Treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis B virus infection

Introduction and Objective: This study aimed to compare the efficacy of treatment with entecavir (ETV) and tenofovir (TDF) in patients with chronic hepatitis B infection. Material and Methods: Cross-sectional, descriptive, retrolective study. Realized in the “Hospital de especialidades Siglo XXI”. W...

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Main Authors: CA González Rodríguez, A Bautista Santos, R Moreno Alcántar
Format: Article
Language:English
Published: Elsevier 2022-12-01
Series:Annals of Hepatology
Online Access:http://www.sciencedirect.com/science/article/pii/S1665268122001697
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author CA González Rodríguez
A Bautista Santos
R Moreno Alcántar
author_facet CA González Rodríguez
A Bautista Santos
R Moreno Alcántar
author_sort CA González Rodríguez
collection DOAJ
description Introduction and Objective: This study aimed to compare the efficacy of treatment with entecavir (ETV) and tenofovir (TDF) in patients with chronic hepatitis B infection. Material and Methods: Cross-sectional, descriptive, retrolective study. Realized in the “Hospital de especialidades Siglo XXI”. We included patients >18 years with chronic hepatitis B infection in treatment and follow-up from January 1st, 2015, to March 1st, 2021. Descriptive statistics were performed and to show differences Wilcoxon test was used. Approved by the institutional ethics committee and informed consent was obtained. Results: We included 33 patients, male gender predominated in 51.5% (17), mean age was 59 years (+/- 11.25). Co-infected with HIV were 18% (6). Median baseline viral load was 2´500,00 (3940 – 191´500,000 copies/ml). Median baseline APRI 0.3 (0.2-1.6) and FIB-4 1.33 (1.0-2.2). Exposure to previous treatments was 45.8% (16). The mean follow-up was 9.48 years (+/-4.82). Current treatment TDF 60.6% (20), ETV 27% (9). Incidence of hepatocellular carcinoma occurred in 3% (1). At 6 and 12 months of treatment, 69% and 64% (16/23 and 16/28), respectively, with undetectable viral load. There was a difference in baseline APRI compared to current p <0.05; there was no difference in APRI throughout treatment. Discussion: Treatment is effective for HBV both in chronic infection and liver cirrhosis, maintaining viral suppression with low seroconversion rates and low incidence of hepatocellular carcinoma. Conclusion: Treatment with nucleotide and nucleoside analogues is effective for the suppression of the hepatitis B virus. Funding: The resources used in this study were from the hospital without any additional financing Declaration of interest: The authors declare no potential conflicts of interest.
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spelling doaj.art-f7468e6376e344d7b0a5490edbe264252022-12-22T04:36:00ZengElsevierAnnals of Hepatology1665-26812022-12-0127100827Treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis B virus infectionCA González Rodríguez0A Bautista Santos1R Moreno Alcántar2Specialty Hospital. Centro Médico Nacional Siglo XXI. Mexico City, Mexico. Instituto Mexicano del Seguro Social, (IMSS)Specialty Hospital. Centro Médico Nacional Siglo XXI. Mexico City, Mexico. Instituto Mexicano del Seguro Social, (IMSS)Specialty Hospital. Centro Médico Nacional Siglo XXI. Mexico City, Mexico. Instituto Mexicano del Seguro Social, (IMSS)Introduction and Objective: This study aimed to compare the efficacy of treatment with entecavir (ETV) and tenofovir (TDF) in patients with chronic hepatitis B infection. Material and Methods: Cross-sectional, descriptive, retrolective study. Realized in the “Hospital de especialidades Siglo XXI”. We included patients >18 years with chronic hepatitis B infection in treatment and follow-up from January 1st, 2015, to March 1st, 2021. Descriptive statistics were performed and to show differences Wilcoxon test was used. Approved by the institutional ethics committee and informed consent was obtained. Results: We included 33 patients, male gender predominated in 51.5% (17), mean age was 59 years (+/- 11.25). Co-infected with HIV were 18% (6). Median baseline viral load was 2´500,00 (3940 – 191´500,000 copies/ml). Median baseline APRI 0.3 (0.2-1.6) and FIB-4 1.33 (1.0-2.2). Exposure to previous treatments was 45.8% (16). The mean follow-up was 9.48 years (+/-4.82). Current treatment TDF 60.6% (20), ETV 27% (9). Incidence of hepatocellular carcinoma occurred in 3% (1). At 6 and 12 months of treatment, 69% and 64% (16/23 and 16/28), respectively, with undetectable viral load. There was a difference in baseline APRI compared to current p <0.05; there was no difference in APRI throughout treatment. Discussion: Treatment is effective for HBV both in chronic infection and liver cirrhosis, maintaining viral suppression with low seroconversion rates and low incidence of hepatocellular carcinoma. Conclusion: Treatment with nucleotide and nucleoside analogues is effective for the suppression of the hepatitis B virus. Funding: The resources used in this study were from the hospital without any additional financing Declaration of interest: The authors declare no potential conflicts of interest.http://www.sciencedirect.com/science/article/pii/S1665268122001697
spellingShingle CA González Rodríguez
A Bautista Santos
R Moreno Alcántar
Treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis B virus infection
Annals of Hepatology
title Treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis B virus infection
title_full Treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis B virus infection
title_fullStr Treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis B virus infection
title_full_unstemmed Treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis B virus infection
title_short Treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis B virus infection
title_sort treatment with nucleoside and nucleotide analogues in patients with chronic hepatitis b virus infection
url http://www.sciencedirect.com/science/article/pii/S1665268122001697
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