Evidence map›Paper›PMID 22484354›Full record

ArticleThe Journal of pediatrics2012

Calcineurin inhibitor treatment of intravenous immunoglobulin-resistant Kawasaki disease.

Adriana H Tremoulet, Paige Pancoast, Alessandra Franco, Matthew Bujold, Chisato Shimizu, Yoshihiro Onouchi, Alyson Tamamoto, Guliz Erdem, Debra Dodd, Jane C Burns

Abstract read
In one paragraph

Article in The Journal of pediatrics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 139 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Kawasaki Disease: an Update.Current rheumatology reports · 2020
    Review
  15. Article
  16. Article
  17. The role of CaScientific reports · 2020
    Article
  18. Antibodies and Immunity During Kawasaki Disease.Frontiers in cardiovascular medicine · 2020
    Review
  19. Article
  20. 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

10 authors at 4 institutions in 2 countries.

Adriana H TremouletDepartment of Pediatrics, University of California at San Diego and Rady Children's Hospital, La Jolla, CA, USA.
Paige Pancoast
Alessandra Franco
Matthew Bujold
Chisato Shimizu
Yoshihiro Onouchi
Alyson Tamamoto
Guliz Erdem
Debra Dodd
Jane C Burns
Rady Children's Hospital-San Diego · USKapiolani Medical Center for Women and Children · USMonroe Carell Jr. Children's Hospital · USRIKEN Center for Integrative Medical Sciences · JP

Funding

SAN DIEGO CLINICAL AND TRANSLATIONAL RESEARCH INSTITUTEUL1RR031980 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI FIRESTEIN, GARY S · 2010 to 2011
$14.0M
Genetic Markers and gene expression in Kawasaki DiseaseR01HL069413 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BURNS, JANE C · 2002 to 2010
$5.5M
Impact of TNFa blockade on immune function in acute Kawasaki diseaseR01HL103536 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BURNS, JANE C, FRANCO, ALESSANDRA I · 2010 to 2013
$1.5M
NCRR NIH HHS 5UL1 RR031980NCRR NIH HHS UL1 RR031980NHLBI NIH HHS HL103536NHLBI NIH HHS HL69413NHLBI NIH HHS R01 HL069413NHLBI NIH HHS R01 HL103536
6 · The paper itself

Abstract

objectiveTo describe the clinical course and outcome of 10 patients with Kawasaki disease (KD) treated with a calcineurin inhibitor after failing to respond to multiple therapies. STUDY

designDemographic and clinical data were prospectively collected using standardized case report forms. T-cell phenotypes were determined by flow cytometry, and KD risk alleles in ITPKC (rs28493229), CASP3 (rs72689236), and FCGR2A (rs1801274) were genotyped.

resultsIntravenous followed by oral therapy with cyclosporine (CSA) or oral tacrolimus was well tolerated and resulted in defervescence and resolution of inflammation in all 10 patients. There were no serious adverse events, and a standardized treatment protocol was developed based on our experiences with this patient population. Analysis of T-cell phenotype by flow cytometry in 2 subjects showed a decrease in circulating activated CD8(+) and CD4(+) T effector memory cells after treatment with CSA. However, suppression of regulatory T-cells was not seen, suggesting targeting of specific, proinflammatory T-cell compartments by CSA.

conclusionTreatment of refractory KD with a calcineurin inhibitor appears to be a safe and effective approach that achieves rapid control of inflammation associated with clinical improvement.

Indexed as

ChildChild, PreschoolClinical ProtocolsCyclosporineFemaleHumansImmunoglobulins, IntravenousImmunologic FactorsImmunosuppressive AgentsInfantMaleMucocutaneous Lymph Node SyndromeTacrolimusT-LymphocytesTreatment FailureCyclosporineImmunoglobulins, IntravenousImmunologic FactorsImmunosuppressive AgentsTacrolimus

Identifiers

PMID22484354
PMCPMC3613150
OpenAlexW1975430314

What OpenQuestion holds

Textmetadata
LicenceTDM
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.