动症状(包括步态),利凡斯的明可能有用,物理治疗具有临床意义;基于运动的运动策略训练和规范化的模式训练可能有用。没有新的研究,也没有改变预防/延缓运动并发症的结论。对于治疗运动波动,大多数非麦角类多巴胺激动剂、培高利特、左旋多巴 ER、左旋多巴肠内输注、恩他卡朋、奥匹卡朋、雷沙吉兰、唑尼沙胺、沙芬酰胺、双侧 STN 和 GPi DBS 均具有临床意义。对于异动症,金刚烷胺、氯氮平、双侧 STN 和 GPi DBS 具有临床意义。

结论

治疗 PD 症状的选择不断扩大。这些推荐意见使治疗医生能够确定向个体患者推荐哪种干预措施。© 2018 国际帕金森病和运动障碍协会。

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