Cost-utility analysis of interferon-free treatments for patients with early-stage genotype 1 hepatitis C virus in Brazil
INTRODUCTIONWe conducted a cost-utility analysis of available interferon-free treatments for patients with early-stage genotype 1 chronic hepatitis C based on a Brazilian public health system perspective. METHODSA Markov model was derived using a cohort of stage F0-F2 patients treated as recommended...
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Published in: | Revista da Sociedade Brasileira de Medicina Tropical Vol. 53; p. e20190594 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
Sociedade Brasileira de Medicina Tropical - SBMT
01-01-2020
Sociedade Brasileira de Medicina Tropical (SBMT) |
Subjects: | |
Online Access: | Get full text |
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Summary: | INTRODUCTIONWe conducted a cost-utility analysis of available interferon-free treatments for patients with early-stage genotype 1 chronic hepatitis C based on a Brazilian public health system perspective. METHODSA Markov model was derived using a cohort of stage F0-F2 patients treated as recommended by the Brazilian national guidelines. RESULTSGlecaprevir plus pibrentasvir was superior to all other treatments, followed by sofosbuvir plus velpatasvir. Sofosbuvir plus daclatasvir was identified as the least cost-effective option. CONCLUSIONSThe above findings were confirmed via probabilistic sensitivity analysis and the tested scenarios. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Authors’ contribution: VLF: designed the study, conducted all analysis, wrote the first draft of the manuscript and approved the final version of the manuscript; LPL: designed the study, analyzed the data, wrote the first draft of the manuscript and approved the final version of the manuscript; MLAP and RP: conceptualized and designed the study, supervised the project and approved the final version of the manuscript. Conflict of Interest: The authors declare that there is no conflict of interest. |
ISSN: | 0037-8682 1678-9849 1678-9849 |
DOI: | 10.1590/0037-8682-0594-2019 |