Title of article :
Ribavirin Impairs Salivary Gland Function in Hepatitis C Patients During Combination Treatment With Pegylated Interferon Alfa-2a
Author/Authors :
Aghemo, Alessio A. M. Migliavacca Center for Liver Disease First - Division of Gastroenterology - IRCCS Fondazione Ca’ Granda Hospital - University of Milan - Milan, Italy , Grazia Rumi, Maria Department of Hepatology - St. Joseph’s Hospital - University of Milan - Milan, Italy , Monico, Sara A. M. Migliavacca Center for Liver Disease First - Division of Gastroenterology - IRCCS Fondazione Ca’ Granda Hospital - University of Milan - Milan, Italy , Banderali, Matteo Department of Clinical Sciences - “L. Sacco“ Hospital - University of Milan - Milan, Italy , Russo, Antonio Departments of Epidemiology and Biostatistics - San Carlo Borromeo Hospital - Milan, Italy , Ottaviani, Francesco Department of Clinical Sciences - “L. Sacco“ Hospital - University of Milan - Milan, Italy , Vigano, Mauro Department of Hepatology - St. Joseph’s Hospital - University of Milan - Milan, Italy , D’Ambrosio, Roberta A. M. Migliavacca Center for Liver Disease First - Division of Gastroenterology - IRCCS Fondazione Ca’ Granda Hospital - University of Milan - Milan, Italy , Colombo, Massimo A. M. Migliavacca Center for Liver Disease First - Division of Gastroenterology - IRCCS Fondazione Ca’ Granda Hospital - University of Milan - Milan, Italy
Pages :
7
From page :
918
To page :
924
Abstract :
Background: Xerostomia is a common adverse event of unknown etiology observed during pegylated interferon (PegIFN)/Ribavirin (Rbv) treatment. Objectives: To assess the frequency and mechanisms of xerostomia during PegIFN/Rbv therapy. Patients and Methods: Thirty-one naïve patients with chronic hepatitis C consecutively received PegIFN-α2a (180 μg/week) plus Rbv (800–1200 mg/day). The controls were 10 patients with chronic hepatitis B who received PegIFN-α2a (180 μg/week). During treatment and follow-up, all patients underwent basal and masticatory stimulated sialometry, otorhinolaryngoiatric (ORL) examination, and a questionnaire survey to subjectively assess symptoms of oral dryness. Results: Twenty-seven patients on PegIFN/Rbv and 4 on PegIFN (87% vs. 40%, P = 0.006) reported xerostomia. Thirty patients on PegIFN/Rbv combination therapy and 2 patients on monotherapy had ORL signs of salivary gland hypofunction (97% vs. 20%, P < 0.0001). Mean basal (A) and stimulated (B) salivary flow rates (mL/min) progressively decreased during PegIFN/Rbv treatment (A, 0.49 at baseline vs. 0.17 at the end of treatment, P < 0.0001; B, 1.24 at baseline vs. 0.53 at the end of treatment, P = 0.0004). At week 24 following PegIFN/Rbv treatment, salivary flow rates were similar to baseline (A, 0.53 at the end of follow-up vs. 0.49 at baseline; B, 1.19 at the end of follow-up vs. 1.24 at baseline). Salivary function was unaffected in monotherapy patients. Conclusions: Rbv causes salivary gland hypofunction in hepatitis C patients receiving PegIFN/Rbv therapy, which promptly reverts to normal upon cessation of treatment.
Keywords :
Ribavirin , Peginterferon Alfa-2a , Salivary Glands , Hepatitis C , Hepatitis B
Journal title :
Astroparticle Physics
Record number :
2424387
Link To Document :
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