痴呆家庭支持的组成部分、影响和成本:包括desant RCT在内的一项研究项目

Q4 Medicine
P. Clarkson, D. Challis, J. Hughes, B. Roe, L. Davies, I. Russell, M. Orrell, F. Poland, D. Jolley, N. Kapur, Catherine A. Robinson, Helen Chester, S. Davies, C. Sutcliffe, J. Peconi, Rosa Pitts, G. Fegan, Saiful Islam, Vincent Gillan, C. Entwistle, Rebecca Beresford, M. Abendstern, C. Giebel, Saima Ahmed, Rowan Jasper, A. Usman, Baber Malik, K. Hayhurst
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引用次数: 4

摘要

超过一半的痴呆症患者住在家里。我们几乎不知道什么样的家庭支持在临床上是有效的或具有成本效益的,可以使他们生活得更好。我们的目标是(1)回顾家庭支持组成部分的证据,确定它们在英国文献和服务中的存在,并制定适当的经济模型;(2)开发并测试早期痴呆的实用记忆支持包,测试常规家庭支持在晚期痴呆中的临床效果和成本效益,并在此基础上设计工具包;(3)得出工作人员、护理人员和痴呆症患者对家庭支持投入和一揽子计划的偏好,并评估这些方法在早期和晚期痴呆症中的成本效益。我们进行了(1)证据综合,国民保健服务和社会护理的全国调查和经济审查;(2)一项多中心实用随机试验[痴呆症早期认知辅助新试验(descan)],以评估为早期痴呆症患者提供记忆辅助和指导(descan干预)的临床效果和成本效益,同时进行过程评估和定性分析,一项对晚期痴呆症现有护理包的观察性研究,并进行定性分析,并开发工具包以总结这一证据;(3)咨询专家、工作人员和护理人员,通过案例小故事探讨非正式和有偿家庭支持之间的平衡,离散选择实验探讨痴呆症患者和护理人员对早期和晚期痴呆症家庭支持方案的偏好,并在试验和观察研究的基础上进行成本效用分析。这项全国性调查描述了英国各地的社区心理健康团队、记忆诊所和社会护理服务。该试验的招募是通过英格兰9个NHS信托机构和威尔士一个健康委员会的记忆服务进行的。观察性研究的招募是通过英格兰17个地方当局的社会服务部门进行的。小短文和偏好研究的招募是通过记忆服务、社区中心和护理机构进行的。年龄> 50岁且在记忆诊所首次就诊一年内患有痴呆症的人符合试验条件。年龄> 60岁且在护理需求评估后3个月内患有晚期痴呆的人符合观察性研究的条件。我们招募了工作人员、护理人员和痴呆症患者进行小短文和偏好研究。所有参与者都必须给予书面知情同意。试验和观察性研究使用布里斯托尔日常生活活动量表作为主要结果,还测量了生活质量、能力、认知、一般心理健康和照顾者的能力感。由于干预措施、方法和结果测量的异质性,我们的证据和经济综述都使用了叙事综合。经济研究的主要来源是NHS经济评估数据库。我们用线性混合模型对试验和观察研究进行了分析。我们通过“分配治疗”来分析试验,并使用倾向评分来最小化观察性研究中的混淆。我们的回顾和调查确定了几种潜在的有益的家庭支持方法。在早期痴呆中,desant试验有468名随机参与者(234名干预参与者和234名对照参与者),其中347名参与者进行了分析。我们发现,在desant干预的6个月的主要终点,对几个参与者的结果测量都没有显著影响。主要结果是布里斯托尔日常生活活动量表,得分范围从0到60,得分越高表明依赖性越强。在基线差异调整后,平均差异为0.38,稍微但不显著地有利于接受常规治疗的比较组。95%置信区间为-0.89 ~ 1.65 (p = 0.56)。没有证据表明对晚期痴呆患者进行更多的重症监护比基本护理更有效。然而,正式的家庭护理似乎有助于让人们呆在家里。工作人员推荐的非正规护理费用为正规护理的88%,但对于非正规护理人员,这一比例仅为62%。痴呆症患者更喜欢社交和娱乐活动,护理人员更喜欢临时护理和定期家庭护理。desant干预在早期痴呆中可能不具有成本效益,重症监护包在晚期痴呆中可能不具有成本效益。从第三部门的角度来看,中等强度的一揽子计划更便宜,但效果较差。某些因素可能是导致这些结果的原因,特别是护理员小组的使用减少。我们选择的结果测量可能不能反映痴呆症患者所重视的微妙结果。痴呆症患者及其护理人员首选的几种方法具有潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Components, impacts and costs of dementia home support: a research programme including the DESCANT RCT
Over half of people with dementia live at home. We know little about what home support could be clinically effective or cost-effective in enabling them to live well. We aimed to (1) review evidence for components of home support, identify their presence in the literature and in services in England, and develop an appropriate economic model; (2) develop and test a practical memory support package in early-stage dementia, test the clinical effectiveness and cost-effectiveness of routine home support in later-stage dementia and design a toolkit based on this evidence; and (3) elicit the preferences of staff, carers and people with dementia for home support inputs and packages, and evaluate the cost-effectiveness of these approaches in early- and later-stage dementia. We undertook (1) an evidence synthesis, national surveys on the NHS and social care and an economic review; (2) a multicentre pragmatic randomised trial [Dementia Early Stage Cognitive Aids New Trial (DESCANT)] to estimate the clinical effectiveness and cost-effectiveness of providing memory aids and guidance to people with early-stage dementia (the DESCANT intervention), alongside process evaluation and qualitative analysis, an observational study of existing care packages in later-stage dementia along with qualitative analysis, and toolkit development to summarise this evidence; and (3) consultation with experts, staff and carers to explore the balance between informal and paid home support using case vignettes, discrete choice experiments to explore the preferences of people with dementia and carers between home support packages in early- and later-stage dementia, and cost–utility analysis building on trial and observational study. The national surveys described Community Mental Health Teams, memory clinics and social care