Literature DB >> 17187538

Bereaved hospice caregivers' perceptions of the end-of-life care communication process and the involvement of health care professionals.

Ellen L Csikai1.   

Abstract

BACKGROUND: This study was conducted to gain an understanding of bereaved hospice family caregivers' perceptions of the communication process from initial discussion of the need for end-of-life care and hospice through the decision to choose hospice and the transition home.
METHODS: One hundred eight bereaved hospice caregivers that were 36 months postpatient death responded to a quantitative mailed survey. Aspects of the end-of-life care communication process, including involvement of health care professionals at each step, were assessed.
RESULTS: Serious illness and the need for hospice care were first mentioned to patients and caregivers by physicians. Often the caregivers recalled only one meeting in which hospice was discussed. Other than the physicians, social workers were the professionals most often present in at least one of these meetings. Nurses and social workers were both perceived to be helpful in the transition to home hospice. Social workers were reported to be most comfortable with discussion of end-of-life care, most knowledgeable, and most available during the communication process that led to a decision about end-of-life care. Suggestions that these caregivers had to improve communication with health care professionals were categorized from responses to an open-ended survey question as: the need to discuss vital information earlier and what to expect for care at end stage; be more forthcoming about reality of death; and treat people as individuals.
CONCLUSIONS: Although many health care professionals play a role in the communication and transition to hospice care, physicians and social workers were found to be pivotal participants in this process. A coordinated team approach to end-of-life communication and decision-making may facilitate the process and possibly lead to increased and earlier referral to hospice.

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Year:  2006        PMID: 17187538     DOI: 10.1089/jpm.2006.9.1300

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  8 in total

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Journal:  Patient Educ Couns       Date:  2018-12-12

2.  Quality of palliative care at US hospices: results of a national survey.

Authors:  Melissa D A Carlson; Colleen Barry; Mark Schlesinger; Ruth McCorkle; R Sean Morrison; Emily Cherlin; Jeph Herrin; Jennifer Thompson; Martha L Twaddle; Elizabeth H Bradley
Journal:  Med Care       Date:  2011-09       Impact factor: 2.983

3.  Challenges Facing Families at the End of Life in Three Settings.

Authors:  Karen A Kehl; Karin T Kirchhoff; Betty J Kramer; Cyndi Hovland-Scafe
Journal:  J Soc Work End Life Palliat Care       Date:  2009-07-01

4.  Development of a Web-based educational intervention to improve cross-cultural communication among hospice providers.

Authors:  Ardith Z Doorenbos; Taryn Lindhorst; Stephanie Myers Schim; Eileen Van Schaik; George Demiris; Hope A Wechkin; J Randall Curtis
Journal:  J Soc Work End Life Palliat Care       Date:  2010

5.  Does caregiver knowledge matter for hospice enrollment and beyond? Pilot study of minority hospice patients.

Authors:  Kyusuk Chung; Elizabeth Lehr Essex; Linda Samson
Journal:  Am J Hosp Palliat Care       Date:  2009-02-19       Impact factor: 2.500

6.  Home Hospice Caregivers' Perceived Information Needs.

Authors:  Ariel Shalev; Veerawat Phongtankuel; M Carrington Reid; Sara J Czaja; Ritchell Dignam; Rosemary Baughn; Matthew Newmark; Holly G Prigerson; Jeanne Teresi; Ronald D Adelman
Journal:  Am J Hosp Palliat Care       Date:  2018-10-09       Impact factor: 2.500

7.  Perspectives of Cardiac Care Unit Nursing Staff about Developing Hospice Services in Iran for Terminally ill Cardiovascular Patients: A Qualitative Study.

Authors:  Saber Azami-Aghdash; Morteza Ghojazadeh; Mohammad Naghavi-Behzad; Shahin Imani; Mir Hossein Aghaei
Journal:  Indian J Palliat Care       Date:  2015 Jan-Apr

8.  Perspective of patients, patients' families, and healthcare providers towards designing and delivering hospice care services in a middle income Country.

Authors:  Saber Azami-Aghdash; Morteza Ghojazadeh; Mir Hossein Aghaei; Mohammad Naghavi-Behzad; Zoleikha Asgarlo
Journal:  Indian J Palliat Care       Date:  2015 Sep-Dec
  8 in total

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