Related Experiment Video
Updated: Dec 6, 2025

Author Spotlight: Enhancing Graft Viability Assessment Through Quantitative Metrics and Innovative Reservoir Systems
Published on: August 2, 2024
Comparing outcomes for infiltrative and restrictive cardiomyopathies under the new heart transplant allocation system
Jan M Griffin1, Ersilia M DeFilippis1, Hannah Rosenblum1
1Milstein Division of Cardiology, Department of Medicine, Columbia University Vagelos College of Physicians and Surgeons, New York, NY, USA.
Insights
The updated heart transplantation policy improved outcomes for cardiomyopathy patients by reducing waitlist times and mortality. This led to increased transplant rates without negatively impacting short-term survival post-surgery.
Area of Science:
- Cardiology
- Transplantation Medicine
- Public Health Policy
Background:
- The introduction of a new heart transplantation (HT) allocation policy on October 18, 2018, prompted an evaluation of its impact.
- Previous allocation systems faced challenges in managing waitlist dynamics and clinical outcomes for specific heart conditions.
Purpose of the Study:
- To compare early outcomes of heart transplantation for patients with restrictive cardiomyopathy, hypertrophic cardiomyopathy, cardiac sarcoidosis, or cardiac amyloidosis under the new policy versus the old system.
- To assess the effects of the revised HT allocation policy on waitlist events and transplantation rates.
Main Methods:
- Utilized the United Network for Organ Sharing (UNOS) registry to analyze data from 1232 HT candidates.
- Categorized patients into two eras: Era 1 (pre-policy, listed before 10/17/2018) and Era 2 (post-policy, listed on or after 10/18/2018).
- The primary endpoint was defined as death on the waitlist or delisting due to clinical deterioration.
Main Results:
- Era 2 demonstrated a significant increase in temporary mechanical circulatory support use.
- A reduction in the primary endpoint was observed in Era 2 (18.6 events per 100 PY) compared to Era 1 (20.9 events per 100 PY).
- Median waitlist time decreased significantly (91 to 58 days), and the transplantation rate increased substantially (119.0 to 204.7 transplants/100 PY).
Conclusions:
- The new heart transplantation allocation policy has successfully decreased waitlist time and mortality/delisting due to clinical deterioration for patients with infiltrative, hypertrophic, and restrictive cardiomyopathies.
- The policy change has led to an increased rate of heart transplantation for these patient groups.
- Importantly, the updated policy did not adversely affect post-transplant 6-month survival rates.
Abstract:
The new heart transplantation (HT) allocation policy was introduced on 10/18/2018. Using the UNOS registry, we examined early outcomes following HT for restrictive cardiomyopathy, hypertrophic cardiomyopathy, cardiac sarcoidosis, or cardiac amyloidosis compared to the old system. Those listed who had an event (transplant, death, or waitlist removal) prior to 10/17/2018 were in Era 1, and those listed on or after 10/18/2018 were in Era 2. The primary endpoint was death on the waitlist or delisting due to clinical deterioration. A total of 1232 HT candidates were included, 855 (69.4%) in Era 1 and 377 (30.6%) in Era 2. In Era 2, there was a significant increase in the use of temporary mechanical circulatory support and a reduction in the primary endpoint, (20.9 events per 100 PY (Era 1) vs. 18.6 events per 100 PY (Era 2), OR 1.98, p = .005). Median waitlist time decreased (91 vs. 58 days, p < .001), and transplantation rate increased (119.0 to 204.7 transplants/100 PY for Era 1 vs Era 2). Under the new policy, there has been a decrease in waitlist time and waitlist mortality/delisting due to clinical deterioration, and an increase in transplantation rates for patients with infiltrative, hypertrophic, and restrictive cardiomyopathies without any effect on post-transplant 6-month survival.
More Related Videos
Related Concept Videos
Kidney Transplant I: Introduction
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy IV: Restrictive Cardiomyopathy

