Evidence map›Paper›PMID 36786810›Full record

ArticlePediatric cardiology2023

COVID-19 Positive Versus Negative Complete Kawasaki Disease: A Study from the International Kawasaki Disease Registry.

Jerin Jose, Elif Seda Selamet Tierney, Ashraf S Harahsheh, Nagib Dahdah, Geetha Raghuveer, Kevin G Friedman, Michael Khoury, Mark D Hicar, Shae A Merves, Frederic Dallaire and 13 more

Open access · bronzeAbstract read
In one paragraph

Article in Pediatric cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Guideline
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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

23 authors at 20 institutions in 3 countries.

Jerin JoseDivision of Pediatric Cardiology, Lucile Packard Children's Hospital, Stanford University Medical Center, Palo Alto, CA, USA. jtj17@alumni.utsw.edu.
Elif Seda Selamet TierneyDivision of Pediatric Cardiology, Lucile Packard Children's Hospital, Stanford University Medical Center, Palo Alto, CA, USA.
Ashraf S HarahshehChildren's National Health System/George Washington University School of Medicine & Health Sciences, Washington, DC, USA.
Nagib DahdahDivision of Pediatric Cardiology, CHU Ste-Justine, University of Montreal, Montreal, Canada.
Geetha RaghuveerChildren's Mercy Hospital, Kansas City, MO, USA.
Kevin G FriedmanBoston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Michael KhouryDepartment of Pediatrics, Stollery Children's Hospital, University of Alberta, Edmonton, AB, Canada.
Mark D HicarJacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, NY, USA.
Shae A MervesUniversity of Arkansas for Medical Sciences/Arkansas Children's Hospital, Little Rock, AR, USA.
Frederic DallaireCentre de recherche du Centre hospitalier universitaire de Sherbrooke, Sherbrooke, QC, Canada.
Pedrom FaridDivision of Cardiology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Cedric ManlhiotDivision of Cardiology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
Kyle RunecklesTed Rogers Computational Program, Peter Munk Cardiac Centre, Ted Rogers Centre for Heart Research, The Hospital for Sick Children, University Health Network, Toronto, ON, Canada.
Nilanjana MisraCohen Children's Medical Center of NY, Northwell Health, Queens, NY, USA.
Michael PortmanSeattle Children's Hospital, Seattle, WA, USA.
Jean A BallwegChildren's Hospital & Medical Center of Omaha, Omaha, NE, USA.
Simon LeeThe Heart Center at Nationwide Children's Hospital, Columbus, OH, USA.
Supriya S JainNew York Medical College/Maria Fareri Children's Hospital at Westchester Medical Center, Valhalla, New York, USA.
Tyler H HarrisUPMC Children's Hospital of Pittsburgh, University of Pittsburgh SOM, Pittsburgh, PA, USA.
Jacqueline R SzmuszkoviczChildren's Hospital of Los Angeles, Los Angeles, CA, USA.
William OrrDivision of Pediatric Cardiology, Department of Pediatrics, Washington University School of Medicine, St. Louis, USA.
Guillermo LariosPontificia Universidad Católica de Chile, Región Metropolitana, Santiago, Chile.
Brian W McCrindleDivision of Cardiology, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada.
SickKids Foundation · CAAPT Therapeutics (United States) · USArkansas Children's Hospital · USBoston Children's Hospital · USCentre Hospitalier Universitaire de Sherbrooke · CAChildren's Hospital & Medical Center · USChildren's Hospital of Los Angeles · USChildren's Mercy Hospital · USGeorge Washington University · USJacobs (United States) · USNationwide Children's Hospital · USNew York Medical College · USNorthwell Health · USPontificia Universidad Católica de Chile · CLSeattle Children's Hospital · USStanford Medicine · USStollery Children's Hospital · CAUniversité de Montréal · CAUniversity Health Network · CAUniversity of Pittsburgh · US

Funding

National Institutes of Health R01HL143130
6 · The paper itself

Abstract

To determine clinical differences for children with complete Kawasaki disease (KD) with and without evidence of preceding SARS-CoV-2 infection. From January 2020, contemporaneous patients with complete KD criteria were classified as either SARS-CoV-2 positive (KDCOVID+; confirmed household exposure, positive PCR and/or serology) or SARS-CoV-2 negative (KDCOVID-; negative testing and no exposure) and compared. Of 744 patients in the International Kawasaki Disease Registry, 52 were KDCOVID- and 61 were KDCOVID+. KDCOVID+ patients were older (median 5.5 vs. 3.7 years; p < 0.001), and all additionally met diagnostic criteria for multisystem inflammatory syndrome in children (MIS-C). They were more likely to have abdominal pain (60% vs. 35%; p = 0.008) and headache (38% vs. 10%; p < 0.001) and had significantly higher CRP, troponin, and BUN/creatinine, and lower hemoglobin, platelets, and lymphocytes. KDCOVID+ patients were more likely to have shock (41% vs. 6%; p < 0.001), ICU admission (62% vs. 10%; p < 0.001), lower left ventricular ejection fraction (mean lowest LVEF 53% vs. 60%; p < 0.001), and to have received inotropic support (60% vs. 10%; p < 0.001). Both groups received IVIG (2 doses in 22% vs. 18%; p = 0.63), but KDCOVID+ were more likely to have received steroids (85% vs. 35%; p < 0.001) and anakinra (60% vs. 10%; p = 0.002). KDCOVID- patients were more likely to have medium/large coronary artery aneurysms (CAA, 12% vs. 0%; p = 0.01). KDCOVID+ patients differ from KDCOVID-, have more severe disease, and greater evidence of myocardial involvement and cardiovascular dysfunction rather than CAA. These patients may be a distinct KD phenotype in the presence of a prevalent specific trigger.

Indexed as

COVID-19Mucocutaneous Lymph Node SyndromeHumansRegistriesSARS-CoV-2Stroke VolumeSystemic Inflammatory Response SyndromeVentricular Function, LeftCOVID-19KawasakiMIS-CMIS-C with KD phenotypeSARS-CoV-2

Identifiers

PMID36786810
PMCPMC9926414
OpenAlexW4320709757

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.