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Cost-effectiveness and system-wide impact of using Hepatitis C-viremic donors for heart transplant
Brian Wayda1, Alexander T Sandhu1, Justin Parizo1
1Division of Cardiology; Stanford Cardiovascular Institute, Department of Medicine, Stanford University School of Medicine, Stanford, California.
Insights
Using Hepatitis C (HCV) donor hearts for transplantation can increase heart transplants and improve outcomes. This strategy is cost-effective, especially where donor organs are scarce.
Area of Science:
- Cardiology
- Transplantation
- Infectious Diseases
Background:
- Direct-acting antiviral (DAA) therapy has transformed Hepatitis C (HCV) treatment.
- This advancement enables the use of HCV-viremic donors for organ transplantation.
- A significant donor organ shortage exists in heart transplantation.
Purpose of the Study:
- To evaluate the impact of using HCV-viremic donors for heart transplantation.
- To assess the cost-effectiveness of this strategy.
- To analyze effects on transplant volume, waitlist outcomes, and quality-adjusted life years (QALYs).
Main Methods:
- A large-scale simulation of adult heart transplant candidates in the U.S. (July 2014-June 2019).
- Modeled outcomes for a cohort of 19,346 patients.
- Simulated an intervention where all candidates accept HCV+ donors (n=472).
Main Results:
- The intervention resulted in 232 additional transplants and reduced waitlist deaths by 50.
- Wait times decreased by 3% to 11%, varying by priority status.
- The strategy was cost-effective, adding 0.08 QALYs per patient at an average cost of $81,892 per QALY.
Conclusions:
- Transplanting hearts from HCV+ donors is a viable and cost-effective strategy.
- This approach can significantly improve waitlist outcomes, particularly in areas with donor scarcity.
- The benefits are most pronounced in subgroups facing high donor organ shortages.
Background:
The advent of direct-acting antiviral therapy for Hepatitis C (HCV) has made using HCV-viremic donors a viable strategy to address the donor shortage in heart transplantation. We employed a large-scale simulation to evaluate the impact and cost-effectiveness of using HCV-viremic donors for heart transplant.
Methods:
We simulated detailed histories from time of listing until death for the real-world cohort of all adults listed for heart transplant in the United States from July 2014 to June 2019 (n = 19,346). This population was imputed using historical data and captures "real-world" heterogeneity in geographic and clinical characteristics. We estimated the impact of an intervention in which all candidates accept HCV+ potential donors (n = 472) on transplant volume, waitlist outcomes, and lifetime costs and quality-adjusted life years (QALYs).
Results:
The intervention produced 232 more transplants, 132 fewer delistings due to deterioration, and 50 fewer waitlist deaths within this 5-year cohort and reduced wait times by 3% to 11% (varying by priority status). The intervention was cost-effective, adding an average of 0.08 QALYs per patient at a cost of $124 million ($81,892 per QALY). DAA therapy and HCV care combined account for 11% this cost, with the remainder due to higher costs of transplant procedures and routine post-transplant care. The impact on transplant volume varied by blood type and region and was correlated with donor-to-candidate ratio (ρ = 0.71).
Conclusions:
Transplanting HCV+ donor hearts is likely to be cost-effective and improve waitlist outcomes, particularly in regions and subgroups experiencing high donor scarcity.
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