Lenox-Smith Alan, Reed Catherine, Lebrec Jeremie, Belger Mark, Jones Roy W
Eli Lilly and Company, Basingstoke, UK.
Eli Lilly and Company, Erl Wood, Windlesham, UK.
BMC Geriatr. 2016 Nov 25;16(1):195. doi: 10.1186/s12877-016-0371-6.
Alzheimer's disease (AD), the commonest cause of dementia, represents a significant cost to UK society. This analysis describes resource utilisation, costs and clinical outcomes in non-institutionalised patients with AD in the UK.
The GERAS prospective observational study assessed societal costs associated with AD for patients and caregivers over 18 months, stratified according to baseline disease severity (mild, moderate, or moderately severe/severe [MS/S]). All patients enrolled had an informal caregiver willing to participate in the study. Healthcare resource utilisation was measured using the Resource Utilization in Dementia instrument, and 18-month costs estimated by applying unit costs of services and products (2010 values). Total societal costs were calculated using an opportunity cost approach.
Overall, 526 patients (200 mild, 180 moderate and 146 MS/S at baseline) were recruited from 24 UK centres. Mini-Mental State Examination (MMSE) scores deteriorated most markedly in the MS/S patient group, with declines of 3.6 points in the mild group, 3.5 points in the moderate group and 4.7 points in the MS/S group; between-group differences did not reach statistical significance. Patients with MS/S AD dementia at baseline were more likely to be institutionalised (Kaplan-Meier probability 28% versus 9% in patients with mild AD dementia; p < 0.001 for difference across all severities) and had a greater probability of death (Kaplan-Meier probability 15% versus 5%; p = 0.013) at 18 months. Greater disease severity at baseline was also associated with concomitant increases in caregiver time and mean total societal costs. Total societal costs of £43,560 over 18 months were estimated for the MS/S group, versus £25,865 for the mild group and £30,905 for the moderate group (p < 0.001). Of these costs, over 50% were related to informal caregiver costs at each AD dementia severity level.
This study demonstrated a mean deterioration in MMSE score over 18 months in patients with AD. It also showed that AD is a costly disease, with costs increasing with disease severity, even when managed in the community: informal caregiver costs represented the main contributor to societal costs.
阿尔茨海默病(AD)是痴呆最常见的病因,给英国社会带来了巨大成本。本分析描述了英国非机构化AD患者的资源利用、成本及临床结局。
GERAS前瞻性观察性研究评估了18个月内AD患者及其照护者的社会成本,根据基线疾病严重程度(轻度、中度或中重度/重度[MS/S])进行分层。所有入组患者均有一名愿意参与研究的非正式照护者。使用痴呆症资源利用工具测量医疗资源利用情况,并通过应用服务和产品的单位成本(2010年数值)估算18个月的成本。使用机会成本法计算总社会成本。
总体而言,从英国24个中心招募了526例患者(基线时200例轻度、180例中度和146例MS/S)。简易精神状态检查表(MMSE)评分在MS/S患者组中恶化最为明显,轻度组下降3.6分,中度组下降3.5分,MS/S组下降4.7分;组间差异未达到统计学显著性水平。基线时患有MS/S AD痴呆的患者更有可能被送入机构(Kaplan-Meier概率,轻度AD痴呆患者为9%,MS/S患者为28%;所有严重程度之间的差异p<0.001),且在18个月时死亡概率更高(Kaplan-Meier概率,轻度AD痴呆患者为5%,MS/S患者为15%;p=0.013)。基线时疾病严重程度越高,照护者时间和平均总社会成本也随之增加。MS/S组18个月的总社会成本估计为43,560英镑,轻度组为25,865英镑,中度组为30,905英镑(p<0.001)。在每个AD痴呆严重程度水平,这些成本中超过50%与非正式照护者成本相关。
本研究表明AD患者在18个月内MMSE评分平均恶化。研究还表明,AD是一种成本高昂的疾病,即使在社区管理,成本也随疾病严重程度增加:非正式照护者成本是社会成本的主要贡献因素。