Evidence map›Paper›PMID 30021610›Full record

Observational studyPediatric rheumatology online journal2018

Kawasaki disease: abnormal initial echocardiogram is associated with resistance to IV Ig and development of coronary artery lesions.

Dima Chbeir, Jean Gaschignard, Ronan Bonnefoy, Constance Beyler, Isabelle Melki, Albert Faye, Ulrich Meinzer

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Pediatric rheumatology online journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
6.6field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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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 4 institutions in 1 country.

Dima ChbeirService de pédiatrie générale, maladies infectieuses et médecine interne, Centre de référence des rhumatismes inflammatoires et maladies auto-immunes systémiques rares de l'enfant (RAISE), Hôpital Robert Debré, Assistance Publique Hôpitaux de Paris, 75019, Paris, France.
Jean GaschignardService de pédiatrie générale, maladies infectieuses et médecine interne, Centre de référence des rhumatismes inflammatoires et maladies auto-immunes systémiques rares de l'enfant (RAISE), Hôpital Robert Debré, Assistance Publique Hôpitaux de Paris, 75019, Paris, France.
Ronan BonnefoyCentre de recherche sur l'inflammation, Institut National de la Santé et de la Recherche Médicale, Université Paris Diderot-Sorbonne Paris-Cité, UMR 1149, 75018, Paris, France.
Constance BeylerCentre de recherche sur l'inflammation, Institut National de la Santé et de la Recherche Médicale, Université Paris Diderot-Sorbonne Paris-Cité, UMR 1149, 75018, Paris, France.
Isabelle MelkiService de pédiatrie générale, maladies infectieuses et médecine interne, Centre de référence des rhumatismes inflammatoires et maladies auto-immunes systémiques rares de l'enfant (RAISE), Hôpital Robert Debré, Assistance Publique Hôpitaux de Paris, 75019, Paris, France.
Albert FayeService de pédiatrie générale, maladies infectieuses et médecine interne, Centre de référence des rhumatismes inflammatoires et maladies auto-immunes systémiques rares de l'enfant (RAISE), Hôpital Robert Debré, Assistance Publique Hôpitaux de Paris, 75019, Paris, France.
Ulrich MeinzerService de pédiatrie générale, maladies infectieuses et médecine interne, Centre de référence des rhumatismes inflammatoires et maladies auto-immunes systémiques rares de l'enfant (RAISE), Hôpital Robert Debré, Assistance Publique Hôpitaux de Paris, 75019, Paris, France. ulrich.meinzer@aphp.fr.
Assistance Publique – Hôpitaux de Paris · FRCentre de Recherche sur l'Inflammation · FRHôpital Robert-Debré · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundKawasaki disease (KD) is an acute febrile systemic vasculitis that affects small and medium blood vessels. Intensified treatments for the most severely affected patients have been proposed recently, and the early identification of KD patients at high risk for coronary artery aneurysms (CAA) is crucial. However, the risk scoring systems developed in Japan have not been validated in European populations, and little data is available concerning the link between initial echocardiogram findings other than high z-scores and cardiac prognosis.

methodsIn order to investigate whether the presence of any abnormalities, other than high z-scores in first echocardiogram, are associated with resistance to IV immunoglobulins and/or subsequent development of CAA, we retrospectively analyzed data from children diagnosed with KD between 2006 and 2016 at a tertiary Hospital in Paris, France.

resultsA total of 157 children were included. The initial echocardiogram was performed after a median of 7 days of fever and was abnormal in 48 cases (31%). The initial presence of any echocardiographic abnormality (coronary artery dilatation, CAA, pericardial effusion, perivascular brightness of the coronary arteries, left-ventricular dysfunction and mitral insufficiency) was strongly associated with resistance to intravenous immunoglobulin (p = 0.005) and development of coronary artery lesions within the first 6 weeks of disease (p = 0.01). All patients (n = 7) with persistent coronary abnormalities at 1 year already had an abnormal initial echocardiogram. Severity scoring systems from Japan had low sensitivity (0-33%) and low specificity (71-82%) for predicting immunoglobulin resistance or cardiac involvement.

conclusionsIn European populations with mixed ethnic backgrounds, the presence of any abnormalities at the initial echocardiogram may contribute to early identification of patients with severe disease.

Indexed as

ChildChild, PreschoolCoronary Artery DiseaseDrug ResistanceEchocardiographyFemaleFranceHumansImmunoglobulins, IntravenousInfantMaleMucocutaneous Lymph Node SyndromePrognosisRetrospective StudiesRisk AssessmentSensitivity and SpecificityImmunoglobulins, Intravenouscoronary arteryKawasaki diseasePediatric RheumatologyVasculitis

Identifiers

PMID30021610
PMCPMC6052519
OpenAlexW2884367917

What OpenQuestion holds

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LicenceCC BY
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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.