Evidence map›Paper›PMID 36282324›Full record

ArticleEuropean journal of pediatrics2023

Treatments for multi-system inflammatory syndrome in children - discharge, fever, and second-line therapies.

Alfredo Tagarro, Sara Domínguez-Rodríguez, Juan Miguel Mesa, Cristina Epalza, Carlos Grasa, María Isabel Iglesias-Bouzas, Elisa Fernández-Cooke, Cristina Calvo, Serena Villaverde, David Torres-Fernández and 17 more

Open access · greenAbstract read
In one paragraph

Article in European journal of pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
2.0field-weighted citation impact, top 14% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 10 citations in OpenAlex.

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

27 authors at 16 institutions in 2 countries.

Alfredo TagarroFundación de Investigación Biomédica Hospital 12 de Octubre, Instituto de Investigación 12 de Octubre (imas12), Madrid, Spain. alfredotagarro@gmail.com.
Sara Domínguez-RodríguezFundación de Investigación Biomédica Hospital 12 de Octubre, Instituto de Investigación 12 de Octubre (imas12), Madrid, Spain.
Juan Miguel MesaPaediatrics Department, Hospital Universitario Infanta Sofía, Madrid, Spain.
Cristina EpalzaPaediatric Infectious Diseases Unit, Department of Paediatrics, Hospital Universitario, Unidad Pediátrica de Investigación y Ensayos Clínicos (UPIC), Instituto de Investigación Hospital 12 Octubre, Madrid, Spain.
Carlos GrasaPaediatrics, Infectious and Tropical Diseases Department, Hospital Universitario La Paz, Instituto Investigación Hospital La Paz (IDIPaz), Madrid, Spain.
María Isabel Iglesias-BouzasPaediatrics Intensive Care Unit, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Elisa Fernández-CookePaediatric Infectious Diseases Unit, Department of Paediatrics, Hospital Universitario, Unidad Pediátrica de Investigación y Ensayos Clínicos (UPIC), Instituto de Investigación Hospital 12 Octubre, Madrid, Spain.
Cristina CalvoPaediatrics, Infectious and Tropical Diseases Department, Hospital Universitario La Paz, Instituto Investigación Hospital La Paz (IDIPaz), Madrid, Spain.
Serena VillaverdeFundación de Investigación Biomédica Hospital 12 de Octubre, Instituto de Investigación 12 de Octubre (imas12), Madrid, Spain.
David Torres-FernándezPaediatric Infectious Diseases Unit, Department of Paediatrics, Hospital Universitario, Unidad Pediátrica de Investigación y Ensayos Clínicos (UPIC), Instituto de Investigación Hospital 12 Octubre, Madrid, Spain.
Ana Méndez-EchevarriaPaediatrics, Infectious and Tropical Diseases Department, Hospital Universitario La Paz, Instituto Investigación Hospital La Paz (IDIPaz), Madrid, Spain.
Inés LeozPaediatrics Intensive Care Unit, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
María Fernández-PascualPaediatrics Department, Hospital Universitario Infanta Sofía, Madrid, Spain.
Jesús Saavedra-LozanoPediatric Infectious Diseases Unit, Department of Pediatrics, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
Beatriz SotoPaediatrics Department, Hospital Universitario de Getafe, Getafe, Madrid, Spain.
David Aguilera-AlonsoFundación de Investigación Biomédica Hospital 12 de Octubre, Instituto de Investigación 12 de Octubre (imas12), Madrid, Spain.
Jacques G RivièreInfectious Diseases and Paediatric Immunology Unit, Department of Paediatrics, Hospital Universitario Vall d'Hebron, Barcelona, Spain.
Victoria FumadóPaediatric Infectious Diseases Unit, Department of Paediatrics, Hospital Universitario Sant Joan de Deu, Barcelona, Spain.
Leticia Martínez-CamposPaediatric Infectious Diseases Unit, Department of Paediatrics, Hospital Universitario Torrecárdenas, Almeria, Spain.
Ana VivancoPaediatrics Intensive Care Unit, Hospital Central de Asturias, Asturias, Spain.
