Long-Term Community Supports for Individuals With Co-Occurring Disabilities After Traumatic Brain Injury: Cost Effectiveness and Project-Based Intervention

2007 ◽  
Vol 8 (3) ◽  
pp. 276-292 ◽  
Author(s):  
Mark Ylvisaker ◽  
Timothy Feeney ◽  
Melissa Capo

AbstractOutcome studies have established that successful community living is compromised in the population of individuals with traumatic brain injury and chronic behavioural difficulties along with a co-occurring diagnosis of substance abuse and/or mental health disorder. Two studies are presented. The first was aimed at describing long-term outcome of a sample of individuals (N = 51) served by the New York State Department of Health TBI Medicaid Waiver Program. Each of the participants was diagnosed with TBI plus either substance abuse or a mental health disorder, or both. Because of significant behavioural challenges, all of the participants were in a restrictive living setting the year before enrolment in the waiver program (e.g., nursing or correctional facility). Data on community living arrangement, self-reported community integration experiences, and costs are presented. Results indicate that most of the participants (41 of the 46 who were alive and living in state) continued to live in the community 8 to 9 years after commencement of community support services. The participants' community integration responses were generally positive and cost data demonstrate substantial savings to the state for this cohort. Comparing prewaiver costs in residential settings with most recent (2005) costs for community supports, there was an average daily cost savings of US$137 per person for the 1996 cohort and US$144 per person for the 1997 cohort. The second study explored the use of project-oriented interventions and supports in an agency that provides community support services to this dual diagnosis population. Project-oriented services are described as meeting many needs common to this dual-diagnosis population. Clinical staff (N = 11) and a sample of waiver participants (N = 7) were surveyed. Results suggest that the use of personally meaningful projects can become a clinical habit for staff and that projects are generally judged by participants to be a meaningful use of time, and significant in giving them an opportunity to play an expert role and to help others.

2016 ◽  
Vol 16 (6) ◽  
pp. 282 ◽  
Author(s):  
Nelly D. Oelke ◽  
Kaela Schill ◽  
Carolyn Szostak ◽  
Betty Brown ◽  
Susana Caxaj ◽  
...  

Curationis ◽  
1988 ◽  
Vol 11 (3) ◽  
Author(s):  
E.S. Malan

Since cancer is a long-term disease it has far-reaching implications for the patient. Nurse and patient are in contact with one another for prolonged periods during treatment. It is important to develop education programmes and community support services during these periods of close patient contact in order to lighten the burden of nursing staff and to encourage patient independence .


2010 ◽  
Vol 18 (1) ◽  
pp. 82-99
Author(s):  
Jacqui O'Riordan ◽  
Féilim O'Hadhmaill ◽  
Helen Duggan

This paper is drawn from research on family carers1 that was carried out in the Cork area of Ireland in 2007–08. The research itself focused on the experiences of family carers and their access to support services in the locality. Key findings indicate that individuals are often caring for family members over the long term, often with minimal access to discretionary community support services. The assumption made by the Irish State, by community services, by carers themselves and by extended family members and friends, is that the onus is and should be on close relatives, and particularly women, to take the major responsibility for caring, when this care takes place in the home (Timonen and McMenamin 2002). This also contributes to the invisibility and undervaluation of family carers (Baker et al. 2004; Lynch 2007). The development of theoretical perspectives on caring can contribute to highlighting the manner in which assumptions about family, domesticity, gender roles and household continue to disadvantage those located primarily within the private sphere.


Inclusion ◽  
2017 ◽  
Vol 5 (1) ◽  
pp. 33-44 ◽  
Author(s):  
Carli Friedman ◽  
Natasha A. Spassiani

Abstract Despite an increased number of community-based services, people with intellectual and developmental disabilities (IDD) continue to struggle with meaningful community participation and often feel they are not valued community members. This study examined how community support services, which support physical placement and community integration, were allocated in Medicaid 1915(c) HCBS waivers, the largest provider of long-term services and supports for people with IDD in the United States. Community support services totaled $447.5 million of projected funding in fiscal year 2014. While community transition services funded expenses required to establish a basic household for the initial transition, community integration services promoted a successful community placement by utilizing natural supports and developing skills necessary to maintain community integration.


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.


CJEM ◽  
2021 ◽  
Author(s):  
Matthew S. Leyenaar ◽  
Brent McLeod ◽  
Aaron Jones ◽  
Audrey-Anne Brousseau ◽  
Eric Mercier ◽  
...  

Abstract Objectives The aim for this study was to provide information about how community paramedicine home visit programs best “navigate” their role delivering preventative care to frequent 9-1-1 users by describing demographic and clinical characteristics of their patients and comparing them to existing community care populations. Methods Our study used secondary data from standardized assessment instruments used in the delivery of home care, community support services, and community paramedicine home visit programs in Ontario. Identical assessment items from each instrument enabled comparisons of demographic, clinical, and social characteristics of community-dwelling older adults using descriptive statistics and z-tests. Results Data were analyzed for 29,938 home care clients, 13,782 community support services clients, and 136 community paramedicine patients. Differences were observed in proportions of individuals living alone between community paramedicine patients versus home care clients and community support clients (47.8%, 33.8%, and 59.9% respectively). We found higher proportions of community paramedicine patients with multiple chronic disease (87%, compared to 63% and 42%) and mental health-related conditions (43.4%, compared to 26.2% and 18.8% for depression, as an example). Conclusion When using existing community care populations as a reference group, it appears that patients seen in community paramedicine home visit programs are a distinct sub-group of the community-dwelling older adult population with more complex comorbidities, possibly exacerbated by mental illness and social isolation from living alone. Community paramedicine programs may serve as a sentinel support opportunity for patients whose health conditions are not being addressed through timely access to other existing care providers. Protocol registration ISRCTN 58273216.


2007 ◽  
Vol 19 (2) ◽  
pp. 229-241 ◽  
Author(s):  
Tien Tay ◽  
Jie Jin Wang ◽  
Richard Lindley ◽  
Ee-Munn Chia ◽  
Peter Landau ◽  
...  

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