Copyright
©The Author(s) 2021.
World J Hepatol. May 27, 2021; 13(5): 522-532
Published online May 27, 2021. doi: 10.4254/wjh.v13.i5.522
Published online May 27, 2021. doi: 10.4254/wjh.v13.i5.522
Drug | Mechanism of action | Impact on CLD management |
Remdesivir | Viral RNA-dependent RNA polymerase inhibitor | Liver toxicity possible; No liver relevant drug-drug interactions |
Lopinavir/ritonavir | Protease inhibitors | mTOR inhibitors (sirolimus, everolimus) should not be co-administered; Close monitoring of drug level is required for calcineurin inhibitors (cyclosporine, tacrolimus); The risk of lopinavir-associated hepatotoxicity in patients with very advanced liver disease is low; Patients with decompensated cirrhosis should not be treated |
Tocilizumab | Humanized monoclonal antibody targeting interleukin-6 receptor | Patients with decompensated cirrhosis should not be treatedConsider risk of HBV reactivation |
Methylprednisolone (steroids) | Bind nuclear receptors todampen proinflammatory cytokines | The risk of other infections (e.g., spontaneous bacterial peritonitis) and viral shedding may increase in patents with decompensated liver cirrhosis; Consider antimicrobial prophylaxis; Consider risk of HBV reactivation |
Favipiravir | Guanine analogue, RNA-dependent RNA polymerase | Elevation of ALT and AST possible; No data in cirrhosis available |
- Citation: Nasa P, Alexander G. COVID-19 and the liver: What do we know so far? World J Hepatol 2021; 13(5): 522-532
- URL: https://www.wjgnet.com/1948-5182/full/v13/i5/522.htm
- DOI: https://dx.doi.org/10.4254/wjh.v13.i5.522