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Hepatitis C virus reinfection in patients on haemodialysis after achieving sustained virologic response with antiviral treatment

  • Chen Hua Liu
  • , Cheng Yuan Peng
  • , Wei Yu Kao
  • , Sheng Shun Yang
  • , Yu Lueng Shih
  • , Chin Lin Lin
  • , Meng Kun Tsai
  • , Chih Yuan Lee
  • , Chun Chao Chang
  • , Jo Hsuan Wu
  • , Chun Jen Liu
  • , Tung Hung Su
  • , Tai Chung Tseng
  • , Pei Jer Chen
  • , Jia Horng Kao

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Data are limited regarding the risk of hepatitis C virus (HCV) reinfection after treatment-induced sustained virologic response (SVR) in patients on haemodialysis. Aims: To assess the risk of HCV reinfection among patients on haemodialysis with treatment-induced SVR. Methods: Patients on haemodialysis patients who achieved SVR12 with interferon (IFN) or direct-acting antiviral (DAA)-based treatment received follow-up at SVR24 and then biannually with HCV RNA measurements. HCV reinfection was defined as the resurgence of viremia by different viral strains beyond SVR12. The low-risk general population who achieved SVR12 and who underwent the same post-SVR12 surveillance served as the reference group. Crude reinfection rates per 100 person-years (PYs) were calculated. Multivariate Cox regression analysis was performed to estimate the relative risk of HCV reinfection between the two groups. Results: We recruited 374 patients on haemodialysis and 1571 reference patients with a mean post-SVR12 follow-up of 4.7 and 6.1 years. All haemodialysis patients who achieved SVR12 also achieved SVR24. The incidence rates of HCV reinfection were 0.23 per 100 PYs (95% confidence interval [CI]: 0.09-0.59) in haemodialysis patients and 0.16 per 100 PYs (95% CI: 0.10-0.26) in the reference group. The risk of HCV reinfection in patients on haemodialysis was comparable to that in the reference patients (hazard ratio [HR]: 1.39; 95% CI: 0.44-4.38, P = 0.57). Conclusions: The risk of HCV reinfection in patients on haemodialysis who achieve SVR12 is low and comparable to that in the low-risk general population. HCV microelimination in this special population is feasible once universal screening and scaled-up treatment are implemented.

Original languageEnglish
Pages (from-to)434-445
Number of pages12
JournalAlimentary Pharmacology and Therapeutics
Volume55
Issue number4
DOIs
Publication statusPublished - Feb 2022

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

ASJC Scopus subject areas

  • Hepatology
  • Gastroenterology
  • Pharmacology (medical)

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