Sofosbuvir and Daclatasvir Bypassing Genotypic Investigation of Chronic Hepatitis C Infection: A Real-Life Experience at Tertiary care center in North Indian Population Sofosbuvir and Daclatasvir Bypassing Genotypic Investigation

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Authors

  • Amar Deep
     Experimental and Public Health Laboratory, Department of Zoology, University of Lucknow, Lucknow – 226007, Uttar Pradesh ,IN ORCID logo http://orcid.org/0000-0002-8253-5169
  • Ajay Kumar
     Department of Medicine, King George's Medical University, Lucknow – 226003, Uttar Pradesh ,IN
  • Sumit Rungta
     Department of Medical Gastroenterology, King George's Medical University, Lucknow – 226003, Uttar Pradesh ,IN
  • Suchit Swaroop
     Experimental and Public Health Laboratory, Department of Zoology, University of Lucknow, Lucknow – 226007, Uttar Pradesh ,IN

DOI:

https://doi.org/10.18311/jeoh/2020/24450

Keywords:

Cirrhosis, End of Treatment Response (ETR), Hepatocellular Carcinoma (HCC), Sofosbuvir and Daclatasvir (SOF DCV), Steatosis, Sustained Virological Response (SVR)
Hepatitis C Infection and its Treatment

Abstract

Background and Aims: The goal of Hepatitis C Virus infection treatment is to remove the virus, to avoid advancement of Hepatitis C Virus (HCV) infection and progression of related disease such as liver cirrhosis and hepatocellular carcinoma and to achieve End of Treatment Response (ETR) with 12-week therapy and Sustained Virological Response (SVR) at post-treatment week 12 (SVR-12), which is defined as undetectable HCV RNA at 12 weeks post ETR. In the Compassionate Use Program (CUP) in Europe, Sofosbuvir (SOF) and Daclatasvir (DCV) were used in all genotypes and achieved SVR-12. Aims: Our aim is to compare the efficacy and effectiveness of Sofosbuvir and Daclatasvir in the treatment of HCV infection in the patients who could not afford for the investigating of HCVGenotype and to those in whom genotyping was done. Methods: Group 1 includes ten patients, given Sofosbuvir and Daclatasvir without genotype and group 2 includes nine patients, given Sofosbuvir and Daclatasvir with genotype. The patient group selection was done using a randomized table generated by using excel. All the patients in the groups completed the twelve weeks treatment with twelve weeks and twenty-four weeks of follow up. All the nineteen patients were given Sofosbuvir and Daclatasvir for twelve weeks and the endpoint of therapy was marked by undetectable HCV-RNA in blood by ETR-12 (end of treatment response), Sustained Virological Response at post-treatment week 12 (SVR-12) and Sustained Virological Response at post-treatment week 24 (SVR- 24). Results: Quantitative HCV-RNA (IU/ml) by RT-PCR was undetectable in all the patients in both groups at the end of treatment (ETR-12) and SVR-12- and SVR-24-weeks follow-up after completion of treatment i.e. Sofosbuvir and Daclatasvir has 100% ETR-12, SVR-12 and SVR-24 in both the groups. Conclusion: If patients do not investigate for genotype and use the Sofosbuvir and Daclatasvir in HCV infected patients, there is no effect on outcome ETR. This will reduce the risk of late stage complications such as liver cirrhosis and hepatocellular carcinoma and will also leads to the economic benefits such as no extra burden on patients.

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Published

2020-06-24

How to Cite

Deep, A., Kumar, A., Rungta, S., & Swaroop, S. (2020). Sofosbuvir and Daclatasvir Bypassing Genotypic Investigation of Chronic Hepatitis C Infection: A Real-Life Experience at Tertiary care center in North Indian Population Sofosbuvir and Daclatasvir Bypassing Genotypic Investigation. Journal of Ecophysiology and Occupational Health, 20(1&2), 70–74. https://doi.org/10.18311/jeoh/2020/24450

Issue

Volume 20, Issue 1&2, June 2020

Section

Articles
Crossref
Scopus
Google Scholar
Europe PMC
Received 2019-11-21
Accepted 2020-02-07
Published 2020-06-24

 

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