Literature DB >> 19779584

Informal Hospice Caregiving: The Toll on Quality of Life.

Hm Wilder, D Parker Oliver, G Demiris, K Washington.   

Abstract

Entities:  

Year:  2008        PMID： 19779584      PMCID： PMC2749275          DOI： 10.1080/15524250903081566

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


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  38 in total

1.  Quality of life instruments for caregivers of patients with cancer: a review of their psychometric properties.

Authors:  Ben Edwards; Lerma Ung
Journal:  Cancer Nurs       Date:  2002-10       Impact factor: 2.592

2.  Health related quality of life: a changing construct?

Authors:  Jürg Bernhard; Adam Lowy; Natascha Mathys; Richard Herrmann; Christoph Hürny
Journal:  Qual Life Res       Date:  2004-09       Impact factor: 4.147

3.  Symptom assessment of patients with advanced cancer and AIDS and their family caregivers: the results of a quality-of-life pilot study.

Authors:  Deborah Witt Sherman; Xiang Y Ye; Christina Beyer McSherry; Valerie Parkas; Miriam Calabrese; Maria Gatto
Journal:  Am J Hosp Palliat Care       Date:  2007 Oct-Nov       Impact factor: 2.500

4.  The use of quality of life data in clinical practice.

Authors:  J Morris; D Perez; B McNoe
Journal:  Qual Life Res       Date:  1998-01       Impact factor: 4.147

5.  Quality-of-life predictors for caregivers at 1 and 6 months poststroke: Results of path analyses.

Authors:  Marieke Van Puymbroeck; Maude R Rittman
Journal:  J Rehabil Res Dev       Date:  2005 Nov-Dec

Review 6.  Coping theory and research: past, present, and future.

Authors:  R S Lazarus
Journal:  Psychosom Med       Date:  1993 May-Jun       Impact factor: 4.312

7.  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

8.  Effects of placement and bereavement on psychological well-being and cardiovascular risk in Alzheimer's caregivers: a longitudinal analysis.

Authors:  Brent T Mausbach; Kirstin Aschbacher; Thomas L Patterson; Roland von Känel; Joel E Dimsdale; Paul J Mills; Sonia Ancoli-Israel; Igor Grant
Journal:  J Psychosom Res       Date:  2007-04       Impact factor: 3.006

9.  Caregiving at the end of life: Perceptions of health care quality and quality of life among patients and caregivers.

Authors:  David A Fleming; Vanessa B Sheppard; Patricia A Mangan; Kathryn L Taylor; Michelle Tallarico; Inez Adams; Jane Ingham
Journal:  J Pain Symptom Manage       Date:  2006-05       Impact factor: 3.612

10.  Family caregiver burden: results of a longitudinal study of breast cancer patients and their principal caregivers.

Authors:  Eva Grunfeld; Doug Coyle; Timothy Whelan; Jennifer Clinch; Leonard Reyno; Craig C Earle; Andrew Willan; Raymond Viola; Marjorie Coristine; Teresa Janz; Robert Glossop
Journal:  CMAJ       Date:  2004-06-08       Impact factor: 8.262
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  11 in total

Review 1.  Hospice caregiver depression: the evidence surrounding the greatest pain of all.

Authors:  Debra Parker Oliver; David L Albright; Karla Washington; Elaine Wittenberg-Lyles; Ashley Gage; Megan Mooney; George Demiris
Journal:  J Soc Work End Life Palliat Care       Date:  2013

Review 2.  Informal caregiving of hospice patients.

Authors:  Colin G Pottie; Karen A Burch; Lori P Montross Thomas; Scott A Irwin
Journal:  J Palliat Med       Date:  2014-07       Impact factor: 2.947

3.  The Social Convoy for Family Caregivers Over the Course of Hospice.

Authors:  David L Albright; Karla Washington; Debra Parker-Oliver; Alexandria Lewis; Robin L Kruse; George Demiris
Journal:  J Pain Symptom Manage       Date:  2015-11-03       Impact factor: 3.612

4.  Behind the doors of home hospice patients: A secondary qualitative analysis of hospice nurse communication with patients and families.

Authors:  Debra Parker Oliver; Jessica Tappana; Karla T Washington; Abigail Rolbiecki; Kevin Craig; George Demiris; Collyn Schafer; Mumeenat Winjobi; Margaret F Clayton; Maija Reblin; Lee Ellington
Journal:  Palliat Support Care       Date:  2019-10

5.  Reciprocal suffering: caregiver concerns during hospice care.

Authors:  Elaine Wittenberg-Lyles; George Demiris; Debra Parker Oliver; Stephanie Burt
Journal:  J Pain Symptom Manage       Date:  2010-12-13       Impact factor: 3.612

6.  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

7.  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

8.  Understanding social support burden among family caregivers.

Authors:  Elaine Wittenberg-Lyles; Karla Washington; George Demiris; Debra Parker Oliver; Sara Shaunfield
Journal:  Health Commun       Date:  2013-12-17

9.  Reporting of "quality of life": a systematic review and quantitative analysis of research publications in palliative care journals.

Authors:  Senthil P Kumar
Journal:  Indian J Palliat Care       Date:  2012-01

Review 10.  Psychometric properties of carer-reported outcome measures in palliative care: A systematic review.

Authors:  Charlotte T J Michels; Mary Boulton; Astrid Adams; Bee Wee; Michele Peters
Journal:  Palliat Med       Date:  2015-09-25       Impact factor: 4.762
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