Literature DB >> 20044332

Caring for the caregiver.

Geline Joy Tamayo1, Anita Broxson, Mark Munsell, Marlene Z Cohen.   

Abstract

PURPOSE/
OBJECTIVES: To describe the quality of life (QOL) and well-being of caregivers of patients receiving outpatient chemotherapy for leukemia and to identify strategies to promote the best possible QOL and well-being for the caregivers.
DESIGN: Descriptive, cross-sectional study.
SETTING: Ambulatory treatment center of a major comprehensive cancer center in the southern United States. SAMPLE: Convenience sample of 194 caregivers of patients receiving chemotherapy for leukemia.
METHODS: Participants completed the Caregiver Quality-of-Life-Cancer Scale, the Caregiver Well-Being Scale, and the Learning Needs Questionnaire developed by the authors. Descriptive statistics were used to summarize the demographic characteristics of the caregivers, and exploratory factor analysis was performed to identify meaningful factors. MAIN RESEARCH VARIABLES: QOL, well-being, and learning needs.
FINDINGS: Caregivers identified burden as their most important concern for QOL. Key factors identified with caregivers' well-being were expression of feelings and household maintenance. Caregivers identified giving medications and managing the side effects as crucial to learning needs. Communication, positive attitudes, support, and education were important in promoting QOL for the caregivers.
CONCLUSIONS: Caregiving for a patient receiving chemotherapy for leukemia influences the QOL and well-being of the caregiver. IMPLICATIONS FOR NURSING: This study highlights the need for better nurse-caregiver communication and education, particularly in the areas of symptom management and medication administration. Additional research should focus on factors that affect caregivers' QOL, their educational needs, and improved interventions for delivering new information or reinforcing old information.

Entities:  

Mesh:

Year:  2010        PMID: 20044332     DOI: 10.1188/10.ONF.E50-E57

Source DB:  PubMed          Journal:  Oncol Nurs Forum        ISSN: 0190-535X            Impact factor:   2.172


  32 in total

1.  The Impact of Family Communication Patterns on Hospice Family Caregivers: A New Typology.

Authors:  Elaine Wittenberg-Lyles; Joy Goldsmith; George Demiris; Debra Parker Oliver; Jacob Stone
Journal:  J Hosp Palliat Nurs       Date:  2012-01       Impact factor: 1.918

2.  Sleep-wake circadian activity rhythms and fatigue in family caregivers of oncology patients.

Authors:  Anand Dhruva; Kathryn Lee; Steven M Paul; Claudia West; Laura Dunn; Marylin Dodd; Bradley E Aouizerat; Bruce Cooper; Patrick Swift; Christine Miaskowski
Journal:  Cancer Nurs       Date:  2012 Jan-Feb       Impact factor: 2.592

3.  How calls from carers, friends and family members of someone affected by cancer differ from those made by people diagnosed with cancer; analysis of 4 years of South Australian Cancer Council Helpline data.

Authors:  Kate M Fennell; L Heckel; C Wilson; M Byrnes; P M Livingston
Journal:  Support Care Cancer       Date:  2016-01-04       Impact factor: 3.603

4.  Quality of life and satisfaction with care among family caregivers of patients with recurrent or metastasized digestive cancer requiring palliative care.

Authors:  Miki Morishita; Kiyoko Kamibeppu
Journal:  Support Care Cancer       Date:  2014-05-01       Impact factor: 3.603

5.  Predictors of depression and anxiety among caregivers of hospitalised advanced cancer patients.

Authors:  Aytül Karabekiroğlu; Esra Yancar Demir; Servet Aker; Birsen Kocamanoğlu; Gamze Sırmalı Karabulut
Journal:  Singapore Med J       Date:  2018-06-07       Impact factor: 1.858

6.  Conveying empathy to hospice family caregivers: team responses to caregiver empathic communication.

Authors:  Elaine Wittenberg-Lyles; Parker Oliver Debra; George Demiris; Anna Rankin; Sara Shaunfield; Robin L Kruse
Journal:  Patient Educ Couns       Date:  2012-05-01

7.  An overview and evaluation of the oncology family caregiver project: improving quality of life and quality of care for oncology family caregivers.

Authors:  Betty Ferrell; Jo Hanson; Marcia Grant
Journal:  Psychooncology       Date:  2012-10-14       Impact factor: 3.894

8.  Exploring spirituality in family caregivers of patients with primary malignant brain tumors across the disease trajectory.

Authors:  Alyssa G Newberry; Chien-Wen Jean Choi; Heidi S Donovan; Richard Schulz; Catherine Bender; Barbara Given; Paula Sherwood
Journal:  Oncol Nurs Forum       Date:  2013-05-01       Impact factor: 2.172

9.  A telephone outcall program to support caregivers of people diagnosed with cancer: utility, changes in levels of distress, and unmet needs.

Authors:  Leila Heckel; Kate M Fennell; Liliana Orellana; Anna Boltong; Monica Byrnes; Patricia M Livingston
Journal:  Support Care Cancer       Date:  2018-05-15       Impact factor: 3.603

10.  Communicating advanced cancer patients' symptoms via the Internet: a pooled analysis of two randomized trials examining caregiver preparedness, physical burden, and negative mood.

Authors:  Ming-Yuan Chih; Lori L DuBenske; Robert P Hawkins; Roger L Brown; Susan K Dinauer; James F Cleary; David H Gustafson
Journal:  Palliat Med       Date:  2012-09-17       Impact factor: 4.762

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