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. 2020 Apr;9(2):583-590.
doi: 10.21037/tau.2020.01.05.

A safety and efficacy analysis of direct-antiviral therapy in patients with chronic hepatitis C after renal transplantation

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A safety and efficacy analysis of direct-antiviral therapy in patients with chronic hepatitis C after renal transplantation

Guanghui Li et al. Transl Androl Urol. 2020 Apr.

Abstract

Background: To explore the safety and efficacy of direct antiviral therapy in patients with hepatitis C virus (HCV) infection after renal transplantation.

Methods: We retrospectively reviewed the medical information of 15 cases of HCV+ patients treated with direct antiviral therapy after renal transplantation in our center. The effectiveness of direct antiviral therapy was evaluated by analyzing the HCV-RNA levels of patients at 1, 4, 12, 24, and 48 weeks before and after antiviral therapy. In addition, parameters including the rejection rate, the blood concentration of anti-rejection drugs, liver function level [alanine aminotransferase (ALT), aspartate transaminase (AST)], estimated glomerular filtration rate (eGFR) and serum creatinine (CREA) levels were used to assess its safety.

Results: A total of 15 patients were enrolled in the study. All patients turned HCV-RNA negative after 12 weeks of direct-antiviral therapy; the serological test of all patients demonstrated an 100% response rate in rapid virological response (RVR) (15/15), 12-week sustained virological response (SVR12), and 24-week sustained virological response (SVR24). In addition, compared to pre-treatment, the liver function within 12, 24, and 48 weeks after treatment was significantly improved. Moreover, eGFR, CREA, and anti-rejection drug concentration remained stable while acute rejection reaction and other obvious side effects were not observed throughout the treatment period.

Conclusions: The direct antiviral therapy was well-tolerated and effective for patients with chronic hepatitis C after renal transplantation.

Keywords: Renal transplantation; chronic hepatitis C; direct antiviral drugs; virological response.

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Conflict of interest statement

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tau.2020.01.05). The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
HCV-RNA in 15 patients before and after DDA treatment. All patients received DAA treatment; HCV-RNA levels decreased to the normal range at about 1 week. HCV, hepatitis C virus; DAA, direct antiviral agent.

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