Literature DB >> 21146356

Reciprocal suffering: caregiver concerns during hospice care.

Elaine Wittenberg-Lyles1, George Demiris, Debra Parker Oliver, Stephanie Burt.   

Abstract

CONTEXT: For many hospice caregivers, the constancy and difficulty of caregiving impact their physical quality of life and cause depression, psychological distress, guilt, loneliness, and restrictions on social activities.
OBJECTIVES: Deviating from traditional unidimensional research on hospice caregivers, this study explored the transactional nature of reciprocal suffering by examining caregiver concerns through four dimensions: physical, psychological, social, and spiritual.
METHODS: Researchers analyzed audiotapes of intervention discussions between hospice caregivers and research social workers.
RESULTS: Results indicated that, of the 125 pain talk utterances, most referenced psychological concern (49%), followed by physical (28%), social (22%), and spiritual (2%) concerns. Reflections on concerns revealed a global perspective of caregiving, which highlighted the patient's needs juxtaposed to the caregiver's recognized limitations.
CONCLUSION: By examining the reciprocal nature of suffering for caregivers, this study reinforced the need for assessing caregivers in hospice care, with specific emphasis on the importance of providing caregiver education on pain management.
Copyright © 2011 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 21146356      PMCID: PMC3053049          DOI: 10.1016/j.jpainsymman.2010.04.026

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


  21 in total

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Authors:  Holly G Prigerson; Emily Cherlin; Joyce H Chen; Stanislav V Kasl; Rosemary Hurzeler; Elizabeth H Bradley
Journal:  Am J Geriatr Psychiatry       Date:  2003 May-Jun       Impact factor: 4.105

Review 2.  The nature of suffering and the goals of nursing.

Authors:  Betty R Ferrell; Nessa Coyle
Journal:  Oncol Nurs Forum       Date:  2008-03       Impact factor: 2.172

Review 3.  ABC of palliative care. Principles of palliative care and pain control.

Authors:  B O'Neill; M Fallon
Journal:  BMJ       Date:  1997-09-27

4.  Caregiver burden and symptom distress in people with cancer receiving hospice care.

Authors:  S C Andrews
Journal:  Oncol Nurs Forum       Date:  2001-10       Impact factor: 2.172

5.  Comparing face-to-face and telehealth-mediated delivery of a psychoeducational intervention: a case comparison study in hospice.

Authors:  Debra Parker Oliver; George Demiris
Journal:  Telemed J E Health       Date:  2010 Jul-Aug       Impact factor: 3.536

6.  Family caregiver quality of life: differences between curative and palliative cancer treatment settings.

Authors:  M A Weitzner; S C McMillan; P B Jacobsen
Journal:  J Pain Symptom Manage       Date:  1999-06       Impact factor: 3.612

7.  Hospice patient and caregiver congruence in reporting patients' symptom intensity.

Authors:  Susan C McMillan; Linda E Moody
Journal:  Cancer Nurs       Date:  2003-04       Impact factor: 2.592

8.  Family caregiving in cancer pain management.

Authors:  B R Ferrell; M Grant; T Borneman; G Juarez; A ter Veer
Journal:  J Palliat Med       Date:  1999       Impact factor: 2.947

9.  Predicting caregiver burden from daily functional abilities of patients with mild dementia.

Authors:  Jill Razani; Bernadette Kakos; Carla Orieta-Barbalace; Jennifer T Wong; Rachel Casas; Po Lu; Cathy Alessi; Karen Josephson
Journal:  J Am Geriatr Soc       Date:  2007-09       Impact factor: 5.562

10.  Barriers to pain management: caregiver perceptions and pain talk by hospice interdisciplinary teams.

Authors:  Debra Parker Oliver; Elaine Wittenberg-Lyles; George Demiris; Karla Washington; Davina Porock; Michele Day
Journal:  J Pain Symptom Manage       Date:  2008-05-20       Impact factor: 3.612

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  7 in total

1.  Perceived mental health status of drug users with HIV: concordance between caregivers and care recipient reports and associations with caregiving burden and reciprocity.

Authors:  Mary M Mitchell; Allysha C Robinson; Jennifer L Wolff; Amy R Knowlton
Journal:  AIDS Behav       Date:  2014-06

2.  Application of the VALUE communication principles in ACTIVE hospice team meetings.

Authors:  Karla T Washington; Elaine Wittenberg-Lyles; Debra Parker Oliver; George Demiris; Sara Shaunfield; Edith Crumb
Journal:  J Palliat Med       Date:  2012-10-04       Impact factor: 2.947

Review 3.  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

4.  Informal Caregiver Characteristics Associated with Viral Load Suppression Among Current or Former Injection Drug Users Living with HIV/AIDS.

Authors:  Mary M Mitchell; Allysha C Robinson; Trang Q Nguyen; Amy R Knowlton
Journal:  AIDS Behav       Date:  2015-11

5.  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

6.  Hospice caregivers' experiences with pain management: "I'm not a doctor, and I don't know if I helped her go faster or slower".

Authors:  Debra Parker Oliver; Elaine Wittenberg-Lyles; Karla Washington; Robin L Kruse; David L Albright; Paula K Baldwin; Amy Boxer; George Demiris
Journal:  J Pain Symptom Manage       Date:  2013-05-31       Impact factor: 3.612

7.  Exploring factors influencing the work-related morale for certified nursing assistants in hospice care: A structural equation modeling study.

Authors:  Jong-Yi Wang; Hui-Lin Zhuang; Jeng-Yuan Chiou; Chia-Woei Wang; Chen-Yu Wang; Li-Fan Liu
Journal:  PLoS One       Date:  2018-10-26       Impact factor: 3.240

  7 in total

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