Francisco Javier Pilar-OrivePaediatrics Department, Hospital Universitario de Cruces, Barakaldo, Spain.
Pedro AlcaláPaediatrics Department, Hospital General de Alicante, Alicante, Spain.
Beatriz RuizPaediatrics Department, Hospital Reina Sofía, Córdoba, Spain.
Ana López-MachínPaediatrics Department, Hospital Son Espasses, Palma, Spain.
Manuel OltraPaediatrics Department, Hospital La Fe, Valencia, Spain.
Cinta MoraledaFundación de Investigación Biomédica Hospital 12 de Octubre, Instituto de Investigación 12 de Octubre (imas12), Madrid, Spain.
EPICO Working Group
Research Institute Hospital 12 de Octubre · ESHospital Universitario 12 De Octubre · ESHospital Universitario La Paz · ESHospital Infantil Universitario Niño Jesús · ESHospital Universitario Infanta Sofía · ESComplejo Hospitalario Torrecárdenas · ESHospital de Cruces · ESHospital General Universitario de Alicante Doctor Balmis · ESHospital General Universitario Gregorio Marañón · ESHospital Sant Joan de Déu Barcelona · ESHospital Universitario Central de Asturias · ESHospital Universitario de Getafe · ESHospital Universitario Reina Sofía · ESLeitat Technological Center · ESUniversidad Europea · ESVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scarce evidence exists about the best treatment for multi-system inflammatory syndrome (MIS-C). We analyzed the effects of steroids, intravenous immunoglobulin (IVIG), and their combination on the probability of discharge over time, the probability of switching to second-line treatment over time, and the persistence of fever 2 days after treatment. We did a retrospective study to investigate the effect of different treatments on children with MIS-C from 1 March 2020 to 1 June 2021. We estimated the time-to-event probability using a Cox model weighted by propensity score to balance the baseline characteristics. Thirty of 132 (22.7%) patients were initially treated with steroids alone, 29/132 (21.9%) with IVIG alone, and 73/132 (55%) with IVIG plus steroids. The probability of early discharge was higher with IVIG than with IVIG plus steroids (hazard ratio [HR] 1.65, 95% CI 1.11-2.45, p = 0.013), but with a higher probability of needing second-line therapy compared to IVIG plus steroids (HR 3.05, 95% CI 1.12-8.25, p = 0.028). Patients on IVIG had a higher likelihood of persistent fever than patients on steroids (odds ratio [OR] 4.23, 95% CI 1.43-13.5, p = 0.011) or on IVIG plus steroids (OR 4.4, 95% CI 2.05-9.82, p < 0.001). No differences were found for this endpoint between steroids or steroids plus IVIG.    Conclusions: The benefits of each approach may vary depending on the outcome assessed. IVIG seemed to increase the probability of earlier discharge over time but also of needing second-line treatment over time. Steroids seemed to reduce persistent fever, and combination therapy reduced the need for escalating treatment. What is Known: • Steroids plus intravenous immunoglobulin, compared with intravenous immunoglobulin alone for multi-system inflammatory syndrome (MIS-C) might reduce the need for hemodynamic support and the duration of fever, but the certainty of the evidence is low. What is New: • Intravenous immunoglobulin, steroids, and their combination for MIS-C may have different outcomes. • In this study, intravenous immunoglobulin increased the probability of discharge over time, steroids reduced persistent fever, while combination therapy reduced the need for second-line treatments.

Indexed as

Immunoglobulins, IntravenousPatient DischargeChildCOVID-19FeverHumansRetrospective StudiesSteroidsSystemic Inflammatory Response SyndromeImmunoglobulins, IntravenousSteroidsChildrenCOVID-19MIS-CSARS-CoV-2

Identifiers

PMID36282324
PMCPMC9595092
OpenAlexW4307208730

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.