N. Drummond, L. Mccleary, L. Garcia, K. McGilton, F. Molnar, W. Dalziel, T. J. Xu, D. Turner, J. Triscott, E. Freiheit
{"title":"Assessing Determinants of Perceived Quality in Transitions for People with Dementia: a Prospective Observational Study","authors":"N. Drummond, L. Mccleary, L. Garcia, K. McGilton, F. Molnar, W. Dalziel, T. J. Xu, D. Turner, J. Triscott, E. Freiheit","doi":"10.5770/cgj.22.332","DOIUrl":null,"url":null,"abstract":"Background The trajectory of dementia through time is characterized by common transitions which are difficult for persons with dementia (PWDs) and their families and friends. Our study sought to identify determinants for the quality of transition outcomes. Method A 24-month, prospective, longitudinal design identified specific transitions as they occurred in 108 person-with-dementia/caregiver dyads, and assessed the perceived transition quality from the perspective of the caregiver and what we denote as the ‘summative’ transition quality outcome variable (as explained in the Data Processing section under Methods). Results Among caregivers and during the authors’ deliberations of the summative transition quality outcomes, good transition quality was associated with the PWD’s baseline Disability Assessment for Dementia (OR 1.04, 95% CI 1.02–1.06 per increase in percent score based on summative assessments), and with the PWD’s higher baseline quality of life scores (OR 1.11, 95% CI 1.05–1.18 per increase in unit of score in QOL-AD based on summative assessments). Caregiver-perceived better outcome quality was associated with lower caregiver burden, (OR 0.97, 95% CI 0.95–0.99 per unit CBI score increase). Conclusion Identifying determinants of successful transitions is feasible and may be translated into practical guidance for use in clinical encounters. Those with worse prior quality of life or worse performance in activities of daily living appear to require specific support during transitions, as do those whose caregivers report higher levels of burden.","PeriodicalId":56182,"journal":{"name":"Canadian Geriatrics Journal","volume":"22 1","pages":"13 - 22"},"PeriodicalIF":1.6000,"publicationDate":"2019-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian Geriatrics Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5770/cgj.22.332","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
引用次数: 7
Abstract
Background The trajectory of dementia through time is characterized by common transitions which are difficult for persons with dementia (PWDs) and their families and friends. Our study sought to identify determinants for the quality of transition outcomes. Method A 24-month, prospective, longitudinal design identified specific transitions as they occurred in 108 person-with-dementia/caregiver dyads, and assessed the perceived transition quality from the perspective of the caregiver and what we denote as the ‘summative’ transition quality outcome variable (as explained in the Data Processing section under Methods). Results Among caregivers and during the authors’ deliberations of the summative transition quality outcomes, good transition quality was associated with the PWD’s baseline Disability Assessment for Dementia (OR 1.04, 95% CI 1.02–1.06 per increase in percent score based on summative assessments), and with the PWD’s higher baseline quality of life scores (OR 1.11, 95% CI 1.05–1.18 per increase in unit of score in QOL-AD based on summative assessments). Caregiver-perceived better outcome quality was associated with lower caregiver burden, (OR 0.97, 95% CI 0.95–0.99 per unit CBI score increase). Conclusion Identifying determinants of successful transitions is feasible and may be translated into practical guidance for use in clinical encounters. Those with worse prior quality of life or worse performance in activities of daily living appear to require specific support during transitions, as do those whose caregivers report higher levels of burden.
随着时间的推移,痴呆症的发展轨迹具有共同的过渡特征,这对痴呆症患者及其家人和朋友来说是困难的。我们的研究试图确定过渡结果质量的决定因素。方法一项为期24个月的前瞻性纵向设计确定了108名痴呆症患者/护理人员的特定过渡,并从护理人员的角度评估了感知的过渡质量,以及我们所说的“总结性”过渡质量结果变量(如方法下的数据处理部分所述)。结果在护理人员中,在作者对总结性过渡质量结果的审议过程中,良好的过渡质量与PWD的痴呆基线残疾评估(基于总结性评估的百分比分数每增加1.04,95% CI 1.02-1.06)和PWD较高的基线生活质量评分(基于总结性评估的QOL-AD评分单位每增加1.11,95% CI 1.05-1.18)相关。照顾者感知更好的结局质量与照顾者负担降低相关(OR 0.97, 95% CI 0.95-0.99 /单位CBI评分增加)。结论确定成功转化的决定因素是可行的,并可转化为临床遭遇使用的实用指导。那些先前生活质量较差或日常生活活动表现较差的人在过渡期间似乎需要特殊的支持,那些照顾者报告负担较高的人也是如此。
期刊介绍:
The Canadian Geriatrics Journal (CGJ) is a peer-reviewed publication that is a home for innovative aging research of a high quality aimed at improving the health and the care provided to older persons residing in Canada and outside our borders. While we gratefully accept submissions from researchers outside our country, we are committed to encouraging aging research by Canadians. The CGJ is targeted to family physicians with training or an interest in the care of older persons, specialists in geriatric medicine, geriatric psychiatrists, and members of other health disciplines with a focus on gerontology.