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阿尔茨海默病负担:新西兰基于人群的估计与2006 - 2031年预测

Burden of Alzheimer's disease: population-based estimates and projections for New Zealand, 2006-2031.

作者信息

Tobias Martin, Yeh Li-Chia, Johnson Elizabeth

机构信息

Public Health Intelligence, New Zealand Ministry of Health, Wellington, New Zealand.

出版信息

Aust N Z J Psychiatry. 2008 Sep;42(9):828-36. doi: 10.1080/00048670802277297.

Abstract

OBJECTIVE

To estimate the burden of Alzheimer's disease (AD, including 'mixed' dementia) in New Zealand in 2006, and project this burden out to 2031.

METHOD

An incidence to prevalence methodology was utilized, the foundation of which is a discrete time Markov model allowing for multiple stages of disease (early vs late). Population estimates and projections, and all-cause mortality rates, were obtained from Statistics New Zealand. In the absence of usable New Zealand data, data on disease incidence and progression were obtained from systematic reviews of the international (mainly European, Australian and North American) literature. Projection scenarios included a demographic scenario in which change resulted only from increases in population size and ageing; a prevention scenario in which incidence rates were reduced by 25% from 2011; a treatment scenario in which disease progression rates were likewise reduced by 25% from 2011; and a combined scenario capturing both interventions.

RESULTS

The model estimated that approximately 28000 people are currently living with AD (whether formally diagnosed or not), approximately 55% in the early and 45% in the late stage of the disease; approximately 6600 people newly develop AD each year; and approximately 2300 people die from (as opposed to with) this condition. The model projected that the prevalence of AD will increase approximately 2.5-fold (to approx. 70,000 people) by 2031, if demographic drivers are unopposed. Plausible improvements in prevention and treatment, however, acting together, could reduce this growth by up to 50%, so that the prevalence of AD only doubles.

CONCLUSION

Even this more optimistic projection has profound implications for the funding and provision of dementia care services, as well as for patients, their families, informal carers and the psychogeriatric workforce. New service configurations and models of care will be necessary. Access, quality and coordination standards for home care, day care, respite care, residential care and specialist services (including memory clinics) will need to respond accordingly.

摘要

目的

估算2006年新西兰阿尔茨海默病(AD,包括“混合型”痴呆)的负担,并预测到2031年的负担情况。

方法

采用发病率到患病率的方法,其基础是一个离散时间马尔可夫模型,该模型考虑了疾病的多个阶段(早期与晚期)。人口估计数和预测数以及全因死亡率数据均取自新西兰统计局。在缺乏可用的新西兰数据的情况下,疾病发病率和进展的数据取自对国际(主要是欧洲、澳大利亚和北美)文献的系统评价。预测方案包括:人口统计学方案,即变化仅源于人口规模的增加和老龄化;预防方案,即从2011年起发病率降低25%;治疗方案,即从2011年起疾病进展率同样降低25%;以及综合方案,涵盖两种干预措施。

结果

该模型估计,目前约有28000人患有AD(无论是否被正式诊断),其中约55%处于疾病早期,45%处于晚期;每年约有6600人新患AD;约有2300人死于这种疾病(而非患这种疾病)。该模型预测,如果不受人口统计学因素影响,到2031年AD的患病率将增加约2.5倍(增至约70000人)。然而,预防和治疗方面合理的改善措施共同作用,可将这种增长降低多达50%,使AD的患病率仅翻倍。

结论

即使是这种较为乐观的预测,对痴呆症护理服务的资金投入和提供,以及对患者、其家人、非正式护理人员和老年精神科工作人员而言,都有着深远的影响。新的服务配置和护理模式将必不可少。家庭护理、日托、临时护理、住院护理和专科服务(包括记忆诊所)的可及性、质量和协调标准都需要做出相应调整。

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