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CHERISH(住院老年人减少住院影响协作组):一项多中心改进项目的方案,旨在减少老年住院患者的老年综合征

CHERISH (collaboration for hospitalised elders reducing the impact of stays in hospital): protocol for a multi-site improvement program to reduce geriatric syndromes in older inpatients.

作者信息

Mudge Alison M, Banks Merrilyn D, Barnett Adrian G, Blackberry Irene, Graves Nicholas, Green Theresa, Harvey Gillian, Hubbard Ruth E, Inouye Sharon K, Kurrle Sue, Lim Kwang, McRae Prue, Peel Nancye M, Suna Jessica, Young Adrienne M

机构信息

Royal Brisbane and Women's Hospital, Metro North Hospital and Health Service, Brisbane, Australia.

Institute of Health and Biomedical Innovation and School of Public Health and Social Work, Queensland University of Technology, Brisbane, Australia.

出版信息

BMC Geriatr. 2017 Jan 9;17(1):11. doi: 10.1186/s12877-016-0399-7.

Abstract

BACKGROUND

Older inpatients are at risk of hospital-associated geriatric syndromes including delirium, functional decline, incontinence, falls and pressure injuries. These contribute to longer hospital stays, loss of independence, and death. Effective interventions to reduce geriatric syndromes remain poorly implemented due to their complexity, and require an organised approach to change care practices and systems. Eat Walk Engage is a complex multi-component intervention with structured implementation, which has shown reduced geriatric syndromes and length of stay in pilot studies at one hospital. This study will test effectiveness of implementing Eat Walk Engage using a multi-site cluster randomised trial to inform transferability of this intervention.

METHODS

A hybrid study design will evaluate the effectiveness and implementation strategy of Eat Walk Engage in a real-world setting. A multisite cluster randomised study will be conducted in 8 medical and surgical wards in 4 hospitals, with one ward in each site randomised to implement Eat Walk Engage (intervention) and one to continue usual care (control). Intervention wards will be supported to develop and implement locally tailored strategies to enhance early mobility, nutrition, and meaningful activities. Resources will include a trained, mentored facilitator, audit support, a trained healthcare assistant, and support by an expert facilitator team using the i-PARIHS implementation framework. Patient outcomes and process measures before and after intervention will be compared between intervention and control wards. Primary outcomes are any hospital-associated geriatric syndrome (delirium, functional decline, falls, pressure injuries, new incontinence) and length of stay. Secondary outcomes include discharge destination; 30-day mortality, function and quality of life; 6 month readmissions; and cost-effectiveness. Process measures including patient interviews, activity mapping and mealtime audits will inform interventions in each site and measure improvement progress. Factors influencing the trajectory of implementation success will be monitored on implementation wards.

DISCUSSION

Using a hybrid design and guided by an explicit implementation framework, the CHERISH study will establish the effectiveness, cost-effectiveness and transferability of a successful pilot program for improving care of older inpatients, and identify features that support successful implementation.

TRIAL REGISTRATION

ACTRN12615000879561 registered prospectively 21/8/2015.

摘要

背景

老年住院患者面临与医院相关的老年综合征风险,包括谵妄、功能衰退、失禁、跌倒和压疮。这些会导致住院时间延长、失去独立生活能力以及死亡。由于其复杂性,减少老年综合征的有效干预措施仍未得到充分实施,需要一种有组织的方法来改变护理实践和系统。“饮食、行走、参与”(Eat Walk Engage)是一种具有结构化实施方式的复杂多成分干预措施,在一家医院的试点研究中已显示出可减少老年综合征和缩短住院时间。本研究将通过多中心整群随机试验来测试实施“饮食、行走、参与”的有效性,以了解该干预措施的可推广性。

方法

采用混合研究设计来评估“饮食、行走、参与”在实际环境中的有效性和实施策略。将在4家医院的8个内科和外科病房进行多中心整群随机研究,每个地点的一个病房随机分配实施“饮食、行走、参与”(干预组),另一个病房继续常规护理(对照组)。将支持干预病房制定并实施因地制宜的策略,以促进早期活动、营养摄入和有意义的活动。资源将包括一名经过培训和指导的协调员、审计支持、一名经过培训的医疗保健助理,以及由一个专家协调团队使用i - PARIHS实施框架提供的支持。将比较干预病房和对照病房干预前后的患者结局和过程指标。主要结局是任何与医院相关的老年综合征(谵妄、功能衰退、跌倒、压疮、新发失禁)和住院时间。次要结局包括出院去向;30天死亡率、功能和生活质量;6个月再入院率;以及成本效益。包括患者访谈、活动映射和用餐时间审计在内的过程指标将为每个地点的干预措施提供信息并衡量改进进展。将在实施病房监测影响实施成功轨迹的因素。

讨论

通过采用混合设计并以明确的实施框架为指导,CHERISH研究将确定一项成功的试点项目在改善老年住院患者护理方面的有效性、成本效益和可推广性,并确定支持成功实施的特征。

试验注册

ACTRN12615000879561,于2015年8月21日前瞻性注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2af4/5223473/cdeb178ed18d/12877_2016_399_Fig1_HTML.jpg

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