Family Caregiver Burden Among Advanced Cancer Patients: Findings from the CONNECT Trial (RP421)

2020 ◽  
Vol 60 (1) ◽  
pp. 226-227
Author(s):  
Wagahta Semere ◽  
Andrew Althouse ◽  
Douglas White ◽  
Robert Arnold ◽  
Thomas Smith ◽  
...  
2009 ◽  
Vol 32 (1) ◽  
pp. 73-81 ◽  
Author(s):  
Karen F. Bowman ◽  
Julia H. Rose ◽  
Rosanne M. Radziewicz ◽  
Elizabeth E. O'Toole ◽  
Rose A. Berila

1999 ◽  
Vol 17 (11) ◽  
pp. 3621-3630 ◽  
Author(s):  
Cheryl L. Nekolaichuk ◽  
Thomas O. Maguire ◽  
Maria Suarez-Almazor ◽  
W. Todd Rogers ◽  
Eduardo Bruera

PURPOSE: The purpose of this study was to examine the reliability of symptom assessments in advanced cancer patients under various conditions, including multiple raters (patients, nurses, and family caregivers), occasions, and symptoms. PATIENTS AND METHODS: The study sample consisted of 32 advanced cancer patients admitted to a tertiary palliative care unit. Symptom assessments were completed for each patient on two separate occasions, approximately 24 hours apart. On each occasion, the patient, the primary care nurse, and a primary family caregiver independently completed an assessment using the Edmonton Symptom Assessment System (ESAS). The ESAS is a nine-item visual analogue scale for assessing symptoms in palliative patients. The reliability of the assessments (r) was examined using generalizability theory. RESULTS: Three important findings emerged from this analysis. First, the analysis of individual symptom ratings provided a more meaningful representation of the symptom experience than total symptom distress ratings. Secondly, patients, nurses, and caregivers varied in their ratings across different patients, as well as in their ratings of shortness of breath, which may have been a result of individual rater variability. Finally, reliability estimates (r), based on a single rater and one occasion, were less than .70 for all symptoms, except appetite. These estimates improved substantially (r ≥ .70) for all symptoms except anxiety and shortness of breath, using three raters on a single occasion or two raters across two occasions. CONCLUSION: The findings from this study reinforce the need for the development of an integrated symptom assessment approach that combines patient and proxy assessments. Further research is needed to explore individual differences among raters.


2003 ◽  
Vol 1 (4) ◽  
pp. 319-329 ◽  
Author(s):  
SHIRLEY S. HWANG ◽  
VICTOR T. CHANG ◽  
YVETTE ALEJANDRO ◽  
PAMELA OSENENKO ◽  
CASAUNDRA DAVIS ◽  
...  

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.


2016 ◽  
Vol 5 (5) ◽  
pp. 853-862 ◽  
Author(s):  
J. Nicholas Dionne‐Odom ◽  
Jay G. Hull ◽  
Michelle Y. Martin ◽  
Kathleen Doyle Lyons ◽  
Anna T. Prescott ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document