Literature DB >> 35028718

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.

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

Abstract

BACKGROUND: National recommendations state that Danish patients with complex palliative needs should have access to specialized palliative care but little is known about the perceived quality of this care or end of life care in general. AIM: To assess how end of life care was evaluated by the bereaved spouses and to investigate whether the perceived quality was associated with (1) quantity of specialized palliative care provided, (2) place of death, and (3) emotional state when completing the questionnaire.
DESIGN: The bereaved spouses of 1584 cancer patients who had received 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) approximately 3-9 months after the patient's death.
RESULTS: A total of 787 (50%) of the 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 83% of the cases and it was significantly associated with place of death (p = 0.0051, fewest considered it "fair" or "poor" if the patient died at home). In total, 93% reported that the patient died at the right place although only 74% died at the patient's preferred place. Higher levels of anxiety (p = 0.01) but not depression at the time of questionnaire completion was associated with lower satisfaction with the overall quality of care.
CONCLUSION: The quality of care was rated very highly by bereaved spouses of patients receiving specialized palliative care.
© 2021. 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

Mesh:

Year:  2022        PMID: 35028718     DOI: 10.1007/s00520-021-06756-y

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


  16 in total

1.  The care experiences of patients who die in residential hospice: A qualitative analysis of the last three months of life from the views of bereaved caregivers.

Authors:  Daryl Bainbridge; Mohanna Giruparajah; Hanyan Zou; Hsien Seow
Journal:  Palliat Support Care       Date:  2017-06-29

2.  Measuring the quality of end-of-life care: Development, testing, and cultural validation of the Danish version of Views of Informal Carers' Evaluation of Services-Short Form.

Authors:  Lone Ross; Mette Asbjoern Neergaard; Morten Aagaard Petersen; Mogens Groenvold
Journal:  Palliat Med       Date:  2017-11-13       Impact factor: 4.762

3.  The Right Place at the Right Time: Medical Oncology Outpatients' Perceptions of Location of End-of-Life Care.

Authors:  Amy Waller; Rob Sanson-Fisher; Nicholas Zdenkowski; Charles Douglas; Alix Hall; Justin Walsh
Journal:  J Natl Compr Canc Netw       Date:  2018-01       Impact factor: 11.908

4.  Exploratory analyses of the Danish Palliative Care Trial (DanPaCT): a randomized trial of early specialized palliative care plus standard care versus standard care in advanced cancer patients.

Authors:  Anna Thit Johnsen; Morten Aagaard Petersen; Per Sjøgren; Lise Pedersen; Mette Asbjoern Neergaard; Anette Damkier; Christian Gluud; Peter Fayers; Jane Lindschou; Annette S Strömgren; Jan Bjoern Nielsen; Irene J Higginson; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2019-08-13       Impact factor: 3.603

5.  Single early palliative care intervention added to usual oncology care for patients with advanced cancer: A randomized controlled trial (SENS Trial).

Authors:  Steffen Eychmüller; Susanne Zwahlen; Monica C Fliedner; Peter Jüni; Daniel M Aebersold; Drahomir Aujesky; Martin F Fey; Maud Maessen; Sven Trelle
Journal:  Palliat Med       Date:  2021-04-28       Impact factor: 4.762

6.  Psychometric properties of the Hospital Anxiety and Depression Scale in family caregivers of palliative care patients.

Authors:  Karla Gough; Peter Hudson
Journal:  J Pain Symptom Manage       Date:  2008-09-11       Impact factor: 3.612

7.  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

8.  The quality of dying and death in cancer and its relationship to palliative care and place of death.

Authors:  Sarah Hales; Aubrey Chiu; Amna Husain; Michal Braun; Anne Rydall; Lucia Gagliese; Camilla Zimmermann; Gary Rodin
Journal:  J Pain Symptom Manage       Date:  2014-04-03       Impact factor: 3.612

9.  What do patients and family-caregivers value from hospice care? A systematic mixed studies review.

Authors:  Nicole Marie Hughes; Jane Noyes; Lindsay Eckley; Trystan Pritchard
Journal:  BMC Palliat Care       Date:  2019-02-08       Impact factor: 3.234

10.  Preferred and actual place of death in haematological malignancy.

Authors:  D A Howell; H I Wang; E Roman; A G Smith; R Patmore; M J Johnson; A Garry; M Howard
Journal:  BMJ Support Palliat Care       Date:  2015-07-08       Impact factor: 3.568

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  1 in total

1.  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.

Authors:  Lone Ross; Mette Asbjoern Neergaard; Morten Aagaard Petersen; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2022-08-18       Impact factor: 3.359

  1 in total

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