Multiparametric cardiovascular magnetic resonance is associated with outcomes in pediatric heart transplant recipients.

J Cardiovasc Magn Reson

Division of Cardiology, Department of Pediatrics, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL, USA, E Chicago Ave, Box 21. Chicago, IL, 60611.

Published: December 2024

Background: Multiparametric cardiovascular magnetic resonance (CMR) has an emerging role in non-invasive surveillance of pediatric heart transplant recipients (PHTR). Higher myocardial T2, higher extracellular volume fraction (ECV), and late gadolinium enhancement (LGE) have been associated with adverse clinical outcomes in adult heart transplant recipients. This study's purpose was to investigate the prognostic value of CMR-derived T1- and T2-mapping, ECV, and LGE for clinical outcomes in PHTR.

Methods: We performed a single-center, retrospective chart review of consecutive, gadolinium-enhanced CMR studies in PHTR over a 7.5-year period, excluding follow-up studies. Standard CMR ventricular volume and function analysis, T1 mapping with ECV, T2 mapping, and LGE assessment were performed. The composite outcome included cardiac death, non-cardiac death, re-transplantation, and cardiac hospitalization.

Results: Among 113 PHTR, mean age was 13.0±5.1y, with 6.0±4.0y since transplant. The indication for CMR was surveillance in 79%. Mean native T1 was 1050±48ms; T2 49.2±3.9ms and ECV 29.7±4.5%. LV LGE was present in 37% (42/113) and RV LGE in 3.5% (4/113). The mean follow-up time was 2.3y, median 1.4y. Cardiac death occurred in 2% (2/113), re-transplantation in 4% (4/113), and cardiac hospitalization in 22% (25/113). Non-cardiac death did not occur. Using Kaplan-Meier analysis, high T1 (≥1061ms), T2 (≥50.0ms), and ECV (≥31.4%) were each associated with decreased freedom from the composite outcome in follow-up. In univariable Cox regression analyses, high T1 was associated with increased risk of the composite outcome (HR 4.0, 95% CI 1.7-9.2, p=0.001), as were high T2 (HR 2.8, 95% CI 1.1-7.1, p=0.026), and high ECV (HR 3.5, 95% CI 1.5-8.1, p=0.004).

Conclusions: T1 and T2 mapping are associated with early differences in adverse cardiac events in PHTR. These data suggest a role for a multicenter study with longer follow-up duration.

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Source
http://dx.doi.org/10.1016/j.jocmr.2024.101138DOI Listing

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