Evidence map›Paper›PMID 30180185›Full record

ArticlePloS one2018

Gastrointestinal presentation of Kawasaki disease: A red flag for severe disease?

Marianna Fabi, Elena Corinaldesi, Luca Pierantoni, Elisa Mazzoni, Chiara Landini, Barbara Bigucci, Gina Ancora, Laura Malaigia, Tetyana Bodnar, Giorgia Di Fazzio and 15 more

Open access · goldAbstract readEvaluation StudyMulticenter Study
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
10.9field-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

51 citing papers in PubMed, 1 synthesis or guideline pooled it, 90 citations in OpenAlex.

  1. Pooled it
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  10. Gut Microbiota Alterations in Patients With Kawasaki Disease.Arteriosclerosis, thrombosis, and vascular biology · 2025
    Review
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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

25 authors at 11 institutions in 1 country.

Marianna FabiPediatric Cardiology and Adult Congenital Unit, University of Bologna, S.Orsola-Malpighi Hospital, Bologna, Italy.
Elena CorinaldesiDepartment of Pediatrics, Ramazzini Hospital, Carpi, Italy.
Luca PierantoniDepartment of Pediatrics, University of Bologna, S.Orsola-Malpighi Hospital, Bologna, Italy.
Elisa MazzoniDepartment of Pediatrics, Maggiore Hospital, Bologna, Italy.
Chiara LandiniDepartment of Pediatrics, Maggiore Hospital, Bologna, Italy.
Barbara BigucciDepartment of Pediatrics, Infermi Hospital, Rimini, Italy.
Gina AncoraDepartment of Pediatrics, Infermi Hospital, Rimini, Italy.
Laura MalaigiaDepartment of Pediatrics, Bufalini Hospital, Cesena, Italy.
Tetyana BodnarDepartment of Pediatrics, University of Bologna, S.Orsola-Malpighi Hospital, Bologna, Italy.ORCID 0000-0002-2727-3506
Giorgia Di FazzioDepartment of Pediatrics, Arcispedale Santa Maria Nuova, IRCCS, Reggio Emilia, Italy.
Francesca LamiDepartment of Pediatric, Department of Medical and Surgical Sciences for Mothers, Children and Adults, University of Modena and Reggio Emilia, Reggio Emilia, Italy.
Enrico VallettaDepartment of Pediatrics, G.B.Morgagni-L. Pierantoni Hospital, AUSL della Romagna, Forlì, Italy.
Cristina CiceroDepartment of Pediatrics, Guglielmo da Saliceto Hospital, AUSL, Piacenza, Italy.
Giacomo BiasucciDepartment of Pediatrics, Guglielmo da Saliceto Hospital, AUSL, Piacenza, Italy.
Lorenzo IughettiDepartment of Pediatric, Department of Medical and Surgical Sciences for Mothers, Children and Adults, University of Modena and Reggio Emilia, Reggio Emilia, Italy.
Federico MarchettiDepartment of Pediatrics, Santa Maria delle Croci Hospital, AUSL della Romagna, Ravenna, Italy.
Paola Sogno ValinDepartment of Pediatrics, Santa Maria della Scaletta Hospital, Imola, Italy.
Sergio AmarriDepartment of Pediatrics, Arcispedale Santa Maria Nuova, IRCCS, Reggio Emilia, Italy.
Sandra BrusaDepartment of Pediatrics, Santa Maria della Scaletta Hospital, Imola, Italy.
Monica SprocatiDepartment of Pediatrics, Arcispedale Sant'Anna, Ferrara, Italy.
Giuseppe MaggioreDepartment of Pediatrics, Arcispedale Sant'Anna, Ferrara, Italy.
Ada DormiDepartment of Medical and Surgical Sciences DIMEC, University of Bologna, Bologna, Italy.
Paolo LanzoniDepartment of Pediatrics, Ramazzini Hospital, Carpi, Italy.
Andrea DontiPediatric Cardiology and Adult Congenital Unit, University of Bologna, S.Orsola-Malpighi Hospital, Bologna, Italy.
Marcello LanariDepartment of Pediatrics, University of Bologna, S.Orsola-Malpighi Hospital, Bologna, Italy.
IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITArcispedale Sant'Anna · ITGuglielmo da Saliceto Hospital · ITIstituto Ramazzini · ITOspedale Infermi di Rimini · ITOspedale Santa Maria · ITUniversity of Modena and Reggio Emilia · ITOspedale G.B. Morgagni - L.Pierantoni · ITOspedale “M. Bufalini” di Cesena · ITOspedale "Santa Maria delle Croci" di Ravenna · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKawasaki disease (KD) is a febrile systemic vasculitis of unknown etiology and the main cause of acquired heart disease among children in the developed world. To date, abdominal involvement at presentation is not recognized as a risk factor for a more severe form of the disease.

objectiveTo evaluate whether presenting abdominal manifestations identify a group at major risk for Intravenous immunoglobulin (IVIG)-resistance and coronary lesions.

methodsRetrospective study of KD patients diagnosed between 2000 and 2015 in 13 pediatric units in Italy. Patients were divided into 2 groups according to the presence or absence of abdominal manifestations at onset. We compared their demographic and clinical data, IVIG-responsiveness, coronary ectasia/aneurysms, laboratory findings from the acute and subacute phases.

results302 patients (181 boys) were enrolled: 106 patients with, and 196 patients without presenting abdominal features. Seasonality was different between the groups (p = 0.034). Patients with abdominal manifestations were younger (p = 0.006) and more frequently underwent delayed treatment (p = 0.014). In the acute phase, patients with abdominal presentation had higher platelet counts (PLT) (p = 0.042) and lower albuminemia (p = 0.009), while, in the subacute phase, they had higher white blood cell counts (WBC) and PLT (p = 0.002 and p < 0.005, respectively) and lower red blood cell counts (RBC) and hemoglobin (Hb) (p = 0.031 and p 0.009). Moreover, the above mentioned group was more likely to be IVIG-resistant (p < 0.005) and have coronary aneurysms (p = 0.007). In the multivariate analysis, presenting abdominal manifestations, age younger than 6 months, IVIG- resistance, delayed treatment and albumin concentration in the acute phase were independent risk factors for coronary aneurysms (respectively p<0.005, <0.005, = 0.005 and 0.009).

conclusionsThis is the first multicenter report demonstrating that presenting gastrointestinal features in KD identify patients at higher risk for IVIG-resistance and for the development of coronary aneurysms in a predominantly Caucasian population. CLINICAL

trial registration8/20014/O/OssN.

Indexed as

Abdominal PainAge FactorsChildChild, PreschoolCohort StudiesCoronary AneurysmDilatation, PathologicDrug ResistanceFemaleHumansImmunoglobulins, IntravenousInfantItalyMaleMucocutaneous Lymph Node SyndromePlatelet CountImmunoglobulins, IntravenousSerum Albumin

Identifiers

PMID30180185
PMCPMC6122791
OpenAlexW2892014593

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.