Evidence map›Paper›PMID 26561332›Full record

Trial reportBMC pediatrics2015

Yersinia pseudotuberculosis infection in Kawasaki disease and its clinical characteristics.

Tomoko Horinouchi, Kandai Nozu, Kiyoshi Hamahira, Yosuke Inaguma, Jun Abe, Hiroshi Nakajima, Masaaki Kugo, Kazumoto Iijima

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC pediatrics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Yersiniosis in New Zealand.Pathogens (Basel, Switzerland) · 2021
    Review
  10. Review
  11. The up-to-date pathophysiology of Kawasaki disease.Clinical & translational immunology · 2021
    Review
  12. Article
  13. Article
  14. Case reports in pediatrics · 2020
    Article
  15. Article
  16. Review
  17. Article
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.

Tomoko HorinouchiDepartment of Pediatrics, Japanese Red Cross Society Himeji Hospital, Hyogo, Japan. tomoko.hatono@gmail.com.
Kandai NozuDepartment of Pediatrics, Kobe University Hospital, Kobe, Japan. nozu@med.kobe-u.ac.jp.
Kiyoshi HamahiraDepartment of Pediatrics, Japanese Red Cross Society Himeji Hospital, Hyogo, Japan. hamahira68@hotmail.com.
Yosuke InagumaDepartment of Pediatrics, Japanese Red Cross Society Himeji Hospital, Hyogo, Japan. yinaguma0709@yahoo.co.jp.
Jun AbeDepartment of Allergy and Immunology, National Research Institute for Child Health and Development, Tokyo, Japan. abe-j@ncchd.go.jp.
Hiroshi NakajimaDepartment of Bacteriology, Okayama Prefectural Institute for Environmental Science and Public Health, Okayama, Japan. hiroshi_nakajima@pref.okayama.lg.jp.
Masaaki KugoDepartment of Pediatrics, Japanese Red Cross Society Himeji Hospital, Hyogo, Japan. m.kugo@hrc-hp.com.
Kazumoto IijimaDepartment of Pediatrics, Kobe University Hospital, Kobe, Japan. iijima@med.kobe-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe etiology of Kawasaki disease (KD) is unknown. Reportedly, there is an association between KD and Yersinia pseudotuberculosis (YPT). Steroid therapy for KD patients with high risk of cardiac sequelae (CS) has been reported; however, the number of reports is limited.

methodsWe conducted a prospective study of 108 patients with newly diagnosed KD in one year to determine how many KD patients have positive anti-YPT antibody titers and/or positive anti-YPT-derived mitogen (YPM) antibody titers. In addition, we tried to identify clinical differences between KD patients in whom YPT infection was or not a contributing factor. We also compared clinical characteristics of patients treated with the protocol of the Randomized controlled trial to Assess Immunoglobulin plus Steroid Efficacy for Kawasaki disease (RAISE) study (RAISE group) and with the conventional Intravenous immunoglobulin (IVIG) protocol (conventional group).

resultsEleven patients (10%) were positive for anti-YPT and/or anti-YPM antibodies (positive group) and 97 (90%) were negative (negative group). Cardiac sequelae (CS) occurred significantly more frequently in the positive than the negative group (two patients, 18% vs one patient, 1%, p = 0.027). Forty patients were in the RAISE group. Two of 40 (5%) in the RAISE group and one of 68 (1.47%) in the conventional group had CS (p = 0.55).

conclusionsKD patients with YPT infection had CS significantly more frequently and treatment with RAISE protocol did not decrease the frequency of CS in our cohort, nor did YPT infection affect risk scores of no response to IVIG. However, our sample size was overly small to draw such conclusions. Further investigation in a larger cohort is necessary to confirm our findings. Additionally, further research is needed to determine whether early diagnosis of YPT can prevent KD from developing and reduce the incidence of CS.

Indexed as

Antibodies, BacterialChild, PreschoolDose-Response Relationship, DrugDrug Therapy, CombinationFemaleFollow-Up StudiesGlucocorticoidsHumansImmunoglobulins, IntravenousImmunologic FactorsInfantMaleMethylprednisoloneMucocutaneous Lymph Node SyndromeProspective StudiesTreatment OutcomeAntibodies, BacterialGlucocorticoidsImmunoglobulins, IntravenousImmunologic FactorsMethylprednisolone

Identifiers

PMID26561332
PMCPMC4642785

What OpenQuestion holds

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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.