Literature DB >> 28188462

Caring for the Caregiver: Identifying the Needs of Those Called to Care Through Partnerships with Congregations.

Panagis Galiatsatos1,2, Katie Nelson3,4, W Daniel Hale3,5.   

Abstract

As the older adult population continues to grow, the prevalence of chronic diseases is also increasing, leading to the need for novel ways of managing this large population of patients. One solution is to focus on informal caregivers. These informal caregivers already make a substantial contribution to our nation's healthcare finances and patient health outcomes. Caregivers also derive benefits from caring for their family member or friend; however, it is not uncommon for these individuals to experience negative health consequences, or what is often called "burden of care." Those called to care are not without their own burdens, and they must frequently make significant lifestyle adjustments that impact their own health. Therefore, for caregivers to be effective, caring for the caregivers must be a focus of medicine in the twenty-first century.

Entities:  

Keywords:  Caregiver; Caregiver burden; Chronic illness management

Mesh:

Year:  2017        PMID: 28188462     DOI: 10.1007/s10943-017-0367-3

Source DB:  PubMed          Journal:  J Relig Health        ISSN: 0022-4197


  10 in total

Review 1.  The 2030 problem: caring for aging baby boomers.

Authors:  James R Knickman; Emily K Snell
Journal:  Health Serv Res       Date:  2002-08       Impact factor: 3.402

2.  Is caregiving hazardous to one's physical health? A meta-analysis.

Authors:  Peter P Vitaliano; Jianping Zhang; James M Scanlan
Journal:  Psychol Bull       Date:  2003-11       Impact factor: 17.737

3.  Well-being in informal caregivers of survivors of acute respiratory distress syndrome.

Authors:  Jill I Cameron; Margaret S Herridge; Catherine M Tansey; Mary Pat McAndrews; Angela M Cheung
Journal:  Crit Care Med       Date:  2006-01       Impact factor: 7.598

4.  The quality of life of male spouses of women with breast cancer: hope, self-efficacy, and perceptions of guilt.

Authors:  Wendy Duggleby; Heather Doell; Dan Cooper; Roanne Thomas; Sunita Ghosh
Journal:  Cancer Nurs       Date:  2014 Jan-Feb       Impact factor: 2.592

5.  The opportunity costs of informal elder-care in the United States: new estimates from the American Time Use Survey.

Authors:  Amalavoyal V Chari; John Engberg; Kristin N Ray; Ateev Mehrotra
Journal:  Health Serv Res       Date:  2014-10-07       Impact factor: 3.402

6.  Relatives of the impaired elderly: correlates of feelings of burden.

Authors:  S H Zarit; K E Reever; J Bach-Peterson
Journal:  Gerontologist       Date:  1980-12

7.  Multiple mediators of the relations between caregiving stress and depressive symptoms.

Authors:  Brent T Mausbach; Susan K Roepke; Elizabeth A Chattillion; Alexandrea L Harmell; Raeanne Moore; Rosa Romero-Moreno; Christopher R Bowie; Igor Grant
Journal:  Aging Ment Health       Date:  2012       Impact factor: 3.658

8.  Measurement and correlates of family caregiver self-efficacy for managing dementia.

Authors:  R H Fortinsky; K Kercher; C J Burant
Journal:  Aging Ment Health       Date:  2002-05       Impact factor: 3.658

9.  Assessing family caregiver's mental health using a statistically derived cut-off score for the Zarit Burden Interview.

Authors:  A S Schreiner; T Morimoto; Y Arai; S Zarit
Journal:  Aging Ment Health       Date:  2006-03       Impact factor: 3.658

10.  End-of-life care and the effects of bereavement on family caregivers of persons with dementia.

Authors:  Richard Schulz; Aaron B Mendelsohn; William E Haley; Diane Mahoney; Rebecca S Allen; Song Zhang; Larry Thompson; Steven H Belle
Journal:  N Engl J Med       Date:  2003-11-13       Impact factor: 91.245

  10 in total
  3 in total

1.  How do clients and (In)formal caregivers experience quality of home care? A qualitative approach.

Authors:  Roy Haex; Theresa Thoma-Lürken; Anna J H M Beurskens; Sandra M G Zwakhalen
Journal:  J Adv Nurs       Date:  2019-11-06       Impact factor: 3.187

2.  Validation of the German version of the Family Reported Outcome Measure (FROM-16) to assess the impact of disease on the partner or family member.

Authors:  Susanne A Elsner; Sam S Salek; Andrew Y Finlay; Anna Hagemeier; Catherine J Bottomley; Alexander Katalinic; Annika Waldmann
Journal:  Health Qual Life Outcomes       Date:  2021-03-24       Impact factor: 3.186

3.  Informal Caregiving in a Medically Underserved Community: Challenges, Construction of Meaning, and the Caregiver-Recipient Dyad.

Authors:  Rita Gorawara-Bhat; Jeffrey Graupner; Jason Molony; Katherine Thompson
Journal:  SAGE Open Nurs       Date:  2019-04-24
  3 in total

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