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左旋多巴-卡比多巴肠凝胶治疗土耳其晚期帕金森病患者的综合评估。

Comprehensive assessment of levodopa-carbidopa intestinal gel for Turkish advanced Parkinson’s disease patients.

机构信息

Department of Neurology, Movement Disorders Clinic, University of Health Sciences, Ankara City Hospital, Ankara, Turkey

Department of Gastroenterology, Ankara City Hospital, Ankara, Turkey

出版信息

Turk J Med Sci. 2021 Feb 26;51(1):84-89. doi: 10.3906/sag-2005-96.

Abstract

BACKGROUND/AIM: Levodopa-carbidopa intestinal gel (LCIG) is an effective treatment modality in the management of advanced Parkinson’s disease (PD) despite frequent adverse events and different rates of dropouts. Efficacy and safety data regarding Turkish patients on LCIG are limited. This study aims to report in detail the efficacy and adverse effect profile of LCIG among advanced PD patients from a Turkish center for movement disorders.

MATERIALS AND METHODS

Twenty-two patients (50% male) who started receiving LCIG between December 2014 and March 2020 were recruited. The efficacy of LCIG was assessed with the Unified Parkinson’s Disease Rating Scale (UPDRS III), Clinical Global İmprovement (CGI) scale, and Quality of Life scale (PDQ8). Improvements in gait disorders and nonmotor features were also questioned. Adverse events (AE) were collated into 3 topics: related to percutaneous endoscopic gastrojejunostomy (PEG-J), device-related, and LCIG infusion-related.

RESULTS

Mean age and pre-LCIG disease duration were 66.7 (8.8) and 13.3 (8.0) years respectively. UPDRS III scores and H-Y scale assessments significantly improved. Better quality of life scores, clinical global improvements, and improvements in dysarthria, dysphagia, and gait were observed. None of our patients dropped out or died during a mean 17.5-month (12.3) period. Overall 20 (90.9%) patients experienced at least one AE. Twelve patients had PEG-J–related complications; three had acute abdomen. Eight (36.4%) patients had device-associated problems. Half of the patients required at least one additional endoscopic procedure and 7 had a device replaced. Mean body weight decreased from 69.5 to 62.5 kg and seven patients had newly onset PNP at a follow-up electromyography. Dyskinesia related to LCIG infusion was observed in 5 (22.7%) patients. There was no significant increase in hallucination among patients.

CONCLUSION

LCIG is an efficient treatment modality in the management of Turkish patients with advanced Parkinson’s disease. Although most of the patients had at least one AE, none of them dropped out. Patient selection, patient compliance, and collaborative management are important steps affecting the success of modality.

摘要

背景/目的:左旋多巴-卡比多巴肠凝胶(LCIG)是治疗晚期帕金森病(PD)的有效治疗方法,尽管不良反应频繁,且退出率不同。关于土耳其 LCIG 患者的疗效和安全性数据有限。本研究旨在详细报告土耳其运动障碍中心接受 LCIG 治疗的晚期 PD 患者的疗效和不良反应概况。

材料和方法

2014 年 12 月至 2020 年 3 月期间,招募了 22 名开始接受 LCIG 治疗的患者(50%为男性)。使用统一帕金森病评定量表(UPDRS III)、临床总体印象(CGI)量表和生活质量量表(PDQ8)评估 LCIG 的疗效。还询问了步态障碍和非运动特征的改善情况。将不良反应(AE)分为 3 个主题:与经皮内镜胃空肠造口术(PEG-J)相关、与器械相关和 LCIG 输注相关。

结果

平均年龄和 LCIG 治疗前的病程分别为 66.7(8.8)和 13.3(8.0)岁。UPDRS III 评分和 H-Y 量表评估显著改善。生活质量评分更好,临床总体改善,言语不清、吞咽困难和步态改善。在平均 17.5 个月(12.3)的随访期间,我们没有患者退出或死亡。20 名(90.9%)患者至少经历了一次 AE。12 名患者发生 PEG-J 相关并发症;3 名患者发生急性腹痛。8 名(36.4%)患者出现器械相关问题。一半的患者至少需要进行一次内镜检查,7 名患者更换了器械。平均体重从 69.5 公斤下降到 62.5 公斤,7 名患者在后续肌电图检查中出现新的 PNP。5 名(22.7%)患者出现与 LCIG 输注相关的运动障碍。患者中没有出现明显的幻觉增加。

结论

LCIG 是治疗土耳其晚期帕金森病患者的有效治疗方法。尽管大多数患者至少经历了一次不良反应,但没有患者退出。患者选择、患者依从性和协作管理是影响治疗成功的重要步骤。

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