Literature DB >> 22795051

A social capital framework for palliative care: supporting health and well-being for people with life-limiting illness and their carers through social relations and networks.

Joanne M Lewis1, Michelle DiGiacomo, Tim Luckett, Patricia M Davidson, David C Currow.   

Abstract

CONTEXT: Social relations and networks are vital for sustaining and enhancing end-of-life care. The social capital concept supports a framework to understand the association between social relations and well-being; yet, to date, there has been very limited investigation of social capital in the palliative care literature. A framework for understanding social contexts in end-of-life care is necessary.
OBJECTIVES: To summarize the literature on social capital, well-being, and quality of life for key outcomes to inform a model of social capital in palliative care.
METHODS: The electronic databases MEDLINE (1997 to March 2011), Embase (1997 to March 2011), CINAHL (1997 to March 2011), and PsycINFO (1997 to March 2011) were searched using key/MeSH search terms of "social capital," "palliative care," and "well-being" and/or "quality of life." The literature was reviewed to identify key concepts to develop and inform a palliative care social capital framework.
RESULTS: A total of 93 articles were included in the literature review, with only two articles identifying discourse on social capital and palliative care. Four key areas integrating the social capital outcomes informed a framework for palliative care.
CONCLUSION: The social capital concept provides a structure for understanding how the organization and meaning of social contexts can potentially enhance or hinder end-of-life care. Research that identifies specificity in application of social capital concepts is fundamental to issues of access to services, sustaining levels of care, quality of life, and well-being. The importance of "bridged" social capital relations and networks for improved resource acquisition and information flow was identified in the literature and outlined within the palliative care social capital framework. Differential access to social capital by disadvantaged groups provides further impetus to engage a model of social capital for palliative care.
Copyright © 2013 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22795051     DOI: 10.1016/j.jpainsymman.2011.12.283

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  9 in total

1.  A Cross-Sectional Relationship Between Social Capital, Self-Compassion, and Perceived HIV Symptoms.

Authors:  Allison R Webel; Dean Wantland; Carol Dawson Rose; Jeanne Kemppainen; William L Holzemer; Wei-Ti Chen; Mallory O Johnson; Patrice Nicholas; Lucille Sanzero Eller; Puangtip Chaiphibalsarisdi; Elizabeth Sefcik; Kathleen Nokes; Inge B Corless; Lynda Tyer-Viola; Kenn Kirksey; Joachim Voss; Kathy Sullivan; Marta Rivero-Méndez; John Brion; Scholastika Iipinge; J Craig Phillips; Carmen Portillo
Journal:  J Pain Symptom Manage       Date:  2015-02-04       Impact factor: 3.612

2.  Social capital in a lower socioeconomic palliative care population: a qualitative investigation of individual, community and civic networks and relations.

Authors:  Joanne M Lewis; Michelle DiGiacomo; David C Currow; Patricia M Davidson
Journal:  BMC Palliat Care       Date:  2014-06-16       Impact factor: 3.234

3.  'Being with' or 'doing for'? How the role of an end-of-life volunteer befriender can impact patient wellbeing: interviews from a multiple qualitative case study (ELSA).

Authors:  Steven Dodd; Matt Hill; Nick Ockenden; Guillermo Perez Algorta; Sheila Payne; Nancy Preston; Catherine Walshe
Journal:  Support Care Cancer       Date:  2018-03-29       Impact factor: 3.603

4.  "Small small interventions, big big roles"- a qualitative study of patient, care-giver and health-care worker experiences of a palliative care programme in Kerala, India.

Authors:  Rekha Rachel Philip; Emilie Venables; Abdulla Manima; Jaya Prasad Tripathy; Sairu Philip
Journal:  BMC Palliat Care       Date:  2019-02-04       Impact factor: 3.234

5.  Exploring a New Model of End-of-Life Care for Older People That Operates in the Space Between the Life World and the Healthcare System: A Qualitative Case Study.

Authors:  Steven Dodd; Nancy Preston; Sheila Payne; Catherine Walshe
Journal:  Int J Health Policy Manag       Date:  2020-08-01

Review 6.  New public health approaches to palliative care, a brave new horizon or an impractical ideal? An Integrative literature review with thematic synthesis.

Authors:  Joseph M Sawyer; Paul Higgs; John D H Porter; Elizabeth L Sampson
Journal:  Palliat Care Soc Pract       Date:  2021-10-06

7.  INSPIRE (INvestigating Social and PractIcal suppoRts at the End of life): Pilot randomised trial of a community social and practical support intervention for adults with life-limiting illness.

Authors:  Kathleen McLoughlin; Jim Rhatigan; Sinead McGilloway; Allan Kellehear; Michael Lucey; Feargal Twomey; Marian Conroy; Emillio Herrera-Molina; Suresh Kumar; Mairead Furlong; Joanne Callinan; Max Watson; David Currow; Christopher Bailey
Journal:  BMC Palliat Care       Date:  2015-11-24       Impact factor: 3.234

8.  How effective are volunteers at supporting people in their last year of life? A pragmatic randomised wait-list trial in palliative care (ELSA).

Authors:  Catherine Walshe; Steven Dodd; Matt Hill; Nick Ockenden; Sheila Payne; Nancy Preston; Guillermo Perez Algorta
Journal:  BMC Med       Date:  2016-12-09       Impact factor: 8.775

9.  Sense of support within the family: a cross-sectional study of family members in palliative home care.

Authors:  Anna Milberg; Maria Liljeroos; Rakel Wåhlberg; Barbro Krevers
Journal:  BMC Palliat Care       Date:  2020-08-07       Impact factor: 3.234

  9 in total

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