Literature DB >> 24992371

Informal caregiving of hospice patients.

Colin G Pottie1, Karen A Burch, Lori P Montross Thomas, Scott A Irwin.   

Abstract

BACKGROUND: Informal caregivers play a critical role in the provision of care to hospice patients. The care they provide often impacts their physical and psychological well-being.
OBJECTIVE: This study synthesized 58 articles pertaining to informal hospice caregiving, focusing on caregivers' satisfaction with hospice services, the physical and psychological well-being of caregivers, the predictors of caregivers' well-being, the direct impact of hospice services on caregivers, and the effectiveness of targeted interventions for hospice caregivers.
METHOD: A systematic literature review of journal articles published between 1985 and 2012 was conducted.
RESULTS: The studies reviewed found hospice caregivers to experience clinically significant levels of anxiety, depression, and stress; however, results for caregiver burden and quality of life were mixed. Caregivers' perceptions regarding the meaningfulness of care as well as their levels of social support were associated with enhanced psychological outcomes.
CONCLUSIONS: Beyond satisfaction with hospice services, the direct impact of standard hospice care on caregivers remains uncertain. Caregiver intervention studies have demonstrated promising outcomes signifying a need for additional investigations into hospice-specific interventions that improve caregiver outcomes. Additional research and resources are needed to assist hospice caregivers, with the ultimate goal of minimizing their psychiatric and physical morbidity and enhancing their caregiving and subsequent bereavement processes.

Entities:  

Mesh:

Year:  2014        PMID: 24992371      PMCID: PMC4842949          DOI: 10.1089/jpm.2013.0196

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


  74 in total

1.  The Stressful Caregiving Adult Reactions to Experiences of Dying (SCARED) Scale: a measure for assessing caregiver exposure to distress in terminal care.

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

2.  'The worst thing about hospice is that they talk about death': contrasting hospice decisions and experience among immigrant Central and South American Latinos with US-born White, non-Latino cancer caregivers.

Authors:  Barbara Kreling; Claire Selsky; Monique Perret-Gentil; Elmer E Huerta; Jeanne S Mandelblatt
Journal:  Palliat Med       Date:  2010-06       Impact factor: 4.762

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

4.  The psychological and physical health of hospice caregivers.

Authors:  Y Chentsova-Dutton; S Shuchter; S Hutchin; L Strause; K Burns; S Zisook
Journal:  Ann Clin Psychiatry       Date:  2000-03       Impact factor: 1.567

Review 5.  Family support in advanced cancer.

Authors:  B A Given; C W Given; S Kozachik
Journal:  CA Cancer J Clin       Date:  2001 Jul-Aug       Impact factor: 508.702

Review 6.  Cancer and caregiving: the impact on the caregiver's health.

Authors:  C Nijboer; R Tempelaar; R Sanderman; M Triemstra; R J Spruijt; G A van den Bos
Journal:  Psychooncology       Date:  1998 Jan-Feb       Impact factor: 3.894

7.  Caregiving as a risk factor for mortality: the Caregiver Health Effects Study.

Authors:  R Schulz; S R Beach
Journal:  JAMA       Date:  1999-12-15       Impact factor: 56.272

8.  Concerns of hospice patient caregivers.

Authors:  Marguerite Newton; Doris Bell; Sharon Lambert; Arleen Fearing
Journal:  ABNF J       Date:  2002 Nov-Dec

9.  Hope in the family caregiver of terminally ill people.

Authors:  K Herth
Journal:  J Adv Nurs       Date:  1993-04       Impact factor: 3.187

10.  Needs and experiences of caregivers for family members dying with Parkinson disease.

Authors:  Elizabeth R Goy; Julie H Carter; Linda Ganzini
Journal:  J Palliat Care       Date:  2008       Impact factor: 2.250

View more
  19 in total

1.  Gender Differences in Caregiving at End of Life: Implications for Hospice Teams.

Authors:  Karla T Washington; Kenneth C Pike; George Demiris; Debra Parker Oliver; David L Albright; Alexandria M Lewis
Journal:  J Palliat Med       Date:  2015-10-20       Impact factor: 2.947

2.  Mobile health technology and home hospice care: promise and pitfalls.

Authors:  Veerawat Phongtankuel; Ronald D Adelman; M C Reid
Journal:  Prog Palliat Care       Date:  2018-04-26

3.  Spousal Caregivers Are Caregiving Alone In The Last Years Of Life.

Authors:  Katherine A Ornstein; Jennifer L Wolff; Evan Bollens-Lund; Omari-Khalid Rahman; Amy S Kelley
Journal:  Health Aff (Millwood)       Date:  2019-06       Impact factor: 6.301

4.  The Prevalence and Risks for Depression and Anxiety in Hospice Caregivers.

Authors:  Debra Parker Oliver; Karla Washington; Jamie Smith; Aisha Uraizee; George Demiris
Journal:  J Palliat Med       Date:  2016-12-02       Impact factor: 2.947

5.  Patterns of stress and support in social support networks of in-home hospice cancer family caregivers.

Authors:  Jia-Wen Guo; Maija Reblin; Djin Tay; Lee Ellington; Anna C Beck; Kristin G Cloyes
Journal:  J Soc Pers Relat       Date:  2021-06-16

6.  New antidepressant utilization pre- and post-bereavement: a population-based study of partners and adult children.

Authors:  Katherine A Ornstein; Melissa Aldridge; Christina Gillezeau; Marie S Kristensen; Tatjana Gazibara; Mogens Groenvold; Lau C Thygesen
Journal:  Soc Psychiatry Psychiatr Epidemiol       Date:  2020-03-17       Impact factor: 4.328

7.  Why Do Home Hospice Patients Return to the Hospital? A Study of Hospice Provider Perspectives.

Authors:  Veerawat Phongtankuel; Benjamin A Scherban; Manney C Reid; Amanda Finley; Angela Martin; Jeanne Dennis; Ronald D Adelman
Journal:  J Palliat Med       Date:  2016-01       Impact factor: 2.947

8.  Positive emotion communication: Fostering well-being at end of life.

Authors:  Alexandra L Terrill; Lee Ellington; Kevin K John; Seth Latimer; Jiayun Xu; Maija Reblin; Margaret F Clayton
Journal:  Patient Educ Couns       Date:  2017-11-28

9.  A National Profile Of End-Of-Life Caregiving In The United States.

Authors:  Katherine A Ornstein; Amy S Kelley; Evan Bollens-Lund; Jennifer L Wolff
Journal:  Health Aff (Millwood)       Date:  2017-07-01       Impact factor: 6.301

10.  Communication among cancer patients, caregivers, and hospice nurses: Content, process and change over time.

Authors:  Lee Ellington; Margaret F Clayton; Maija Reblin; Gary Donaldson; Seth Latimer
Journal:  Patient Educ Couns       Date:  2017-09-22
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.