Evidence map›Paper›PMID 35759535›Full record

ArticleACR open rheumatology2022

Treatment of Multisystem Inflammatory Syndrome in Children: Understanding Differences in Results of Comparative Effectiveness Studies.

Michael Melgar, Eleanor G Seaby, Andrew J McArdle, Cameron C Young, Angela P Campbell, Nancy L Murray, Manish M Patel, Michael Levin, Adrienne G Randolph, Mary Beth F Son and 1 more

Abstract 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 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. 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

11 authors.

Michael MelgarCOVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia.ORCID https://orcid.org/0000-0003-3243-9854
Eleanor G SeabyImperial College London, London, UK, University of Southampton, Southampton, UK, and Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge.
Andrew J McArdleImperial College of London, London, UK.
Cameron C YoungBoston Children's Hospital, Boston, Massachusetts.
Angela P CampbellCOVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia.ORCID https://orcid.org/0000-0002-2576-482X
Nancy L MurrayCOVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia.
Manish M PatelCOVID-19 Response Team, Centers for Disease Control and Prevention, Atlanta, Georgia, and Commissioned Corps of the US Public Health Service, Rockville, Maryland.
Michael LevinImperial College Healthcare National Health Service Trust and Imperial College London, London, UK.
Adrienne G RandolphHarvard Medical School and Boston Children's Hospital, Boston.
Mary Beth F SonHarvard Medical School and Boston Children's Hospital, Boston.
BATS Consortium and the Overcoming COVID-19 Investigators

Funding

Validation of Biomarkers of Pediatric TB and further development for use in diagnosis of childhood TBR01AI128765 · NIAID · IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE · PI LEVIN, MICHAEL · 2017 to 2021
$5.0M
CDC HHS 75D30120C07725Horizon 2020 Framework Programme 668303 PERFORMHorizon 2020 Framework Programme 848196 DIAMONDSLee Family FoundationMRF MRF-160-0008-ELP-KAFO-C0801National Institute for Health Research ACL-2018-021-007NIAID NIH HHS R01 AI128765NIH HHS GA5R01AI128765NIHR Imperial Biomedical Research CentreWellcome TrustWellcome Trust 203928/Z/16/ZWellcome Trust 206508/Z/17/ZWellcome Trust RDA02
6 · The paper itself

Abstract

objectiveTwo cohort studies in patients with multisystem inflammatory syndrome in children (MIS-C) demonstrated contrasting results regarding the benefit of initial immunomodulatory treatment with intravenous immunoglobulin (IVIG) alone versus IVIG and glucocorticoids. We sought to determine whether application of different MIS-C definitions and differing disease severity between cohorts underlay discrepant results.

methodsThe Overcoming COVID-19 Public Health Surveillance Registry (OC-19) included patients meeting the US Centers for Disease Control and Prevention (CDC) MIS-C definition, whereas the Best Available Treatment Study (BATS) applied the World Health Organization (WHO) definition. We applied the WHO definition to the OC-19 cohort and the CDC definition to the BATS cohort and determined the proportion that did not meet the alternate definition. We compared illness severity indicators between cohorts.

resultsOf 349 OC-19 patients, 9.5% did not meet the WHO definition. Of 350 BATS patients, 10.3% did not meet the CDC definition. Most organ system involvement was similar between the cohorts, but more OC-19 patients had WHO-defined cardiac involvement (87.1% vs 79.4%, P = 0.008). OC-19 patients were more often admitted to intensive care (61.0% vs 44.8%, P < 0.001) and more often received vasopressors or inotropes (39.5% vs 22.9%, P < 0.001) before immunomodulatory treatment.

conclusionGreater illness severity and cardiovascular involvement in the OC-19 cohort compared with the BATS cohort, and not use of different MIS-C case definitions, may have contributed to differing study conclusions about optimal initial treatment for MIS-C. Disease severity should be considered in future MIS-C study designs and treatment recommendations to identify patients who would benefit from aggressive immunomodulatory treatment.

Identifiers

PMID35759535
PMCPMC9469482

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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.