services across England. Recruitment to the trial was through memory services in nine NHS trusts in England and one health board in Wales. Recruitment to the observational study was through social services in 17 local authorities in England. Recruitment for the vignette and preference studies was through memory services, community centres and carers’ organisations. People aged > 50 years with dementia within 1 year of first attendance at a memory clinic were eligible for the trial. People aged > 60 years with later-stage dementia within 3 months of a review of care needs were eligible for the observational study. We recruited staff, carers and people with dementia for the vignette and preference studies. All participants had to give written informed consent. The trial and observational study used the Bristol Activities of Daily Living Scale as the primary outcome and also measured quality of life, capability, cognition, general psychological health and carers’ sense of competence. Owing to the heterogeneity of interventions, methods and outcome measures, our evidence and economic reviews both used narrative synthesis. The main source of economic studies was the NHS Economic Evaluation Database. We analysed the trial and observational study by linear mixed models. We analysed the trial by ‘treatment allocated’ and used propensity scores to minimise confounding in the observational study. Our reviews and surveys identified several home support approaches of potential benefit. In early-stage dementia, the DESCANT trial had 468 randomised participants (234 intervention participants and 234 control participants), with 347 participants analysed. We found no significant effect at the primary end point of 6 months of the DESCANT intervention on any of several participant outcome measures. The primary outcome was the Bristol Activities of Daily Living Scale, for which scores range from 0 to 60, with higher scores showing greater dependence. After adjustment for differences at baseline, the mean difference was 0.38, slightly but not significantly favouring the comparator group receiving treatment as usual. The 95% confidence interval ran from –0.89 to 1.65 (p = 0.56). There was no evidence that more intensive care packages in later-stage dementia were more effective than basic care. However, formal home care appeared to help keep people at home. Staff recommended informal care that cost 88% of formal care, but for informal carers this ratio was only 62%. People with dementia preferred social and recreational activities, and carers preferred respite care and regular home care. The DESCANT intervention is probably not cost-effective in early-stage dementia, and intensive care packages are probably not cost-effective in later-stage dementia. From the perspective of the third sector, intermediate intensity packages were cheaper but less effective. Certain elements may be driving these results, notably reduced use of carers’ groups. Our chosen outcome measures may not reflect subtle outcomes valued by people with dementia. Several approaches preferred by people with dementia and their carers have potential. However, memory aids aiming to affect daily living activities in early-stage dementia or intensive packages compared with basic care in later-stage dementia were not clinically effective or cost-effective. Further work needs to identify what people with dementia and their carers prefer and develop more sensitive outcome measures. Current Controlled Trials ISRCTN12591717. The evidence synthesis is registered as PROSPERO CRD42014008890. This project was funded by the National Institute for Health Research (NIHR) Programme Grants for Applied Research programme and will be published in full in Programme Grants for Applied Research; Vol. 9, No. 6. See the NIHR Journals Library website for further project information.
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