Literature DB >> 16594221

Caregiver unmet needs, burden, and satisfaction in symptomatic advanced cancer patients at a Veterans Affairs (VA) medical center.

Shirley S Hwang1, Victor T Chang, Yvette Alejandro, Pamela Osenenko, Casaundra Davis, Janet Cogswell, Shanthi Srinivas, Basil Kasimis.   

Abstract

OBJECTIVES: Caregiver outcomes among those caring for symptomatic advanced cancer patients at VA Medical Centers have not been well reported. The purposes of this study were (1) to identify the caregiver characteristics and their unmet needs; (2) to examine the association between caregiver unmet needs, caregiver burden, and caregiver satisfaction; and (3) to identify the independent predictors of different caregiver outcomes.
METHODS: One hundred caregivers completed three caregiver outcomes instruments: Family Inventory of Needs (FIN), Care Strain Index (CSI), and Family Satisfaction with Advanced Cancer Care (FAMCARE). The caregivers' demographics and their function, depression, health status, and social support status as well as the caregivers' perception of the patients' unmet needs (PPUN) were obtained. Principal component analysis was performed to examine the underlying dimensions of caregiver outcome measures. Pearson correlation and stepwise multivariate regression analyses were performed.
RESULTS: The median number of unmet needs was 2 and the median CSI score was 4. Most of unmet needs were related to information needs (needing more information related to home care, finding help with the problems at home, and disease prognosis) and symptom management. The majority of caregivers were satisfied or very satisfied by the care patients received. Spouse caregivers (N = 60, 60%) were significantly older (p = 0.006) with higher unemployment rates (p = 0.001), higher depression scores (p = 0.04), and lower social support scores (p < 0.0001) than nonspouse caregivers (N = 40, 40%). The PPUN predicted caregiver burden and the presence of caregiver unmet needs independently. The presence of caregiver unmet needs was the only independent predictor of caregiver satisfaction. Caregivers with a high PPUN and higher depression score experienced a higher burden. SIGNIFICANCE OF THE RESEARCH: The caregiver outcome model is proposed and needs to be further validated in a new cohort of caregivers.

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Year:  2003        PMID: 16594221     DOI: 10.1017/s1478951503030475

Source DB:  PubMed          Journal:  Palliat Support Care        ISSN: 1478-9515


  31 in total

1.  Using mixed methods to assess how cancer patients' needs in relation to their relatives are met in the Danish health care system: a report from the population-based study "The Cancer Patient's World".

Authors:  Lone Ross; Morten Aagaard Petersen; Anna Thit Johnsen; Louise Hyldborg Lundstrøm; Line Lund; Mogens Groenvold
Journal:  Support Care Cancer       Date:  2012-04-25       Impact factor: 3.603

2.  Caregiver involvement in hospice interdisciplinary team meetings: a case study.

Authors:  Elaine Wittenberg-Lyles; Debra Parker Oliver; George Demiris; Bethany Petty; Michele Day
Journal:  J Palliat Care       Date:  2008       Impact factor: 2.250

3.  Psychometric Properties of a Spanish-Language Version of a Short-Form FAMCARE: Applications to Caregivers of Patients With Alzheimer's Disease and Related Dementias.

Authors:  Jeanne A Teresi; Katja Ocepek-Welikson; Mildred Ramirez; Katherine A Ornstein; Suzanne Bakken; Albert Siu; José A Luchsinger
Journal:  J Fam Nurs       Date:  2019-08-17       Impact factor: 3.818

4.  Managing Medications During Home Hospice Cancer Care: The Needs of Family Caregivers.

Authors:  Jennifer Tjia; Lee Ellington; Margaret F Clayton; Celeste Lemay; Maija Reblin
Journal:  J Pain Symptom Manage       Date:  2015-07-06       Impact factor: 3.612

5.  Satisfaction with oncology care among patients with advanced cancer and their caregivers.

Authors:  Breffni Hannon; Nadia Swami; Monika K Krzyzanowska; Natasha Leighl; Gary Rodin; Lisa W Le; Camilla Zimmermann
Journal:  Qual Life Res       Date:  2013-02-23       Impact factor: 4.147

6.  Family caregiver burden, skills preparedness, and quality of life in non-small cell lung cancer.

Authors:  Marcia Grant; Virginia Sun; Rebecca Fujinami; Rupinder Sidhu; Shirley Otis-Green; Gloria Juarez; Linda Klein; Betty Ferrell
Journal:  Oncol Nurs Forum       Date:  2013-07       Impact factor: 2.172

7.  Measuring patient satisfaction in oncology palliative care: psychometric properties of the FAMCARE-patient scale.

Authors:  Christopher Lo; Debika Burman; Gary Rodin; Camilla Zimmermann
Journal:  Qual Life Res       Date:  2009-06-10       Impact factor: 4.147

8.  A pilot study on the influence of an individualized and experiential training on cancer caregiver's self-efficacy in home care and symptom management.

Authors:  Cristina C Hendrix; Amy Abernethy; Rick Sloane; Joey Misuraca; Joseph Moore
Journal:  Home Healthc Nurse       Date:  2009-05

9.  The heart of the matter: health status of aged care clients receiving home- and community-based care.

Authors:  Deborah Yarmo-Roberts; Rosanne Laura Freak-Poli; Brad Cooper; Tim Noonan; Just Stolewinder; Christopher M Reid
Journal:  J Aging Res       Date:  2010-07-12

10.  Modifiable factors associated with caregiver burden among family caregivers of terminally ill Korean cancer patients.

Authors:  Seok-Joon Yoon; Jong-Sung Kim; Jin-Gyu Jung; Sung-Soo Kim; Samyong Kim
Journal:  Support Care Cancer       Date:  2014-01-16       Impact factor: 3.603

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