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在日常临床实践中,左旋多巴与恩他卡朋联用对单用左旋多巴治疗效果欠佳的帕金森病患者的疗效及安全性:一项国际多中心开放标签研究

Efficacy and safety of levodopa with entacapone in Parkinson's disease patients suboptimally controlled with levodopa alone, in daily clinical practice: an international, multicentre, open-label study.

作者信息

Gershanik Oscar, Emre Murat, Bernhard Gudrun, Sauer Dirk

机构信息

Hospital Frances La Rioja 951, Buenos Aires, Argentina.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2003 Sep;27(6):963-71. doi: 10.1016/S0278-5846(03)00156-8.

Abstract

The combination of entacapone with levodopa is effective in the treatment of Parkinson's disease (PD), providing significant improvements in 'on' time and Unified Parkinson's Disease Rating Scale (UPDRS) motor and ADL scores in controlled clinical trials. This multicentre, open-label study was designed to further evaluate the effectiveness of levodopa combined with entacapone 200 mg in routine clinical practice. Patients experiencing end-of-dose wearing-off were treated for 8 weeks (treatment phase), with an optional extension phase up to 20 weeks. The primary efficacy parameter was the Investigators' Global Assessment of Change; secondary efficacy parameters included UPDRS, 'off' time (from patient diaries), Patients' Global Assessment of Change, quality of life (QoL), SF-36 Health Assessment Questionnaire and Parkinson's Disease Questionnaire 39 (PDQ-39). Of the 479 patients who entered this study, 427 (89.1%) completed the treatment phase and 374 (78.1%) continued into the extension phase. Based on the Investigators' Assessment of Change, 380 (79.7%) patients showed an improvement with entacapone during the treatment phase. This improvement was maintained into the extension phase, and at Week 20, 301 (82.2%) patients continued to show an improvement. A positive treatment effect with entacapone was also seen with all secondary efficacy parameters, including QoL. Mean change in the total PDQ-39 scores showed improvements from baseline of -4.0 score points to the end of the treatment phase (n=182) and -3.1 score points at the end of the extension phase (n=152). Entacapone in combination with levodopa was generally well tolerated: 40 patients (8.4%) discontinued treatment due to adverse events (AEs) by the end of the extension phase. This study in a daily clinical practice setting confirmed the efficacy of coadministering entacapone with levodopa shown in controlled clinical trials and suggests that the combination is useful in improving the disability and QoL in patients with PD.

摘要

恩他卡朋与左旋多巴联合使用对帕金森病(PD)的治疗有效,在对照临床试验中,能显著改善“开”期时间以及统一帕金森病评定量表(UPDRS)的运动和日常生活活动(ADL)评分。这项多中心、开放标签研究旨在进一步评估左旋多巴联合200毫克恩他卡朋在常规临床实践中的有效性。经历剂末疗效减退的患者接受了8周的治疗(治疗阶段),还有一个长达20周的可选延长期。主要疗效参数是研究者的整体变化评估;次要疗效参数包括UPDRS、“关”期时间(来自患者日记)、患者的整体变化评估、生活质量(QoL)、SF - 36健康评估问卷和帕金森病问卷39(PDQ - 39)。在进入本研究的479例患者中,427例(89.1%)完成了治疗阶段,374例(78.1%)进入了延长期。根据研究者的变化评估,380例(79.7%)患者在治疗阶段使用恩他卡朋后有改善。这种改善在延长期得以维持,到第20周时,301例(82.2%)患者仍持续有改善。在所有次要疗效参数(包括QoL)方面,恩他卡朋也显示出积极的治疗效果。PDQ - 39总分的平均变化显示,从基线到治疗阶段结束(n = 182)改善了4.0分,到延长期结束时改善了3.1分(n = 152)。恩他卡朋与左旋多巴联合使用总体耐受性良好:到延长期结束时,40例患者(8.4%)因不良事件(AE)停药。这项在日常临床实践环境中的研究证实了对照临床试验中显示的恩他卡朋与左旋多巴联合使用的疗效,并表明该联合用药有助于改善PD患者的残疾状况和生活质量。

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