Literature DB >> 9205653

Support needs in the last year of life: patient and carer dilemmas.

G E Grande1, C J Todd, S I Barclay.   

Abstract

The aim of this study was to identify needs for support and problems in the introduction of support to terminally ill patients and their carers. The design involved semistructured interviews with patients and carers as well as a survey of general practitioners' (GPs) views, and took place in GP practices and homes of patients in Cambridgeshire. The subjects comprised 43 terminally ill patients, 30 carers, 80 GPs and 13 of their GP partners. The main outcome measures were quantitative data about additional help required and qualitative data on reasons for reluctance to seek help. Needs for help with transport, personal care and housework were identified. Carers may also need reassurance from health professionals. The need for outside help may at times conflict with the need to preserve independence, dignity and familiar aspects of life. Sometimes carers may feel that there is need for more help, but that this conflicts with patients' wishes. There may also be reluctance to seek help because of a perceived lack of resources and professionals time. In conclusion, an increase in services is necessary but not sufficient to meet patients' needs fully. Services should be introduced in ways that help patients to preserve independence, dignity and familiar aspects of life. The perception of accessibility to health professionals may need to be improved. Carers' needs should be assessed separately from patients' needs.

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Year:  1997        PMID: 9205653     DOI: 10.1177/026921639701100304

Source DB:  PubMed          Journal:  Palliat Med        ISSN: 0269-2163            Impact factor:   4.762


  8 in total

1.  Primary care group commissioning of services: the differing priorities of general practitioners and district nurses for palliative care services.

Authors:  S Barclay; C Todd; J McCabe; T Hunt
Journal:  Br J Gen Pract       Date:  1999-03       Impact factor: 5.386

2.  Good end-of-life care according to patients and their GPs.

Authors:  Sander D Borgsteede; Corrie Graafland-Riedstra; Luc Deliens; Anneke L Francke; Jacques Thm van Eijk; Dick L Willems
Journal:  Br J Gen Pract       Date:  2006-01       Impact factor: 5.386

3.  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

4.  "Non-palliative care" - a qualitative study of older cancer patients' and their family members' experiences with the health care system.

Authors:  Marianne Fjose; Grethe Eilertsen; Marit Kirkevold; Ellen Karine Grov
Journal:  BMC Health Serv Res       Date:  2018-09-29       Impact factor: 2.655

5.  The extent and predictors of discrepancy between provider and recipient reports of informal caregiving.

Authors:  Sean Urwin; Yiu-Shing Lau; Gunn Grande; Matt Sutton
Journal:  Soc Sci Med       Date:  2021-04-02       Impact factor: 5.379

6.  The impact on the family carer of motor neurone disease and intervention with noninvasive ventilation.

Authors:  Susan K Baxter; Wendy O Baird; Sue Thompson; Stephen M Bianchi; Stephen J Walters; Ellen Lee; Sam H Ahmedzai; Alison Proctor; Pamela J Shaw; Christopher J McDermott
Journal:  J Palliat Med       Date:  2013-11-16       Impact factor: 2.947

7.  Providing supportive care to cancer patients: a study on inter-organizational relationships.

Authors:  Kevin Brazil; Daryl Bainbridge; Jonathan Sussman; Tim Whelan; Mary Ann O'Brien; Nancy Pyette
Journal:  Int J Integr Care       Date:  2008-02-11       Impact factor: 5.120

8.  Needs of informal caregivers across the caregiving course in amyotrophic lateral sclerosis: a qualitative analysis.

Authors:  Miriam Galvin; Sile Carney; Bernie Corr; Iain Mays; Niall Pender; Orla Hardiman
Journal:  BMJ Open       Date:  2018-01-27       Impact factor: 2.692

  8 in total

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