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Less Invasive Acute Rejection Surveillance After Pediatric Heart Transplantation: Experiences From a Low-intensity
Lisa-Maria Rosenthal1,2,3,4, Luisa M Müller1,2, Michaela M Freitag5
1The Department for Congenital Heart Disease - Pediatric Cardiology, Deutsches Herzzentrum der Charité, Berlin, Germany.
Less invasive rejection surveillance using echocardiography in pediatric heart transplant recipients did not compromise graft survival. This approach may reduce complications and costs associated with invasive biopsies.
Area of Science:
- Pediatric Cardiology
- Transplantation Immunology
- Graft Monitoring
Background:
- Acute rejection is a major cause of morbidity and mortality post-pediatric heart transplantation (HT).
- Current guidelines rely solely on endomyocardial biopsies (EMB) for rejection surveillance.
- This study explored outcomes of less invasive surveillance in a low-biopsy center setting.
Purpose of the Study:
- To evaluate clinical outcomes of less invasive rejection surveillance in pediatric heart transplant recipients.
- To determine if echocardiography can effectively supplement or replace routine EMB.
- To assess the impact on graft survival and complications.
Main Methods:
- Retrospective analysis of 46 pediatric heart recipients (2011-2021).
- Frequent clinical and echocardiographic evaluations, including tissue Doppler imaging (TDI).
- Protocol EMB at 1 and 2 years post-HT, with additional biopsies based on clinical/echocardiographic changes.
Main Results:
- Graft survival was high (97.8% at 1 year, 95.7% at 2 years) with less invasive surveillance.
- Acute rejection detected in 8.5% of EMB; no protocol EMB in asymptomatic patients showed rejection.
- Absence of reduced TDI velocities and normal clinical status correlated with non-rejection.
Conclusions:
- Combining clinical follow-up with TDI echocardiography is a viable, less invasive rejection surveillance method.
- This approach did not compromise long-term clinical outcomes in pediatric heart transplant recipients.
- Further validation in larger cohorts could reduce invasive biopsies, associated risks, and costs.
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