Evidence map›Paper›PMID 39435719›Full record

ArticleJournal of the American Heart Association2024

Longitudinal Assessment of T1 Mapping Trends Disease in Pediatric Patients With Heart Transplant.

Nicolle M Ceneri, Ravi Vegulla, Nicholas Mouzakis, Karin Hamann, Devika Richmann, Joshua Kanter, John Berger, Tacy Downing, Yue-Hin Loke, Steven J Staffa and 3 more

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2024. 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

13 authors.

Nicolle M CeneriChildren's National Hospital Washington DC.ORCID 0000-0003-0478-6250
Ravi VegullaChildren's National Hospital Washington DC.
Nicholas MouzakisChildren's National Hospital Washington DC.
Karin HamannChildren's National Hospital Washington DC.ORCID 0000-0001-6921-2640
Devika RichmannColumbia University, Morgan Stanley Children's Hospital New York NY.
Joshua KanterChildren's National Hospital Washington DC.ORCID 0000-0002-9773-4566
John BergerChildren's National Hospital Washington DC.
Tacy DowningChildren's National Hospital Washington DC.ORCID 0000-0002-2577-0074
Yue-Hin LokeChildren's National Hospital Washington DC.ORCID 0000-0003-1003-1903
Steven J StaffaDepartment of Anesthesiology and Surgery, Boston Children's Hospital Harvard Medical School Boston MA.ORCID 0000-0002-7588-7596
David ZurakowskiDepartment of Anesthesiology and Surgery, Boston Children's Hospital Harvard Medical School Boston MA.ORCID 0000-0003-3610-6942
Russell CrossNemours Children's Hospital Wilmington DE.ORCID 0000-0003-2219-8049
Laura J OlivieriUPMC Children's Hospital of Pittsburgh Pittsburgh PA.ORCID 0000-0002-3783-0783

Funding

Cardiac MRI Increases Accuracy and Decreases Risk of Evaluation of Children with Cardiomyopathy and Cardiac TransplantationR01HL144494 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI OLIVIERI, LAURA J · 2019 to 2023
$3.6M
Children’s National Stimulating Access to Research in Residency (CNStARR) Program (NHLBI)R38HL167247 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI Andrea Leigh Hahn · 2023 to 2026
$1.7M
NHLBI NIH HHS R01 HL144494NHLBI NIH HHS R38 HL167247
6 · The paper itself

Abstract

backgroundSurveillance for heart transplant rejection by endomyocardial biopsy is invasive and may yield false negatives. T1 and T2 mapping from cardiac magnetic resonance can demonstrate elevations with rejection. We sought to evaluate longitudinal changes in T1 and T2 mapping in pediatric patients with heart transplant. METHODS AND

resultsA cohort study was performed of pediatric patients with heart transplant who underwent concurrent endomyocardial biopsy and cardiac magnetic resonance with T1 and T2 mapping from December 2019 to July 2024. Segmental values were measured and subsegmental elevations (ie, hotspots) were identified. Subjects were categorized as either treated rejection or no rejection. Peak and mean T1 and T2 values and number of hotspots at/between each time point for patient dyads were compared between the groups. A total of 21 subjects (7 treated rejection, 14 no rejection) with 68 total encounters met inclusion criteria. Peak and mean T1 values were higher in treated rejection patients during the rejection period and decreased with treatment (peak, 1086 versus 1052; mean, 1028 versus 1021), such that at last follow-up when their rejection had resolved, there was no significant difference in values when compared with no rejection patients (peak, 1066; mean, 1016). The number of T1 hotspots decreased after rejection treatment (2 versus 1). There were no changes in peak or mean T2 values in the treated rejection group despite treatment, and peak and mean T2 values were similar to patients with no rejection through last follow-up.

conclusionsElevated T1 values and hotspots observed during cardiac allograft rejection decline in response to treatment. Cardiac magnetic resonance may serve as a noninvasive monitoring tool for the development and resolution of rejection, as well as the effectiveness of rejection therapy.

Indexed as

Graft RejectionHeart TransplantationMyocardiumAdolescentBiopsyChildChild, PreschoolFemaleHumansLongitudinal StudiesMagnetic Resonance Imaging, CineMaleRetrospective Studiescardiac magnetic resonanceheart transplantparametric mappingpediatrics

Identifiers

PMID39435719
PMCPMC11935723

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Registered trials

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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.