Three approaches to determining clinically meaningful benefit on the Cohen-Mansfield Agitation Inventory in dementia clinical trials for agitation

IF 4.9 Q1 CLINICAL NEUROLOGY
Kathy Y. Liu, Chineze Ivenso, Rebecca Howard, Penny Rapaport, Suzanne Reeves, Sube Banerjee, Lon S. Schneider, Maria I. Lapid, Agitation MCID Study Group, Robert Howard
{"title":"Three approaches to determining clinically meaningful benefit on the Cohen-Mansfield Agitation Inventory in dementia clinical trials for agitation","authors":"Kathy Y. Liu,&nbsp;Chineze Ivenso,&nbsp;Rebecca Howard,&nbsp;Penny Rapaport,&nbsp;Suzanne Reeves,&nbsp;Sube Banerjee,&nbsp;Lon S. Schneider,&nbsp;Maria I. Lapid,&nbsp;Agitation MCID Study Group,&nbsp;Robert Howard","doi":"10.1002/trc2.70099","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> INTRODUCTION</h3>\n \n <p>There is a need to understand the clinical meaningfulness of symptom score changes in treatment trials of dementia-related agitation. We estimated minimal clinically important differences (MCIDs) for commonly employed agitation scales and contextualized their clinical application.</p>\n </section>\n \n <section>\n \n <h3> METHODS</h3>\n \n <p>We employed anchor- and distribution-based approaches to determine changes in scores corresponding to minimal symptom improvement. An opinion-based approach assessed expert clinicians’ agreement on the meaningfulness of score changes through three clinical vignettes.</p>\n </section>\n \n <section>\n \n <h3> RESULTS</h3>\n \n <p>Minimal symptom improvement for Cohen-Mansfield Agitation Inventory total score ranged from −4 (over &lt;1 month) to −11 (over 1 to 3 months) points. Greater symptom severity correlated with higher MCID estimates. The clinical importance of score changes was influenced by treatment duration, pharmacological side effects, and impacts on caregiver distress/time resources.</p>\n </section>\n \n <section>\n \n <h3> DISCUSSION</h3>\n \n <p>The clinical meaningfulness of agitation scale MCIDs is influenced by trial-specific and clinical factors. Shorter trial durations and measuring caregiver distress/time resources enhance the clinical interpretation of agitation treatment outcomes.</p>\n </section>\n \n <section>\n \n <h3> Highlights</h3>\n \n <div>\n <ul>\n \n <li>For the CMAI total score, the MCID was −4 points over shorter time scales and −11 points for longer time scales.</li>\n \n <li>Worse agitation severity was associated with higher MCID estimates.</li>\n \n <li>There was high expert consensus that a noticeable treatment benefit was not worthwhile if it occurred after 12 weeks or had no impact on caregiver/staff distress/time resources.</li>\n </ul>\n </div>\n </section>\n </div>","PeriodicalId":53225,"journal":{"name":"Alzheimer''s and Dementia: Translational Research and Clinical Interventions","volume":"11 2","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/trc2.70099","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alzheimer''s and Dementia: Translational Research and Clinical Interventions","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/trc2.70099","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

INTRODUCTION

There is a need to understand the clinical meaningfulness of symptom score changes in treatment trials of dementia-related agitation. We estimated minimal clinically important differences (MCIDs) for commonly employed agitation scales and contextualized their clinical application.

METHODS

We employed anchor- and distribution-based approaches to determine changes in scores corresponding to minimal symptom improvement. An opinion-based approach assessed expert clinicians’ agreement on the meaningfulness of score changes through three clinical vignettes.

RESULTS

Minimal symptom improvement for Cohen-Mansfield Agitation Inventory total score ranged from −4 (over <1 month) to −11 (over 1 to 3 months) points. Greater symptom severity correlated with higher MCID estimates. The clinical importance of score changes was influenced by treatment duration, pharmacological side effects, and impacts on caregiver distress/time resources.

DISCUSSION

The clinical meaningfulness of agitation scale MCIDs is influenced by trial-specific and clinical factors. Shorter trial durations and measuring caregiver distress/time resources enhance the clinical interpretation of agitation treatment outcomes.

Highlights

  • For the CMAI total score, the MCID was −4 points over shorter time scales and −11 points for longer time scales.
  • Worse agitation severity was associated with higher MCID estimates.
  • There was high expert consensus that a noticeable treatment benefit was not worthwhile if it occurred after 12 weeks or had no impact on caregiver/staff distress/time resources.
确定Cohen-Mansfield躁动量表在痴呆临床试验中有临床意义的益处的三种方法
有必要了解痴呆相关躁动治疗试验中症状评分变化的临床意义。我们估计了常用躁动量表的最小临床重要差异(MCIDs),并将其临床应用背景化。方法:我们采用基于锚点和分布的方法来确定最小症状改善对应的评分变化。一种基于意见的方法通过三个临床小插曲评估专家临床医生对评分变化意义的同意。结果:Cohen-Mansfield躁动量表总分最小症状改善范围为- 4分(超过1个月)至- 11分(超过1至3个月)。更严重的症状与更高的MCID估计值相关。评分变化的临床重要性受治疗时间、药物副作用和对护理者痛苦/时间资源的影响。躁动量表MCIDs的临床意义受试验特异性和临床因素的影响。较短的试验持续时间和测量护理者的痛苦/时间资源可以增强对躁动治疗结果的临床解释。对于CMAI总分,较短时间尺度的MCID为−4分,较长时间尺度的MCID为−11分。较差的躁动严重程度与较高的MCID估计值相关。专家一致认为,如果在12周后才出现明显的治疗效果,或者对护理人员/工作人员的痛苦/时间资源没有影响,那么就不值得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信