Literature DB >> 17298263

Bereavement services for family caregivers: how often used, why, and why not.

Emily J Cherlin1, Colleen L Barry, Holly G Prigerson, Dena Schulman Green, Rosemary Johnson-Hurzeler, Stanislav V Kasl, Elizabeth H Bradley.   

Abstract

BACKGROUND: Bereavement services are central to high-quality end-of-life care, however, little is known about how frequently and why such bereavement services are used and not used. We examined family caregiver reports about how often they used bereavement services, predictors of their use, and reported reasons for not using bereavement services.
METHODS: Prospective cohort study of family caregivers (n = 161) of patients with cancer enrolled with hospice between October 1999 and September 2001. We conducted bivariate and multivariable analyses to determine predictors of bereavement service use, adjusted for a broad range of factors including caregiving experiences, major depressive disorder (MDD), relationship with the deceased, and demographic factors. We used content analysis to summarize responses to open-ended questions concerning why individuals did not use bereavement services.
RESULTS: We found that approximately 30% of family caregivers used bereavement services in the year postloss, and the majority of these caregivers used services in the first 6 months postloss. Even among bereaved caregivers with MDD, less than half (47.6%) used bereavement services. Factors associated with using bereavement services included being a spouse caregiver, younger age, having MDD at study enrollment, witnessing highly distressing events pertaining to the patient's death, having assisted the patient with more Instrumental Activities of Daily Living (IADLs) prior to the patient's death, having greater availability of instrumental support for oneself, and physician communication with the caregiver about the patient's prognosis before the patient's death. The most common given reason for nonuse was the perception that bereavement services were not needed or would not help.
CONCLUSION: Addressing caregiver receptivity to bereavement services will be an important aspect of increasing appropriate use of such services. Future studies might examine specific interventions for reducing barriers and increasing receptivity to bereavement service use.

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Year:  2007        PMID: 17298263     DOI: 10.1089/jpm.2006.0108

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  16 in total

1.  Randomized controlled trial of a collaborative care intervention to manage cancer-related symptoms: lessons learned.

Authors:  Jennifer Steel; David A Geller; Allan Tsung; J Wallis Marsh; Mary Amanda Dew; Michael Spring; Jonathan Grady; Sonja Likumahuwa; Andrea Dunlavy; Michael Youssef; Michael Antoni; Lisa H Butterfield; Richard Schulz; Richard Day; Vicki Helgeson; Kevin H Kim; T Clark Gamblin
Journal:  Clin Trials       Date:  2011-06       Impact factor: 2.486

2.  Spiritual and emotional support of primary informal end-of-life caregivers in Nova Scotia.

Authors:  Leila Sloss; Beverley Lawson; Frederick I Burge
Journal:  J Palliat Care       Date:  2012       Impact factor: 2.250

3.  Time for change? A national audit on bereavement care in intensive care units.

Authors:  M Berry; E Brink; V Metaxa
Journal:  J Intensive Care Soc       Date:  2016-06-17

4.  Primary Care for the Elderly Bereaved: Recommendations for Medical Education.

Authors:  Sue Morris; Kristen Schaefer; Erlene Rosowsky
Journal:  J Clin Psychol Med Settings       Date:  2018-12

5.  Survey of bereavement practices of cancer care and palliative care physicians in the Pacific Northwest United States.

Authors:  Aaron S Kusano; Tawni Kenworthy-Heinige; Charles R Thomas
Journal:  J Oncol Pract       Date:  2012-06-05       Impact factor: 3.840

6.  Underutilization of mental health services among bereaved caregivers with prolonged grief disorder.

Authors:  Wendy G Lichtenthal; Matthew Nilsson; David W Kissane; William Breitbart; Elizabeth Kacel; Eric C Jones; Holly G Prigerson
Journal:  Psychiatr Serv       Date:  2011-10       Impact factor: 3.084

7.  Factors Predicting Bereaved Caregiver Perception of Quality of Care in the Final Week of Life: Implications for Health Care Providers.

Authors:  Philip C Higgins; Melissa M Garrido; Holly G Prigerson
Journal:  J Palliat Med       Date:  2015-07-17       Impact factor: 2.947

8.  Preliminary study of themes of meaning and psychosocial service use among informal cancer caregivers.

Authors:  Allison J Applebaum; Carol J Farran; Allison M Marziliano; Anna R Pasternak; William Breitbart
Journal:  Palliat Support Care       Date:  2013-08-07

9.  Bereavement among hospice caregivers of cancer patients one year following loss: predictors of grief, complicated grief, and symptoms of depression.

Authors:  Jessica Y Allen; William E Haley; Brent J Small; Ron S Schonwetter; Susan C McMillan
Journal:  J Palliat Med       Date:  2013-05-22       Impact factor: 2.947

10.  Hospice Services for Complicated Grief and Depression: Results from a National Survey.

Authors:  Angela R Ghesquiere; Melissa D Aldridge; Rosemary Johnson-Hürzeler; Daniel Kaplan; Martha L Bruce; Elizabeth Bradley
Journal:  J Am Geriatr Soc       Date:  2015-10-12       Impact factor: 5.562

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