Evidence map›Paper›PMID 31493782›Full record

ArticleBMC pediatrics2019

Kawasaki disease in infants less than one year of age: an Italian cohort from a single center.

Greta Mastrangelo, Rolando Cimaz, Giovani Battista Calabri, Gabriele Simonini, Donatella Lasagni, Massimo Resti, Sandra Trapani

Open access · goldAbstract read
In one paragraph

Article in BMC pediatrics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
4.0field-weighted citation impact, top 6% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  8. Atypical Kawasaki Disease in a 5-month-old Infant.Annals of African medicine · 2025
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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

7 authors at 2 institutions in 1 country.

Greta MastrangeloPediatric Residency program, Meyer Children's Hospital, University of Florence, Florence, Italy. greta.mastrangelo@gmail.com.ORCID 0000-0002-3455-7304
Rolando CimazDepartment of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
Giovani Battista CalabriCardiology Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
Gabriele SimoniniRheumatology Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
Donatella LasagniDepartment of Pediatrics, Meyer Children's Hospital, University of Florence, Florence, Italy.
Massimo RestiDepartment of Pediatrics, Meyer Children's Hospital, University of Florence, Florence, Italy.
Sandra TrapaniDepartment of Pediatrics, Meyer Children's Hospital, University of Florence, Florence, Italy.
Meyer Children's Hospital · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsFew data are currently available for Kawasaki disease (KD) below 12 months especially in Caucasians. This study aims to analyze clinical and laboratory features of KD among an Italian cohort of infants.

methodsA retrospective chart review of KD children aged less than 1 year at time of disease onset between January 2008-December 2017 was performed. Clinical data, laboratory parameters, instrumental findings, treatment and outcome were collected in a customized database.

resultsAmong 113 KD patients, 32 (28.3%) were younger than 1 year. Nineteen patients aged below 6 months, and three below 3 months. The median age was 5.7 ± 2.7 months. The mean time to diagnosis was 7 ± 3 days and was longer in the incomplete forms (8 ± 4 vs 6 ± 1 days). Conjunctival injection was present in 26 patients (81.2%); rash in 25 (78.1%); extremity changes in 18 (56.2%); mucosal changes in 13 (40.6%,) and lymphadenopathy only in 7 (21.8%). Mucosal changes were the least common features in incomplete forms (18.2%). Twenty-two patients (68.7%) had incomplete KD. Nineteen (59.4%) had cardiac involvement, of whom 13 (59.0%) had incomplete form. ESR, PCR and platelet values were higher in complete KD; especially, ESR resulted significantly higher in complete forms (80 ± 25.7 mm/h vs 50 ± 28.6 mm/h; p = 0.01). Conversely, AST level was statistically significant higher in patients with incomplete forms (95.4 ± 132.7 UI/L vs 29.8 ± 13.2 UI/L; p = 0.03). All patients received IVIG. Response was reported in 26/32 patients; 6 cases needed a second dose of IVIG and one required a dose of anakinra.

conclusionIn our cohort, incomplete disease was commonly found, resulting in delayed diagnoses and poor cardiac prognosis. Infants with incomplete KD seem to have a more severe disease and a greater predilection for coronary involvement than those with complete KD. AST was significantly higher in incomplete forms, thus AST levels might be a new finding in incomplete forms' diagnosis. Eventually, we highlight a higher resistance to IVIG treatment. To our knowledge this is the first study involving an Italian cohort of patients with KD below 12 months.

Indexed as

Mucocutaneous Lymph Node SyndromeAnti-Inflammatory Agents, Non-SteroidalAspirinCohort StudiesConjunctivitisDelayed DiagnosisExanthemaFemaleHeart DiseasesHumansImmunoglobulins, IntravenousInfantInfant, NewbornItalyLymphadenopathyMaleAnti-Inflammatory Agents, Non-SteroidalAspirinImmunoglobulins, IntravenousASTCaucasiansCoronary artery aneurysmsInfantKawasaki disease

Identifiers

PMID31493782
PMCPMC6731567
OpenAlexW2971877810

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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.