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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Heart transplantation in children after mechanical circulatory support with pulsatile pneumatic assist device
Brigitte Stiller1, Roland Hetzer, Yuguo Weng
1Department of Pediatric Cardiology, Deutsches Herzzentrum Berlin, Berlin, Germany. stiller@dhzb.de
Insights
Bridging pediatric patients with a pulsatile pneumatic ventricular assist device (VAD) to heart transplantation (HTx) is safe. Survival outcomes after VAD-supported HTx are comparable to other pre-transplant support methods.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Surgery
- Transplantation Medicine
Background:
- Mechanical circulatory support using pulsatile pneumatic ventricular assist devices (VADs) is a critical intervention for children with severe cardiogenic shock.
- The long-term impact of VAD support on survival following heart transplantation (HTx) in pediatric patients requires further investigation.
Purpose of the Study:
- To evaluate the safety and efficacy of using pulsatile pneumatic VADs as a bridge to heart transplantation in children.
- To compare early and long-term survival rates and clinical outcomes in pediatric patients undergoing HTx after VAD support versus other pre-transplant management strategies.
Main Methods:
- A retrospective review of 95 pediatric patients who underwent heart transplantation.
- Patients were categorized into three groups: elective HTx (Group A), emergency HTx without VAD (Group B), and VAD-supported HTx (Group C).
- Comparison of survival rates, neurologic outcomes, acute cardiac rejection, and transplant failure across the groups.
Main Results:
- Overall 5-year survival after HTx was 78%, with no significant differences among the three groups (Group A: 80%, Group B: 79%, Group C: 72%).
- Pediatric patients with cardiomyopathy showed significantly better survival rates compared to those with congenital heart defects (p = 0.014).
- No significant differences were observed in neurologic outcomes, acute cardiac rejection, or transplant failure between the groups.
Conclusions:
- Bridging to heart transplantation with a pulsatile pneumatic VAD is a safe and effective strategy for pediatric patients with end-stage heart failure.
- Survival following HTx in VAD-supported pediatric patients is comparable to those bridged with inotropes or awaiting transplantation electively.
Background:
Mechanical support with a pulsatile pneumatic ventricular assist device (VAD) is a complex rescue procedure performed in children with untreatable cardiogenic shock. Its impact on early and long-term survival after subsequent heart transplantation (HTx) remains to be determined.
Methods:
We reviewed retrospectively the course of 95 children (median age, 8 years; range, 8 days-17 years; body weight, 24 kg; range, 3-110 kg) who underwent HTx. Group A, the elective-HTx group, consists of 33 children who were treated as outpatients before transplantation. Group B, the emergency-HTx group, has 44 children who were critically ill and hospitalized before transplantation but without ventricular assist devices, whereas Group C, the VAD-HTx group, consists of 18 children resuscitated and supported with pulsatile pneumatic VADs for a median time of 20 days.
Results:
Overall actuarial survival after cardiac transplantation was 86% at 1 month, 82% at 1 year, and 78% at 5 years, without significant differences among the 3 sub-groups. Group A had the best long-term survival rate, 88% at 1 month, 88% at 1 year, and 80% at 5 years. Group B had a survival rate of 88% at 1 month, 82% at 1 year, and 79% at 5 years. Group C had a survival rate of 72% at 1 month, 72% at 1 year, and 72% at 5 years. We found no differences in neurologic outcome, acute cardiac rejection, or transplant failure. The survival rate was significantly better in the children with cardiomyopathy compared with those with congenital heart defects (p = 0.014).
Conclusions:
Bridging to HTx with a pulsatile pneumatic VAD is a safe procedure in pediatric patients. After HTx, overall survival of these children is similar to that of patients who were bridged with inotropes or who were awaiting heart transplantation electively.
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