Abstract
Objective: To evaluate the safety and efficacy of sofosbuvir-based therapy in end-stage renal disease patients undergoing hemodialysis complicated with acute hepatitis C. Methods: Totally 33 subjects who met the inclusion criteria received a half dose of sofosbuvir (200 mg) and a full dose of daclatasvir (90 mg) daily for 24 weeks. Then we detected the levels of HCV RNA, ALT, and TBil at 0, 4, 8, 12, 16, 20, 24, 28, 32 and 36 weeks respectively and evaluated the adverse drug reactions. Results: All the patients made a sustained virological response at 12 weeks after the end of treatment, and there were no drug-related serious adverse events. Conclusion: A half dose of sofosbuvir (200 mg once daily) plus a full dose of daclatasvir (90 mg once daily) was safe and effective for treatment of acute HCV infection in patients who were undergoing ESRD and were on hemodialysis.
| Translated title of the contribution | Safety and efficacy of sofosbuvir-based treatment of acute hepatitis C in end-stage renal disease patients undergoing hemodialysis |
|---|---|
| Original language | Chinese (Traditional) |
| Pages (from-to) | 406-410 and 431 |
| Journal | Journal of Xi'an Jiaotong University (Medical Sciences) |
| Volume | 40 |
| Issue number | 3 |
| DOIs | |
| State | Published - May 2019 |