Partial Heart Transplant for Congenital Heart Disease.

Abstract

Importance

Partial heart transplant, or living valve replacement, has the potential to advance surgical management of irreparable valvular disease by providing a viable option with capacity for growth.

Objectives

To describe the early experience and assess the feasibility, safety, and efficacy of partial heart transplant in patients with congenital heart valve disease.

Design, setting, and participants

Case series of the first 19 patients to undergo partial heart transplant at a single high-volume pediatric cardiac surgery and transplant center in the US between April 2022 and December 2024. No patients were excluded or lost to follow-up.

Exposures

Partial heart transplant using semilunar valves from donor hearts. Maintenance immunosuppression consisted of tacrolimus monotherapy with a trough level goal of 4 to 8 ng/mL.

Main outcomes and measures

Efficacy was defined as growth of the transplanted valve annulus and leaflets over time. Secondary outcomes included valve dysfunction and complications related to immunosuppression.

Results

Among the 19 participants with irreparable congenital heart valve dysfunction, 53% were male and 47% female. The median age at the time of transplant was 97 days. The median follow-up was 26 weeks. Three patients received partial heart transplant of both semilunar valves, 7 underwent living pulmonary valve replacement in the pulmonary position, 2 had a living aortic valve allograft in the aortic position, and 7 had a living aortic valve allograft in the pulmonary position. Nine patients constituting the initial cohort of partial heart transplant recipients had their annular diameter and valve leaflet length longitudinally analyzed for growth. All valves functioned well and demonstrated growth along appropriate z scores. Annular diameter increased from medians of 7 mm (aortic valve) and 9 mm (pulmonary valve) to 14 mm (aortic valve) and 17 mm (pulmonary valve), respectively. Leaflet length similarly increased from medians of 0.5 mm (aortic valve) and 0.49 mm (pulmonary valve) to 1 mm (aortic valve) and 0.675 mm (pulmonary valve), respectively. One patient required reoperation unrelated to the implanted valve. No significant complications related to immunosuppression were observed.

Conclusions and relevance

Partial heart transplant appears feasible, safe, and efficacious. All transplanted valves demonstrated growth based on annular and leaflet length measurements. Careful follow-up and monitoring are crucial to support the continued expansion of this novel technique.

Department

Description

Provenance

Subjects

Aortic Valve, Pulmonary Valve, Humans, Heart Defects, Congenital, Heart Valve Diseases, Tacrolimus, Immunosuppressive Agents, Treatment Outcome, Aftercare, Heart Transplantation, Retrospective Studies, Feasibility Studies, Graft Rejection, Adolescent, Adult, Child, Child, Preschool, Infant, Infant, Newborn, Female, Male

Citation

Published Version (Please cite this version)

10.1001/jama.2025.13580

Publication Info

Overbey, Douglas M, Berk Aykut, John A Kucera, Cathlyn K Medina, Neeta J Sethi, Piers CA Barker, Erin V Shea, Joseph W Turek, et al. (2025). Partial Heart Transplant for Congenital Heart Disease. JAMA, 334(12). pp. 1077–1083. 10.1001/jama.2025.13580 Retrieved from https://hdl.handle.net/10161/33802.

This is constructed from limited available data and may be imprecise. To cite this article, please review & use the official citation provided by the journal.

Scholars@Duke

Overbey

Douglas Overbey

Assistant Professor of Surgery
Aykut

Berk Aykut

House Staff

College/University: Ruprecht Karl University of Heidelberg

Medical School: Ruprecht Karl University of Heidelberg

Sethi

Neeta Jain Sethi

Assistant Professor of Pediatrics
Barker

Piers Christopher Andrew Barker

Professor of Pediatrics

Improving parent/infant bonding in prenatally diagnosed congenital heart disease
 
Analysis of advanced cardiac mechanics (strain, strain rate, torsion) in congenital and acquired heart disease by echo and cardiac MRI

Development of novel uses of 3D/4D echo for fetal and congenital heart disease

Sub-maximal exercise testing in congenital and maternal heart disease

Cardiac Mechanics during exercise in pediatrics

Outcome improvement in patients with Functional Single Ventricle and fetal cardiac disease

Application of novel imaging technologies (ultrasound, cardiac MRI, cardiac CT) in fetal, congenital and acquired heart disease

Characterization of rheumatic heart disease and HIV-related cardiomyopathy in developing countries

Cost Effectivess of screening for immune-mediated fetal heart block

Dyssynchrony analysis in pediatric patients

3D printing and computational fluid dynamics in congenital heart disease

Shea

Erin V Shea

Assistant Professor of Pediatrics

Pediatric transplant cardiology
Heart failure and cardiomyopathy in children

Turek

Joseph W Turek

Professor of Surgery

Joseph W. Turek, MD, PhD, MBA is an academic pediatric cardiac surgeon at Duke University in Durham, North Carolina. Since 2017, Dr. Turek has served as chief of pediatric cardiac surgery. Prior to Duke, he served in a similar leadership role at the University of Iowa Stead Family Children’s Hospital from 2012-2017.

Dr. Turek attended the Illinois Mathematics and Science Academy for secondary education. He then graduated from Northwestern University with a degree in biochemistry and received his MD/PhD (pharmacology) from the University of Illinois in Chicago with Alpha Omega Alpha distinction. He completed his general surgery education at Duke University, where he also finished a cardiothoracic surgery residency. During this time, he served as a visiting congenital heart surgery fellow at Texas Children’s Hospital. Dr. Turek completed a congenital cardiac surgery fellowship at the Children’s Hospital of Philadelphia in 2011. He received his MBA with a concentration in Health Sector Management from Duke’s Fuqua School of Business in 2020.

Board certified in general surgery, thoracic surgery and congenital cardiac surgery, Dr. Turek has been one of the foremost innovators of the last decade in congenital heart surgery, developing novel operations, modifying techniques and introducing new products and procedures to children and adults with congenital cardiac disease. Most notably, he performed the world’s first co-transplant of a heart and cultured thymus tissue, in an operation that could usher in an era in which solid organ transplant recipients can develop tolerance to their newly transplanted organ, recognizing them as “self”. In another highly innovative operation, he performed the world’s first partial heart transplant for a newborn without functioning aortic or pulmonary valves, maintaining growth capacity of the newly implanted valves. Additionally, he led the team at Duke in completing the nation’s first pediatric donation after circulatory death heart transplant with ex vivo reanimation and with normothermic regional perfusion, as a means to expand the already limited donor pool of available organs. His clinical passion and expertise lies in high complexity neonatal heart surgery.

Academically, Dr. Turek has published over 200 peer-reviewed manuscripts and numerous book chapters. He maintains an active and well-funded research laboratory with projects spanning from basic science to translational to clinical research, in areas such as heart transplant tolerance with thymus-heart co-transplant, partial heart transplantation, xenotransplantation, Marfan syndrome, and the role of alpha-gal sensitization in biologic valve degradation. He maintains active leadership roles in national and international cardiothoracic surgery societies.


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