Literature DB >> 18495415

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

Debra Parker Oliver1, Elaine Wittenberg-Lyles, George Demiris, Karla Washington, Davina Porock, Michele Day.   

Abstract

As patients are cared for in their homes by family caregivers, several challenges arise in effective pain and symptom management. Despite hospice's reputation as the gold standard for terminal care, there is still a need to improve pain management practices, including challenges that caregivers face, related to pain assessment, reluctance and fear of administering medication, noncompliance with pain medicine regimens, and hesitance to report pain. The hospice philosophy of care promotes service for both patients and their family by an interdisciplinary team, and total pain management is a goal of this care. The aim of this control phase of a larger National Cancer Institute-funded mixed methods study was to understand the current practice of hospice assessment and collaboration on informal caregiver issues related to pain management. This study of 30 hospice caregiver--patient dyads from one rural hospice found that 87% of caregivers indicated concern with at least one question on the Caregiver Pain Medicine Questionnaire. Interdisciplinary team discussions for 23 of the dyads were recorded over nine months for a total of 86 sessions. Although caregiver concerns were identified with the Caregiver Pain Medicine Questionnaire by the research team, there was only one discussion of caregiver pain-related concerns during the hospice team meeting. This despite the finding that 38% of the time involved in a patient discussion is spent on pain-related talk. These findings indicate an opportunity for improvement by hospice teams through focusing on caregiver assessment and intervention.

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Year:  2008        PMID: 18495415      PMCID: PMC2581443          DOI: 10.1016/j.jpainsymman.2007.11.005

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


  24 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

2.  Pain management at the end of life: often a difficult call.

Authors:  Michel Y Dubois; Perry G Fine; Daniel Fischberg; Betty Ferrell; Mary Lou Taylor
Journal:  Pain Med       Date:  2003-03       Impact factor: 3.750

3.  Is good 'quality of life' possible at the end of life? An explorative study of the experiences of a group of cancer patients in two different care cultures.

Authors:  E Sahlberg-Blom; B M Ternestedt; J E Johansson
Journal:  J Clin Nurs       Date:  2001-07       Impact factor: 3.036

4.  Pain management autobiographies and reluctance to use opioids for cancer pain management.

Authors:  Karen L Schumacher; Claudia West; Marylin Dodd; Steven M Paul; Debu Tripathy; Peter Koo; Christine A Miaskowski
Journal:  Cancer Nurs       Date:  2002-04       Impact factor: 2.592

5.  How are you feeling? Who wants to know? Patients' and oncologists' preferences for discussing health-related quality-of-life issues.

Authors:  S B Detmar; N K Aaronson; L D Wever; M Muller; J H Schornagel
Journal:  J Clin Oncol       Date:  2000-09-15       Impact factor: 44.544

6.  "Pain talk" in hospice and palliative care team meetings: an ethnography.

Authors:  Anne Arber
Journal:  Int J Nurs Stud       Date:  2006-06-09       Impact factor: 5.837

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.  Caregiver responses and needs. An ambulatory bone marrow transplant model.

Authors:  P M Grimm; K L Zawacki; V Mock; S Krumm; B B Frink
Journal:  Cancer Pract       Date:  2000 May-Jun

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.  Family perspectives on end-of-life care at the last place of care.

Authors:  Joan M Teno; Brian R Clarridge; Virginia Casey; Lisa C Welch; Terrie Wetle; Renee Shield; Vincent Mor
Journal:  JAMA       Date:  2004-01-07       Impact factor: 56.272

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  25 in total

1.  Effectiveness of a clinical intervention to eliminate barriers to pain and fatigue management in oncology.

Authors:  Tami Borneman; Marianna Koczywas; Virginia Sun; Barbara F Piper; Cynthia Smith-Idell; Benjamin Laroya; Gwen Uman; Betty Ferrell
Journal:  J Palliat Med       Date:  2011-01-27       Impact factor: 2.947

2.  Informal Hospice Caregiving: The Toll on Quality of Life.

Authors:  Hm Wilder; D Parker Oliver; G Demiris; K Washington
Journal:  J Soc Work End Life Palliat Care       Date:  2008-01-01

3.  Caregiver participation in hospice interdisciplinary team meetings via videophone technology: A pilot study to improve pain management.

Authors:  Debra Parker Oliver; George Demiris; Elaine Wittenberg-Lyles; Davina Porock; Jacqueline Collier; Antony Arthur
Journal:  Am J Hosp Palliat Care       Date:  2010-03-18       Impact factor: 2.500

Review 4.  YouTube as a tool for pain management with informal caregivers of cancer patients: a systematic review.

Authors:  Elaine Wittenberg-Lyles; Debra Parker Oliver; George Demiris; Jeff Swarz; Matthew Rendo
Journal:  J Pain Symptom Manage       Date:  2014-04-30       Impact factor: 3.612

5.  Perceptions about hospice from a community-based pilot study: lessons and findings.

Authors:  Daniel Van Dussen; Krystal L Culler; John G Cagle
Journal:  Am J Hosp Palliat Care       Date:  2011-01-04       Impact factor: 2.500

6.  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

7.  Informal hospice caregiver pain management concerns: a qualitative study.

Authors:  Marjorie Kelley; George Demiris; Huong Nguyen; Debra P Oliver; Elaine Wittenberg-Lyles
Journal:  Palliat Med       Date:  2013-04-23       Impact factor: 4.762

8.  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

9.  EMPOWER: an intervention to address barriers to pain management in hospice.

Authors:  John G Cagle; Sheryl Zimmerman; Lauren W Cohen; Laura S Porter; Laura C Hanson; David Reed
Journal:  J Pain Symptom Manage       Date:  2014-05-28       Impact factor: 3.612

10.  Conducting the ACTIVE randomized trial in hospice care: keys to success.

Authors:  Robin L Kruse; Debra Parker Oliver; Elaine Wittenberg-Lyles; George Demiris
Journal:  Clin Trials       Date:  2012-10-25       Impact factor: 2.486

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