Safety and Efficacy of Direct-acting Antiviral Therapies for Chronic HCV Infection in Hemodialysis Patients.

Autor:	Droc G; Department of Anesthesiology and Intensive Care, Fundeni Clinical Institute, Bucharest, Romania.; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania., Istrate M; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania; mircea.istrate@rez.umfcd.ro.; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania., Mercan-Stanciu A; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania., Dodot M; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania., Isac T; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania., Toma L; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania., Zgura A; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania., Trifan A; Grigore T. Popa University of Medicine and Pharmacy, Iasi, Romania.; Gastroenterology and Hepatology Institute, Iasi, Romania., Serbanica AN; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania.; Pediatrics Department, Fundeni Clinical Institute, Bucharest, Romania., Iliescu L; Carol Davila University of Medicine and Pharmacy, Bucharest, Romania.; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania., Micu L; Department of Internal Medicine, Fundeni Clinical Institute, Bucharest, Romania.
Jazyk:	angličtina
Zdroj:	In vivo (Athens, Greece) [In Vivo] 2022 Nov-Dec; Vol. 36 (6), pp. 2918-2922.
DOI:	10.21873/invivo.13033
Abstrakt:	Background/aim: The aim of this study was to determine the safety and efficacy of a direct-acting antiviral treatment, ombitasvir/paritaprevir/ritonavir and dasabuvir, without ribavirin, in a real-life setting. Patients and Methods: We performed a prospective observational study including 108 patients undergoing hemodialysis for end-stage kidney disease, referred to our clinic for antiviral therapy for chronic hepatitis C virus infection. Patients received treatment with ombitasvir/paritaprevir/ritonavir and dasabuvir, for 12 weeks. Sustained virologic response (SVR) was defined as undetectable viremia at 12 weeks after the end of therapy. For safety analysis, we monitored serum levels of hemoglobin, albumin, total bilirubin, alanine-aminotransferase and aspartate- aminotransferase at the beginning and end of therapy, as well as at SVR. Verbal Numeric Rating Scale was used to assess the presence of nausea, headaches and fatigue. Results: We noted a high prevalence of diabetic and hypertensive nephropathy as the underlying cause of chronic kidney disease. Most of the patients had F2 and F3 liver fibrosis (32.40% and 34.25%, respectively). The SVR rate was 96.2% (103/107 patients). We recorded an unrelated death after the completion of antiviral therapy. We found increased levels of nausea, headaches and fatigue at the end of therapy compared to at initiation, The presence and degree of symptoms did not correlate with the underlying cause of renal disease (p=0.72) nor with the degree of fibrosis (p=0.08). Minimal increases in transaminases and bilirubin were recorded at the end of treatment, with no statistical significance. Conclusion: Oral antiviral therapy with ombitasvir/paritaprevir/ritonavir and dasabuvir can be safely used in hemodialysis patients, with similar response rates compared to the general population. (Copyright © 2022, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)
Databáze:	MEDLINE
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