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Updated: Sep 10, 2025

A Porcine Heterotopic Heart Transplantation Protocol for Delivery of Therapeutics to a Cardiac Allograft
Published on: February 14, 2022
Cardiomyopathy as indication for pediatric heart transplantation
Alireza Raissadati1, Drishti Tolani2, Elizabeth L Profita1
1Department of Pediatrics (Cardiology), Stanford University, Palo Alto, California.
Pediatric cardiomyopathy (CMP) is a serious heart condition in children, often leading to heart failure and the need for transplantation. Ventricular assist devices (VADs) improve survival rates for these young patients.
Area of Science:
- Pediatric Cardiology
- Cardiovascular Research
- Transplantation Medicine
Background:
- Pediatric cardiomyopathy (CMP) affects 1 in 100,000 children, frequently progressing to end-stage heart failure.
- CMP is the leading cause for pediatric heart transplantation, necessitating careful management of etiologies and listing criteria.
- Navigating waitlist complexities and understanding specific CMP subtypes are crucial for successful outcomes.
Purpose of the Study:
- To provide a comprehensive review of pediatric cardiomyopathy progressing to end-stage heart failure requiring transplantation.
- To synthesize current knowledge on CMP etiologies, clinical presentations, and transplant evaluation.
- To highlight the impact of ventricular assist devices (VADs) and contemporary post-transplant management.
Main Methods:
- Literature review synthesizing current knowledge on pediatric cardiomyopathy and heart transplantation.
- Analysis of etiologies, clinical presentations, and transplant evaluation strategies.
- Examination of the role of mechanical circulatory support, specifically VADs, in bridging to transplant.
Main Results:
- Pediatric CMP is a critical challenge, often leading to heart failure and transplantation.
- Ventricular assist devices (VADs) have significantly improved survival rates for pediatric heart transplant candidates.
- Post-transplant outcomes show continuous improvement with refined long-term management strategies.
Conclusions:
- This review offers an updated framework for clinicians managing pediatric cardiomyopathy and heart failure.
- Optimizing decision-making for transplant evaluation and VAD use is essential for this high-risk population.
- Continued advancements in post-transplant care are improving survival and quality of life.
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Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy IV: Restrictive Cardiomyopathy
Kidney Transplant I: Introduction

