Literature DB >> 17387080

Family-centered care: a resource for social work in end-of-life and palliative care.

Pamela J Kovacs1, Melissa Hayden Bellin, David P Fauri.   

Abstract

Recent trends in medicine reflect an attempt to be more patient-centered and while this is progress from the disease- or provider- focused model familiar in healthcare, the experiences and contributions of family as caregivers continue to be overlooked in some settings. The family-centered care model, developed most notably in pediatrics, but emerging in HIV, cancer, and aging, is presented as a resource to increase family involvement at the end of life. In this paper, family-centered care is defined, caregiving trends including support needs of formal and informal caregivers are discussed, and barriers to family-centered services are identified. Reintroducing family into the focus of care at the end of life is the primary goal of this paper. The family- centered model of care offers an appropriate framework for understanding the value of family in end-of-life care and fits well with social work perspectives that understand individuals in the context of their family system and greater environment.

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Mesh:

Year:  2006        PMID: 17387080     DOI: 10.1300/J457v02n01_03

Source DB:  PubMed          Journal:  J Soc Work End Life Palliat Care        ISSN: 1552-4264


  10 in total

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2.  Predictors of Palliative Care Knowledge: Findings from the Health Information National Trends Survey.

Authors:  Motolani E Ogunsanya; Elizabeth A Goetzinger; Oluwatomi F Owopetu; Paulette D Chandler; Lauren E O'Connor
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3.  Family presence during resuscitation: attitudes of Yale-New Haven Hospital staff.

Authors:  Zohar Lederman; Oren Wacht
Journal:  Yale J Biol Med       Date:  2014-03-05

4.  "Hope for the best, prepare for the worst": A qualitative interview study on parents' needs and fears in pediatric advance care planning.

Authors:  Julia Desiree Lotz; Marion Daxer; Ralf J Jox; Gian Domenico Borasio; Monika Führer
Journal:  Palliat Med       Date:  2016-11-24       Impact factor: 4.762

5.  Effects of family group conferences among high-risk patients of chronic disability and their significant others: study protocol for a multicentre controlled trial.

Authors:  Chantal F Hillebregt; Eline W M Scholten; Marjolijn Ketelaar; Marcel W M Post; Johanna M A Visser-Meily
Journal:  BMJ Open       Date:  2018-03-08       Impact factor: 2.692

6.  Influences on Care Preferences of Older People with Advanced Illness: A Systematic Review and Thematic Synthesis.

Authors:  Simon N Etkind; Anna E Bone; Natasha Lovell; Irene J Higginson; Fliss E M Murtagh
Journal:  J Am Geriatr Soc       Date:  2018-03-07       Impact factor: 5.562

7.  Health and social care services for people with dementia at home at the end of life: A qualitative study of bereaved informal caregivers' experiences.

Authors:  Caroline Mogan; Karen Harrison Dening; Christopher Dowrick; Mari Lloyd-Williams
Journal:  Palliat Med       Date:  2022-04-23       Impact factor: 5.713

8.  Primary care providers' perceptions and experiences of family-centered care for older adults: a qualitative study of community-based diabetes management in China.

Authors:  Jiong Tu; Jing Liao
Journal:  BMC Geriatr       Date:  2021-07-23       Impact factor: 3.921

9.  Pediatric palliative care for youth with HIV/AIDS: systematic review of the literature.

Authors:  Megan L Wilkins; Ronald H Dallas; Kathleen E Fanone; Maureen E Lyon
Journal:  HIV AIDS (Auckl)       Date:  2013-07-29

10.  Development and pilot evaluation of a home-based palliative care training and support package for young children in southern Africa.

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  10 in total

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