Background
Patient navigation (PN) may improve cancer care by identifying and removing patient-reported barriers to care. In 2012, the American College of Surgeons Commission on Cancer (CoC) announced that healthcare facilities seeking CoC-accreditation must have PN processes in place starting January 1, 2015. Given the unfunded mandates, hospitals are looking for cost-effective ways to implement PN. This study examined demographic and psychosocial predictors of barriers to diagnostic resolution among individuals with a cancer screening abnormality enrolled in the Ohio Patient Navigation Research Project (OPNRP).
Methods
Data were obtained from patients who received care at one of nine OPNRP intervention clinics. Descriptive statistics and logistic regression models were used.
Results
Of 424 participants, 151 (35.6%) reported a barrier to diagnostic resolution within 90 days of study consent. The most commonly reported barriers were misconception about a test or treatment (16.4%), difficulty communicating with their provider (15.0%), and scheduling problems (11.5%). Univariate analyses indicated that race, education, employment, income, insurance, clinic type, friend support, and physical and psychological functioning were significantly associated with reporting a barrier to diagnostic resolution. Multivariate analyses found having a comorbidity (OR=1.25, 95% CI=1.04, 2.61) and higher intrusive thoughts and feelings (OR=1.25, 95% CI=1.10,1.41) were significantly associated with reporting a barrier to diagnostic resolution.
Conclusion
Results suggest demographic and psychosocial factors are associated with barriers to diagnostic resolution. To assure CoC mandate compliance and provide timely care for all patients, CoC-accredited facilities can systematically identify patients most likely to have barriers to care, and assign them to PN.