Unknown

Dataset Information

0

Treatment outcomes and costs of a simplified antiretroviral treatment strategy for hepatitis C among Hepatitis C Virus and Human Immuno deficiency Virus co-infected patients in Ukraine.


ABSTRACT:

Background and aim

To demonstrate the use of a standard dose of ledipasvir (LDV) and sofosbuvir (SOF), with or without ribavirin, to treat hepatitis C and hepatitis C/HIV co-infection in Ukraine.

Methods

Eligible HCV viraemic adults from two clinics in Kyiv were treated with LDV/SOF with or without weight-based ribavirin for 12 weeks. Clinical assessments were performed at screening and at week 24, and as needed; treatment was dispensed every 4 weeks. The primary outcome was sustained virologic response (SVR) 12 weeks after treatment, with analysis by intention to treat. Cost per patient was estimated in USD (2018) over the 24-week period.

Results

Of 868 patients included in the study and initiated on therapy, 482 (55.5%) were co-infected with HIV. The common genotypes were 1 (74.1%) and 3 (22%). Overall, SVR was achieved in 831 of the 868 patients (95.7%). SVR in patients with hepatitis C alone and hepatitis C/HIV co-infection was 98.4% and 93.6%, respectively. Adverse events were infrequent and usually mild. Using generic medication, cost per patient was estimated at US$680.

Conclusion

A standard dose of LDV and SOF, with ribavirin as per protocol, resulted in good outcomes for patients with both hepatitis C alone and co-infected with hepatitis C/HIV. Program costs in Ukraine were modest using generic medication.

SUBMITTER: Antoniak S 

PROVIDER: S-EPMC9730727 | biostudies-literature | 2022 Dec

REPOSITORIES: biostudies-literature

altmetric image

Publications


<h4>Background and aim</h4>To demonstrate the use of a standard dose of ledipasvir (LDV) and sofosbuvir (SOF), with or without ribavirin, to treat hepatitis C and hepatitis C/HIV co-infection in Ukraine.<h4>Methods</h4>Eligible HCV viraemic adults from two clinics in Kyiv were treated with LDV/SOF with or without weight-based ribavirin for 12 weeks. Clinical assessments were performed at screening and at week 24, and as needed; treatment was dispensed every 4 weeks. The primary outcome was susta  ...[more]

Similar Datasets

| S-EPMC7746582 | biostudies-literature
| S-EPMC7371238 | biostudies-literature
| S-EPMC4214386 | biostudies-literature
| S-EPMC516776 | biostudies-literature
| S-EPMC4254786 | biostudies-literature
| S-EPMC5565933 | biostudies-literature
| S-EPMC10276322 | biostudies-literature
| S-EPMC2814776 | biostudies-literature
| S-EPMC3369565 | biostudies-literature
| S-EPMC8364824 | biostudies-literature