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Published on: May 7, 2019
Acute rejection after paediatric heart transplantation: far less common and less severe
Astrid E Lammers1, Philip Roberts, Katherine L Brown
1Department of Paediatric Cardiology, Great Ormond Street Hospital for Children, London, UK.
Insights
Pediatric heart transplant rejection is a serious concern. Tacrolimus and mycophenolate mofetil-based immunosuppression show the best protective effect against rejection episodes.
Area of Science:
- Pediatric Cardiology
- Transplantation Immunology
- Immunosuppression Therapy
Background:
- Rejection remains a significant cause of morbidity and mortality in pediatric heart transplant recipients.
- Despite advancements in immunosuppression, understanding risk factors for rejection is crucial.
Purpose of the Study:
- To determine the incidence and outcomes of rejection in children post-heart transplantation.
- To identify risk factors associated with significant rejection episodes.
Main Methods:
- Retrospective analysis of 105 children undergoing heart transplantation between 2002 and 2007.
- Multivariate modeling to assess risk factors for rejection.
- Analysis of patient-years of follow-up and rejection episodes (grade >=3A).
Main Results:
- Twenty-three episodes of significant rejection occurred in 21 patients (20%) over 271.9 patient-years.
- Rejection was more common in older children, boys, and those treated with sirolimus.
- Tacrolimus-containing immunosuppression was associated with a significantly lower risk of rejection (P < 0.002).
- None of the patients with severe rejection requiring extracorporeal membrane oxygenation support were on mycophenolate mofetil.
Conclusions:
- Rejection is a serious complication after pediatric heart transplantation, although incidence may be lower than registry data.
- Sirolimus monotherapy was associated with increased rejection episodes.
- Tacrolimus and mycophenolate mofetil appear to offer the most effective protective profile against rejection.
Abstract:
Despite improved immunosuppression, rejection accounts for significant morbidity and mortality in children after heart transplantation. We report the incidence and outcome of rejection of 105 children (male = 50; mean age of 8.3 +/- 5.8 years) following heart transplantation between January 2002 and August 2007. A multi-variant model was constructed for risk factors associated with significant rejection. In 271.9 patient-years of follow-up, there were 23 episodes of significant rejection (>or=3A) in 21 patients (20%). Five presented in haemodynamic collapse requiring extracorporeal membrane oxygenation support 1.6-35.9 months after transplantation; four of five survived the rejection episode. Overall rejection episodes were more common in older children, boys and those treated with sirolimus. Whereas the risk for rejection in patients on an immunosuppression regime containing tacrolimus was significantly lower. The latter finding persisted on multivariate analysis (P < 0.002). Interestingly, none of the patients who presented with haemodynamic collapse was on mycophenolate mofetil. While our experience is of a far lower incidence of rejection than registry data, rejection remains a serious problem after paediatric heart transplantation. Sirolimus without a calcineurin inhibitor was associated with more rejection episodes, whereas tacrolimus and mycophenolate appeared to provide the best protective profile.
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