Caregiver Stress as Experienced by Wives of Institutionalized and In-home Dementia Husbands PDF Download

Author: Patricia Lynne Lee
Publisher:
ISBN:
Category :
Languages : en
Pages : 732

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Author: National Academies of Sciences, Engineering, and Medicine
Publisher: National Academies Press
ISBN: 0309448093
Category : Medical
Languages : en
Pages : 367

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Book Description
Family caregiving affects millions of Americans every day, in all walks of life. At least 17.7 million individuals in the United States are caregivers of an older adult with a health or functional limitation. The nation's family caregivers provide the lion's share of long-term care for our older adult population. They are also central to older adults' access to and receipt of health care and community-based social services. Yet the need to recognize and support caregivers is among the least appreciated challenges facing the aging U.S. population. Families Caring for an Aging America examines the prevalence and nature of family caregiving of older adults and the available evidence on the effectiveness of programs, supports, and other interventions designed to support family caregivers. This report also assesses and recommends policies to address the needs of family caregivers and to minimize the barriers that they encounter in trying to meet the needs of older adults.

Author: Ronda Hughes
Publisher: Department of Health and Human Services
ISBN:
Category : Medical
Languages : en
Pages : 592

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"Nurses play a vital role in improving the safety and quality of patient car -- not only in the hospital or ambulatory treatment facility, but also of community-based care and the care performed by family members. Nurses need know what proven techniques and interventions they can use to enhance patient outcomes. To address this need, the Agency for Healthcare Research and Quality (AHRQ), with additional funding from the Robert Wood Johnson Foundation, has prepared this comprehensive, 1,400-page, handbook for nurses on patient safety and quality -- Patient Safety and Quality: An Evidence-Based Handbook for Nurses. (AHRQ Publication No. 08-0043)." - online AHRQ blurb, http://www.ahrq.gov/qual/nurseshdbk/

Author: Phyllis Jean Pallett
Publisher:
ISBN:
Category : Adaptability (Psychology)
Languages : en
Pages : 246

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Author: Carol S. Aneshensel
Publisher: Elsevier
ISBN: 0080539831
Category : Medical
Languages : en
Pages : 406

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Given medical advances and greater understanding of healthful living habits, people are living longer lives. Proportionally speaking, a greater percentage of the population is elderly. Despite medical advances, there is still no cure for dementia, and as elderly individuals succumb to Alzheimer's Disease or related dementia, more and more people are having to care their elderly parents and /or siblings. Profiles in Caregiving is practical source of information for anyone who teaches caregiving, acts as a caregiver, or studies caregiving. This book discusses recent research on stress factors associated with caregiving, and what factors impact on successful versus non-successful adaptation to the care-giving role. This is an expanding field in gerontology, and is also of interest to personality and social psychologists studying stress and interpersonal relations. Although there are many books on the cause and treatment of dementia, there has been a book that provides a research investigation into the factors associated with effective caregiving to dementia patients. - Conceptualizes caregiving as a multistage career whose impact on the caregiver continues to be felt after in-home care has ceased - Based upon a longitudinal survey of a demographically diverse sample of principal caregivers over a three-year period - Identifies caregivers who are most at-risk for adverse adaptation to the role - Describes preventative and clinical intervention strategies - Identifies post-care risk and issues - Identifies antecedents to successful adaptation - State of the art analytic techniques - Graphic presentation of empirical findings - Renowned multidisciplinary research team

Author: Betty J. Kramer, PhD
Publisher: Springer Publishing Company
ISBN: 0826197213
Category : Social Science
Languages : en
Pages : 407

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Today, more and more caregivers are male. Despite this fact, the vast majority of research on caregiving has centered on the experience of the female caregiver. This volume addresses the fundamental gap in our knowledge and theories about the growing male subpopulation of caregivers. The authors identify the serious limitations that result from viewing men caregivers through the lens of women's experiences and call for an unbiased and fresh perspective in future research. Special consideration is given to men who care for a family member with dementia; fathers of adult children with mental retardation; gay male caregivers for partners with AIDS; and sons and parent care.

