Abstract 4367893: Growing Use, Evolving Risk: A Contemporary Profile of Heart-Liver Transplantation

A Alexander Berg (Stanford, Stanford, California, United States) A Aravind Krishnan E Elbert Heng S Sofia Hu (Stanford, Stanford, California, United States) D Danielle Mullis (Stanford Medical School, Palo Alto, California, United States) N Nataly Vargas (Stanford, Stanford, California, United States) A Andre Vu (Stanford University, Palo Alto, California, United States) A Alyssa Garrison D Daniel Alnasir (Stanford University, Palo Alto, California, United States) D Daniel Clark (Stanford University, Palo Alto, California, United States) C Christiane Haeffele (STANFORD UNIVERSITY, Pacifica, California, United States) G George Lui (Stanford University, Palo Alto, California, United States) J Jeffrey Teuteberg (Division of Cardiovascular Medicine and Stanford Cardiovascular Institute, Stanford University, CA (W.F.F., K.T., K.T., A.S., H.I.L., C.A.L., T.H., K.S., A.Y., J.W.K., Y.H., J.T., K.K.K.).) Y Y Joseph Woo (STANFORD UNIV SCHOOL MEDICINE, Stanford, California, United States) J John Macarthur (Stanford University, Stanford, California, United States)

Abstract

Background: Combined heart–liver transplantation (CHLT) offers long-term survival comparable with isolated heart transplantation. National use keeps rising, and 2019 was the first year adults with congenital heart disease (ACHD) represented > 50 % of all CHLTs. Whether these modern ACHD candidates reach transplant in poorer condition—and how their increasing complexity affects outcomes—remains uncertain. Methods: UNOS STAR files captured every adult CHLT (2000-2024). A Pre-modern era (2000-2018) was contrasted with a Modern era (2019-2024). Wilcoxon and Chi-squared tests compared characteristics; Kaplan–Meier curves and multivariable Cox models—including a prespecified Modern era × ACHD interaction—evaluated 90-day and 1-year mortality. Thirty-day conditional survival localised excess risk. Results: Among 586 heart-liver transplants from 2000–2024, annual volume more than doubled after 2019, rising from ~30 to over 70 per year (Image 1) . ACHD recipients also increased from 28% to 55% in 2019. Modern recipients were younger (median 43 vs 48 y) yet markedly sicker: ventricular-assist device 8.1 % vs 3.8 %, extracorporeal membrane oxygenation 2.7 % vs 0 %, prior sternotomy 60 % vs 36 % (all P < 0.05). Procurement distance quadrupled (198 vs 51 nm) and cold-ischemic time lengthened (3.7 vs 3.0 h; P < 0.001). Kaplan–Meier curves (Image 2) showed higher Modern-era mortality for the full cohort at 90 days (13.5 % vs 6.2 %) and 1 year (17.5 % vs 12.1 %; both P ≤ 0.007); ACHD-only curves revealed an even wider Modern-era deficit at 90 days (P = 0.003) and 1 year (P = 0.007). Each additional ischemic hour increased 1-year hazard 22 % (HR 1.22, P = 0.007). The Modern era × ACHD term was strong (HR 3.9, P = 0.009), indicating nearly four-fold excess risk for Modern-era ACHD recipients. Conditional curves equalised beyond day 30 (P = 0.36) ( Image 3). Deaths shifted toward cerebrovascular events (15 % vs 3 %), organ failure (23% vs 15% and primary graft failure (11 % vs 3 %) Conclusions: Survival has declined in the Modern era for CHLT overall and—most strikingly—for ACHD recipients, likely driven by greater physiologic and surgical complexity and longer cold ischemia. Because deaths cluster within the peri-operative window, earlier ACHD referral, cold-ischemia reduction, and ACHD-focused peri-operative pathways are essential. Allocation policies that broadened sharing expanded access but now require refinement to safeguard this vulnerable ACHD CHLT population.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (15)

A

Alexander Berg

Stanford, Stanford, California, United States

A

Aravind Krishnan

E

Elbert Heng

S

Sofia Hu

Stanford, Stanford, California, United States

D

Danielle Mullis

Stanford Medical School, Palo Alto, California, United States

N

Nataly Vargas

Stanford, Stanford, California, United States

A

Andre Vu

Stanford University, Palo Alto, California, United States

A

Alyssa Garrison

D

Daniel Alnasir

Stanford University, Palo Alto, California, United States

D

Daniel Clark

Stanford University, Palo Alto, California, United States

C

Christiane Haeffele

STANFORD UNIVERSITY, Pacifica, California, United States

G

George Lui

Stanford University, Palo Alto, California, United States

J

Jeffrey Teuteberg

Division of Cardiovascular Medicine and Stanford Cardiovascular Institute, Stanford University, CA (W.F.F., K.T., K.T., A.S., H.I.L., C.A.L., T.H., K.S., A.Y., J.W.K., Y.H., J.T., K.K.K.).

Y

Y Joseph Woo

STANFORD UNIV SCHOOL MEDICINE, Stanford, California, United States

J

John Macarthur

Stanford University, Stanford, California, United States