Evidence map›Paper›PMID 40864436›Full record

ArticleJAMA2025

Partial Heart Transplant for Congenital Heart Disease.

Douglas M Overbey, Berk Aykut, John A Kucera, Cathlyn K Medina, Neeta J Sethi, Piers C A Barker, Erin V Shea, Joseph W Turek

Abstract readEvaluation StudyComment
In one paragraph

Article in JAMA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Douglas M OverbeyCongenital Heart Surgery Research and Training Laboratory, Duke University, Durham, North Carolina.
Berk AykutCongenital Heart Surgery Research and Training Laboratory, Duke University, Durham, North Carolina.
John A KuceraCongenital Heart Surgery Research and Training Laboratory, Duke University, Durham, North Carolina.
Cathlyn K MedinaCongenital Heart Surgery Research and Training Laboratory, Duke University, Durham, North Carolina.
Neeta J SethiDuke Children's Pediatric and Congenital Heart Center, Duke University, Durham, North Carolina.
Piers C A BarkerDuke Children's Pediatric and Congenital Heart Center, Duke University, Durham, North Carolina.
Erin V SheaDuke Children's Pediatric and Congenital Heart Center, Duke University, Durham, North Carolina.
Joseph W TurekCongenital Heart Surgery Research and Training Laboratory, Duke University, Durham, North Carolina.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Heart Defects, CongenitalHeart TransplantationHeart Valve DiseasesAdolescentAdultAftercareAortic ValveChildChild, PreschoolFeasibility StudiesFemaleGraft RejectionHumansImmunosuppressive AgentsInfantInfant, NewbornImmunosuppressive AgentsTacrolimus

Identifiers

PMID40864436
PMCPMC12457970

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.