Evidence map›Paper›PMID 30332473›Full record

ArticlePloS one2018

Profile of resistance to IVIG treatment in patients with Kawasaki disease and concomitant infection.

Audrey Dionne, Cathie-Kim Le, Steffany Poupart, Julie Autmizguine, Léamarie Meloche-Dumas, Jean Turgeon, Anne Fournier, Nagib Dahdah

Open access · goldAbstract read
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 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
  7. Combined Single Nucleotide Variants ofChildren (Basel, Switzerland) · 2021
    Article
  8. Correct identification of incomplete Kawasaki disease.The Journal of international medical research · 2021
    Review
  9. Kawasaki Disease Complicated byCase reports in pediatrics · 2021
    Article
  10. Article
  11. Article
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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

8 authors at 2 institutions in 2 countries.

Audrey DionneDepartment of Cardiology, CHU Ste-Justine, Montreal, Canada.
Cathie-Kim LeDepartment of Cardiology, CHU Ste-Justine, Montreal, Canada.
Steffany PoupartDepartment of Cardiology, CHU Ste-Justine, Montreal, Canada.
Julie AutmizguineDepartment of Pharmacology, University of Montreal, Montreal, Canada.
Léamarie Meloche-DumasDepartment of Cardiology, CHU Ste-Justine, Montreal, Canada.
Jean TurgeonDepartment of pediatrics, CHU Ste-Justine, Montreal, Canada.
Anne FournierDepartment of Cardiology, CHU Ste-Justine, Montreal, Canada.
Nagib DahdahDepartment of Cardiology, CHU Ste-Justine, Montreal, Canada.ORCID 0000-0001-7715-3169
Centre Hospitalier Universitaire Sainte-Justine · CABoston Children's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionKawasaki disease (KD) can be associated with concomitant viral or bacterial infections. Children with persistent or recurrent fever 36 hours after the end of intravenous immunoglobulin (IVIG) are considered to be resistant to treatment and are at increased risk for coronary complications. Although concomitant infection does not affect coronary outcome, it is unknown how it influences the response to IVIG treatment. METHODOLOGY: Retrospective cohort study between 2008 and 2016 in a tertiary pediatric university hospital, including 154 children, of which 59 (38%) had concomitant infection.

resultsChildren with concomitant infection were more likely to have fever 48 hours after initial IVIG treatment (36% vs 20%, p = 0.05) and to be treated with a second dose (33% vs 18%, p = 0.04). Children with infection had higher C-reactive protein at the time of diagnosis (148 vs 112 mg/L, p = 0.04), and 48 hours after IVIG administration (111 vs 59 mg/L, p = 0.003). Nevertheless, there was no statistically significant difference in the prevalence of coronary complications (Z-score > 2.5) between children with and without concomitant infection (36% vs 39%, p = 0.68).

conclusionChildren with KD and concomitant infection are more likely to have persistent fever and elevated inflammatory markers after treatment. This association increases the likelihood of receiving a second dose of IVIG but not the risk of coronary complication. Accordingly, prospective studies to distinguish true IVIG resistance from infection induced persistent fever is warranted.

Indexed as

Drug ResistanceChild, PreschoolCommunicable DiseasesCoronary Artery DiseaseC-Reactive ProteinFemaleFeverHumansImmunoglobulins, IntravenousMaleMucocutaneous Lymph Node SyndromeTreatment OutcomeC-Reactive ProteinImmunoglobulins, Intravenous

Identifiers

PMID30332473
PMCPMC6192641
OpenAlexW2897460544

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.