Literature DB >> 23731855

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

Debra Parker Oliver1, Elaine Wittenberg-Lyles, Karla Washington, Robin L Kruse, David L Albright, Paula K Baldwin, Amy Boxer, George Demiris.   

Abstract

CONTEXT: Those caring for their loved ones in hospice experience tremendous stress, being faced with numerous decisions as they work to manage the pain experienced by their loved one. Although hospice care teams create pain management strategies, it is the role of the caregiver to implement these plans.
OBJECTIVES: The purpose of this study was to further understand the hospice caregiver experience relating to pain management.
METHODS: Semistructured interviews with 146 caregivers provided data for the study. Responses to seven questions asking for a ranking of end-of-life pain management indicated a less than ideal experience. Available narratives from 38 caregivers were analyzed for themes related to further understanding of the concerns.
RESULTS: Five themes were identified in the data including difficulty with administration of pain medicines, concerns about side effects of medications, insecurity with pain assessment, frustrations with communication among health care team members, and memories of unrelieved pain.
CONCLUSION: These findings should raise concern among hospice professionals, whose commitment is to the management of pain, including emotional pain, with a focus on both the patient and the family as a unit of care. These data clearly suggest that hospice providers have an opportunity to be sensitive to perceptions held by caregivers regarding pain management. Effective planning for pain control must incorporate the values and beliefs not only of each patient but also of the family caregiver.
Copyright © 2013 U.S. Cancer Pain Relief Committee. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Hospice; caregivers; pain

Mesh:

Year:  2013        PMID: 23731855      PMCID: PMC3795892          DOI: 10.1016/j.jpainsymman.2013.02.011

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


  35 in total

1.  Symptom burden at the end of life: hospice providers' perceptions.

Authors:  J S Kutner; C T Kassner; D E Nowels
Journal:  J Pain Symptom Manage       Date:  2001-06       Impact factor: 3.612

Review 2.  Differences between caregivers and noncaregivers in psychological health and physical health: a meta-analysis.

Authors:  Martin Pinquart; Silvia Sörensen
Journal:  Psychol Aging       Date:  2003-06

Review 3.  Access to opioid analgesics and pain relief for patients with cancer.

Authors:  Shalini Dalal; Eduardo Bruera
Journal:  Nat Rev Clin Oncol       Date:  2013-01-15       Impact factor: 66.675

4.  Hospice home care pain management. Four critical variables.

Authors:  C Austin; C P Cody; P J Eyres; E A Hefferin; R W Krasnow
Journal:  Cancer Nurs       Date:  1986-04       Impact factor: 2.592

5.  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

6.  Is opiate compliance a problem in cancer pain? A survey of health-care professionals' views.

Authors:  Syed Q Abbas; Zafar Abbas
Journal:  Int J Palliat Nurs       Date:  2003-02

7.  Family caregiving in hospice: effects on psychological and health functioning among spousal caregivers of hospice patients with lung cancer or dementia.

Authors:  W E Haley; L A LaMonde; B Han; S Narramore; R Schonwetter
Journal:  Hosp J       Date:  2001

8.  The influence of cancer patients' symptoms and functional states on patients' depression and family caregivers' reaction and depression.

Authors:  C W Given; M Stommel; B Given; J Osuch; M E Kurtz; J C Kurtz
Journal:  Health Psychol       Date:  1993-07       Impact factor: 4.267

9.  The self-efficacy of family caregivers for helping cancer patients manage pain at end-of-life.

Authors:  Francis J Keefe; Tim A Ahles; Laura S Porter; Linda M Sutton; Colleen M McBride; Mary Susan Pope; Elizabeth T McKinstry; Charlotte P Furstenberg; JoAnn Dalton; Donald H Baucom
Journal:  Pain       Date:  2003-05       Impact factor: 6.961

10.  Barriers to caregiver administration of pain medication in hospice care.

Authors:  Marijo Letizia; Steve Creech; Ellen Norton; Marie Shanahan; Lori Hedges
Journal:  J Pain Symptom Manage       Date:  2004-02       Impact factor: 3.612

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  11 in total

1.  Managing Medications During Home Hospice Cancer Care: The Needs of Family Caregivers.

Authors:  Jennifer Tjia; Lee Ellington; Margaret F Clayton; Celeste Lemay; Maija Reblin
Journal:  J Pain Symptom Manage       Date:  2015-07-06       Impact factor: 3.612

2.  RDOS-family: a guided learning tool for layperson assessment of respiratory distress.

Authors:  Margaret L Campbell; Thomas N Templin
Journal:  J Palliat Med       Date:  2014-08-12       Impact factor: 2.947

3.  Communicating Caregivers' Challenges With Cancer Pain Management: An Analysis of Home Hospice Visits.

Authors:  Claire J Han; Nai-Ching Chi; Soojeong Han; George Demiris; Debra Parker-Oliver; Karla Washington; Margaret F Clayton; Maija Reblin; Lee Ellington
Journal:  J Pain Symptom Manage       Date:  2018-01-31       Impact factor: 3.612

4.  Pain Management Concerns From the Hospice Family Caregivers' Perspective.

Authors:  Nai-Ching Chi; George Demiris; Kenneth C Pike; Karla Washington; Debra Parker Oliver
Journal:  Am J Hosp Palliat Care       Date:  2017-09-06       Impact factor: 2.500

5.  Pain in Hospice Patients With Dementia: The Informal Caregiver Experience.

Authors:  Robin Tarter; George Demiris; Kenneth Pike; Karla Washington; Debra Parker Oliver
Journal:  Am J Alzheimers Dis Other Demen       Date:  2016-06-14       Impact factor: 2.035

6.  Hospice Family Caregiver Involvement in Care Plan Meetings: A Mixed-Methods Randomized Controlled Trial.

Authors:  Debra Parker Oliver; George Demiris; Karla Washington; Robin L Kruse; Greg Petroski
Journal:  Am J Hosp Palliat Care       Date:  2016-07-27       Impact factor: 2.500

7.  Testing the factorial validity of scores from the caregiver pain medicine questionnaire.

Authors:  David L Albright; Robin L Kruse; Debra Parker Oliver; Karla Washington; John Cagle; George Demiris
Journal:  J Pain Symptom Manage       Date:  2013-11-15       Impact factor: 3.612

8.  Associations Between Hospice Care and Scary Family Caregiver Experiences.

Authors:  Elizabeth A Luth; Paul K Maciejewski; Veerawat Phongtankuel; Jiehui Xu; Holly G Prigerson
Journal:  J Pain Symptom Manage       Date:  2020-10-07       Impact factor: 3.612

9.  Survival in hospice patients with dementia: the effect of home hospice and nurse visits.

Authors:  Elizabeth A Luth; David J Russell; Jiehui Cici Xu; Bonnie Lauder; Miriam B Ryvicker; Ritchell R Dignam; Rosemary Baughn; Kathryn H Bowles; Holly G Prigerson
Journal:  J Am Geriatr Soc       Date:  2021-02-19       Impact factor: 7.538

Review 10.  The Experience of Caregivers Living with Cancer Patients: A Systematic Review and Meta-Synthesis.

Authors:  Peeranuch LeSeure; Supaporn Chongkham-Ang
Journal:  J Pers Med       Date:  2015-11-19
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