Overcoming the Health–Social Care Divide and the Formal–Informal Care Divide

Keyword(s):  
2015 ◽  
Vol 86 (11) ◽  
pp. e4.14-e4
Author(s):  
Jacob Howells ◽  
Waqar Rashid

BackgroundMultiple sclerosis (MS) is the most common disabling illness of young adults in the UK causing significant social and economical cost. The aim of this study was to ascertain further detail of the characteristics of the MS population in an area of Sussex representing about 25% of the whole region.MethodsThe following was obtained from community databases: (a) demographics; (b) employment status; (c) DMT use; (d) walking aid use and (e) utilisation of social care.ResultsN=665. The mean (SD) age was 54 (13.2) years; Relapsing-Remitting MS 51%, Secondary Progressive MS 29% and Primary Progressive MS 15%. Of participants <65 years: 56% were unemployed, 44% worked part or full-time; 57.8% of participants required walking aids to mobilise, 23.3% were on a DMT, 35.1% required informal care and 20.2% required external social care. We found associations (at α level=0.05) between unemployment and: SPMS, walking aid use, informal care and external social care.DiscussionThis study highlights the needs of people with MS in Sussex. Of note is the impact on employment and the need for walking aids and additional care associated with MS. This knowledge will allow us to better develop services for people with MS with commissioners.


2019 ◽  
Vol 32 (1) ◽  
pp. 97-109
Author(s):  
Violeta De Vera ◽  
Daniel Ondé ◽  
Martín Martín-González

Care work encompasses a series of tasks of distinct social and economic importance; however, it has not been a traditional object of study in Economics. The main objective of this article is to analyze the factors that intervene in informal care work in Spain. To approach this, an econometric analysis will be conducted using the National Health Survey (ENS as its Spanish acronym) carried out by the Instituto Nacional de Estadística (INE) of Spain. The results show that, in Spain, dependent adults do not receive the institutional support they need to perform basic daily activities. In fact, practically all of the care they receive is informal. This article will demonstrate that, within the household, women are responsible for informal care work whenever a family member is in need of such services. Our research shows that this is a consistent pattern regardless of the carer’s personal characteristics and level of education as well as the characteristics of the dependent adult living in the household. These findings reveal the necessity of reorienting public policies in order to help reduce gender inequalities caused by this socio-economic reality.


2016 ◽  
Vol 38 (4) ◽  
pp. 766-793 ◽  
Author(s):  
BO HU ◽  
SAI MA

ABSTRACTThis paper examines the factors affecting the receipt of informal care among older people in China. It uses the second wave data of the China Health and Retirement Longitudinal Survey, which collected ageing and health-related information on a nationally representative sample of 8,906 older people aged 60 and over in 2013. Apart from the factors that have been examined in the contexts of developed countries, the paper further investigates two factors specific to Chinese society: rural–urban residence and regular financial assistance from children. Based on binary and multinomial logit regression analyses, the research findings are threefold: the determinants of receiving informal care differ remarkably according to the sources of care; disability and living arrangements are the most important determinants; rural–urban residence plays a vital role in the Chinese context, but regular financial assistance from children makes little difference. It is estimated that 53 million older people are receiving informal care each year, a figure equivalent to the entire population of England. With continuous population ageing, Chinese society will face huge pressure to meet the demand for social care among older people in the future. The Chinese government needs to build a well-rounded welfare system that tackles this challenge from multiple dimensions. The formal care services should aim to complement informal care in the short run and reduce inequality in social care in the long run.


1985 ◽  
Vol 5 (1) ◽  
pp. 1-18 ◽  
Author(s):  
Philip Abrams ◽  
Martin Bulmer

ABSTRACTPolicies to promote informal social care have particular importance for elderly people, since a substantial minority of them are in receipt of informal care from kin, neighbours and friends, and the majority of those living in their own homes who receive informal care are themselves elderly. Yet informal care has not had the attention it deserves, compared to care provided by statutory, commercial or organised voluntary effort. This paper focuses on neighbourhood care, drawing on the results of a five-year research programme. Three types of neighbourhood care are examined: voluntary action for neighbourhood involvement, voluntary action for informal care, and voluntary action for neighbourhood care. Neighbourhood involvement is increasingly a political matter, with local organisation tied to specific local issues. Informal care has little directly to do with local involvement. Nine-tenths of such care is provided by kin, though there is scope for greater local action. Voluntary action for neighbourhood care is encouraged particularly by pressure-group activism, self-help organisations and support for carers. Effective informal care requires a higher degree of competence and the establishment of contexts for reciprocity. Policies in this area need to provide modest financial resources, greater information exchange and support for carers.


