Abstract
Background
Disparities in receipt of hepatocellular carcinoma (HCC) surveillance contribute to disparities in overall survival outcomes.
Aim
We aim to evaluate disparities in receipt of routine HCC surveillance among patients with cirrhosis in a large urban safety-net hospital.
Methods
Consecutive adults (age ≥ 18) with cirrhosis from July 1, 2014, to December 31, 2015, were retrospectively evaluated to determine rates of receiving appropriate HCC surveillance within 6 months and 1 year after diagnosis of cirrhosis. Rates of HCC surveillance were stratified by sex, race/ethnicity, and liver disease etiology. Multivariate Cox proportional hazards models were utilized to evaluate for predictors of receiving appropriate HCC surveillance.
Results
Among 157 cirrhosis patients enrolled [hepatitis C virus (HCV): 29.9%, hepatitis B virus: 13.4%, alcoholic cirrhosis: 44.6%, nonalcoholic steatohepatitis (NASH): 8.9%], mean age of cirrhosis diagnosis was 53.8 ± 9.0 years. Among these patients, 49% received (n = 77) HCC surveillance within 6 months and 78% (n = 123) were surveyed within 1 year of cirrhosis diagnosis. On multivariate analyses, patients with NASH cirrhosis were significantly less likely to receive HCC surveillance compared with chronic HCV cirrhosis patients (HR 0.44, 95% CI 0.19–0.99, p < 0.05). No significant sex-specific or race/ethnicity-specific disparities in receipt of HCC surveillance were observed.
Conclusion
Among a diverse safety-net hospital population, sub-optimal HCC surveillance rates were observed: Only 49% of cirrhosis patients received HCC surveillance within 6 months, and 78% of cirrhosis patients received HCC surveillance within 1 year. Differences in rates of HCC screening by liver disease etiology were observed.
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Abbreviations
- AASLD:
-
American association for the study of liver disease
- AFP:
-
Alpha-fetoprotein
- EASL:
-
European association for the study of the liver
- HBV:
-
Hepatitis B virus
- HCC:
-
Hepatocellular carcinoma
- HCV:
-
Hepatitis C virus
- MELD:
-
Model for end stage liver disease
- NAFLD:
-
Nonalcoholic fatty liver disease
- NASH:
-
Nonalcoholic steatohepatitis
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Hesam Tavakoli: None. Ann Robinson: None. Benny Liu: None. Taft Bhuket: None. Zobair Younossi: Consultant—Gilead, Abbvie, Bristol Myers Squibb, Glaxo Smith Kline, Tobira. Sammy Saab: Consultant and speaker’s bureau—Gilead and Bristol Myers Squibb. Aijaz Ahmed: Consultant, advisory board, and research grants—Gilead. Robert Wong: Consultant, advisory board, research grants, and speaker’s bureau—Gilead.
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Tavakoli, H., Robinson, A., Liu, B. et al. Cirrhosis Patients with Nonalcoholic Steatohepatitis Are Significantly Less Likely to Receive Surveillance for Hepatocellular Carcinoma. Dig Dis Sci 62, 2174–2181 (2017). https://doi.org/10.1007/s10620-017-4595-x
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DOI: https://doi.org/10.1007/s10620-017-4595-x