English

The Carers and Disabled Children Act (2000) has the potential to fundamentally change carers services and the way they are currently delivered. As yet, there is little published work that considers the implications of this Act either for local authorities or informal carers themselves. This paper examines the practical issues involved in the implementation of the Act in terms of: providing equitable services, defining terms, young carers and care package limits, local authority eligibility criteria and whether funding is adequate.

The overall aim of the A.C.T.I.O.N. research project (Assisting Carers using Telematic Interventions to meet Older person's Needs) is to maintain or enhance the autonomy, independence and quality of life of frail older and disabled people and their family carers by providing information, advice and support in the home. The authors report on the first phase of evaluation conducted using a case-study approach to test the A.C.T.I.O.N. system in several family carers' homes in Sheffield, England.

Phillipa Hare offers some practical advice on how general practices can identify and record carers within their areas. 3 refs. [Introduction]

A project worker who identified gaps in services for ethnic minority carers of people with mental health difficulties provided the catalyst for Birmingham's Pamela Project, which won a Community Care Award. Anabel Unity Sale reports. [Introduction]

This study aims to measure the causal effect of informal caregiving on the health and health care use of women who are caregivers, using instrumental variables. We use data from South Korea, where daughters and daughters-in-law are the prevalent source of caregivers for frail elderly parents and parents-in-law.

This paper summarises findings of a review of research evidence and current service provision of support of carers of people with mental health problems (Arksey et al., 2002). Research consisting of (i) a literature review and (ii) a consultation exercise was carried out between October 2001 and March 2002. The research was commissioned by the National Co-ordinating Centre for NHS Service Delivery and Organisation Research and Development (NCCSDO)

BACKGROUND: Informal caregivers of people with dementia are challenged in managing the consequences of dementia in daily life. The objective of this meta-review was to synthesize evidence from previous systematic reviews about professional self-management support interventions for this group.

Objectives: To determine the problems and issues of accessing specialist palliative care by patients, informal carers and health and social care professionals involved in their care in primary and secondary care settings. Data sources: Eleven electronic databases (medical, health-related and social science) were searched from the beginning of 1997 to October 2003.

The 24th chapter of 35 in this book on ageing and disability from research and clinical perspectives viewpoints appears in the sixth part (of 12) on loss and end of life issues. It reviews the role of the carer in chronic disease and end of life care, and how positive or otherwise caring, particularly long term, may be. Following an introduction there are five main sections.

Despite evidence of high psychological distress and unmet needs, evaluated interventions for informal caregivers in palliative care are few. This study involved an observational outcome evaluation of attendees, and a comparison group, in specialist home palliative care. The measures included carer psychological status and patient physical status at baseline, 8 weeks, and 20 weeks. Qualitative data were collected regarding content, satisfaction with, and impact of intervention. Process data described the uptake, resources, and group activity.