Livingston Gill, Barber Julie, Marston Louise, Stringer Aisling, Panca Monica, Hunter Rachael, Cooper Claudia, Laybourne Anne, La Frenais Francesca, Reeves Suzanne, Manela Monica, Lambe Katie, Banerjee Sube, Rapaport Penny
Division of Psychiatry, University College London, London, UK; Camden and Islington NHS Foundation Trust, St Pancras Hospital, London, UK.
UCL Statistical Science and PRIMENT Clinical Trials Unit, University College London, London, UK.
Lancet Psychiatry. 2019 Apr;6(4):293-304. doi: 10.1016/S2215-0366(19)30045-8. Epub 2019 Mar 11.
Many people with dementia living in care homes have distressing and costly agitation symptoms. Interventions should be efficacious, scalable, and feasible.
We did a parallel-group, cluster-randomised controlled trial in 20 care homes across England. Care homes were eligible if they had 17 residents or more with dementia, agreed to mandatory training for all eligible staff and the implementation of plans, and more than 60% of eligible staff agreed to participate. Staff were eligible if they worked during the day providing face-to-face care for residents with dementia. Residents were eligible if they had a known dementia diagnosis or scored positive on screening with the Noticeable Problems Checklist. A statistician independent of the study randomised care homes (1:1) to the Managing Agitation and Raising Quality of Life (MARQUE) intervention or treatment as usual (TAU) using computer-generated randomisation in blocks of two, stratified by type of home (residential or nursing). Care home staff were not masked to the intervention but were asked not to inform assessors. Residents with dementia, family carers, outcome assessors, statisticians, and health economists were masked to allocation until the data were analysed. MARQUE is an evidence-based manualised intervention, delivered by supervised graduate psychologists to staff in six interactive sessions. The primary outcome was agitation score at 8 months, measured using the Cohen-Mansfield Agitation Inventory (CMAI). Analysis of the primary outcome was done in the modified intention-to-treat population, which included all randomly assigned residents for whom CMAI data was available at 8 months. Mortality was assessed in all randomly assigned residents. This study is registered with the ISRCTN registry, number ISRCTN96745365.
Between June 14, 2016, and July 4, 2017, we randomised ten care homes (189 residents) to the MARQUE intervention and ten care homes (215 residents) to TAU. At 8 months, primary outcome data were available for 155 residents in the MARQUE group and 163 residents in the TAU group. At 8 months, no significant differences in mean CMAI scores were identified between the MARQUE and TAU groups (adjusted difference -0·40 [95% CI -3·89 to 3·09; p=0·8226]). In the intervention care homes, 84% of all eligible staff completed all sessions. The mean difference in cost between the MARQUE and TAU groups was £204 (-215 to 623; p=0·320) and mean difference in quality-adjusted life-years was 0·015 (95% CI -0·004 to 0·034; p=0·127). At 8 months, 27 (14%) of 189 residents in the MARQUE group and 41 (19%) of 215 residents in the TAU group had died. The prescription of antipsychotic drugs was not significantly different between the MARQUE group and the TAU group (odds ratio 0·66; 95% CI 0·26 to 1·69, p=0·3880).
The MARQUE intervention was not efficacious for agitation although feasible and cost-effective in terms of quality of life. Addressing agitation in care homes might require resourcing for delivery by professional staff of a more intensive intervention, implementing social and activity times, and a longer time to implement change.
UK Economic and Social Research Council and the National Institute of Health Research.
许多住在养老院的痴呆症患者有令人痛苦且成本高昂的激越症状。干预措施应有效、可扩展且可行。
我们在英格兰的20家养老院进行了一项平行组、整群随机对照试验。如果养老院有17名或更多患有痴呆症的居民,同意对所有符合条件的工作人员进行强制性培训并实施相关计划,且超过60%的符合条件的工作人员同意参与,则该养老院符合条件。工作人员符合条件的前提是他们在白天为患有痴呆症的居民提供面对面护理。居民符合条件的前提是他们有已知的痴呆症诊断或在使用《明显问题清单》进行筛查时呈阳性。一名独立于该研究的统计学家使用计算机生成的随机分组法,按养老院类型(寄宿型或护理型)分层,以2个一组的区组将养老院(1:1)随机分配至管理激越与提高生活质量(MARQUE)干预组或常规治疗(TAU)组。养老院工作人员未对干预措施进行盲法处理,但被要求不得告知评估人员。患有痴呆症的居民、家庭照顾者、结果评估人员、统计学家和卫生经济学家在数据分析之前对分组情况不知情。MARQUE是一种基于证据的手册化干预措施,由受监督的研究生心理学家对工作人员进行6次互动式培训。主要结局是8个月时的激越评分,使用科恩-曼斯菲尔德激越量表(CMAI)进行测量。主要结局的分析在改良意向性分析人群中进行,该人群包括所有随机分配且在8个月时有CMAI数据的居民。对所有随机分配的居民进行死亡率评估。本研究已在国际标准随机对照试验编号注册库注册,编号为ISRCTN96745365。
在2016年6月14日至2017年7月4日期间,我们将10家养老院(189名居民)随机分配至MARQUE干预组,10家养老院(215名居民)随机分配至TAU组。在8个月时,MARQUE组有155名居民和TAU组有163名居民可获得主要结局数据。在8个月时,MARQUE组和TAU组之间的平均CMAI评分无显著差异(调整后差异为-0·40 [95%置信区间为-3·89至3·09;p = 0·8226])。在干预养老院中,所有符合条件的工作人员中有84%完成了所有培训课程。MARQUE组和TAU组之间的成本平均差异为204英镑(-215至623;p = 0·320),质量调整生命年的平均差异为0·015(95%置信区间为-0·004至0·034;p = 0·127)。在8个月时,MARQUE组189名居民中有27名(14%)死亡,TAU组215名居民中有41名(19%)死亡。MARQUE组和TAU组之间抗精神病药物的处方无显著差异(比值比为0·66;95%置信区间为0·26至1·69,p = 0·3880)。
MARQUE干预措施对激越症状无效,尽管在生活质量方面可行且具有成本效益。解决养老院中的激越问题可能需要为专业工作人员提供资源,以实施更强化的干预措施、安排社交和活动时间,以及更长的时间来实现改变。
英国经济和社会研究委员会以及国家卫生研究院。