| AASLD | American Association for the Study of Liver Diseases |
| AE | Adverse Events |
| AH | Arterial Hypertension |
| AZA | Azathioprine |
| bDNA | Branched DNA signal amplification |
| CI | Confidence intervals |
| CKD | Chronic kidney disease |
| CKD-EPI | Chronic kidney disease epidemiology collaboration equation |
| CMV | Cytomegalovirus |
| CNI | Calcineurin inhibitor |
| DAA | Direct-acting antiviral agent |
| DCV | Daclatasvir |
| DDI | Drug-drug interaction |
| DM | Diabetes mellitus |
| DSV | Dasabuvir |
| eGFR | Estimated glomerular filtration rate |
| EOT | End-of-treatment |
| ESRD | End-stage renal disease |
| FDA | Food and Drug administration |
| GI | Gastrointestinal |
| GN | Glomerulonephritis |
| HBV | Hepatitis B virus |
| HCV | Hepatitis C virus |
| HD | Haemodialysis |
| IDSA | Infectious Disease Society of America |
| IFN | Interferon |
| IQR | Interquartile range |
| IRB | Institutional review board |
| ITT | Intention-to-treat |
| KDIGO | Kidney Disease: Improving Global Outcomes |
| LDV | Ledipasvir |
| LT | Liver transplant |
| MMF | Mycophenolate mofetil |
| mTOR | Mammalian target of rapamycin |
| NA | Not available |
| NAT | Nucleic acid testing |
| OBV | Ombitasvir |
| OPTN | Organ Procurement Transplantation Network |
| OR | Odds ratio |
| PCR | Polymerase chain reaction |
| PegIFN | Pegylated interferon |
| PHS | Public health service |
| PI | Protease inhibitors |
| PTV | Paritaprevir |
| R | Ritonavir |
| RBV | Ribavirin |
| RR | Relative risk |
| RT | Renal transplant |
| RRT | Renal replacement therapy |
| SAE | Serious adverse event |
| SOF | Sofosbuvir |
| SVR | Sustained Virological Response |
| TAC | Tacrolimus |
| TMA | Transcription-mediated amplification |
| UNOS | United Network for Organ Sharing |
| USA | United States of America |
| VEL | Velpatasvir |
| WKS | Weeks |
| W12 | 12 weeks after antiviral therapy ended |