2020 ◽  
pp. 1-18
Author(s):  
Valentina Zigante ◽  
Jose-Luis Fernandez ◽  
Fernanda Mazzotta

Abstract Informal care plays a crucial role in the social care system in England and is increasingly recognised as a cornerstone of future sustainability of the long-term care (LTC) system. This paper explores the variation in informal care provision over time, and in particular, whether the considerable reduction in publicly-funded formal LTC after 2008 had an impact on the provision of informal care. We used small area data from the 2001 and 2011 English censuses to measure the prevalence and intensity (i.e. the number of hours of informal care provided) of informal care in the population. We controlled for changes in age structure, health, deprivation, income, employment and education. The effects of the change in formal social care provision on informal care were analysed through instrumental variable models to account for the well-known endogeneity. We found that informal care provision had increased over the period, particularly among high-intensity carers (20+ hours per week). We also found that the reduction in publicly-funded formal care provision was associated with significant increases in high-intensity (20+ hours per week) informal care provision, suggesting a substitutive relationship between formal and informal care of that intensity in the English system.


2020 ◽  
Author(s):  
Jackie Buck ◽  
Rehana Di Rico ◽  
Fiona Scheibl ◽  
Stephen Barclay ◽  
Morag Farquhar ◽  
...  

Abstract Background: The ‘oldest old’ are amongst the largest recipients of social care services and informal care, yet they are under-represented in research and service-user experience surveys. The aim of this study was to understand experiences of receiving social care from formal services and informal carers amongst very old people living in the community. Method: Framework analysis of qualitative data from 36 interviews with community-dwelling people aged 95-101 (n=24) and/or their relatives/carers participating in the UK population-based Cambridge City over-75s Cohort (CC75C) study.Results: Fifty-eight percent lived alone, 75% were disabled, and 42% moderately or severely cognitively impaired. Sixty-seven percent had contact with formal care services and 85% with relatives at least weekly. Informal care mainly supported instrumental activities of daily living, though substituted for, and complemented, formal care at low and higher disability levels respectively. Impractical service delivery and lack of awareness of social care processes and entitlements caused unnecessary distress. Lack of meaningful social interaction, difficulties with bathing and management of continence were key areas of unmet need. Poor continuity of service and frequent changes of formal carers posed a threat to older people’s autonomy, dignity and safety.Conclusions: This study revealed a rich complexity of older old care recipients’ responses and attitudes not adequately captured in national surveys. As the urgent need to review social care provision receives more attention, there are valuable opportunities to incorporate the views of older old people into service design and delivery, honouring policy directives for person-centred care and improved quality of life.


2020 ◽  
Vol 32 (3) ◽  
pp. 359-370 ◽  
Author(s):  
A. Buylova Gola ◽  
S. Morris ◽  
B. Candy ◽  
S. Davis ◽  
M. King ◽  
...  

ABSTRACTObjective:Nearly half of care home residents with advanced dementia have clinically significant agitation. Little is known about costs associated with these symptoms toward the end of life. We calculated monetary costs associated with agitation from UK National Health Service, personal social services, and societal perspectives.Design:Prospective cohort study.Setting:Thirteen nursing homes in London and the southeast of England.Participants:Seventy-nine people with advanced dementia (Functional Assessment Staging Tool grade 6e and above) residing in nursing homes, and thirty-five of their informal carers.Measurements:Data collected at study entry and monthly for up to 9 months, extrapolated for expression per annum. Agitation was assessed using the Cohen-Mansfield Agitation Inventory (CMAI). Health and social care costs of residing in care homes, and costs of contacts with health and social care services were calculated from national unit costs; for a societal perspective, costs of providing informal care were estimated using the resource utilization in dementia (RUD)-Lite scale.Results:After adjustment, health and social care costs, and costs of providing informal care varied significantly by level of agitation as death approached, from £23,000 over a 1-year period with no agitation symptoms (CMAI agitation score 0–10) to £45,000 at the most severe level (CMAI agitation score >100). On average, agitation accounted for 30% of health and social care costs. Informal care costs were substantial, constituting 29% of total costs.Conclusions:With the increasing prevalence of dementia, costs of care will impact on healthcare and social services systems, as well as informal carers. Agitation is a key driver of these costs in people with advanced dementia presenting complex challenges for symptom management, service planners, and providers.


1990 ◽  
Vol 10 (3) ◽  
pp. 331-347 ◽  
Author(s):  
Ann Netten ◽  
Bleddyn Davies

ABSTRACTThe social production of welfare provides a theoretical framework for the analysis of the consumption of social services and the impact of welfare policies. Based on the new home economics, it represents the unit of consumption as a unit of production of commodities. With the advent of disability this unit extends from the household to the informal care network. Social care agencies become involved when the production of basic commodities, such as nutrition and personal care, fall below threshold levels which threaten the survival of the informal care network. The social production of welfare allows comparisons across systems and provides the starting point for the development of tools for empirical analysis.


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