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Updated: Aug 14, 2026

Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
Successful cardiac resynchronization therapy in a 9-year-old boy with dilated cardiomyopathy
J-H Nürnberg1, C Butter, H Abdul-Khaliq
1Abteilung für Angeborene Herzfehler/Kinderkardiologie, Klinikum Links der Weser, Senator-Weissling-Str. 1, 28277 Bremen, Germany. jan-hendrik.nuernberg@klinikum-bremen-ldw.de
Insights
Cardiac resynchronization therapy (CRT) effectively improved a child with dilated cardiomyopathy (DCMP) and left bundle branch block (LBBB). This pediatric CRT case study shows significant hemodynamic and functional gains, potentially delaying heart transplantation.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Electrophysiology
- Medical Device Technology
Background:
- Dilated cardiomyopathy (DCMP) and left bundle branch block (LBBB) in children present significant challenges.
- Cardiac resynchronization therapy (CRT) is established in adults but less experienced in pediatric populations.
- Heart transplantation (HTX) is often considered for pediatric patients with end-stage heart failure.
Observation:
- A 9-year-old boy with DCMP and LBBB, who met criteria for HTX, underwent transvenous CRT implantation.
- The implantation procedure was technically successful with an uneventful recovery.
- Optimized AV-interval pacing demonstrated significant hemodynamic improvements.
Findings:
- Pacing increased pulse pressure by 16% and left ventricular (LV) dp/dt by 63%.
- Tissue Doppler imaging confirmed complete LV resynchronization.
- The patient experienced enhanced physical capacity, allowing for the delay of HTX.
Implications:
- Transvenous CRT is a viable and effective treatment option for pediatric patients with DCMP and LBBB.
- CRT can significantly improve hemodynamic function and physical capacity in children.
- Successful CRT may reduce the need for or delay pediatric heart transplantation.
Abstract:
Despite increasing clinical impact of cardiac resynchronization therapy (CRT) with av-synchronous biventricular pacing in adults with dilated cardiomyopathy (DCMP), an ejection fraction (EF) of less than 35% and left bundle branch block (LBBB), there is still only little experience in children. We report on a 9-year-old boy with histologically proven DCMP and LBBB who had fulfilled the criteria for heart transplantation (HTX) after cardiac decompensation including catecholamine therapy. A transvenous CRT pacing system was implanted without technical difficulties. The healing process was uneventful. With optimized AV-interval invasive evaluation during implantation indicated a 16% pulse pressure increase and a 63% augmentation of LV dp/dt by pacing the LV 20 ms prior to the RV. Tissue Doppler imaging demonstrated complete LV resynchronization. Physical capacity increased and HTX could be delayed.
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