Literature DB >> 21242762

Informal caregivers of hematopoietic cell transplant patients: a review and recommendations for interventions and research.

Robin Gemmill1, Liz Cooke, Anna Cathy Williams, Marcia Grant.   

Abstract

BACKGROUND: Informal caregivers (ICs) for medically fragile hematopoietic cell transplantation (HCT) patients are a vital unrecognized population supporting the transplant patient along the illness continuum. The long transplant recovery period shifts a greater burden of care to the patient's IC. Assessment of HCT caregivers' quality of life (QOL) and health status is critical to implementation of timely intervention and support.
METHODS: A literature search using several search strategies covering 1980 to 2010 identified studies on ICs of HCT patients. These studies were summarized within the caregiver concepts of QOL, role, and resources. Findings of this review were used to create recommended interventions and identify implications for further research.
RESULTS: Although limited, research on ICs of hematopoietic call transplant patients provides beginning evidence for clinical interventions to support this caregiver population. Interventions created focus on education, psychosocial support, and self-care.
CONCLUSIONS: Although limited randomized trials of interventions have been reported, descriptive studies provide evidence for creating intervention content that addresses the needs of ICs of HCT patients. Testing of these interventions and additional areas of research are identified. IMPLICATIONS FOR PRACTICE: Beginning descriptive evidence provides the basis for interventions for ICs of HCT patients. These interventions support caregiver QOL and role implementation, depending on individual caregivers' resources and needs. Further evaluation and clinical research are needed.

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Year:  2011        PMID: 21242762      PMCID: PMC3123439          DOI: 10.1097/NCC.0b013e31820a592d

Source DB:  PubMed          Journal:  Cancer Nurs        ISSN: 0162-220X            Impact factor:   2.592


  43 in total

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  28 in total

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Review 2.  The Effect of Psychosocial Interventions on Outcomes for Caregivers of Hematopoietic Cell Transplant Patients.

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3.  Engaging Patients in Setting a Patient-Centered Outcomes Research Agenda in Hematopoietic Cell Transplantation.

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Journal:  Biol Blood Marrow Transplant       Date:  2018-02-03       Impact factor: 5.742

4.  Identifying unmet informational needs in the inpatient setting to increase patient and caregiver engagement in the context of pediatric hematopoietic stem cell transplantation.

Authors:  Elizabeth Kaziunas; David A Hanauer; Mark S Ackerman; Sung Won Choi
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5.  A qualitative exploration of the informed consent process in hematopoietic cell transplantation clinical research and opportunities for improvement.

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6.  Caregiver availability and patient access to hematopoietic cell transplantation: social worker perspectives inform practice.

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Journal:  Support Care Cancer       Date:  2019-03-09       Impact factor: 3.603

Review 7.  National Institutes of Health Hematopoietic Cell Transplantation Late Effects Initiative: The Patient-Centered Outcomes Working Group Report.

Authors:  Margaret Bevans; Areej El-Jawahri; D Kathryn Tierney; Lori Wiener; William A Wood; Flora Hoodin; Erin E Kent; Paul B Jacobsen; Stephanie J Lee; Matthew M Hsieh; Ellen M Denzen; Karen L Syrjala
Journal:  Biol Blood Marrow Transplant       Date:  2016-09-19       Impact factor: 5.742

8.  A problem-solving education intervention in caregivers and patients during allogeneic hematopoietic stem cell transplantation.

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Review 9.  A scoping review of caregiver burden during allogeneic HSCT: lessons learned and future directions.

Authors:  A J Applebaum; M Bevans; T Son; K Evans; M Hernandez; S Giralt; K DuHamel
Journal:  Bone Marrow Transplant       Date:  2016-06-13       Impact factor: 5.483

10.  The need to support caregivers during pediatric bone marrow transplantation (BMT): A case report.

Authors:  Christina Mangurian; Wendy Packman; Nicholas S Riano; Julia Kearney
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