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BackgroundSupporting persons with dementia and their caregivers is a global public health priority. However, current research typically relies on subjective caregiver reports, lacking the integration of objective physiological indicators.ObjectiveTo identify the determinants of caregiver burden among family caregivers of persons with dementia, guided by a biopsychosocial framework.MethodsSeventy-five dyads of persons with dementia and their caregivers participated in this study. The determinants of caregiver burden, including biological, psychological, and social factors, were assessed using sweat patches, actigraphy, and surveys, and analyzed using hierarchical multiple regression analysis.ResultsThe mean caregiver burden score was 42.32. Hierarchical multiple regression analysis showed that psychological factors explained 39.3% of the variance in caregiver burden. A 17.5% increase was observed by the addition of biological factors, accounting for 56.8% of the variance. Among the biological factors, high level of pro-inflammatory cytokine tumor necrosis factor-α in persons with dementia was significantly associated with increased caregiver burden. In contrast, long total sleep time was associated with decreased caregiver burden. Amidst psychological factors, not only increased depressive symptoms but also severe behavioral and psychological symptoms of dementia in individuals with dementia were significantly associated with increased caregiver burden.ConclusionsThese findings highlight the importance of tailored interventions that address both biological and psychological factors to reduce caregiver burden and improve care outcomes. Additionally, by alleviating caregiver burden, these interventions may also support ageing-in-place, allowing persons with dementia to remain in familiar environments within their communities.
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http://dx.doi.org/10.1177/13872877251365642 | DOI Listing |
Int Urol Nephrol
September 2025
Division of Nursing, Singapore General Hospital, Singapore, Singapore.
Objective: To explore healthcare professionals' perceptions on the implementation of home hemodialysis and self-assisted hemodialysis in Singapore and to identify the perceived barriers, facilitators, and actionable strategies for increasing uptake.
Methods: This is a qualitative explorative study based on semi-structured face-to-face interviews conducted with a multidisciplinary group of 12 healthcare professionals at an acute teaching hospital in Singapore. Thematic analysis was used for data analysis.
J Hosp Palliat Care
September 2025
Department of Family Medicine, Korea University Guro Hospital, Seoul, Korea.
Purpose: This study investigated the association between spiritual well-being and care burden among family caregivers of patients with terminal cancer.
Methods: Data from 172 family caregivers from nine hospice care units in South Korea were analyzed using multivariate regression models. Spiritual well-being was measured using the Functional Assessment of Chronic Illness Therapy - Spiritual Well-being questionnaire, and the subjective care burden on family caregivers was assessed using the Caregiver Reaction Assessment tool.
J Hosp Palliat Care
September 2025
Department of Family Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
Home-based palliative care (HBPC) has emerged as a critical model to address the complex needs of individuals with life-limiting illnesses, particularly in super-aged societies. This review explored the key components of HBPC and elaborated on its benefits, challenges, opportunities, and future directions, drawing on international evidence and practical frameworks. HBPC is reported to enhance the quality of life, reduce unnecessary hospitalizations, and increase the likelihood of patients dying in their preferred settings.
View Article and Find Full Text PDFNeurol Clin Pract
October 2025
Departments of Neurology and Radiology, University of Texas Southwestern Medical Center, Dallas.
Background And Objectives: With more women entering the medical workforce, caregiving challenges and family-work conflicts are of growing importance to today's neurologists. The aim of this study was to assess the impact of caregiver (CG) status on academic achievements in neurology, analyze the division of labor and time devoted to domestic responsibilities, and measure family-work conflict in US academic neurology faculty.
Methods: A total of 19 US neurology departments completed a survey on baseline demographics, academic achievements, CG status, division of domestic time and labor, and responses on a FWC scale.
Front Public Health
September 2025
Institute of Public Health, Guangzhou Center for Disease Control and Prevention, Guangzhou Medical University, Guangzhou, China.
Objective: This study aims to investigate the current status of disability among older adults and analyze factors influencing the burden on their family caregivers in southern China.
Methods: A cross-sectional survey was conducted among 334 pairs of disabled older adults (≥65 years) and their primary family caregivers across three districts in Guangzhou. Face-to-face interviews using standardized questionnaires assessed disability levels via the "Long-term Care Disability Level Assessment" scale and caregiver burden via the Zarit Burden Interview (ZBI) scale.