Literature DB >> 16505131

Length of hospice enrollment and subsequent depression in family caregivers: 13-month follow-up study.

Alison E Kris1, Emily J Cherlin, Holly Prigerson, Melissa D A Carlson, Rosemary Johnson-Hurzeler, Stanislav V Kasl, Elizabeth H Bradley.   

Abstract

OBJECTIVE: Although more people are using hospice than ever before, the average length of hospice enrollment is decreasing. Little is known about the effect of hospice length of enrollment on surviving family caregivers. The authors examine the association between patient length of hospice enrollment and major depressive disorder (MDD) among the surviving primary family caregivers 13 months after the patient's death.
METHODS: The authors conducted a three-year longitudinal study of 175 primary family caregivers of patients with terminal cancer who consecutively enrolled in the participating hospice from October 1999 through September 2001. Interviews were conducted with the primary family caregiver when the patient first enrolled with hospice and again 13 months after the patient's death. The authors used multivariate logistic regression models to estimate caregivers' adjusted risk at 13 months postloss for MDD, assessed using the Structured Clinical Interview for the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (SCID).
RESULTS: The effect of very short hospice length of enrollment (three days or less) compared with longer lengths of enrollment on caregiver MDD 13 months after their loss was nonsignificant in unadjusted analyses. The adjusted risk of MDD was significantly elevated for caregivers of patients who had very short hospice enrollments (adjusted odds ratio: 8.76, 95%confidence interval: 1.09-70.19) only after adjusting for baseline MDD, caregiver gender, caregiver age, kinship relationship to patient, caregiver education, caregiver chronic conditions, and caregiver burden. The adjustment for caregiver burden resulted in the greatest increase in odds ratio for very short hospice length of enrollment on risk of caregiver MDD 13 months after the loss.
CONCLUSIONS: This study identifies a potential target group of family caregivers, characterized by hospice length of enrollment and several caregiver features, who might be most in need of mental health interventions.

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Year:  2006        PMID: 16505131     DOI: 10.1097/01.JGP.0000194642.86116.ce

Source DB:  PubMed          Journal:  Am J Geriatr Psychiatry        ISSN: 1064-7481            Impact factor:   4.105


  31 in total

1.  Psychological states and coping strategies after bereavement among spouses of cancer patients: a quantitative study in Japan.

Authors:  Mariko Asai; Nobuya Akizuki; Maiko Fujimori; Yutaka Matsui; Kuniaki Itoh; Masafumi Ikeda; Ryuichi Hayashi; Taira Kinoshita; Atsushi Ohtsu; Kanji Nagai; Hiroya Kinoshita; Yosuke Uchitomi
Journal:  Support Care Cancer       Date:  2012-04-18       Impact factor: 3.603

2.  Hospice Utilization in Elderly Patients With Brain Metastases.

Authors:  Elie K Mehanna; Paul J Catalano; Daniel N Cagney; Daphne A Haas-Kogan; Brian M Alexander; James A Tulsky; Ayal A Aizer
Journal:  J Natl Cancer Inst       Date:  2020-12-14       Impact factor: 13.506

3.  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

4.  Meaning-Centered Psychotherapy for Cancer Caregivers (MCP-C): Rationale and Overview.

Authors:  Allison J Applebaum; Julia R Kulikowski; William Breitbart
Journal:  Palliat Support Care       Date:  2015-05-22

5.  Geographic Variation of Hospice Use Patterns at the End of Life.

Authors:  Shi-Yi Wang; Melissa D Aldridge; Cary P Gross; Maureen Canavan; Emily Cherlin; Rosemary Johnson-Hurzeler; Elizabeth Bradley
Journal:  J Palliat Med       Date:  2015-07-14       Impact factor: 2.947

6.  Perspectives Regarding Hospice Services and Transfusion Access: Focus Groups With Blood Cancer Patients and Bereaved Caregivers.

Authors:  Catherine Henckel; Anna Revette; Scott F Huntington; James A Tulsky; Gregory A Abel; Oreofe O Odejide
Journal:  J Pain Symptom Manage       Date:  2020-01-09       Impact factor: 3.612

Review 7.  Informal caregiving of hospice patients.

Authors:  Colin G Pottie; Karen A Burch; Lori P Montross Thomas; Scott A Irwin
Journal:  J Palliat Med       Date:  2014-07       Impact factor: 2.947

8.  Association between survival time with metastatic breast cancer and aggressive end-of-life care.

Authors:  Melissa K Accordino; Jason D Wright; Sowmya Vasan; Alfred I Neugut; Tal Gross; Grace C Hillyer; Dawn L Hershman
Journal:  Breast Cancer Res Treat       Date:  2017-07-27       Impact factor: 4.872

9.  Retrospective evaluation of palliative care and hospice utilization in hospitalized patients with metastatic breast cancer.

Authors:  Jennifer A Shin; Amanda Parkes; Areej El-Jawahri; Lara Traeger; Helen Knight; Emily R Gallagher; Jennifer S Temel
Journal:  Palliat Med       Date:  2016-03-15       Impact factor: 4.762

Review 10.  Care for the cancer caregiver: a systematic review.

Authors:  Allison J Applebaum; William Breitbart
Journal:  Palliat Support Care       Date:  2012-10-10
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