Literature DB >> 16716871

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

David A Fleming1, Vanessa B Sheppard, Patricia A Mangan, Kathryn L Taylor, Michelle Tallarico, Inez Adams, Jane Ingham.   

Abstract

This study explored the association between perceptions of health care quality and quality of life in patients with advanced metastatic cancer and their informal caregivers (n=39). Patients' and caregivers' perceptions of health care quality, mental health, health-related quality of life, symptoms, and burden were measured. The key findings included the following: 1) patients' mental health and depression scores correlated with those of caregivers, suggesting that the mental health of patients and their caregivers are associated; 2) patients and caregivers shared similar perceptions regarding health care quality; 3) the presence of depression in caregivers correlated with caregivers being less satisfied with the health care being given to their patients (this correlation did not exist for patients, a finding that may be due in part to the protective buffering effect that caregivers provide their patients as illness progresses); and 4) a modified Primary Care Assessment Survey, originally designed for primary care patients, was a useful measure of health care assessment for both patients and caregivers. These data suggest that patients with advanced disease and their caregivers share similar perceptions and evolve as a "unit of care," and caregivers, as unique and important members of the patient's health care team, are also in need of care. When depressed, caregivers may unilaterally lose trust by becoming less satisfied with the quality of health care being provided to their patients.

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Year:  2006        PMID: 16716871     DOI: 10.1016/j.jpainsymman.2005.09.002

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


  20 in total

1.  Dyadic coping in metastatic breast cancer.

Authors:  Hoda Badr; Cindy L Carmack; Deborah A Kashy; Massimo Cristofanilli; Tracey A Revenson
Journal:  Health Psychol       Date:  2010-03       Impact factor: 4.267

Review 2.  Caregiver Well-being and the Quality of Cancer Care.

Authors:  Kristin Litzelman
Journal:  Semin Oncol Nurs       Date:  2019-06-20       Impact factor: 2.315

3.  Support needs of informal hospice caregivers: a qualitative study.

Authors:  Jean Kutner; Kristin M Kilbourn; Allison Costenaro; Courtney A Lee; Carolyn Nowels; Jenny L Vancura; Derek Anderson; Tarah Ellis Keech
Journal:  J Palliat Med       Date:  2009-12       Impact factor: 2.947

4.  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

Review 5.  Measuring Experience With End-of-Life Care: A Systematic Literature Review.

Authors:  Jessica Penn Lendon; Sangeeta C Ahluwalia; Anne M Walling; Karl A Lorenz; Oluwatobi A Oluwatola; Rebecca Anhang Price; Denise Quigley; Joan M Teno
Journal:  J Pain Symptom Manage       Date:  2014-12-24       Impact factor: 3.612

6.  Nonsymptomatic Factors More Strongly Associated with High-Quality End-of-Life Care than Symptomatic Factors for Community-Dwelling Older Adults with Multiple Chronic Conditions.

Authors:  Gayle Kricke; Donna Woods; Alicia Arbaje; Neil Jordan
Journal:  J Palliat Med       Date:  2019-01-07       Impact factor: 2.947

7.  Correlates of Triple Negative Breast Cancer and Chemotherapy Patterns in Black and White Women With Breast Cancer.

Authors:  Vanessa B Sheppard; Luciane R Cavalli; Chiranjeev Dash; Yasmine M Kanaan; Asma A Dilawari; Sara Horton; Kepher H Makambi
Journal:  Clin Breast Cancer       Date:  2017-01-06       Impact factor: 3.225

Review 8.  Schizophrenia: Impact on Family Dynamics.

Authors:  Alejandra Caqueo-Urízar; Mar Rus-Calafell; Thomas K J Craig; Matias Irarrazaval; Alfonso Urzúa; Laurent Boyer; David R Williams
Journal:  Curr Psychiatry Rep       Date:  2017-01       Impact factor: 5.285

9.  How much do cancer-related symptoms contribute to health-related quality of life in lung and colorectal cancer patients? A report from the Cancer Care Outcomes Research and Surveillance (CanCORS) Consortium.

Authors:  Kelly M Kenzik; Patricia A Ganz; Michelle Y Martin; Laura Petersen; Ron D Hays; Neeraj Arora; Maria Pisu
Journal:  Cancer       Date:  2015-04-17       Impact factor: 6.860

10.  Narrowing racial gaps in breast cancer chemotherapy initiation: the role of the patient-provider relationship.

Authors:  Vanessa B Sheppard; Claudine Isaacs; George Luta; Shawna C Willey; Marc Boisvert; Felicity W K Harper; Karen Smith; Sara Horton; Minetta C Liu; Yvonne Jennings; Fikru Hirpa; Felicia Snead; Jeanne S Mandelblatt
Journal:  Breast Cancer Res Treat       Date:  2013-04-16       Impact factor: 4.872

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