Evidence map›Paper›PMID 40162860›Full record

Observational studyCritical care explorations2025

Prothrombotic Microvesicle Generation in Pediatric Cardiopulmonary Bypass: A Pilot Observational Study.

Andrew D Meyer, Anjana Rishmawi, Alia Elkhalili, David Rupert, Joshua Walker, John Calhoon, Andrew P Cap, Lauren Kane

Abstract readObservational Study
In one paragraph

Observational study in Critical care explorations, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Andrew D MeyerDivision of Critical Care, Department of Pediatrics, Long School of Medicine, University of Texas Health Science Center, San Antonio, TX.ORCID 0000-0001-8121-2619
Anjana RishmawiDivision of Critical Care, Department of Pediatrics, Long School of Medicine, University of Texas Health Science Center, San Antonio, TX.
Alia ElkhaliliDivision of Critical Care, Department of Pediatrics, Long School of Medicine, University of Texas Health Science Center, San Antonio, TX.
David RupertDivision of Critical Care, Department of Pediatrics, Long School of Medicine, University of Texas Health Science Center, San Antonio, TX.
Joshua WalkerDepartment of Cardiothoracic Surgery, Long School of Medicine, University of Texas Health Science Center, San Antonio, TX.
John CalhoonDepartment of Cardiothoracic Surgery, Long School of Medicine, University of Texas Health Science Center, San Antonio, TX.
Andrew P CapDepartment of Organ Support & Automated Technologies, U.S. Army Institute of Surgical Research, Fort Sam Houston, TX.
Lauren KaneDepartment of Cardiothoracic Surgery, Childrens Hospital of New Orleans, New Orleans, LA.

Funding

Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
Pro-thrombotic Microparticles Generated by Pediatric Cardiopulmonary BypassK23HL124336 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI MEYER, ANDREW DUNCAN JOSEPH · 2015 to 2018
$725k
NCATS NIH HHS UL1 TR001120NHLBI NIH HHS K23 HL124336
6 · The paper itself

Abstract

importanceOver 10% of children develop thrombosis after cardiac surgery for congenital heart disease. Children with a single ventricle physiology have the highest risk of thrombosis associated with increased length of the postoperative stay, neurologic complications, and mortality. To decrease these complications, research is needed to understand the mechanisms that promote cardiopulmonary bypass (CPB) surgery-induced thrombin generation and clot formation.

objectivesThe objective of this pilot observational study was to measure the generation of prothrombotic microvesicles (MVs) and thrombin generation in 21 children collected 5 minutes after initiation of CPB, at the end of CPB, upon arrival in the pediatric congenital cardiac unit (PCCU), and 20 to 24 hours after arrival in the PCCU. DESIGN, SETTING, AND

participantsAn observational pilot study measured platelet and leukocyte MV, platelet aggregation, coagulation, and thrombin generation in 21 children undergoing CPB surgery. The study setting was a tertiary pediatric hospital. Inclusion criteria included age between birth to 5 years and weight on the day of surgery greater than three kilograms. MAIN OUTCOMES AND MEASURES: Bleeding outcomes were measured by chest tube output and thrombotic outcomes were measured by surveillance ultrasound. Laboratory outcomes of prothrombotic MVs and thrombin generation were measured by high-resolution flow cytometry and calibrated automated thrombogram, respectively.

resultsTime on CPB correlated with a significant increase in WBCs and phosphatidylserine-expressing MVs. Children with single ventricle physiology had increased levels of prothrombotic MVs (p = 0.017), platelet aggregation, peak thrombin (p = 0.019), and d-dimer (p = 0.029) upon arrival to the ICU compared with children with a dual ventricle. Only single ventricle children had a positive correlation between generation of platelet MV with peak thrombin (p = 0.010). CONCLUSIONS AND RELEVANCE: Larger prospective studies are needed to determine if prothrombotic MVs can predict children with congenital heart disease at risk for thrombotic events.

Indexed as

Cardiopulmonary BypassCell-Derived MicroparticlesHeart Defects, CongenitalThrombosisChild, PreschoolFemaleHumansInfantInfant, NewbornMalePilot ProjectsPlatelet AggregationThrombinThrombin

Identifiers

PMID40162860
PMCPMC11960801

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.