Evidence map›Paper›PMID 34052147›Full record

ReviewArchives of cardiovascular diseases2021

Severe acute respiratory syndrome coronavirus 2-related multisystem inflammatory syndrome in children mimicking Kawasaki disease.

Jean-Christophe Mercier, Naim Ouldali, Isabelle Melki, Romain Basmaci, Michael Levy, Luigi Titomanlio, Constance Beyler, Ulrich Meinzer

Abstract readComparative StudyReview
In one paragraph

Review in Archives of cardiovascular diseases, 2021. 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
–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

5 citing papers in PubMed.

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

8 authors.

Jean-Christophe MercierUniversité de Paris, 75006 Paris, France; AP-HP et ARS Île de France, 93200 Saint-Denis, France. Electronic address: jean-christophe.mercier@sfr.fr.
Naim OuldaliService de Pédiatrie Générale, Hôpital Robert Debré, 75019 Paris, France.
Isabelle MelkiService de Pédiatrie Générale, Hôpital Robert Debré, 75019 Paris, France; Centre de Référence pour les Maladies Rhumatologiques Auto-Immunes et Systémiques (RAISE), Institut IMAGINE, 75015 Paris, France.
Romain BasmaciService de Pédiatrie-Urgences, Hôpital Louis-Mourier, AP-HP, 92700 Colombes, France; Université de Paris, Inserm, Infection-Antimicrobials-Modelling-Evolution (IAME), UMR-1137, Université de Paris, Hôpital Bichat, 75018 Paris, France.
Michael LevyService de Médecine Intensive-Réanimation Pédiatriques, Hôpital Robert-Debré, 75019 Paris, France.
Luigi TitomanlioService des Urgences Pédiatriques, Hôpital Robert-Debré, 75019 Paris, France.
Constance BeylerService de Cardiologie Pédiatrique, Hôpital Robert-Debré, 75019 Paris, France.
Ulrich MeinzerService de Pédiatrie Générale, Hôpital Robert Debré, 75019 Paris, France; Centre de Recherche sur l'Inflammation, Inserm UMR-1149, 75018 Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has been characterized by high transmission rates and high mortality in adults with predisposing factors, including age>70 years, obesity, diabetes, systemic hypertension and other underlying diseases. During the second week of viral pneumonia, acute respiratory distress syndrome can occur and carries high mortality. Unlike most common respiratory viruses, children seem to be less susceptible to SARS-CoV-2 infection, and generally develop mild disease with low mortality. However, clusters of severe shock associated with high levels of cardiac biomarkers and unusual vasoplegia requiring inotropes, vasopressors and volume loading have recently been described. Both the clinical symptoms (i.e. high and persistent fever, gastrointestinal disorders, skin rash, conjunctival injection and dry cracked lips) and the biological signs (e.g. elevated C-reactive protein/procalcitonin and high levels of ferritinaemia) mimicked Kawasaki disease. In most cases, intravenous immunoglobin therapy improved cardiac function and led to full recovery within a few days. Adjunctive steroid therapy and sometimes biotherapy (e.g. anti-interleukin 1Ra and anti-interleukin 6 monoclonal antibodies) were often necessary. Although almost all children fully recovered within a week, some of them later developed coronary artery dilation or aneurysm. Thus, a new "multisystem inflammatory syndrome in children" related to SARS-CoV-2 has recently been described. Similarities with Kawasaki disease and the physiopathology of this syndrome still need further exploration.

Indexed as

SARS-CoV-2AdolescentBiomarkersChildCOVID-19Diagnosis, DifferentialDisease SusceptibilityFemaleHumansImmunoglobulins, IntravenousImmunologic FactorsLength of StayMaleMucocutaneous Lymph Node SyndromeShock, CardiogenicShock, SepticBiomarkersImmunoglobulins, IntravenousImmunologic FactorsCardiogenic shockChildrenChoc cardiogéniqueCOVID-19EnfantKawasaki syndromeMultisystem inflammatory syndrome temporally associated with SARS-CoV-2Syndrome de KawasakiSyndrome inflammatoire multi-systémique temporellement associé à SARS-CoV-2

Identifiers

PMID34052147
PMCPMC8141693

What OpenQuestion holds

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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.