Literature DB >> 1913486

Caregiver burden and unmet patient needs.

K Siegel1, V H Raveis, P Houts, V Mor.   

Abstract

Four-hundred eighty-three patients with cancer and their informal caregivers were studied. Patients reported on met and unmet needs in personal care activities (bathing and dressing), instrumental activities (heavy and light housekeeping, cooking, shopping), transportation (medical and general), and home health care (health/treatment assistance). A minority (18.9%) experienced an unmet need. Hierarchical logistic regression was used to identify significant predictors of any unmet need. Patients were more likely to report any unmet needs when their illness/treatment resulted in restricted activity days, when their financial resources were reduced enough for them to apply for Medicaid or Public Assistance, or when their caregivers were not their spouses. Although in general, the likelihood of an unmet need decreased as the number of domains of assistance provided by the caregiver increased, if that care was associated with a high level of burden, the odds of a patient reporting an unmet need actually increased.

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Year:  1991        PMID: 1913486     DOI: 10.1002/1097-0142(19910901)68:5<1131::aid-cncr2820680541>3.0.co;2-n

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  33 in total

1.  Korean version of the caregiver quality of life index-cancer (CQOLC-K).

Authors:  Young Sun Rhee; Dong Ok Shin; Kwang Mi Lee; Han Jin Yu; Joung Wha Kim; Soon Ok Kim; Ran Lee; Yeon Ok Lee; Nam Shin Kim; Young Ho Yun
Journal:  Qual Life Res       Date:  2005-04       Impact factor: 4.147

2.  Confirmatory and exploratory factor analysis of the caregiver quality of life index-cancer with Turkish samples.

Authors:  Zeynep C Ozer; Mehmet Z Firat; Hicran A Bektas
Journal:  Qual Life Res       Date:  2009-06-25       Impact factor: 4.147

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.  Role recognition and changes to self-identity in family caregivers of people with advanced cancer: a qualitative study.

Authors:  Anna Ugalde; Meinir Krishnasamy; Penelope Schofield
Journal:  Support Care Cancer       Date:  2011-05-25       Impact factor: 3.603

Review 5.  Pain management in the home.

Authors:  Nessa Coyle
Journal:  Curr Pain Headache Rep       Date:  2005-08

6.  A psychometric validation study of the Quality of Life and FAMCARE scales in Turkish cancer family caregivers.

Authors:  Gulbeyaz Can; Semiha Akin; Adnan Aydiner; Kursat Ozdilli; Umran Oskay; Zehra Durna
Journal:  Qual Life Res       Date:  2011-02-23       Impact factor: 4.147

7.  Rapid assessment of psychosocial well-being: are computers the way forward in a clinical setting?

Authors:  Allison Boyes; Sallie Newell; Afaf Girgis
Journal:  Qual Life Res       Date:  2002-02       Impact factor: 4.147

8.  Unmet needs of patients with systemic lupus erythematosus.

Authors:  Sharon Danoff-Burg; Fred Friedberg
Journal:  Behav Med       Date:  2009       Impact factor: 3.104

Review 9.  Care for the cancer caregiver: a systematic review.

Authors:  Allison J Applebaum; William Breitbart
Journal:  Palliat Support Care       Date:  2012-10-10

10.  The formal mental health care burden among recently deinstitutionalized patients.

Authors:  P Deb; A M Holmes
Journal:  J Behav Health Serv Res       Date:  1998-08       Impact factor: 1.505

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