©The Author(s) 2017.
World J Hepatol. Jul 8, 2017; 9(19): 833-839
Published online Jul 8, 2017. doi: 10.4254/wjh.v9.i19.833
Published online Jul 8, 2017. doi: 10.4254/wjh.v9.i19.833
Table 2 Direct acting antiviral agent options for patients with kidney disease
| HCV/kidney disease consideration | Complications and observations from HCV infection | DAA options | Other DAA options/notes |
| HCV related acute glomerulonephritis with or without cryoglobulinemia | HCV has tropism for B-cells with subsequent: Mixed cryoglobulinemia | Sofosbuvir 400 mg/d combined with | Can use: Grazoprevir 100 mg/elbasvir 50 mg/d |
| Simeprivir 150 mg/d | |||
| Daclastavir 60 mg/d | Ombitasvir 12.5 mg/paritaprevir 75 mg/ritonavir 50 mg × 2 tabs/dasabuvir 250 mg × 2 tabs | ||
| Glomerulonephritis with distinct histological patterns: Membranous nephropathy | Velpatasvir 100 mg/d | ||
| Ledipasvir 90 mg/d | |||
| Membranoproliferative GN | |||
| The HCV-infected patient with stage 1-3a chronic kidney disease (GFR > 45 mL/min) | Increased risk for CKD development | Sofosbuvir 400 mg/d combined with | Can use |
| Increased rate of CKD progression to ESRD | Simeprivir 150 mg/d | Grazoprevir 100 mg/elbasvir 50 mg/d | |
| Daclastavir 60 mg/d | |||
| Higher mortality rate | Velpatasvir 100 mg/d | Ombitasvir 12.5 mg/paritaprevir 75 mg/ritonavir 50 mg × 2 tabs/dasabuvir 250 mg × 2 tabs | |
| Ledipasvir 90 mg/d | |||
| The patient with advanced stage 3 and stage 4/5 chronic kidney disease (GFR < 45 mL/min) | Receiving an anti-HCV positive allograft decreases waiting times for a deceased donor kidney | Sofosbuvir 400 mg/d combined with | Sofosbuvir not recommended with GFR < 30 mL/min |
| Simeprivir 150 mg/d | |||
| Daclastavir 60 mg/d | Can use | ||
| Velpatasvir 100 mg/d | Grazoprevir 100 mg/Elbasvir 50 mg/d | ||
| Ledipasvir 90 mg/d | |||
| Ombitasvir 12.5 mg/Paritaprevir 75 mg/ritonavir 50 mg × 2 tabs/dasabuvir 250 mg × 2 tabs | |||
| The ESRD patient on dialysis | Increased risk of mortality and poor clinical outcomes in ESRD patients Increased cardiovascular risk | Grazoprevir 100 mg/Elbasvir 50 mg/d | Grazoprevir/elbasvir, ombitasvir/paritaprevir/ritonavir/dasabuvir, Dialysis population studied |
| Ombitasvir 12.5 mg/Paritaprevir 75 mg/ritonavir 50 mg × 2 tabs/dasabuvir 250 mg × 2 tabs | |||
| Minimal adverse events in patients with advanced CKD and ESRD on hemodialysis | |||
| The kidney transplant recipient with eGFR > 30 mL/min | DAA use after kidney transplant is safe and well tolerated with SVR > 97% | Sofosbuvir 400 mg/d combined with | Can use |
| Simeprivir 150 mg/d | Grazoprevir 100 mg/elbasvir 50 mg/d (caution with cyclosporin) | ||
| Daclastavir 60 mg/d | |||
| Velpatasvir 100 mg/d | Ombitasvir 12.5 mg/paritaprevir 75 mg/ritonavir 50 mg × 2 tabs/dasabuvir 250 mg × 2 tabs | ||
| Ledipasvir 90 mg/d |
- Citation: Ladino M, Pedraza F, Roth D. Opportunities for treatment of the hepatitis C virus-infected patient with chronic kidney disease. World J Hepatol 2017; 9(19): 833-839
- URL: https://www.wjgnet.com/1948-5182/full/v9/i19/833.htm
- DOI: https://dx.doi.org/10.4254/wjh.v9.i19.833