@article {4816,
	title = {Predicting Risk of End-Stage Liver Disease in Antiretroviral-Treated Human Immunodeficiency Virus/Hepatitis C Virus-Coinfected Patients.},
	journal = {Open forum infectious diseases},
	volume = {2},
	year = {2015},
	month = {2015 Sep},
	pages = {ofv109},
	abstract = {Background.   End-stage liver disease (ESLD) is an important cause of morbidity among human immunodeficiency virus (HIV)/hepatitis C virus (HCV)-coinfected patients. Quantifying the risk of this outcome over time could help determine which coinfected patients should be targeted for risk factor modification and HCV treatment. We evaluated demographic, clinical, and laboratory variables to predict risk of ESLD in HIV/HCV-coinfected patients receiving antiretroviral therapy (ART). Methods.   We conducted a retrospective cohort study among 6016 HIV/HCV-coinfected patients who received ART within the Veterans Health Administration between 1997 and 2010. The main outcome was incident ESLD, defined by hepatic decompensation, hepatocellular carcinoma, or liver-related death. Cox regression was used to develop prognostic models based on baseline demographic, clinical, and laboratory variables, including FIB-4 and aspartate aminotransferase-to-platelet ratio index, previously validated markers of hepatic fibrosis. Model performance was assessed by discrimination and decision curve analysis. Results.   Among 6016 HIV/HCV patients, 532 (8.8\%) developed ESLD over a median of 6.6 years. A model comprising FIB-4 and race had modest discrimination for ESLD (c-statistic, 0.73) and higher net benefit than alternative strategies of treating no or all coinfected patients at relevant risk thresholds. For FIB-4 >3.25, ESLD risk ranged from 7.9\% at 1 year to 26.0\% at 5 years among non-blacks and from 2.4\% at 1 year to 14.0\% at 5 years among blacks. Conclusions.   Race and FIB-4 provided important predictive information on ESLD risk among HIV/HCV patients. Estimating risk of ESLD using these variables could help direct HCV treatment decisions among HIV/HCV-coinfected patients.},
	issn = {2328-8957},
	doi = {10.1093/ofid/ofv109},
	author = {Lo Re, Vincent and Kallan, Michael J and Tate, Janet P and Lim, Joseph K and Goetz, Matthew Bidwell and Klein, Marina B and Rimland, David and Rodriguez-Barradas, Maria C and Butt, Adeel A and Gibert, Cynthia L and Brown, Sheldon T and Park, Lesley S and Dubrow, Robert and Reddy, K Rajender and Kostman, Jay R and Justice, Amy C and Localio, A Russell}
}
