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Viusid, a nutritional supplement, increases survival and reduces disease progression in HCV-related decompensated cirrhosis: a randomised and controlled trial

OBJECTIVES: Viusid is a nutritional supplement with recognised antioxidant and immunomodulatory properties which could have beneficial effects on cirrhosis-related clinical outcomes such as survival, disease progression and development of hepatocellular carcinoma (HCC). This study evaluated the effi...

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Autores principales: Vilar Gomez, Eduardo, Sanchez Rodriguez, Yoan, Torres Gonzalez, Ana, Calzadilla Bertot, Luis, Arus Soler, Enrique, Martinez Perez, Yadina, Yasells Garcia, Ali, Abreu Vazquez, Maria del Rosario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191588/
https://www.ncbi.nlm.nih.gov/pubmed/22021873
http://dx.doi.org/10.1136/bmjopen-2011-000140
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author Vilar Gomez, Eduardo
Sanchez Rodriguez, Yoan
Torres Gonzalez, Ana
Calzadilla Bertot, Luis
Arus Soler, Enrique
Martinez Perez, Yadina
Yasells Garcia, Ali
Abreu Vazquez, Maria del Rosario
author_facet Vilar Gomez, Eduardo
Sanchez Rodriguez, Yoan
Torres Gonzalez, Ana
Calzadilla Bertot, Luis
Arus Soler, Enrique
Martinez Perez, Yadina
Yasells Garcia, Ali
Abreu Vazquez, Maria del Rosario
author_sort Vilar Gomez, Eduardo
collection PubMed
description OBJECTIVES: Viusid is a nutritional supplement with recognised antioxidant and immunomodulatory properties which could have beneficial effects on cirrhosis-related clinical outcomes such as survival, disease progression and development of hepatocellular carcinoma (HCC). This study evaluated the efficacy and safety of viusid in patients with HCV-related decompensated cirrhosis. DESIGN: A randomised double-blind and placebo-controlled study was conducted in a tertiary care academic centre (National Institute of Gastroenterology, Havana, Cuba). The authors randomly assigned 100 patients with HCV-related decompensated cirrhosis to receive viusid (three oral sachets daily, n=50) or placebo (n=50) during 96 weeks. The primary outcome of the study was overall survival at 96 weeks, and the secondary outcomes included time to disease progression, time to HCC diagnosis, time to worsening of the prognostic scoring systems Child–Pugh and Model for End-Stage Liver Disease, and time to a new occurrence or relapse for each one of the main clinical complications secondary to portal hypertension at 96 weeks. RESULTS: Viusid led to a significant improvement in overall survival (90%) versus placebo (74%) (HR 0.27, 95% CI 0.08 to 0.92; p=0.036). A similar improvement in disease progression was seen in viusid-treated patients (28%), compared with placebo-treated patients (48%) (HR 0.47, 95% CI 0.22 to 0.89; p=0.044). However, the beneficial effects of viusid were wholly observed among patients with Child–Pugh classes B or C, but not among patients with Child–Pugh class A. The cumulative incidence of HCC was significantly reduced in patients treated with viusid (2%) as compared with placebo (12%) (HR 0.15, 95% CI 0.019 to 0.90; p=0.046). Viusid was well tolerated. CONCLUSIONS: The results indicate that treatment with viusid leads to a notable improvement in overall clinical outcomes such as survival, disease progression and development of HCC in patients with HCV-related decompensated cirrhosis. TRIAL REGISTRATION NUMBER: http://ClinicalTrials.gov (NCT00502086).
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spelling pubmed-31915882011-10-13 Viusid, a nutritional supplement, increases survival and reduces disease progression in HCV-related decompensated cirrhosis: a randomised and controlled trial Vilar Gomez, Eduardo Sanchez Rodriguez, Yoan Torres Gonzalez, Ana Calzadilla Bertot, Luis Arus Soler, Enrique Martinez Perez, Yadina Yasells Garcia, Ali Abreu Vazquez, Maria del Rosario BMJ Open Gastroenterology and Hepatology OBJECTIVES: Viusid is a nutritional supplement with recognised antioxidant and immunomodulatory properties which could have beneficial effects on cirrhosis-related clinical outcomes such as survival, disease progression and development of hepatocellular carcinoma (HCC). This study evaluated the efficacy and safety of viusid in patients with HCV-related decompensated cirrhosis. DESIGN: A randomised double-blind and placebo-controlled study was conducted in a tertiary care academic centre (National Institute of Gastroenterology, Havana, Cuba). The authors randomly assigned 100 patients with HCV-related decompensated cirrhosis to receive viusid (three oral sachets daily, n=50) or placebo (n=50) during 96 weeks. The primary outcome of the study was overall survival at 96 weeks, and the secondary outcomes included time to disease progression, time to HCC diagnosis, time to worsening of the prognostic scoring systems Child–Pugh and Model for End-Stage Liver Disease, and time to a new occurrence or relapse for each one of the main clinical complications secondary to portal hypertension at 96 weeks. RESULTS: Viusid led to a significant improvement in overall survival (90%) versus placebo (74%) (HR 0.27, 95% CI 0.08 to 0.92; p=0.036). A similar improvement in disease progression was seen in viusid-treated patients (28%), compared with placebo-treated patients (48%) (HR 0.47, 95% CI 0.22 to 0.89; p=0.044). However, the beneficial effects of viusid were wholly observed among patients with Child–Pugh classes B or C, but not among patients with Child–Pugh class A. The cumulative incidence of HCC was significantly reduced in patients treated with viusid (2%) as compared with placebo (12%) (HR 0.15, 95% CI 0.019 to 0.90; p=0.046). Viusid was well tolerated. CONCLUSIONS: The results indicate that treatment with viusid leads to a notable improvement in overall clinical outcomes such as survival, disease progression and development of HCC in patients with HCV-related decompensated cirrhosis. TRIAL REGISTRATION NUMBER: http://ClinicalTrials.gov (NCT00502086). BMJ Group 2011-09-30 /pmc/articles/PMC3191588/ /pubmed/22021873 http://dx.doi.org/10.1136/bmjopen-2011-000140 Text en © 2011, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Gastroenterology and Hepatology
Vilar Gomez, Eduardo
Sanchez Rodriguez, Yoan
Torres Gonzalez, Ana
Calzadilla Bertot, Luis
Arus Soler, Enrique
Martinez Perez, Yadina
Yasells Garcia, Ali
Abreu Vazquez, Maria del Rosario
Viusid, a nutritional supplement, increases survival and reduces disease progression in HCV-related decompensated cirrhosis: a randomised and controlled trial
title Viusid, a nutritional supplement, increases survival and reduces disease progression in HCV-related decompensated cirrhosis: a randomised and controlled trial
title_full Viusid, a nutritional supplement, increases survival and reduces disease progression in HCV-related decompensated cirrhosis: a randomised and controlled trial
title_fullStr Viusid, a nutritional supplement, increases survival and reduces disease progression in HCV-related decompensated cirrhosis: a randomised and controlled trial
title_full_unstemmed Viusid, a nutritional supplement, increases survival and reduces disease progression in HCV-related decompensated cirrhosis: a randomised and controlled trial
title_short Viusid, a nutritional supplement, increases survival and reduces disease progression in HCV-related decompensated cirrhosis: a randomised and controlled trial
title_sort viusid, a nutritional supplement, increases survival and reduces disease progression in hcv-related decompensated cirrhosis: a randomised and controlled trial
topic Gastroenterology and Hepatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3191588/
https://www.ncbi.nlm.nih.gov/pubmed/22021873
http://dx.doi.org/10.1136/bmjopen-2011-000140
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