Literature DB >> 35982298

The quality of end-of-life care for Danish cancer patients who have received non-specialized palliative care: a national survey using the Danish version of VOICES-SF.

Lone Ross1, Mette Asbjoern Neergaard2, Morten Aagaard Petersen3, Mogens Groenvold3,4.   

Abstract

PURPOSE: About half of Danish patients dying from cancer have never been in contact with specialized palliative care. Non-specialized palliative care in Denmark, i.e., somatic hospital departments, community nurses, and general practitioners, has rarely been described or evaluated. We aim to assess how non-specialized palliative care was evaluated by bereaved spouses, and to test whether distress when completing the questionnaire and ratings of aspects of end-of-life care was associated with satisfaction with place of death and overall quality of end-of-life care.
METHODS: Bereaved spouses of 792 cancer patients who had received non-specialized palliative care were invited to answer the Views of Informal Carers-Evaluation of Services-Short Form (VOICES-SF) and the Hospital Anxiety and Depression Scale (HADS) 3-9 months after the patient's death.
RESULTS: A total of 280 (36%) of invited spouses participated. In the last 3 months of the patient's life, the quality of all services taken together was rated as good, excellent, or outstanding in 70% of the cases. Satisfaction was associated with respondent's current distress (p = 0.0004). Eighty percent of bereaved spouses believed that the patient had died in the right place. Satisfaction with place of death was associated with place of death (p = 0.012) and the respondent's current distress (p = 0.0016).
CONCLUSION: Satisfaction with place of death and overall quality of services was generally high but was rated lower by spouses reporting higher levels of distress when completing the questionnaire. Distress should be taken into account whenever services are evaluated by bereaved relatives.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Cancer; End-of-life care; Palliative care; Place of death; Satisfaction with care; Spouses

Year:  2022        PMID: 35982298     DOI: 10.1007/s00520-022-07302-0

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.359


  29 in total

1.  Lay carers' satisfaction with community palliative care: results of a postal survey. South Tyneside MAAG Palliative Care Study Group.

Authors:  J Lecouturier; A Jacoby; C Bradshaw; T Lovel; M Eccles
Journal:  Palliat Med       Date:  1999-07       Impact factor: 4.762

Review 2.  Measuring end-of-life care outcomes retrospectively.

Authors:  Joan M Teno
Journal:  J Palliat Med       Date:  2005       Impact factor: 2.947

3.  Dying from cancer in community hospitals or a hospice: closest lay carers' perceptions.

Authors:  D A Seamark; S Williams; M Hall; C J Lawrence; J Gilbert
Journal:  Br J Gen Pract       Date:  1998-06       Impact factor: 5.386

4.  The culture of general palliative nursing care in medical departments: an ethnographic study.

Authors:  Heidi Bergenholtz; Lene Jarlbaek; Bibi Hølge-Hazelton
Journal:  Int J Palliat Nurs       Date:  2015-04

5.  Is Care for the Dying Improving in the United States?

Authors:  Joan M Teno; Vicki A Freedman; Judith D Kasper; Pedro Gozalo; Vincent Mor
Journal:  J Palliat Med       Date:  2015-04-29       Impact factor: 2.947

6.  The quality of end of life care for Danish cancer patients who have received specialized palliative: a national survey using the Danish version of VOICES-SF.

Authors:  Lone Ross; Mette Asbjoern Neergaard; Morten Aagaard Petersen; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2022-01-14       Impact factor: 3.603

7.  Symptoms and problems in a nationally representative sample of advanced cancer patients.

Authors:  A T Johnsen; M A Petersen; L Pedersen; M Groenvold
Journal:  Palliat Med       Date:  2009-05-14       Impact factor: 4.762

8.  Do advanced cancer patients in Denmark receive the help they need? A nationally representative survey of the need related to 12 frequent symptoms/problems.

Authors:  Anna Thit Johnsen; Morten Aagaard Petersen; Lise Pedersen; Lise Jul Houmann; Mogens Groenvold
Journal:  Psychooncology       Date:  2012-10-08       Impact factor: 3.894

9.  The CaregiverVoice Survey: A Pilot Study Surveying Bereaved Caregivers To Measure the Caregiver and Patient Experience at End of Life.

Authors:  Hsien Seow; Daryl Bainbridge; Deanna Bryant; Dawn Guthrie; Sara Urowitz; Victoria Zwicker; Denise Marshall
Journal:  J Palliat Med       Date:  2016-06-02       Impact factor: 2.947

10.  Developing the methods and questionnaire (VOICES-SF) for a national retrospective mortality follow-back survey of palliative and end-of-life care in England.

Authors:  Katherine J Hunt; Alison Richardson; Anne-Sophie E Darlington; Julia M Addington-Hall
Journal:  BMJ Support Palliat Care       Date:  2017-11-03       Impact factor: 3.568

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