Patient-Reported Quality of Supportive Care Among Patients With Colorectal Cancer in the Veterans Affairs Health Care System
- Michelle van Ryn⇑,
- Sean M. Phelan,
- Neeraj K. Arora,
- David A. Haggstrom,
- George L. Jackson,
- S. Yousuf Zafar,
- Joan M. Griffin,
- Leah L. Zullig,
- Dawn Provenzale,
- Mark W. Yeazel,
- Rahul M. Jindal and
- Steven B. Clauser
+ Author Affiliations
- Corresponding author: Michelle van Ryn, PhD, MPH, Division of Health Care Policy and Research, Mayo Clinic, 200 First St SW, Rochester, MN 55905; e-mail: vanryn.michelle@mayo.edu.
Abstract
Purpose High-quality
supportive care is an essential component of comprehensive cancer care.
We implemented a patient-centered quality
of cancer care survey to examine and identify
predictors of quality of supportive care for bowel problems, pain,
fatigue,
depression, and other symptoms among 1,109
patients with colorectal cancer.
Patients and Methods
Patients with new diagnosis of colorectal cancer at any Veterans Health
Administration medical center nationwide in 2008
were ascertained through the Veterans Affairs
Central Cancer Registry and sent questionnaires assessing a variety of
aspects
of patient-centered cancer care. We received
questionnaires from 63% of eligible patients (N = 1,109). Descriptive
analyses
characterizing patient experiences with
supportive care and binary logistic regression models were used to
examine predictors
of receipt of help wanted for each of the five
symptom categories.
Results There were
significant gaps in patient-centered quality of supportive care,
beginning with symptom assessment. In multivariable
modeling, the impact of clinical factors and
patient race on odds of receiving wanted help varied by symptom.
Coordination
of care quality predicted receipt of wanted help
for all symptoms, independent of patient demographic or clinical
characteristics.
Conclusion This study
revealed substantial gaps in patient-centered quality of care, difficult
to characterize through quality measurement
relying on medical record review alone. It
established the feasibility of collecting patient-reported quality
measures. Improving
quality measurement of supportive care and
implementing patient-reported outcomes in quality-measurement systems
are high
priorities for improving the processes and
outcomes of care for patients with cancer.
Footnotes
-
Supported by the Interagency Quality of Cancer Care Committee, Applied Research Branch, National Cancer Institute (NCI), through an interagency agreement with the Veterans Health Administration and by NCI Grant No. 5R25CA116339 (L.L.Z.).
- Authors' disclosures of potential conflicts of interest and author contributions are found at the end of this article.© 2014 by American Society of Clinical Oncology
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