Literature DB >> 22248787

The nature and timing of family-provider communication in late-stage cancer: a qualitative study of caregivers' experiences.

Deborah P Waldrop1, Mary Ann Meeker, Christopher Kerr, Judith Skretny, John Tangeman, Robert Milch.   

Abstract

CONTEXT: Family members of people with advanced cancer can experience intensified distress and uncertainty during the final stages of their loved one's illness. Enhanced comprehension about disease progression, symptom management, and options for care can help families adapt, cope, and plan for the future.
OBJECTIVES: Guided by concepts from the Sense of Coherence Theory, which illuminates factors that contribute to adaptation in stressful situations, the objective of this study was to explore and describe family caregivers' accounts of the nature and timing of communication they had with a loved one's health care provider(s) during the advanced stages of cancer and before hospice enrollment.
METHODS: Retrospective in-depth interviews were conducted with caregivers of 46 people who died of cancer. Interviews were audiotaped, transcribed, and submitted to an iterative process of qualitative data analysis that included 1) systematic coding, 2) the use of data matrices to display summarized results and collapse the codes into themes, 3) and axial coding to characterize the nature of the themes.
RESULTS: Overall, communication with providers was found to be either 1) satisfactory or 2) unsatisfactory. Satisfactory communication was 1) compassionate, 2) responsive, and/or 3) dedicated. Unsatisfactory communication was described as 1) sparse, 2) conflicted, 3) contradictory, and/or 4) brink of death.
CONCLUSION: Communication with health care providers is critical for helping family caregivers understand and manage the changes that accompany a life-limiting illness. Timely communication with information and meaningful discussion about disease progression can help families prepare for the advanced stages of an illness and approaching death.
Copyright © 2012 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22248787     DOI: 10.1016/j.jpainsymman.2011.04.017

Source DB:  PubMed          Journal:  J Pain Symptom Manage        ISSN: 0885-3924            Impact factor:   3.612


  8 in total

1.  The interaction between informal cancer caregivers and health care professionals: a survey of caregivers' experiences of problems and unmet needs.

Authors:  Line Lund; Lone Ross; Morten Aagaard Petersen; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2014-11-29       Impact factor: 3.603

2.  Family caregivers' perspectives on communication with cancer care providers.

Authors:  Karla T Washington; Kevin W Craig; Debra Parker Oliver; Jeffrey S Ruggeri; Samantha R Brunk; Andrea K Goldstein; George Demiris
Journal:  J Psychosoc Oncol       Date:  2019-06-16

3.  Spirituality alleviates the burden on family members caring for patients receiving palliative care exclusively.

Authors:  Paula Menis Vigna; Isac de Castro; Renata Rego Lins Fumis
Journal:  BMC Palliat Care       Date:  2020-06-03       Impact factor: 3.234

4.  A sense of security in palliative homecare in a Norwegian municipality; dyadic comparisons of the perceptions of patients and relatives - a quantitative study.

Authors:  Reidun Hov; Bente Bjørsland; Bente Ødegård Kjøs; Bodil Wilde-Larsson
Journal:  BMC Palliat Care       Date:  2020-01-11       Impact factor: 3.234

Review 5.  Concerns and potential improvements in end-of-life care from the perspectives of older patients and informal caregivers: a scoping review.

Authors:  Mina Motamedi; Caitlin Brandenburg; Mina Bakhit; Zoe A Michaleff; Loai Albarqouni; Justin Clark; Meidelynn Ooi; Danial Bahudin; Danielle Ní Chróinín; Magnolia Cardona
Journal:  BMC Geriatr       Date:  2021-12-20       Impact factor: 3.921

6.  Survey on the effectiveness of telephone-based communication with relatives of hospitalized cancer patients in COVID-19 era in Italy.

Authors:  Beatrice Riccò; Claudia Fiorani; Leonardo Ferrara; Leonardo Potenza; Alessia Saviola; Norma Malavasi; Gloria Acquaviva; Chiara Carboni; Laura Scarabelli; Massimo Dominici; Mario Luppi; Giuseppe Longo
Journal:  Support Care Cancer       Date:  2022-04-11       Impact factor: 3.603

7.  The second patient? Family members of cancer patients and their role in end-of-life decision making.

Authors:  Katsiaryna Laryionava; Timo A Pfeil; Mareike Dietrich; Stella Reiter-Theil; Wolfgang Hiddemann; Eva C Winkler
Journal:  BMC Palliat Care       Date:  2018-02-17       Impact factor: 3.234

8.  Managing uncertainty and references to time in prognostic conversations with family members at the end of life: A conversation analytic study.

Authors:  Rebecca J Anderson; Patrick C Stone; Joseph T S Low; Steven Bloch
Journal:  Palliat Med       Date:  2020-04-01       Impact factor: 4.762

  8 in total

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