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社区居住的痴呆症患者的卫生系统使用轨迹和生存情况:一项队列研究。

Trajectories of health system use and survival for community-dwelling persons with dementia: a cohort study.

作者信息

Bronskill Susan E, Maclagan Laura C, Walker Jennifer D, Guan Jun, Wang Xuesong, Ng Ryan, Rochon Paula A, Yates Erika A, Vermeulen Marian J, Maxwell Colleen J

机构信息

ICES, Toronto, Ontario, Canada

Women's College Research Institute, Women's College Hospital, Toronto, Ontario, Canada.

出版信息

BMJ Open. 2020 Jul 23;10(7):e037485. doi: 10.1136/bmjopen-2020-037485.

Abstract

OBJECTIVES

To determine the long-term trajectories of health system use by persons with dementia as they remain in the community over time.

DESIGN

Population-based cohort study using health administrative data.

SETTING

Ontario, Canada from 1 April 2007 to 31 March 2014.

PARTICIPANTS

62 622 community-dwelling adults aged 65+ years with prevalent dementia on 1 April 2007 matched 1:1 to persons without dementia based on age, sex and comorbidity.

MAIN OUTCOME MEASURES

Rates of health service use, long-term care placement and mortality over time.

RESULTS

After 7 years, 49.0% of persons with dementia had spent time in long-term care (6.8% without) and 64.5% had died (30.0% without). Persons with dementia were more likely than those without to use home care (rate ratio (RR) 3.02, 95% CI 2.93 to 3.11) and experience hospitalisations with a discharge delay (RR 2.36, 95% CI 2.30 to 2.42). As they remained in the community, persons with dementia used home care at a growing rate (10.7%, 95% CI 10.0 to 11.3 increase per year vs 6.7%, 95% CI 4.3 to 9.0 per year among those without), but rates of acute care hospitalisation remained constant (0.6%, 95% CI -0.6 to 1.9 increase per year).

CONCLUSIONS

While persons with dementia used more health services than those without dementia over time, the rate of change in use differed by service type. These results, particularly enumerating the increased intensity of home care service use, add value to capacity planning initiatives where limited budgets require balancing services.

摘要

目的

确定痴呆症患者随着时间推移留在社区期间卫生系统使用情况的长期轨迹。

设计

基于人群的队列研究,使用卫生行政数据。

背景

2007年4月1日至2014年3月31日期间的加拿大安大略省。

参与者

2007年4月1日,62622名年龄在65岁及以上、患有痴呆症的社区居住成年人,根据年龄、性别和合并症与无痴呆症的人1:1匹配。

主要观察指标

随着时间推移的卫生服务使用率、长期护理安置率和死亡率。

结果

7年后,49.0%的痴呆症患者曾在长期护理机构接受护理(无痴呆症者为6.8%),64.5%的患者死亡(无痴呆症者为30.0%)。与无痴呆症者相比,痴呆症患者更有可能使用家庭护理(率比(RR)3.02,95%可信区间2.93至3.11),且经历出院延迟的住院治疗(RR 2.36,95%可信区间2.30至2.42)。随着他们留在社区,痴呆症患者使用家庭护理的比例逐年上升(每年增加10.7%,95%可信区间10.0至11.3%,而无痴呆症者为每年6.7%,95%可信区间4.3至9.0%),但急性护理住院率保持不变(每年增加0.6%,95%可信区间-0.6至1.9%)。

结论

随着时间推移,痴呆症患者比无痴呆症者使用更多的卫生服务,但使用的变化率因服务类型而异。这些结果,特别是列举了家庭护理服务使用强度的增加,为预算有限需要平衡服务的能力规划举措增添了价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f45/7380876/b26a55f9129b/bmjopen-2020-037485f01.jpg

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