Transitional Palliative Care for Family Caregivers: Outcomes From a Randomized Controlled Trial

被引:2
作者
Griffin, Joan M. [1 ]
Mandrekar, Jay N. [2 ]
Vanderboom, Catherine E.
Harmsen, William S. [2 ]
Kaufman, Brystana G. [3 ,4 ,5 ]
Wild, Ellen M. [6 ]
Dose, Ann Marie
Ingram, Cory J.
Taylor, Erin E. [7 ]
Stiles, Carole J. [7 ]
Gustavson, Allison M. [8 ,9 ]
Holland, Diane E.
机构
[1] Mayo Clin, Div Hlth Care Delivery Res, Rochester, MN USA
[2] Mayo Clin, Dept Quantitat Hlth Sci, Rochester, MN USA
[3] Duke Univ, Sch Med, Dept Populat Hlth Sci, Durham, NC USA
[4] Duke Univ, Margolis Inst Hlth Policy, Durham, NC USA
[5] Durham US Dept Vet Affairs, Durham Ctr Innovat Accelerate Discovery & Practice, Durham, NC USA
[6] Mayo Clin, Dept Community Internal Med Geriatr & Palliat Care, Rochester, MN USA
[7] Mayo Clin, Dept Social Work, Rochester, MN USA
[8] Minneapolis Vet Affairs Hlth Care Syst, Ctr Care Delivery & Outcomes Res, Minneapolis, MN USA
[9] Univ Minnesota, Dept Med, Minneapolis, MN USA
基金
美国国家卫生研究院;
关键词
Family caregiving; transitional care; palliative care; depression; quality of life; randomized controlled trial; PATIENTS AFTER-DISCHARGE; QUALITY-OF-LIFE; PSYCHOSOCIAL INTERVENTIONS; ADVERSE EVENTS; OLDER-ADULTS; CANCER; PATIENT; IMPACT; PREPAREDNESS; READMISSIONS;
D O I
10.1016/j.jpainsymman.2024.07.030
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Context. Patients receiving inpatient palliative care often face physical and psychological uncertainties during transitions out of the hospital. Family caregivers often take on responsibilities to ensure patient safety, quality of care, and extend palliative care principles, but often without support or training, potentially compromising their health and well-being. Objectives. This study tested an eight-week intervention using video visits between palliative care nurse interventionists and caregivers to assess changes in caregiver outcomes and patient quality of life. Methods. This randomized controlled trial, conducted from 2018 to 2022, enrolled adult caregivers in rural or medically underserved areas in Minnesota, Wisconsin, and Iowa. Eligible caregivers included those caring for patients who received inpatient palliative care and transitioned out of the hospital. The intervention group received teaching, guidance, and counseling from a palliative care nurse before and for eight weeks after hospital discharge. The control group received monthly phone calls but no intervention. Caregiver outcomes included changes in depression, burden, and quality of life, and patient quality of life, as reported by the caregiver. Results. Of those consented, 183 completed the intervention, and 184 completed the control arm; 158 participants had complete baseline and eight-week data. In unadjusted analyses, the intervention group and their care recipients showed statistically significant fi cant improvements in quality of life compared to the control group. Improvements persisted in adjusted analyses, and depression significantly fi cantly improved. No differences in caregiver burden were observed. Conclusion. Addressing rural caregivers' ' needs during transitions in care can enhance caregiver outcomes and improve patient quality of life. J Pain Symptom Manage 2024;68:456-466. - 466. (c) 2024 The Authors. Published by Elsevier Inc. on behalf of American Academy of Hospice and Palliative Medicine. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/ licenses/by-nc-nd/4.0/).
引用
收藏
页码:456 / 466
页数:11
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