PROs for RARE:为患有遗传性智力障碍的个人开发核心患者报告结果集的协议
Nadia Y van Silfhout1,2,3,4,5, Maud M van Muilekom1,4, Clara D van Karnebeek2,3,5
1Department of Child and Adolescent Psychiatry & Psychosocial Care, Emma Children's Hospital, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands.
Orphanet journal of rare diseases
|September 28, 2024
概括
研究人员正在为遗传性智力障碍 (GID) 开发一套核心患者报告结果 (PRO). 这旨在标准化研究和护理GID患者的结果测量.
科学领域:
- 神经科学是一个神经科学.
- 遗传学 是一个遗传学.
- 患者报告的结果
背景情况:
- 遗传智力障碍 (GID) 涵盖了影响日常功能的罕见神经发育障碍.
- 对患者报告结果 (PROs) 的标准化测量对于了解GID的影响至关重要.
- 目前GID的PRO多种多样,需要采用统一的方法.
研究的目的:
- 为患有GID的儿童和成年人开发一套通用核心PRO套件.
- 建立一个标准化患者报告结果测量 (PROM) 的基础,用于GID.
主要方法:
- 进行范围审查和定性研究,以确定相关的PRO.
- 将已识别的 PRO 集成和概念化为一个试点通用核心 PRO 集.
- 通过欧洲Delphi调查和共识会议优先考虑PRO.
主要成果:
- 已经建立了一个开发GID通用核心PRO集的协议.
- 该过程涉及全面的文献评论,定性研究和专家共识.
- 开发的套件将指导特定患者报告的结果措施 (PROM) 的选择.
结论:
- 该协议概述了GID.的通用核心PRO集的开发.
- 下一阶段涉及选择和验证GID群体的特定PROM.
- 在护理和研究中实施将增强数据聚合和以患者为中心的护理.
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