Evidence map›Paper›PMID 40384737›Full record

ReviewMethodist DeBakey cardiovascular journal2025

Multi-Organ Transplantation in Adult Congenital Heart Disease: Navigating the Unique Challenges of a Distinct Patient Population.

Valeria E Duarte, Marcus A Urey, Eric D Adler, Brenda Merkelz, Mark J Hobeika, Erik E Suarez, Andrea G Quarti, Rayan Yousefzai

Abstract readReview
In one paragraph

Review in Methodist DeBakey cardiovascular journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Valeria E DuarteHouston Methodist DeBakey Heart & Vascular Center, Houston Methodist, Houston, Texas, US.ORCID https://orcid.org/0000-0001-6616-5412
Marcus A UreyUniversity of California, San Diego, California, US.ORCID https://orcid.org/0000-0001-8311-5003
Eric D AdlerUniversity of California, San Diego, California, US.ORCID https://orcid.org/0000-0002-4765-0188
Brenda MerkelzJ.C. Walter Jr. Transplant Center, Houston Methodist, Houston, Texas, US.
Mark J HobeikaHouston Methodist Hospital, Houston, Texas, US.ORCID https://orcid.org/0000-0002-7444-7097
Erik E SuarezHouston Methodist, Houston, Texas, US.
Andrea G QuartiHouston Methodist, Houston, Texas, US.ORCID https://orcid.org/0000-0002-0040-7084
Rayan YousefzaiHouston Methodist DeBakey Heart & Vascular Center, Houston Methodist, Houston, Texas, US.ORCID https://orcid.org/0000-0002-1759-8892

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The prevalence of adult congenital heart disease (ACHD) is increasing, with heart failure being the leading cause of death. For many ACHD patients, heart transplantation is the only treatment option for advanced heart failure, though significant extracardiac involvement may require multi-organ transplantation. Despite the rising number of ACHD transplants, multi-organ transplants in this population remain challenging, and a substantial gap remains between those in need and those who receive a transplant. While short-term outcomes may be worse for ACHD patients, long-term outcomes are comparable and even superior to other cardiomyopathies. Extracardiac organ dysfunction is common in ACHD patients, often precluding heart-alone transplantation. Fontan-associated liver disease, pulmonary vascular and restrictive lung disease, and renal dysfunction frequently necessitate multi-organ transplantation. ACHD patients have a unique immunological and sensitization profile, increasing their risk for infection, rejection, and malignancies, requiring specialized pretransplant desensitization and post-transplant immunosuppression strategies. ACHD transplantation presents unique surgical challenges, including chest reentry, vascular access issues, bleeding risks, extensive anatomical reconstruction, the need for longer vascular segments from donors, and prolonged ischemic times. Decisions regarding heart-alone versus heart-liver, heart-lung, or heart-kidney transplantation demand careful evaluation. These complex surgical plans require extensive multimodal imaging and collaboration with ACHD cardiac imaging specialists and abdominal transplant teams. Comprehensive coordination and psychosocial support are crucial for ACHD patients throughout the transplant process. A dedicated multidisciplinary team and an established and separate pathway for pre-, peri-, and postoperative care in centers with ACHD and multi-organ transplant expertise are essential. There is need for a revised organ allocation system to ensure timely access to transplantation for ACHD patients.

Indexed as

Heart Defects, CongenitalHeart TransplantationKidney TransplantationLiver TransplantationAdultClinical Decision-MakingHeart-Lung TransplantationHumansPatient SelectionRisk AssessmentRisk FactorsTreatment Outcomeadult congenital heart diseasecomplication associated with adult congenital heart diseaseheart transplantmulti-organ transplant

Identifiers

PMID40384737
PMCPMC12082638

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.