Literature DB >> 24295096

Hospice caregiver depression: the evidence surrounding the greatest pain of all.

Debra Parker Oliver1, David L Albright, Karla Washington, Elaine Wittenberg-Lyles, Ashley Gage, Megan Mooney, George Demiris.   

Abstract

Terminal illness affects the entire family, both the one with the illness and their loved ones. These loved ones must deal not only with the loss but with the challenges of managing daily care. The purpose of the systematic review of the peer-reviewed literature was to identify and explore depression and related interventions for caregivers of hospice patients. While the prevalence of depression reported in the identified studies of hospice caregivers ranges from 26-57%, few interventions specific to this population have been tested and the research methods have been only moderately rigorous.

Entities:  

Mesh:

Year:  2013        PMID: 24295096      PMCID: PMC3849709          DOI: 10.1080/15524256.2013.846891

Source DB:  PubMed          Journal:  J Soc Work End Life Palliat Care        ISSN: 1552-4264


  15 in total

1.  Assessing and managing depression in the terminally ill patient. ACP-ASIM End-of-Life Care Consensus Panel. American College of Physicians - American Society of Internal Medicine.

Authors:  S D Block
Journal:  Ann Intern Med       Date:  2000-02-01       Impact factor: 25.391

Review 2.  Informal primary carers of stroke survivors living at home-challenges, satisfactions and coping: a systematic review of qualitative studies.

Authors:  Nan Greenwood; Ann Mackenzie; Geoffrey C Cloud; Nikki Wilson
Journal:  Disabil Rehabil       Date:  2009       Impact factor: 3.033

3.  Feasibility of a telephone-based counseling program for informal caregivers of hospice patients.

Authors:  Kristin M Kilbourn; Allison Costenaro; Shannon Madore; Kate Deroche; Derek Anderson; Tarah Keech; Jean S Kutner
Journal:  J Palliat Med       Date:  2011-10-03       Impact factor: 2.947

4.  Exploring factors that influence informal caregiving in medication management for home hospice patients.

Authors:  Denys T Lau; Rebecca Berman; Leslie Halpern; A Simon Pickard; Robert Schrauf; Whitney Witt
Journal:  J Palliat Med       Date:  2010-09       Impact factor: 2.947

5.  Improving hospice outcomes through systematic assessment: a clinical trial.

Authors:  Susan C McMillan; Brent J Small; William E Haley
Journal:  Cancer Nurs       Date:  2011 Mar-Apr       Impact factor: 2.592

6.  Hospice providers' key approaches to support informal caregivers in managing medications for patients in private residences.

Authors:  Denys T Lau; Brian Joyce; Marla L Clayman; Sydney Dy; Linda Ehrlich-Jones; Linda Emanuel; Joshua Hauser; Judith Paice; Joseph W Shega
Journal:  J Pain Symptom Manage       Date:  2012-06       Impact factor: 3.612

7.  Psychometric properties of the Hospital Anxiety and Depression Scale in family caregivers of palliative care patients.

Authors:  Karla Gough; Peter Hudson
Journal:  J Pain Symptom Manage       Date:  2008-09-11       Impact factor: 3.612

8.  Closing the quality gap: revisiting the state of the science (vol. 8: improving health care and palliative care for advanced and serious illness).

Authors:  Sydney M Dy; Rebecca Aslakson; Renee F Wilson; Oluwakemi A Fawole; Brandyn D Lau; Kathryn A Martinez; Daniela Vollenweider; Colleen Apostol; Eric B Bass
Journal:  Evid Rep Technol Assess (Full Rep)       Date:  2012-10

Review 9.  Interventions to facilitate family caregiving at the end of life.

Authors:  Susan C McMillan
Journal:  J Palliat Med       Date:  2005       Impact factor: 2.947

10.  Depression symptomatology and diagnosis: discordance between patients and physicians in primary care settings.

Authors:  Chizobam Ani; Mohsen Bazargan; David Hindman; Douglas Bell; Muhammad A Farooq; Lutful Akhanjee; Francis Yemofio; Richard Baker; Michael Rodriguez
Journal:  BMC Fam Pract       Date:  2008-01-03       Impact factor: 2.497

View more
  15 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.  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

3.  Unique characteristics of informal hospice cancer caregiving.

Authors:  Karla T Washington; Kenneth C Pike; George Demiris; Debra Parker Oliver
Journal:  Support Care Cancer       Date:  2014-12-30       Impact factor: 3.603

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.  Anxiety, Depression, Quality of Life, Caregiver Burden, and Perceptions of Caregiver-Centered Communication among Black and White Hospice Family Caregivers.

Authors:  Lauren T Starr; Karen Bullock; Karla Washington; Subhash Aryal; Debra Parker Oliver; George Demiris
Journal:  J Palliat Med       Date:  2021-11-18       Impact factor: 2.947

6.  Reaction to Caregiving by Hospice Caregivers Upon Enrollment.

Authors:  David L Albright; Debra Parker Oliver; George Demiris
Journal:  Am J Hosp Palliat Care       Date:  2014-04-16       Impact factor: 2.500

7.  Psychological distress, health, and socio-economic factors in caregivers of terminally ill patients: a nationwide population-based cohort study.

Authors:  Mette Kjaergaard Nielsen; Mette Asbjoern Neergaard; Anders Bonde Jensen; Flemming Bro; Mai-Britt Guldin
Journal:  Support Care Cancer       Date:  2016-02-18       Impact factor: 3.603

8.  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

9.  Reflections of Hospice Staff Members About Educating Hospice Family Caregivers Through Telenovela.

Authors:  Dulce M Cruz-Oliver; Martha Abshire; Chakra Budhathoki; Debra Parker Oliver; Angelo Volandes; Thomas J Smith
Journal:  Am J Hosp Palliat Care       Date:  2020-07-08       Impact factor: 2.500

10.  Perceived Benefits and Burdens of Participation for Caregivers of Cancer Patients in Hospice Clinical Trials: A Pilot Study.

Authors:  Debra Parker Oliver; Jacquelyn J Benson; Connie Ulrich; Karla T Washington; Abigail J Rolbiecki; Patrick White; Jamie B Smith; Christina Lero; Olivia J Landon; George Demiris
Journal:  J Pain Symptom Manage       Date:  2020-11-06       Impact factor: 5.576

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.