Evidence map›Paper›PMID 36855438›Full record

ArticleThe Lancet. Rheumatology2023

Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study.

Samuel Channon-Wells, Ortensia Vito, Andrew J McArdle, Eleanor G Seaby, Harsita Patel, Priyen Shah, Ekaterina Pazukhina, Clare Wilson, Claire Broderick, Giselle D'Souza and 16 more

Open access · hybridAbstract read
In one paragraph

Article in The Lancet. Rheumatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 3 pooled it
14.0field-weighted citation impact, top 1% 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

27 citing papers in PubMed, 3 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Observational
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

26 authors at 11 institutions in 5 countries.

Samuel Channon-WellsCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Ortensia VitoCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Andrew J McArdleCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Eleanor G SeabyDepartment of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
Harsita PatelCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Priyen ShahCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Ekaterina PazukhinaIstanbul, Türkiye.
Clare WilsonCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Claire BroderickCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Giselle D'SouzaCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Ilana KerenDepartment of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
Ruud G NijmanCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Adriana TremouletDepartment of Paediatrics, University of California San Diego-Rady Children's Hospital San Diego, San Diego, CA, USA.
Daniel MunblitInflammation, Repair, and Development Section, National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK.
Rolando Ulloa-GutierrezServicio de Infectologia Pediatrica, Hospital Nacional de Niños "Dr. Carlos Sáenz Herrera", Centro de Ciencias Médicas, Caja Costarricense de Seguro Social (CCSS), San José, Costa Rica.
Michael J CarterDepartment of Women and Children's Health, School of Life Course Sciences, King's College London, St Thomas' Hospital, London, UK.
Padmanabhan RamnarayanAnaesthetics, Pain Medicine, and Intensive Care (APMIC) Division, Department of Surgery and Cancer, Faculty of Medicine, Imperial College London, London, UK.
Tisham DeDepartment of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, London, UK.
Clive HoggartDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York City, NY, USA.
Elizabeth WhittakerCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Jethro A HerbergCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Myrsini KaforouCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Aubrey J CunningtonCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Oleg BlyussWolfson Institute of Population Health, Queen Mary University of London, London, UK.
Michael LevinCentre for Paediatrics and Child Health, Faculty of Medicine, Imperial College London, London, UK.
Best Available Treatment Study (BATS) consortium
Imperial College London · GBRoyal College of Paediatrics and Child Health · GBUniversidad de Ciencias Medicas · CRKing's College London · GBSechenov University · RUHospital Nacional de Niños · CRIcahn School of Medicine at Mount Sinai · USImperial College Healthcare NHS Trust · GBQueen Mary University of London · GBTürkisch-Deutsche Universität · TRUniversity of Southampton · GB

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
MRF_ MRF-160-0008-ELP-KAFO-C0801NIAID NIH HHS R01 AI128765Wellcome Trust
6 · The paper itself

Abstract

Background: Multisystem inflammatory syndrome in children (MIS-C), a hyperinflammatory condition associated with SARS-CoV-2 infection, has emerged as a serious illness in children worldwide. Immunoglobulin or glucocorticoids, or both, are currently recommended treatments. Methods: The Best Available Treatment Study evaluated immunomodulatory treatments for MIS-C in an international observational cohort. Analysis of the first 614 patients was previously reported. In this propensity-weighted cohort study, clinical and outcome data from children with suspected or proven MIS-C were collected onto a web-based Research Electronic Data Capture database. After excluding neonates and incomplete or duplicate records, inverse probability weighting was used to compare primary treatments with intravenous immunoglobulin, intravenous immunoglobulin plus glucocorticoids, or glucocorticoids alone, using intravenous immunoglobulin as the reference treatment. Primary outcomes were a composite of inotropic or ventilator support from the second day after treatment initiation, or death, and time to improvement on an ordinal clinical severity scale. Secondary outcomes included treatment escalation, clinical deterioration, fever, and coronary artery aneurysm occurrence and resolution. This study is registered with the ISRCTN registry, ISRCTN69546370. Findings: We enrolled 2101 children (aged 0 months to 19 years) with clinically diagnosed MIS-C from 39 countries between June 14, 2020, and April 25, 2022, and, following exclusions, 2009 patients were included for analysis (median age 8·0 years [IQR 4·2-11·4], 1191 [59·3%] male and 818 [40·7%] female, and 825 [41·1%] White). 680 (33·8%) patients received primary treatment with intravenous immunoglobulin, 698 (34·7%) with intravenous immunoglobulin plus glucocorticoids, 487 (24·2%) with glucocorticoids alone; 59 (2·9%) patients received other combinations, including biologicals, and 85 (4·2%) patients received no immunomodulators. There were no significant differences between treatments for primary outcomes for the 1586 patients with complete baseline and outcome data that were considered for primary analysis. Adjusted odds ratios for ventilation, inotropic support, or death were 1·09 (95% CI 0·75-1·58; corrected p value=1·00) for intravenous immunoglobulin plus glucocorticoids and 0·93 (0·58-1·47; corrected p value=1·00) for glucocorticoids alone, versus intravenous immunoglobulin alone. Adjusted average hazard ratios for time to improvement were 1·04 (95% CI 0·91-1·20; corrected p value=1·00) for intravenous immunoglobulin plus glucocorticoids, and 0·84 (0·70-1·00; corrected p value=0·22) for glucocorticoids alone, versus intravenous immunoglobulin alone. Treatment escalation was less frequent for intravenous immunoglobulin plus glucocorticoids (OR 0·15 [95% CI 0·11-0·20]; p<0·0001) and glucocorticoids alone (0·68 [0·50-0·93]; p=0·014) versus intravenous immunoglobulin alone. Persistent fever (from day 2 onward) was less common with intravenous immunoglobulin plus glucocorticoids compared with either intravenous immunoglobulin alone (OR 0·50 [95% CI 0·38-0·67]; p<0·0001) or glucocorticoids alone (0·63 [0·45-0·88]; p=0·0058). Coronary artery aneurysm occurrence and resolution did not differ significantly between treatment groups. Interpretation: Recovery rates, including occurrence and resolution of coronary artery aneurysms, were similar for primary treatment with intravenous immunoglobulin when compared to glucocorticoids or intravenous immunoglobulin plus glucocorticoids. Initial treatment with glucocorticoids appears to be a safe alternative to immunoglobulin or combined therapy, and might be advantageous in view of the cost and limited availability of intravenous immunoglobulin in many countries. Funding: Imperial College London, the European Union's Horizon 2020, Wellcome Trust, the Medical Research Foundation, UK National Institute for Health and Care Research, and National Institutes of Health.

Identifiers

PMID36855438
PMCPMC9949883
OpenAlexW4320716074

What OpenQuestion holds

Textmetadata
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.