Literature DB >> 16703333

Expectations to and evaluation of a palliative home-care team as seen by patients and carers.

Dorthe Goldschmidt1, Lone Schmidt, Allan Krasnik, Ulla Christensen, Mogens Groenvold.   

Abstract

OBJECTIVES: Although the number of palliative home-care teams is increasing, knowledge of what patients and principal informal carers expect from a home-care team is sparse. We aimed to elucidate this as well as evaluate a home-care team. PATIENTS AND METHODS: Individual semi-structured interviews with nine patients and six carers before receiving home care and 2-4 weeks after. In total, 26 interviews were conducted. Interviews were analysed with Template Analysis. Peer debriefing was performed. MAIN
RESULTS: Patients and carers expected the team members to have specialised knowledge in palliative care and to improve their sense of security being at home. They also expected respite for carers and activities for patients. They evaluated the team positively but missed respite for carers and 24-h on-call service.
CONCLUSIONS: Patients and carers found the home-care team essential to their sense of security being at home. Primary health care professionals must receive any necessary training outside patients' homes. Offering respite for carers and 24-h on-call service would be an improvement.

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Year:  2006        PMID: 16703333     DOI: 10.1007/s00520-006-0082-1

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  55 in total

1.  Working with ambivalence: informal caregivers of patients at the end of life.

Authors:  R Harding; I Higginson
Journal:  Support Care Cancer       Date:  2001-11       Impact factor: 3.603

Review 2.  Judging the quality of care at the end of life: can proxies provide reliable information?

Authors:  C J McPherson; J M Addington-Hall
Journal:  Soc Sci Med       Date:  2003-01       Impact factor: 4.634

3.  Palliative care: views of patients and their families.

Authors:  I Higginson; A Wade; M McCarthy
Journal:  BMJ       Date:  1990-08-04

4.  Identifying the concerns of informal carers in palliative care.

Authors:  S Payne; P Smith; S Dean
Journal:  Palliat Med       Date:  1999-01       Impact factor: 4.762

5.  Home palliative care for terminal cancer patients: a survey on the final week of life.

Authors:  C Peruselli; P Di Giulio; F Toscani; M Gallucci; C Brunelli; M Costantini; M Tamburini; E Paci; G Miccinesi; J M Addington-Hall; I J Higginson
Journal:  Palliat Med       Date:  1999-05       Impact factor: 4.762

6.  Intervention development for enhanced lay palliative caregiver support - the use of focus groups.

Authors:  P Hudson; S Aranda; N McMurray
Journal:  Eur J Cancer Care (Engl)       Date:  2002-12       Impact factor: 2.520

7.  Valued aspects of primary palliative care: content analysis of bereaved carers' descriptions.

Authors:  Gunn E Grande; Morag C Farquhar; Stephen Ig Barclay; Chris J Todd
Journal:  Br J Gen Pract       Date:  2004-10       Impact factor: 5.386

8.  Toward a theory of patient satisfaction.

Authors:  S U Linder-Pelz
Journal:  Soc Sci Med       Date:  1982       Impact factor: 4.634

9.  Advanced home care for cancer patients at the end of life: a qualitative study of hopes and expectations of family caregivers.

Authors:  Agneta Wennman-Larsen; Carol Tishelman
Journal:  Scand J Caring Sci       Date:  2002-09

10.  Place of death: hospital-based advanced home care versus conventional care. A prospective study in palliative cancer care.

Authors:  Marianne Ahlner-Elmqvist; Marit S Jordhøy; Magnus Jannert; Peter Fayers; Stein Kaasa
Journal:  Palliat Med       Date:  2004-10       Impact factor: 4.762

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  5 in total

1.  A systematic review of interventions for family caregivers who care for patients with advanced cancer at home.

Authors:  Soojung Ahn; Rafael D Romo; Cathy L Campbell
Journal:  Patient Educ Couns       Date:  2020-03-12

2.  A qualitative study of bereaved family caregivers: feeling of security, facilitators and barriers for rural home care and death for persons with advanced cancer.

Authors:  Anne Sæle Barlund; Beate André; Kari Sand; Anne-Tove Brenne
Journal:  BMC Palliat Care       Date:  2021-01-08       Impact factor: 3.234

3.  An examination of advanced cancer caregivers' support provided by staff interventions at hospices in Argentina.

Authors:  Natalia Luxardo; Eugenia Brage; Cynthia Alvarado
Journal:  Ecancermedicalscience       Date:  2012-11-27

4.  Caregivers' active role in palliative home care - to encourage or to dissuade? A qualitative descriptive study.

Authors:  Anna Weibull; Frede Olesen; Mette Asbjoern Neergaard
Journal:  BMC Palliat Care       Date:  2008-09-16       Impact factor: 3.234

5.  The Utility of Template Analysis in Qualitative Psychology Research.

Authors:  Joanna Brooks; Serena McCluskey; Emma Turley; Nigel King
Journal:  Qual Res Psychol       Date:  2014-09-02
  5 in total

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