Treatment outcomes and costs of a simplified antiviral treatment strategy for hepatitis C among monoinfected and HIV and/or hepatitis B virus‐co‐infected patients in Myanmar
Abstract:Access to hepatitis C virus (HCV) testing and treatment is limited in Myanmar. We assessed an integrated HIV and viral hepatitis testing and HCV treatment strategy. Sofosbuvir/velpatasvir (SOF/VEL) ± weight‐based ribavirin for 12 weeks was provided at three treatment sites in Myanmar and sustained virologic response (SVR) assessed at 12 weeks after treatment. Participants co‐infected with HBV were treated concurrently with tenofovir. Cost estimates in 2018 USD were made at Yangon and Mandalay using standard mi… Show more
“…Low proportions of LTFUs were also reported by workers in other countries [44,45]. At present, we have to concede that the observed results were largely unexpected because treatment in these facilities is offered for free.…”
Background
Reliable real-world data on direct acting anti-retroviral (DAA) uptake and treatment outcomes are lacking for patients with hepatitis C virus (HCV) in Sub-Saharan Africa (SSA). This study provides data on HCV DAA-based treatment outcomes, mortality, loss-to-follow up, and associated factors among patients in Eritrea.
Methodology:
A multicenter retrospective observational cohort study was conducted in two tertiary hospitals in Asmara, Eritrea. A structured checklist was used to collect data from patients’ cards. Descriptive and inferential statistics used included means, medians, chi-squire, Kaplan–Meier estimates, and multivariate Cox proportional hazard models.
Results
Out of 238 patients enrolled in the study, 227 were initiated on treatment. 125 patients had viral load at 12 weeks EOT whereas 102 patients had no viral load at 12 weeks EOT. Out of these patients with HCV RNA data post EOT, 116 (92.8%) had SVR12. The prevalence of death and lost-to-follow up (LTFU) were (7.5%, 95% CI: 1.7–4.1) and 67 (28.1%, 95% CI: 22.3–33.9) and 1.1 (95%CI: 0.8–1.5) per 10,000 person days, respectively. Independent predictors of LTFU included the enrollment year (2020: aHR = 2.2, 95% CI: 1-4.7; p-value = 0.04); Hospital (Hospital B: aHR = 2.2, 95% CI: 1-4.7; p-value = 0.03) and the FIB-4 score (FIB-Score < 1.45: aHR = 3.7, 95% CI: 1.2–11.5; p-value = 0.02).
Conclusion
The SVR rates achieved in this cohort were high. However, high mortality, late presentation and suboptimal population screening/case finding were uncovered. These challenges can be addressed by test-and-treat programs that simultaneously prioritize programmatic screening, decentralization of care, and better patient tracking in the HCV care cascade.
“…Low proportions of LTFUs were also reported by workers in other countries [44,45]. At present, we have to concede that the observed results were largely unexpected because treatment in these facilities is offered for free.…”
Background
Reliable real-world data on direct acting anti-retroviral (DAA) uptake and treatment outcomes are lacking for patients with hepatitis C virus (HCV) in Sub-Saharan Africa (SSA). This study provides data on HCV DAA-based treatment outcomes, mortality, loss-to-follow up, and associated factors among patients in Eritrea.
Methodology:
A multicenter retrospective observational cohort study was conducted in two tertiary hospitals in Asmara, Eritrea. A structured checklist was used to collect data from patients’ cards. Descriptive and inferential statistics used included means, medians, chi-squire, Kaplan–Meier estimates, and multivariate Cox proportional hazard models.
Results
Out of 238 patients enrolled in the study, 227 were initiated on treatment. 125 patients had viral load at 12 weeks EOT whereas 102 patients had no viral load at 12 weeks EOT. Out of these patients with HCV RNA data post EOT, 116 (92.8%) had SVR12. The prevalence of death and lost-to-follow up (LTFU) were (7.5%, 95% CI: 1.7–4.1) and 67 (28.1%, 95% CI: 22.3–33.9) and 1.1 (95%CI: 0.8–1.5) per 10,000 person days, respectively. Independent predictors of LTFU included the enrollment year (2020: aHR = 2.2, 95% CI: 1-4.7; p-value = 0.04); Hospital (Hospital B: aHR = 2.2, 95% CI: 1-4.7; p-value = 0.03) and the FIB-4 score (FIB-Score < 1.45: aHR = 3.7, 95% CI: 1.2–11.5; p-value = 0.02).
Conclusion
The SVR rates achieved in this cohort were high. However, high mortality, late presentation and suboptimal population screening/case finding were uncovered. These challenges can be addressed by test-and-treat programs that simultaneously prioritize programmatic screening, decentralization of care, and better patient tracking in the HCV care cascade.
“…While lower than other cohorts in SSA, the rate of SVR among our participants is comparable to cohorts of PWID in other LMICs. PWID in an HCV treatment cohort in Myanmar achieved an overall SVR rate of 80% 7 . Similarly, 87% of a Bangladeshi HCV treatment cohort of PWID accessing harm services achieved SVR 8 .…”
Section: Discussionmentioning
confidence: 96%
“…PWID in an HCV treatment cohort in Myanmar achieved an overall SVR rate of 80%. 7 Similarly, 87% of a Bangladeshi HCV treatment cohort of PWID accessing harm services achieved SVR. 8 Furthermore, in an intent-to-treat analysis of HCV treatment services for high-risk groups in Ukraine, 78% of currently injecting PWIDs achieved SVR.…”
“…While adherence to HCV treatment was not measured, there was minimal loss to follow up; this may have been because of the Community Based Treatment model of care that incorporates a social worker into the clinical management team 18,19 and also provides harm reduction services at a community level. Even among PWID, who typically have high rate of loss to follow up 20 , there were few losses, due perhaps to the Community Based Treatment harm reduction program in Ukraine 19 . Other studies have demonstrated high rates of success with HCV treatment co-located with substance use treatment services and amongst PWID receiving OST 21,22 .…”
Background: We conducted a demonstration project of an integrated HIV and viral hepatitis testing and treatment strategy using generic ledipasvir/sofosbuvir (LDV/SOF).
Methods: Eligible HCV viraemic adults from two clinics in Kyiv were treated with LDV/SOF +/- weight-based ribavirin for 12 weeks. Clinical assessments were performed at screening and week 24 and as needed; treatment was dispensed every 4 weeks. The primary outcome was sustained virologic response (SVR)12 weeks after treatment. Program costs in 2018 USD were estimated per patient treated using observed resource utilization, local unit, and antiretroviral therapy (ART) costs over the 24-week period.
Results: 868 participants initiated on treatment, 87% (755) were PWID and 55.5% (482) were HIV co-infected. The common genotypes were 1 (74.1%) and 3 (22%) and SVR was achieved in 831/868 (95.7%) by intention-to-treat analysis. The average cost per patient treated was $680, assuming generic LDV/SOF and ribavirin pricing and standard quantitative HCV viral load testing. Medications comprised 38% of the average cost/patient, laboratory tests 26%, events (clinic visits, counselling) 10%, and indirect costs 26%. ART accounted for 60% of all drug costs, with HCV medications just 40%.
Conclusion: Generic LDV/SOF +/- ribavirin provided produced exceptionally good outcomes including amongst patients with genotype 3 HCV and PWID at an average cost of <$700/patient year, including ART for those with HIV. Under the assumptions of generic drug pricing but higher laboratory costs, an average cost of $750/patient is likely a reasonable estimate for this intervention in Ukraine, excluding costs for scaling or maintaining the treatment program.
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