Device-aided therapies (DATs) in Parkinson's disease (PD). The DATs-PD GETM Spanish Registry Protocol Study.

IF 2.9 3区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
PLoS ONE Pub Date : 2025-03-31 eCollection Date: 2025-01-01 DOI:10.1371/journal.pone.0316052
Diego Santos-García, Guillermo González-Ortega, Pilar Sánchez-Alonso, Anna Planas-Ballvé, Rocío García-Ramos, Iria Cabo, Marta Blázquez-Estrada, Álvaro Sánchez-Ferro
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引用次数: 0

Abstract

Background and objective: Device-aided therapies (DATs) are treatments indicated for people with Parkinson´s disease (PwP) experiencing clinical fluctuations that remain suboptimal despite conventional medication. New DATs have recently emerged such as levodopa-entacapone-carbidopa intestinal gel infusion (LECIG) and subcutaneous infusion of foslevodopa/foscarbidopa (fLD/fCD). Understanding the differences between various DATs is essential.

Patients and methods: We present here the protocol study of the DATs-PD GETM Spanish Registry. This is a descriptive, observational, prospective, multicenter, open study that is proposed as a clinical registry with progressive inclusion of PwP treated with a DAT in daily clinical practice conditions in more 40 centers from Spain for 10 years. The principal aim is to know the type of DAT that PwP in our country (Spain) receive. Specific objectives are to compare the clinical characteristics of the patients, the effectiveness, safety and tolerability, to identify predictors of a good response and to analyze the response by groups (gender, disease duration, phenotype, etc.). There is a baseline visit (V1; indication of the therapy), start visit (V2; initiation of the therapy) and follow-up visits at 6 months ±  3 months (V3_6M) and after this annually ±  3 months for 10 years (V3_12M, V3_24M, etc.).

Results: The registry is on going. The first patient was included on April 10, 2024. Patient recruitment and follow-up will be conducted until 31/DEC/2033. It is estimated that the registry will include a minimum of 3,000 patients.

Conclusion: The present study will help improve the care of PD patients treated with a DAT.

背景和目的:器械辅助疗法(DATs)是针对帕金森病(PwP)患者的治疗方法,帕金森病患者在接受常规药物治疗后仍会出现临床症状波动。最近出现了一些新的辅助疗法,如左旋多巴-恩他卡朋-卡比多巴肠道凝胶输注疗法(LECIG)和福舍伏多巴/福斯卡比多巴皮下注射疗法(fLD/fCD)。了解各种 DAT 之间的差异至关重要:我们在此介绍 DATs-PD GETM 西班牙登记处的方案研究。这是一项描述性、观察性、前瞻性、多中心、开放式研究,拟作为一项临床登记,逐步纳入西班牙 40 多个中心 10 年来日常临床实践中接受 DAT 治疗的患者。主要目的是了解我国(西班牙)接受 DAT 治疗的 PwP 的类型。具体目标是比较患者的临床特征、有效性、安全性和耐受性,确定良好反应的预测因素,并按组别(性别、病程、表型等)分析反应情况。登记包括基线访视(V1;治疗指征)、起始访视(V2;开始治疗)和 6 个月±3 个月的随访(V3_6M),此后每年±3 个月随访一次,为期 10 年(V3_12M、V3_24M 等):登记正在进行中。第一例患者于 2024 年 4 月 10 日纳入登记。患者招募和随访将持续到 2033 年 12 月 31 日。据估计,登记处将至少纳入 3000 名患者:本研究将有助于改善对接受 DAT 治疗的帕金森病患者的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PLoS ONE
PLoS ONE 生物-生物学
CiteScore
6.20
自引率
5.40%
发文量
14242
审稿时长
3.7 months
期刊介绍: PLOS ONE is an international, peer-reviewed, open-access, online publication. PLOS ONE welcomes reports on primary research from any scientific discipline. It provides: * Open-access—freely accessible online, authors retain copyright * Fast publication times * Peer review by expert, practicing researchers * Post-publication tools to indicate quality and impact * Community-based dialogue on articles * Worldwide media coverage
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