Evidence map›Paper›PMID 31107862›Full record

ArticlePloS one2019

Epidemiological and clinical features of Kawasaki disease in Spain over 5 years and risk factors for aneurysm development. (2011-2016): KAWA-RACE study group.

Elisa Fernandez-Cooke, Ana Barrios Tascón, Judith Sánchez-Manubens, Jordi Antón, Carlos Daniel Grasa Lozano, Javier Aracil Santos, Enrique Villalobos Pinto, Daniel Clemente Garulo, Beatriz Mercader Rodríguez, Matilde Bustillo Alonso and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 2% 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, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

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  19. COVID-19 ocular findings in children: a case series.World journal of pediatrics : WJP · 2021
    Observational
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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

15 authors at 10 institutions in 2 countries.

Elisa Fernandez-CookeDepartment of Pediatrics, Hospital Universitario Doce de Octubre, Madrid, Spain.ORCID 0000-0002-5921-8261
Ana Barrios TascónDepartment of Pediatrics, Hospital Universitario Infanta Sofia, Madrid, Spain.
Judith Sánchez-ManubensDepartment of Pediatric Rheumatology, Hospital Sant Joan de Deu, Barcelona, Spain.
Jordi AntónDepartment of Pediatric Rheumatology, Hospital Sant Joan de Deu, Barcelona, Spain.
Carlos Daniel Grasa LozanoDepartment of Pediatrics, Hospital Universitario Doce de Octubre, Madrid, Spain.ORCID 0000-0002-9323-2024
Javier Aracil SantosDepartment of Pediatrics, Hospital Universitario La Paz, Madrid, Spain.
Enrique Villalobos PintoDepartment of Pediatrics, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Daniel Clemente GaruloDepartment of Pediatrics, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
Beatriz Mercader RodríguezDepartment of Pediatrics, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.ORCID 0000-0002-6706-408X
Matilde Bustillo AlonsoDepartment of Pediatrics, Hospital Universitario Miguel Servet, Zaragoza, Spain.
Esmeralda Nuñez CuadrosDepartment of Pediatrics, Hospital Regional Universitario de Malaga, Andalucia, Spain.ORCID 0000-0003-1938-1678
Maria Luisa Navarro GómezDepartment of Pediatrics, Hospital Universitario Gregorio Marañon, Madrid, Spain.
Sara Domínguez-RodríguezFundación de Investigación Hospital 12 Octubre (Madrid, Spain), Fondazione PENTA ONLUS, Padova, Italy.
Cristina CalvoDepartment of Pediatrics, Hospital Universitario La Paz, Madrid, Spain.
KAWA-RACE study group
Hospital Infantil Universitario Niño Jesús · ESHospital Sant Joan de Déu Barcelona · ESHospital Universitario 12 De Octubre · ESHospital Universitario La Paz · ESHospital General Universitario Gregorio Marañón · ESHospital Regional Universitario de Málaga · ESHospital Universitario Infanta Sofía · ESHospital Universitario Miguel Servet · ESHospital Universitario Virgen de la Arrixaca · ESPENTA Foundation · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKawasaki disease (KD) is an acute self-limited systemic vasculitis of unknown etiology affecting mainly children less than 5 years of age. Risk factors for cardiac involvement and resistance to treatment are insufficiently studied in non-Japanese children.

objectiveThis study aimed to investigate the epidemiology, clinical features and risk factors for resistance to treatment and coronary artery lesions (CAL) in KD in Spain.

methodsRetrospective study (May 2011-June 2016) of all patients less than 16 years of age diagnosed with KD included in KAWA-RACE network (84 Spanish hospitals).

resultsA total of 625 cases were analyzed, 63% were males, 79% under 5 year-olds and 16.8% younger than 12 months. On echocardiographic examination CAL were the most frequent findings (23%) being ectasia the most common (12%). Coronary aneurysms were diagnosed in 9.6%, reaching 20% in infants under 12 months (p<0.001). A total of 97% of the patients received intravenous immunoglobulin (IVIG) with a median number of days from fever onset to IVIG administration of 7.2. A second dose was given to 15.7% and steroids to 14.5% patients. Only 1.4% patients received infliximab. No deaths were reported. A multivariate analysis identified anemia, hypoalbuminemia, hyponatremia, higher creatinine and procalcitonin as independent risk factors for treatment failure and length under 103 cm, hemoglobin < 10.2 mg/dL, platelets > 900,000 cells/mm3, maximum temperature < 39.5°C, total duration of fever > 10 days and fever before treatment ≥ 8 days as independent risk factors for developing coronary aneurysms.

conclusionsIn our population, children under 12 months develop coronary aneurysms more frequently and children with KD with anemia and leukocytosis have high risk of cardiac involvement. Adding steroids early should be considered in those patients, especially if the treatment is not started before 8 days of fever. A score applicable to non-Japanese children able to predict the risk of aneurysm development and IVIG resistance is necessary.

Indexed as

AdolescentChildChild, PreschoolCoronary AneurysmFemaleHumansInfantMaleMucocutaneous Lymph Node SyndromePrognosisRisk FactorsSpainTreatment Outcome

Identifiers

PMID31107862
PMCPMC6527399
OpenAlexW2945816963

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.