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With the increasing population of people over 65 years of age, escalating rates of chronic disease and disability, a continued emphasis on community-based care, and the economic ramifications of an ever-growing demand for health care services, the burden on family caregivers is increasing. While family caregivers can gain a great deal of satisfaction from their caring role, research is showing they have poorer health and quality of life than noncaregivers. Respite care is a generic term that entails a range of services designed to allow family caregivers temporary relief or time out from their ongoing care commitments, which may be provided on a planned regular basis or in emergencies. Respite care services help caregivers regain or maintain their physical and emotional health so that they can continue to provide care to a family member with a chronic illness or disability. Indeed, respite care is one of the few services available that has a primary focus on supporting family caregivers.

Most developed countries embraced the notion of respite care as an extension of health care service provision, and the scope and diversity of respite care services continue to expand. Despite its widespread use and popularity, research findings are limited on its effectiveness and efficacy on the outcomes associated with caregivers and their care recipients. This entry describes what is known about respite care and discusses key issues concerning the impact of respite care on caregivers and care recipients, the contemporary issues in the use of respite care, and recommendations for practice and policy in the context of family health.

The Scope and Types of Respite Care

Respite care started almost 50 years ago in the United Kingdom, where it was provided mainly in institutional settings, when either frail older people or children with special needs were admitted to hospitals for “relief care” on an informal basis. In some countries such as the United Kingdom, short-term care has been a preferred term to respite care due to perceived negative connotations. However, respite care is now an internationally accepted term and will be used throughout this entry. Literature focusing on respite care began to appear in the early 1970s and has been steadily increasing, mostly from the United States, the United Kingdom, and Canada. A small proportion of work originates from Australia, continental Europe (outside the United Kingdom), and Asia.

Respite care has long been recognized as potentially the most important service for caregivers of frail older people with or without dementia; young people and adults with physical, learning, intellectual, and developmental disabilities; and more recently, people with severe mental illness and chronic disease. Respite care is also offered to caregivers of autistic children and people with brain injury, cancer, and stroke.

Types of respite care vary depending on its intended need (planned versus emergency or crisis), duration (overnight or short-term versus long-term), and location of services (in-home versus out-of-home or an institutional setting, such as hospital, day care, and residential care). Respite care can also be packaged to suit individual caregivers’ needs where caregivers can have a combination of multiple respite care services and/or respite care plus other support services, such as counseling training, support groups, and relaxation therapies.

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