Author: Tamara Sussman
Publisher:
ISBN: 9780494220467
Category :
Languages : en
Pages : 388

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Book Description
The study employed a survey design with a convenience sample of 85 spousal caregivers who lived with their partners and who were using some form of community long-term care services. The face-to-face administration of the study questionnaires allowed caregivers to offer further remarks regarding their experiences with both the service system and caregiving in general. These comments were valuable in extending interpretations of the quantitative data. The objectives of this study are twofold: (a) to examine the relationship between the long-term community care system and spousal caregivers' mental health and (b) to explore the associations between different types of community long-term care services and caregivers' mental health. Informed by an ecological systems framework, this dissertation aims to depict the relationship between, a complex, market-oriented, resource-limited, long-term community care system and caregiving spouses' mental health. The results of this study highlight that adult day programs offer spousal caregivers a unique form of respite. Of three different types of respite services including; day program services, in-home community support workers' services, and institutional respite services, only the frequency of day program use significantly correlated with caregiver burden. Multiple regression analysis showed that caregivers whose spouse used more days of a day program experienced less burden. Comments made by caregivers in this study reinforced the important respite afforded by adult day programs. The results of this study further demonstrate that new or substitute in-home community support workers, who are not informed about the needs of caregivers and persons with dementia, negatively contribute to spousal caregivers' perceptions of services. Specifically, a multiple regression analysis demonstrated that, the less informed in-home community support workers were the more spousal caregivers experienced service discontinuity. Finally, the findings from this research suggest that spousal caregivers do not currently have access to ongoing one-on-one professional support for case coordination, and for information and guidance. Consequently, these caregivers are isolated in their provision of some of the most complex and emotionally challenging types of care. This study offers practice and policy implications that look to close the gap between spousal caregivers' needs and the long-term community care system.

Author: Mary Patricia Gallant
Publisher:
ISBN:
Category :
Languages : en
Pages : 446

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Author: National Academies of Sciences Engineering and Medicine
Publisher:
ISBN: 9780309495035
Category :
Languages : en
Pages :

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Book Description
As the largest generation in U.S. history - the population born in the two decades immediately following World War II - enters the age of risk for cognitive impairment, growing numbers of people will experience dementia (including Alzheimer's disease and related dementias). By one estimate, nearly 14 million people in the United States will be living with dementia by 2060. Like other hardships, the experience of living with dementia can bring unexpected moments of intimacy, growth, and compassion, but these diseases also affect people's capacity to work and carry out other activities and alter their relationships with loved ones, friends, and coworkers. Those who live with and care for individuals experiencing these diseases face challenges that include physical and emotional stress, difficult changes and losses in their relationships with life partners, loss of income, and interrupted connections to other activities and friends. From a societal perspective, these diseases place substantial demands on communities and on the institutions and government entities that support people living with dementia and their families, including the health care system, the providers of direct care, and others. Nevertheless, research in the social and behavioral sciences points to possibilities for preventing or slowing the development of dementia and for substantially reducing its social and economic impacts. At the request of the National Institute on Aging of the U.S. Department of Health and Human Services, Reducing the Impact of Dementia in America assesses the contributions of research in the social and behavioral sciences and identifies a research agenda for the coming decade. This report offers a blueprint for the next decade of behavioral and social science research to reduce the negative impact of dementia for America's diverse population. Reducing the Impact of Dementia in America calls for research that addresses the causes and solutions for disparities in both developing dementia and receiving adequate treatment and support. It calls for research that sets goals meaningful not just for scientists but for people living with dementia and those who support them as well. By 2030, an estimated 8.5 million Americans will have Alzheimer's disease and many more will have other forms of dementia. Through identifying priorities social and behavioral science research and recommending ways in which they can be pursued in a coordinated fashion, Reducing the Impact of Dementia in America will help produce research that improves the lives of all those affected by dementia.

Author: Steven H. Zarit
Publisher: NYU Press
ISBN: 081479663X
Category : Medical
Languages : en
Pages : 231

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Book Description
An invaluable resource guide for anyone working with persons suffering from Alzheimer's disease, this is the first book to present a step-by-step program to help families cope with the day-to-day problems arising from this disease. Using detailed case examples, the authors offer unique and effective strategies to help the family—and the patient—have enjoyable and more productive lives. "Well written and eminently practical guide for families struggling with the burdens of Alzheimer's disease." —Peter V. Rabins, M.D., John Hopkins University School of Medicine, author of Thirty-Six Hour Day "An outstanding book dealing knowledgeably and sensitively with a painful disease affecting millions of American familes." —Robert N. Butler, M.D., Brookdale Professor of Geriatrics and Adult Development, Mount Sinai School of Medicine, New York