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A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
Similar Goals, Divergent Paths: Exploring Approaches to Hepatitis C Treatment Protocols in Heart Transplantation
Roopa A Rao1, Sonu Abraham2, Amanda R Vest3
1Division of Cardiovascular Medicine, Indiana University School of Medicine, Indianapolis, IN.
Insights
Management of heart transplant recipients from hepatitis C-positive donors varies widely. Most centers use direct antiviral therapies, but timing and protocols differ, highlighting the need for standardized guidelines and research.
Area of Science:
- Transplantation Medicine
- Hepatology
- Infectious Diseases
Background:
- Increasing use of hepatitis C virus (HCV)-positive donors for heart transplantation.
- Lack of consensus on optimal management strategies for recipients.
Purpose of the Study:
- To survey current practices in managing heart transplant recipients from HCV NAT-positive donors.
- To identify variations in direct antiviral therapy (DAA) protocols and monitoring.
Main Methods:
- Online survey of US and Canadian heart transplant centers (Jan 2023-Feb 2024).
- Data collected on DAA use, timing, duration, viral load testing, adverse effects, and immunosuppression.
- Analysis focused on US adult programs with HCV transplant protocols.
Main Results:
- 35 of 122 (28.7%) centers responded; 689 transplants using HCV NAT-positive donors identified.
- Among US centers, 16.7% used prophylactic, 30% preemptive, and 53.3% reactive DAA treatment.
- Pan-genotype DAA therapies used for a median of 12 weeks; significant heterogeneity in protocols observed.
Conclusions:
- Significant practice pattern variations exist for managing HCV NAT-positive donor hearts.
- Need for patient registries and randomized controlled trials to guide future clinical practice.
Background:
Heart transplantation from hepatitis C-positive donors is on the rise, yet there exists divergence in approaches to managing recipients of these organs. Practices range from prophylactic treatment of recipients prior to transplantation to delayed treatment following the detection of viremia, with no established consensus on the optimal approach.
Methods:
An online survey was conducted among the heart transplant centers in the United States and Canada from January 2023-February 2024. The survey gathered comprehensive information from the institutions regarding direct antiviral (DAA) therapies used, timing and duration of DAA, frequency of viral load testing, adverse effects, virological response, and immunosuppressive therapy modifications. The treatment pathways were categorized based on the timing of treatment initiation into prophylactic, preemptive or reactive approaches. Analysis was restricted to adult transplant programs in the U.S. that had an HCV transplant protocol and performed at least 1 HCV NAT-positive transplant. The Scientific Registry of Transplant Recipients database was queried for total heart transplants using hepatitis C virus nucleic acid testing (HCV NAT)-positive donors.
Results:
Of 122 heart transplant programs, 35 (28.7%) institutions responded; 689 heart transplants (49.1%) using HCV NAT-positive donors were captured across institutions. Among 30 U.S. institutions performing adult heart transplantation with HCV NAT-positive donor hearts, 5 (16.7%) used prophylactic, 9 (30%) preemptive and 16 (53.3%) reactive treatment pathways. Most employed pan-genotype DAA therapies for a median of 12 weeks. Significant heterogeneity existed in treatment and monitoring protocols.
Conclusion:
Practice patterns for management of HCV NAT-positive donor hearts vary significantly. Establishing registries and randomized control trials for these patients is crucial for guiding future practices.
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