对谁有意义?最小的临床重要差异和痴呆症患者日常功能的优先级

IF 4.9 Q1 CLINICAL NEUROLOGY
Andrea Gilmore-Bykovskyi, Kayla Dillon, Beth Fields, Clark Benson, Dorothy Farrar Edwards
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引用次数: 0

摘要

阿尔茨海默病和阿尔茨海默病相关痴呆(AD/ADRD)对个体的功能性认知能力有显著影响,这凸显了在评估AD/ADRD研究中最低临床重要差异(MCID)阈值时优先考虑功能测量的必要性。在MCID讨论中,缺乏AD/ADRD患者对功能测量的直接输入,包括AD/ADRD患者意味着什么,以及在整个疾病连续体中哪种类型和程度的改善最有意义。在AD/ADRD试验中,大多数评估功能的措施主要集中在日常生活的基本和工具性活动(BADL, IADL)上,缺乏对AD/ADRD患者最重要的日常功能方面。将结果评估扩展到日常功能的其他维度,并使测量方法多样化,对于优化纳入AD/ADRD患者优先考虑的日常功能的个人有意义的方面,以及改进对潜在的更敏感的功能变化的检测至关重要。这一观点概述了四个方向,将对AD/ADRD患者最重要的因素扩展和整合到试验结果评估中,包括(1)考虑对AD/ADRD患者最重要的因素如何在从轻度到晚期痴呆的整个疾病连续体中发生变化,(2)围绕优势领域(如社会参与)识别和评估目标,而不仅仅是强调缺陷和损失。(3)利用目标实现尺度来更具体地匹配个人特定的功能目标;(4)加强对自我报告和基于绩效的功能测量的纳入和使用,并将这些测量与举报人报告测量进行三角测量。阿尔茨海默病和阿尔茨海默病相关痴呆(AD/ADRD)对个体的功能性认知能力有显著影响,这些能力的变化通过检测最小临床重要差异(MCID)阈值来衡量,以确定AD/ADRD临床试验的有效性。在AD/ADRD试验中,广泛用于评估MCID阈值的措施侧重于日常生活的基本和工具性活动,这为扩展MCID的测量提供了机会,以考虑AD/ADRD患者优先考虑的日常功能的其他维度。为了扩大结果评估并改善对AD/ADRD患者最重要的功能方面的整合,我们确定了通过目标实现缩放、自我报告和基于绩效的措施来纳入更多样化策略的机会。我们还强调纳入社会参与等基于优势的领域的重要性,超越以缺陷为重点的功能评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meaningful to whom? Minimal clinically important differences and the priorities of individuals living with dementia for everyday function

Alzheimer's disease and Alzheimer's disease related dementias (AD/ADRD) have a significant impact on an individual's functional cognitive abilities, highlighting the need to prioritize measures of function in evaluating minimally clinically important difference (MCID) thresholds in AD/ADRD research. Input directly from individuals living with AD/ADRD on measures of function are lacking in MCID discussions, including what it means to live with AD/ADRD and what type and degree of improvements are most meaningful across the disease continuum. Most measures for assessing function in AD/ADRD trials are largely focused on basic and instrumental activities of daily living (BADL, IADL), which lack aspects of everyday function that matter most to individuals living with AD/ADRD. Expanding outcome evaluation to other dimensions of everyday function and diversifying measurement approaches is essential for optimizing inclusion of personally meaningful aspects of everyday function prioritized by individuals living with AD/ADRD and improving detection of potentially more sensitive changes in functioning. This perspective outlines four directions to expand and integrate what matters most to individuals living with AD/ADRD into trial outcome evaluation, including (1) consideration of how what matters most to individuals living with AD/ADRD may change across the disease continuum from mild to advanced dementia, (2) identification and evaluation of goals around strengths-based domains such as social participation rather than solely emphasizing deficits and losses, (3) utilization of goal-attainment scaling to more specifically match individually-specific functional goals, and (4) strengthening the inclusion and use of self-report and performance-based measures of function and triangulating these measures with informant-report measures.

Highlights

  • Alzheimer's disease and Alzheimer's disease related dementias (AD/ADRD) have a significant impact on an individual’ functional cognitive abilities, of which changes in these abilities are measured through detection of minimally clinically important difference (MCID) thresholds to determine the effectiveness of AD/ADRD clinical trials.
  • Widely used measures for assessing MCID thresholds in AD/ADRD trials focus on basic and instrumental activities of daily living, presenting opportunities to expand measurement of MCID to account for other dimensions of everyday function that are prioritized by individuals living with AD/ADRD.
  • To expand outcome evaluation and improve integration of aspects of functioning that matter most to people living with AD/ADRD, we identify opportunities to incorporate more diverse strategies via goal-attainment scaling, self-report, and performance-based measures as appropriate. We also highlight the importance of incorporating strengths-based domains such as social participation, moving beyond deficit-focused assessment of functioning.
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来源期刊
CiteScore
10.10
自引率
2.10%
发文量
134
审稿时长
10 weeks
期刊介绍: Alzheimer''s & Dementia: Translational Research & Clinical Interventions (TRCI) is a peer-reviewed, open access,journal from the Alzheimer''s Association®. The journal seeks to bridge the full scope of explorations between basic research on drug discovery and clinical studies, validating putative therapies for aging-related chronic brain conditions that affect cognition, motor functions, and other behavioral or clinical symptoms associated with all forms dementia and Alzheimer''s disease. The journal will publish findings from diverse domains of research and disciplines to accelerate the conversion of abstract facts into practical knowledge: specifically, to translate what is learned at the bench into bedside applications. The journal seeks to publish articles that go beyond a singular emphasis on either basic drug discovery research or clinical research. Rather, an important theme of articles will be the linkages between and among the various discrete steps in the complex continuum of therapy development. For rapid communication among a multidisciplinary research audience involving the range of therapeutic interventions, TRCI will consider only original contributions that include feature length research articles, systematic reviews, meta-analyses, brief reports, narrative reviews, commentaries, letters, perspectives, and research news that would advance wide range of interventions to ameliorate symptoms or alter the progression of chronic neurocognitive disorders such as dementia and Alzheimer''s disease. The journal will publish on topics related to medicine, geriatrics, neuroscience, neurophysiology, neurology, psychiatry, clinical psychology, bioinformatics, pharmaco-genetics, regulatory issues, health economics, pharmacoeconomics, and public health policy as these apply to preclinical and clinical research on therapeutics.
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