Helping Older Adults Assess Their Need for Future Home-Support Services

Author(s):  
Lee Lindquist ◽  
Kenzie Cameron ◽  
Jody Ciolino ◽  
Chris Forcucci ◽  
Dianne Campbell ◽  
...  
2019 ◽  
Vol 3 (4) ◽  
pp. 501-515 ◽  
Author(s):  
Anne McDonald ◽  
Luciana Lolich ◽  
Virpi Timonen ◽  
Austin Warters

This article explores perceptions of time reported by service users, family carers, care workers, nurses, social workers and agency managers across home support services for older adults in Ireland. The findings are organised around: time spent waiting for care; time spent ‘processing’ care across primary and secondary care boundaries; time and person-centred care; and time, technology and communication. Time emerges as a problematic aspect of all processes and structures around formal home care, suggesting that addressing issues around time is central to resolving systemic challenges. Greater flexibility in time allocation and effective communication among stakeholders could improve experiences of care.


2020 ◽  
Vol 4 (Supplement_1) ◽  
pp. 910-911
Author(s):  
Matthew Yau ◽  
Christine Sheppard ◽  
Jocelyn Charles ◽  
Andrea Austen ◽  
Sander Hitzig

Abstract Community support services are an integral component of aging in place. In social housing, older adult tenants struggle to access these services due to the siloed nature of housing and health services. This study aims to describe the relationship between community support services and social housing for older adults and examine ways to optimize delivery. Data on government-funded community support services delivered to 74 seniors’ social housing buildings in Toronto, Ontario was analyzed. Neighbourhood profile data for each building was also collected, and correlational analyses were used to examine the link between neighbourhood characteristics and service delivery. Fifty-six community agencies provided 5,976 units of services across 17 service categories, most commonly mental health supports, case management and congregate dining. On average, each building was supported by nine agencies that provided 80 units of service across 10 service categories. Buildings in neighbourhoods with a higher proportion of low-income older adults had more agencies providing on-site services (r = .275, p < .05), while those in neighbourhoods with more immigrants (r = -.417, p < .01), non-English speakers (r = -.325, p < .01), and visible minorities (r = -.381, p < .01) received fewer services. Findings point to a lack of coordination between service providers, with multiple agencies offering duplicative services within the same building. Vulnerable seniors from equity-seeking groups, including those who do not speak English and recent immigrants, may be excluded from many services, and future service delivery for seniors should strive to address disparities in availability and access.


2020 ◽  
Vol 222 (1) ◽  
pp. S710-S711
Author(s):  
Deborah R. Berman ◽  
Ashley Hesson ◽  
Katherine Kowalk

2017 ◽  
Vol 55 (2) ◽  
pp. 97-109 ◽  
Author(s):  
Iulia Mihaila ◽  
Sigan L. Hartley ◽  
Benjamin L. Handen ◽  
Peter D. Bulova ◽  
Rameshwari V. Tumuluru ◽  
...  

Abstract The present study examined leisure activity and its association with caregiver involvement (i.e., residence and time spent with primary caregiver) in 62 middle-aged and older adults with Down syndrome (aged 30–53 years). Findings indicated that middle-aged and older adults with Down syndrome frequently participated in social and passive leisure activities, with low participation in physical and mentally stimulating leisure activities. Residence and time spent with primary caregiver were associated with participation in physical leisure activity. The findings suggest a need for support services aimed at increasing opportunities for participating in physical and mentally stimulating leisure activity by middle-aged and older adults with Down syndrome. These support services should partner with primary caregivers in order to best foster participation in physical leisure activity.


2011 ◽  
Vol 19 (6) ◽  
pp. 661-672 ◽  
Author(s):  
J. Tindale ◽  
M. Denton ◽  
J. Ploeg ◽  
J. Lillie ◽  
B. Hutchison ◽  
...  

Author(s):  
Cristina Hendrix ◽  
Sara Tepfer ◽  
Sabrina Forest ◽  
Karen Ziegler ◽  
Valerie Fox ◽  
...  

2020 ◽  
Vol 23 (4) ◽  
pp. 289-296
Author(s):  
Fabrice Immanuel Mowbray ◽  
Komal Aryal ◽  
Eric Mercier ◽  
George Heckman ◽  
Andrew P. Costa

Background Little is known about the prognostic differences between older emergency department (ED) patients who present with different formal support requirements in the community. We set out to describe and compare the patient profiles and patterns of health service use among three older ED cohorts: home care clients, nursing home residents and those receiving no formal support. Methods We conducted a secondary analysis of the Canadian cohort from the interRAI multinational ED study. Data were collected using interRAI ED contact assessment on patients 75 years of age and older (n = 2,274), in eight ED sites across Canada. A series of descriptive statistics were reported. Adjusted as­sociations were determined using logistic regression. Results Older adults receiving no formal support services were most stable. However, they were most likely to be hospitalized. Older home care clients were most likely to report depressive symptoms and distressed caregivers. They also had the great­est odds of frequent ED visitation post-discharge (OR=1.9; 95% CI=1.39–2.59). Older adults transferred from a nursing home were the frailest but had the lowest odds of hospital admission (OR=0.14; 95% CI=0.09–0.23). Conclusion We demonstrated the importance of inquiring about commu­nity-based formal support services and provide data to support decision-making in the ED.  


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