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Comparing Outcomes of Heartmate 3 and Heart Transplantation in Older Children With Dilated Cardiomyopathy-Can
Waldemar F Carlo1, Luz A Padilla2, James K Kirklin3
1Department of Pediatrics, University of Alabama, Birmingham, USA.
Insights
Adolescents with dilated cardiomyopathy (DCM) showed excellent survival with Heartmate 3 (HM3) or heart transplant. Many HM3 patients were transplanted early, suggesting HM3 can support patients while awaiting transplant.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Surgery
- Medical Devices
Background:
- End-stage dilated cardiomyopathy (DCM) in children typically requires heart transplantation or temporary ventricular assist devices.
- Limited pediatric data exists for the Heartmate 3 (HM3) device as a longer-term option for DCM.
- This study compares HM3 and heart transplantation outcomes in adolescents with DCM.
Purpose of the Study:
- To evaluate the survival and adverse event rates of adolescents (ages 10-18) with DCM treated with HM3 versus heart transplantation.
- To assess the feasibility of using HM3 as a longer-term support or bridge to transplant in this population.
Main Methods:
- Analysis of two clinical registries: Pedimacs and Pediatric Heart Transplant Society.
- Inclusion criteria: DCM patients aged 10-18 years, treated with HM3 or transplant between 2017-2022.
- Data collected on mortality and adverse events.
Main Results:
- Ninety HM3 patients and 306 transplant patients were analyzed.
- Similar 12- and 36-month survival rates: 94.4% for HM3 and 99.3%/95.6% for transplant.
- HM3 cohort had a higher proportion of Black patients (40% vs. 30%).
- Sixty-six HM3 patients (73%) were transplanted early (median 2.8 months); 3 late explants for recovery, 3 early deaths.
- Low rates of bleeding, stroke, and device malfunction (<0.1 events/patient/year) in the HM3 group.
Conclusions:
- Adolescents with DCM treated with HM3 or transplant demonstrated excellent 3-year outcomes.
- Early transplantation was common for HM3 patients, indicating HM3's role in supporting patients awaiting transplant.
- HM3 offers potential for delaying or avoiding transplantation, improving long-term survival, and preserving donor organs.
Background:
Children with end-stage dilated cardiomyopathy (DCM) usually undergo heart transplantation or a short-term bridge with a ventricular assist device. Heartmate 3 (HM3) may represent an appealing longer-term option, though pediatric data are limited. We analyzed two clinical registries and hypothesized that adolescents with DCM treated with either HM3 or transplant would present similar survival.
Methods:
The Pedimacs and Pediatric Heart Transplant Society registries were queried for DCM patients ages 10-18 years treated with HM3 or transplant, between 2017 and 2022. Mortality and adverse events were reported.
Results:
Ninety HM3 and 306 transplant patients were reported within the respective registries. There was a higher proportion of Black patients in the HM3 cohort (40% vs. 30% in the transplant cohort, p = 0.03). Twelve- and 36-month survival rates were both 94.4% for HM3 patients and were 99.3% and 95.6% for transplant patients. In the HM3 group, there were 66 transplants (median time of 2.8 months), 3 late explants for recovery, and 3 early deaths. Conditional 1-year survival for HM3 and transplant was 100% and 96.3%, respectively, at 3 years. In the HM3 group, bleeding, stroke, and device malfunction rates were low at 0.1 events per patient per year.
Conclusions:
Adolescents with DCM treated with either HM3 or transplant had excellent 3-year outcomes, though many HM3 pediatric patients are transplanted early after device placement. Safely supporting this group of patients for an extended duration with HM3 has implications for delaying/avoiding transplantation, longer-term patient survival, and donor organ availability.
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