Evidence map›Paper›PMID 36319189›Full record

ArticleACR open rheumatology2022

A Diagnostic Prediction Model to Distinguish Multisystem Inflammatory Syndrome in Children.

Matthew T Clark, Danielle A Rankin, Lauren S Peetluk, Alisa Gotte, Alison Herndon, William McEachern, Andrew Smith, Daniel E Clark, Edward Hardison, Adam J Esbenshade and 4 more

Open access · goldAbstract read
In one paragraph

Article in ACR open rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 20% of its field
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

5 citing papers in PubMed, 8 citations in OpenAlex.

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  4. Review
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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

14 authors at 2 institutions in 1 country.

Matthew T ClarkVanderbilt University Medical Center, Tennessee, Nashville.ORCID https://orcid.org/0000-0002-1158-8124
Danielle A RankinVanderbilt University Medical Center and Vanderbilt University School of Medicine, Tennessee, Nashville.ORCID https://orcid.org/0000-0003-3018-3373
Lauren S PeetlukVanderbilt University Medical Center, Tennessee, Nashville.
Alisa GotteVanderbilt University Medical Center, Tennessee, Nashville.
Alison HerndonVanderbilt University Medical Center, Tennessee, Nashville.
William McEachernVanderbilt University Medical Center, Tennessee, Nashville.
Andrew SmithJohns Hopkins All Children's Hospital, Florida, St. Petersburg.
Daniel E ClarkVanderbilt University Medical Center, Tennessee, Nashville.
Edward HardisonVanderbilt University Medical Center, Tennessee, Nashville.
Adam J EsbenshadeVanderbilt University Medical Center, Tennessee, Nashville.
Anna PatrickVanderbilt University Medical Center, Tennessee, Nashville.ORCID https://orcid.org/0000-0003-1625-2598
Natasha B HalasaVanderbilt University Medical Center, Tennessee, Nashville.
James A ConnellyVanderbilt University Medical Center, Tennessee, Nashville.
Sophie E KatzVanderbilt University Medical Center, Tennessee, Nashville.
Vanderbilt University Medical Center · USJohns Hopkins University · US

Funding

Pathogenesis, Targeted Therapeutics, and New Vaccines for Childhood DiseaseK12HD087023 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Michael R. DeBaun, Juan C Salazar · 2016 to 2026
$4.1M
NICHD NIH HHS K12 HD087023
6 · The paper itself

Abstract

objectiveFeatures of multisystem inflammatory syndrome in children (MIS-C) overlap with other syndromes, making the diagnosis difficult for clinicians. We aimed to compare clinical differences between patients with and without clinical MIS-C diagnosis and develop a diagnostic prediction model to assist clinicians in identification of patients with MIS-C within the first 24 hours of hospital presentation.

methodsA cohort of 127 patients (<21 years) were admitted to an academic children's hospital and evaluated for MIS-C. The primary outcome measure was MIS-C diagnosis at Vanderbilt University Medical Center. Clinical, laboratory, and cardiac features were extracted from the medical record, compared among groups, and selected a priori to identify candidate predictors. Final predictors were identified through a logistic regression model with bootstrapped backward selection in which only variables selected in more than 80% of 500 bootstraps were included in the final model.

resultsOf 127 children admitted to our hospital with concern for MIS-C, 45 were clinically diagnosed with MIS-C and 82 were diagnosed with alternative diagnoses. We found a model with four variables-the presence of hypotension and/or fluid resuscitation, abdominal pain, new rash, and the value of serum sodium-showed excellent discrimination (concordance index 0.91; 95% confidence interval: 0.85-0.96) and good calibration in identifying patients with MIS-C.

conclusionA diagnostic prediction model with early clinical and laboratory features shows excellent discrimination and may assist clinicians in distinguishing patients with MIS-C. This model will require external and prospective validation prior to widespread use.

Identifiers

PMID36319189
PMCPMC9746665
OpenAlexW4307968634

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

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 OpenQuestion graph.