Evidence map›Paper›PMID 41284641›Full record

ArticleBlood2025

Multisite Validation of a Venous Thrombosis Risk Model in Critically Ill Children Through the CHAT Consortium.

Julie Jaffray, Brian R Branchford, Maua Mosha Alleyne, Ernest Amankwah, E Vincent S Faustino, Neil A Zakai, Anthony A Sochet, Amy Stillings, Emily Krava, Guy Young and 1 more

Abstract read
In one paragraph

Article in Blood, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Julie JaffrayRady Children's Hospital, University of California, San Diego, San Diego, California, United States.ORCID 0000-0002-1175-7266
Brian R BranchfordVersiti Blood Research Institute, Wauwatosa, Wisconsin, United States.
Maua Mosha AlleyneJohns Hopkins All Children's Hospital, St Petersburg, Florida, United States.ORCID 0000-0002-9797-2644
Ernest AmankwahJohns Hopkins University School of Medicine, United States.
E Vincent S FaustinoYale School of Medicine, New Haven, Connecticut, United States.
Neil A ZakaiUniversity of Vermont College of Medicine, Burlington, Vermont, United States.ORCID 0000-0001-8824-4410
Anthony A SochetJohns Hopkins All Children's Hospital, St. Petersburg, California, United States.ORCID 0000-0002-6290-4975
Amy StillingsUniversity of California, San Diego, San Diego, California, United States.ORCID 0000-0002-0153-0279
Emily KravaUniversity of California San Diego, United States.
Guy YoungChildren's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, California, United States.ORCID 0000-0001-6013-1254
Neil A GoldenbergJohns Hopkins University School of Medicine, St. Petersburg, Florida, United States.

Funding

Southern California Clinical and Translational Science InstituteUL1TR001855 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Thomas A Buchanan, Michele D. Kipke · 2016 to 2026
$81.3M
Age-dependent heterogeneity in the efficacy of prophylaxis with enoxaparin against catheter-associated thrombosis in critically ill childrenR01HD106326 · NICHD · YALE UNIVERSITY · PI FAUSTINO, EDWARD VINCENT · 2021 to 2025
$3.7M
Validation of a pediatric thrombosis risk assessment model and characterization of bleeding in hospitalized children through the Children's Hospital Acquired Thrombosis (CHAT) ConsortiumK23HL163330 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Julie Ann Jaffray · 2022 to 2026
$926k
NCATS NIH HHS UL1 TR001855NHLBI NIH HHS K23 HL163330NICHD NIH HHS R01 HD106326
6 · The paper itself

Abstract

Critically ill children have a high risk of hospital associated venous thromboembolism (HA-VTE). Developing a validated risk assessment model (RAM) to identify children who may benefit from thromboprophylaxis is essential. We aimed to prospectively validate the Children's Healthcare Advancements in Thrombosis (CHAT) intensive care unit (ICU) VTE RAM containing five clinically significant variables: CVC, immobility, congenital heart disease, autoimmune or inflammatory conditions and hospital stay of ≥3 days in a multicenter cohort study. Randomly selected patients aged 0-21 years admitted to a pediatric ICU (PICU) at 32 institutions were monitored via medical record review for HA-VTE. Discrimination was assessed using the area under the receiver operating characteristic (AUROC) curve. Calibration was assessed using calibration plots. Complete case and imputed analyses were performed and model risk scores were generated along with post-test probability. The RAM was validated in 4,674 patients with an AUROC of 0.71 [95% CI:0.64-0.78], calibration slope of 1.0 (95% CI:0.87-1.14) and intercept of 1.81x10-5 (95% CI: -5.40x10-3-5.44x10- 3). The AUROC for the imputed model was 0.69 (95% CI:0.68-0.70) with the calibration slope of 1.03 (95% CI: 0.85-1.21) and intercept of 1.22x10-3 (95% CI: -7.80x10-3-5.36x10-3). Calculated risk scores were 1 or 2 for each variable in the RAM with a total risk score ranging from 0 to 6. The estimated probability for developing HA-VTE ranged from 1% to 17.4% depending on the total score. In conclusion, the CHAT-ICU RAM has good discriminatory validity, is well-calibrated and reliably identifies children in the PICU at high and low risk of HA-VTE.

Identifiers

PMID41284641
PMCPMC13000931

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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.