Department of Epidemiology, Biostatistics, and Occupational Health, Faculty of Medicine, McGill University, 2001 McGill College, Suite 1200, Montreal, Qc, H3A 1G1, Canada.
Department of Family Medicine, Faculty of Medicine and Health Sciences, Faculty of Medicine, McGill University, 5858 Chemin de La Côte-Des-Neiges, Montreal, Qc, H3S 1Z1, Canada.
BMC Geriatr. 2023 Apr 27;23(1):250. doi: 10.1186/s12877-023-03926-x.
The type and level of healthcare services required to address the needs of persons living with dementia fluctuate over disease progression. Thus, their trajectories of care (the sequence of healthcare use over time) may vary significantly. We aimed to (1) propose a typology of trajectories of care among community-dwelling people living with dementia; (2) describe and compare their characteristics according to their respective trajectories; and (3) evaluate the association between trajectories membership, socioeconomic factors, and self-perceived health.
This is an observational study using the data of the innovative Care Trajectories -Enriched Data (TorSaDE) cohort, a linkage between five waves of the Canadian Community Health Survey (CCHS), and health administrative data from the Quebec provincial health-insurance board. We analyzed data from 690 community-dwelling persons living with dementia who participated in at least one cycle of the CCHS (the date of the last CCHS completion is the index date). Trajectories of care were defined as sequences of healthcare use in the two years preceding the index date, using the following information: 1) Type of care units consulted (Hospitalization, Emergency department, Outpatient clinic, Primary care clinic); 2) Type of healthcare care professionals consulted (Geriatrician/psychiatrist/neurologist, Other specialists, Family physician).
Three distinct types of trajectories describe healthcare use in persons with dementia: 1) low healthcare use (n = 377; 54.6%); 2) high primary care use (n = 154; 22.3%); 3) high overall healthcare use (n = 159; 23.0%). Group 3 membership was associated with living in urban areas, a poorer perceived health status and higher comorbidity.
Further understanding how subgroups of patients use healthcare services over time could help highlight fragility areas in the allocation of care resources and implement best practices, especially in the context of resource shortage.
为满足痴呆患者的需求而提供的医疗保健服务的类型和水平会随着疾病的进展而波动。因此,他们的护理轨迹(随着时间推移医疗保健使用的顺序)可能会有很大的差异。我们旨在:(1)提出一种社区居住的痴呆患者护理轨迹的分类法;(2)根据各自的轨迹描述和比较他们的特征;(3)评估轨迹成员资格、社会经济因素和自我感知健康之间的关联。
这是一项观察性研究,使用了创新的护理轨迹-丰富数据(TorSaDE)队列的数据,该队列是加拿大社区健康调查(CCHS)五个波次的链接,以及魁北克省健康保险委员会的健康管理数据。我们分析了 690 名至少参加过一次 CCHS 周期的社区居住的痴呆患者的数据(最后一次 CCHS 完成日期为索引日期)。护理轨迹被定义为索引日期前两年内医疗保健使用的序列,使用以下信息:1)就诊的护理单位类型(住院、急诊、门诊、初级保健诊所);2)就诊的医疗保健专业人员类型(老年病学家/精神科医生/神经病学家、其他专家、家庭医生)。
三种不同类型的轨迹描述了痴呆患者的医疗保健使用情况:1)低医疗保健使用(n=377;54.6%);2)高初级保健使用(n=154;22.3%);3)高整体医疗保健使用(n=159;23.0%)。第 3 组的成员与居住在城市地区、健康状况较差和合并症较多有关。
进一步了解不同亚组患者随时间推移如何使用医疗保健服务,可以帮助突出医疗资源分配中的脆弱领域,并实施最佳实践,特别是在资源短缺的情况下。