Literature DB >> 28660841

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.

Daryl Bainbridge1, Mohanna Giruparajah2, Hanyan Zou2, Hsien Seow1.   

Abstract

OBJECTIVE: Despite the increasing prominence of residential hospices as a place of death and that, in many regards, this specialized care represents a gold standard, little is known about the care experience in this setting. Using qualitative survey data, we examined the positive and negative perceptions of care in hospices and in other prior settings.
METHOD: Qualitative comments were extracted from the CaregiverVoice survey completed by bereaved caregivers of decedents who had died in 16 residential hospices in Ontario, Canada. On this survey, caregivers reported what was good and bad about the services provided during the last three months of life as separate open-text questions. A constant-comparison method was employed to derive themes from the responses.
RESULTS: A total of 550 caregivers completed the survey, 94% (517) of whom commented on either something good (84%) and/or bad (49%) about the care experience. In addition to residential hospice, the majority of patients represented also received palliative care in the home (69%) or hospital (59%). Overall, most positive statements were about care in hospice (71%), whereas the negative statements tended to refer to other settings (81%). The hospice experience was found to exemplify care that was compassionate and holistic, in a comforting environment, offered by providers who were personable, dedicated, and informative. These humanistic qualities of care and the extent of support were generally seen to be lacking from the other settings. SIGNIFICANCE OF
RESULTS: Our examination of the good and bad aspects of palliative care received is unique in qualitatively exploring palliative care experiences across multiple settings, and specifically that in hospices. Investigation of these perspectives affirmed the elements of care that dying patients and their family caregivers most value and that the hospices were largely effective at addressing. These findings highlight the need for reinforcing these qualities in other end-of-life settings to create comforting and supportive environments.

Entities:  

Keywords:  Homecare; Hospital; Inpatient hospice; Palliative care; Quality

Mesh:

Year:  2017        PMID: 28660841     DOI: 10.1017/S147895151700058X

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  6 in total

1.  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

Review 2.  Patient reported outcomes in oncology: changing perspectives-a systematic review.

Authors:  Augusta Silveira; Teresa Sequeira; Joaquim Gonçalves; Pedro Lopes Ferreira
Journal:  Health Qual Life Outcomes       Date:  2022-05-21       Impact factor: 3.077

3.  Health Care Utilization and End-of-Life Care Outcomes for Patients With Decompensated Cirrhosis Based on Transplant Candidacy.

Authors:  Nneka N Ufere; Jennifer L Halford; Joshua Caldwell; Min Young Jang; Sunil Bhatt; John Donlan; Janet Ho; Vicki Jackson; Raymond T Chung; Areej El-Jawahri
Journal:  J Pain Symptom Manage       Date:  2019-10-23       Impact factor: 3.612

4.  Palliative Care Experience in the Last 3 Months of Life: A Quantitative Comparison of Care Provided in Residential Hospices, Hospitals, and the Home From the Perspectives of Bereaved Caregivers.

Authors:  Daryl Bainbridge; Hsien Seow
Journal:  Am J Hosp Palliat Care       Date:  2017-06-14       Impact factor: 2.500

5.  The development of specialized palliative care in the community: A qualitative study of the evolution of 15 teams.

Authors:  Hsien Seow; Daryl Bainbridge
Journal:  Palliat Med       Date:  2018-05-08       Impact factor: 4.762

6.  A gap between the philosophy and the practice of palliative healthcare: sociological perspectives on the practice of nurses in specialised palliative homecare.

Authors:  Stinne Glasdam; Frida Ekstrand; Maria Rosberg; Ann-Margrethe van der Schaaf
Journal:  Med Health Care Philos       Date:  2020-03
  6 in total

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