Evidence map›Paper›PMID 40314766›Full record

Trial reportPediatric cardiology2026

Reexploring the STRESS Trial: Subgroup Postoperative Outcomes Following Methylprednisolone for Infant Heart Surgery.

Sudeep D Sunthankar, Kevin D Hill, Jeffrey P Jacobs, H Scott Baldwin, Marshall L Jacobs, Jennifer S Li, Eric M Graham, Ashraf M Resheidat, Venugopal Amula, Mark S Bleiweis and 8 more

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Pediatric cardiology, 2026. 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. Article
  2. Article
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

18 authors.

Sudeep D SunthankarDivision of Pediatric Cardiology and Center for Pediatric Precision Medicine, Department of Pediatrics, Vanderbilt University Medical Center, 2220 Children's Way; Suite 5230, Nashville, TN, 37232, USA. sudeep.sunthankar@vumc.org.
Kevin D HillDivision of Pediatric Cardiology, Duke University Medical Center, Durham, NC, USA.
Jeffrey P JacobsDivision of Cardiac Surgery, University of Florida, Gainesville, FL, USA.
H Scott BaldwinDivision of Pediatric Cardiology and Center for Pediatric Precision Medicine, Department of Pediatrics, Vanderbilt University Medical Center, 2220 Children's Way; Suite 5230, Nashville, TN, 37232, USA.
Marshall L JacobsDivision of Cardiac Surgery, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Jennifer S LiDivision of Pediatric Cardiology, Duke University Medical Center, Durham, NC, USA.
Eric M GrahamDivision of Pediatric Cardiology, Medical University of South Carolina, Charleston, SC, USA.
Ashraf M ResheidatDivision of Pediatric Cardiac Anesthesiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Venugopal AmulaDivision of Critical Care, Department of Pediatrics, Primary Children's Hospital, Salt Lake City, UT, USA.
Mark S BleiweisDivision of Cardiac Surgery, University of Florida, Gainesville, FL, USA.
Eric L WaldDivision of Pediatric Cardiology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Pirooz EghtesadyDivision of Cardiac Surgery, Washington University School of Medicine, St. Louis, MO, USA.
John P ScottDivision of Pediatric Cardiology, Medical College of Wisconsin, Madison, WI, USA.
Brett R AndersonDivision of Pediatric Cardiology, Icahn School of Medicine at Mt Sinai, New York, NY, USA.
Michael F SwartzDivision of Cardiac Surgery, University of Rochester, Rochester, NY, USA.
Alexis BenscoterDivision of Pediatric Cardiology, Cincinnati Children's Hospital, Cincinnati, OH, USA.
William RavekesDivision of Pediatric Cardiology, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Prince J KannankerilDivision of Pediatric Cardiology and Center for Pediatric Precision Medicine, Department of Pediatrics, Vanderbilt University Medical Center, 2220 Children's Way; Suite 5230, Nashville, TN, 37232, USA.

Funding

COVID-19 Supplement - Center for Innovative TRIals in ChilDrEN and AdulTs (TRIDENT)U24TR001608 · NCATS · DUKE UNIVERSITY · PI BENJAMIN, DANIEL K., HERNANDEZ, ADRIAN · 2016 to 2022
$177.0M
Vanderbilt Integrated Center of Excellence in Maternal and Pediatric Precision Therapeutics (VICE-MPRINT)P50HD106446 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PRINCE Joseph KANNANKERIL, Digna R Velez Edwards · 2021 to 2026
$9.7M
Leveraging existing registry resources to facilitate clinical trialsU01TR001803 · NCATS · DUKE UNIVERSITY · PI BALDWIN, H SCOTT, JACOBS, JEFFREY PHILLIP · 2016 to 2020
$5.5M
Burroughs Wellcome Fund 1018894Eunice Kennedy Shriver National Institute of Child Health and Human Development P50HD106446FDA HHS U18 FD006298NCATS NIH HHS U01 TR001803NCATS NIH HHS U01TR-001803-01NCATS NIH HHS U24 TR001608NICHD NIH HHS HHSN275201800003INICHD NIH HHS P50 HD106446
6 · The paper itself

Abstract

Objective Assess the association between intraoperative methylprednisolone and specific postoperative outcomes among subgroups undergoing infant heart surgery.

designSubpopulation analyses of The Steroids to Reduce Systemic Inflammation after Infant Heart Surgery trial, a double-blind randomized placebo-controlled trial.

setting24 congenital heart centers. PATIENTS: Infants (< 1 year old) undergoing heart surgery with cardiopulmonary bypass. Patients stratified by Society of Thoracic Surgeons-European Association for Cardio-Thoracic Surgery Congenital Heart Surgery (STAT) Mortality Category, age, gestational age, and presence of chromosomal or syndromic diagnosis (CSD).

interventionsMethylprednisolone (30 mg/kg) versus placebo administered into cardiopulmonary bypass pump-priming fluid. MEASUREMENTS AND MAIN

resultsOutcomes included death, heart transplantation, mechanical circulatory support, reinterventions, and hospital length of stay. Ranked composite outcome (death, transplant, or one of 13 major complications) was compared between placebo and methylprednisolone for each subgroup using the win ratio. Methylprednisolone did not reduce odds of death, transplant, or mechanical circulatory support for any subgroup. Those receiving methylprednisolone had fewer catheterization or surgical reinterventions after STAT Category 1-3 operations [OR 0.50 (0.29-0.86)]; and fewer reoperations for bleeding among patients undergoing STAT Category 1-3 operations [OR 0.28 (0.09-0.87)], term infants [OR 0.30 (0.12-0.76)], and those without CSD [OR 0.22 (0.07-0.68)]. Length of stay was no different between methylprednisolone versus placebo. Those without chromosomal or syndromic diagnosis demonstrated a favorable association for methylprednisolone [win ratio 1.28 (1.01-1.61)] for the composite outcome.

conclusionExploratory subpopulation analyses, although underpowered, suggest that methylprednisolone is not associated with significant harm and may benefit certain subpopulations.

Indexed as

Anti-Inflammatory AgentsCardiac Surgical ProceduresHeart Defects, CongenitalMethylprednisolonePostoperative ComplicationsCardiopulmonary BypassDouble-Blind MethodFemaleGlucocorticoidsHumansInfantInfant, NewbornLength of StayMaleTreatment OutcomeAnti-Inflammatory AgentsGlucocorticoidsMethylprednisoloneCardiac surgeryCongenital heart diseaseCritical careMethylprednisolone

Identifiers

PMID40314766
PMCPMC12354065

What Socratic holds

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LicenceCC BY
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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 Socratic graph.