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Temporal Clusters of Kawasaki Disease Cases Share Distinct Phenotypes That Suggest Response to Diverse Triggers.
Burns, Jane C; DeHaan, Laurel L; Shimizu, Chisato; Bainto, Emelia V; Tremoulet, Adriana H; Cayan, Daniel R; Burney, Jennifer A.
Afiliação
  • Burns JC; Department of Pediatrics, University of California San Diego, La Jolla, CA; Rady Children's Hospital San Diego, San Diego, CA. Electronic address: jcburns@health.ucsd.edu.
  • DeHaan LL; Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA.
  • Shimizu C; Department of Pediatrics, University of California San Diego, La Jolla, CA.
  • Bainto EV; Department of Pediatrics, University of California San Diego, La Jolla, CA.
  • Tremoulet AH; Department of Pediatrics, University of California San Diego, La Jolla, CA; Rady Children's Hospital San Diego, San Diego, CA.
  • Cayan DR; Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA.
  • Burney JA; School of Global Policy and Strategy, University of California San Diego, La Jolla, CA.
J Pediatr ; 229: 48-53.e1, 2021 02.
Article em En | MEDLINE | ID: mdl-32976897
ABSTRACT

OBJECTIVE:

To test the hypothesis that cases of Kawasaki disease within a temporal cluster have a similar pattern of host response that is distinct from cases of Kawasaki disease in different observed clusters and randomly constructed clusters. STUDY

DESIGN:

We designed a case-control study to analyze 47 clusters derived from 1332 patients with Kawasaki disease over a 17-year period (2002-2019) from a single clinical site and compared the cluster characteristics with those of 2 control groups of synthetic Kawasaki disease clusters. We defined a "true" Kawasaki disease cluster as at least 5 patients within a 7-day moving window. The observed and synthetic Kawasaki disease clusters were compared with respect to demographic and clinical characteristics and median values for standard laboratory data using univariate analysis and a multivariate, rotated empirical orthogonal function analysis.

RESULTS:

In a univariate analysis, the median values for age, coronary artery z-score, white blood cell count, erythrocyte sedimentation rate, C-reactive protein, and age-adjusted hemoglobin for several of the true Kawasaki disease clusters exceeded the 95th percentile for the 2 synthetic clusters. REOF analyses revealed distinct patterns of demographic and clinical measures within clusters.

CONCLUSIONS:

Cases of Kawasaki disease within a cluster were more similar with respect to demographic and clinical features and levels of inflammation than would be expected by chance. These observations suggest that different triggers and/or different intensities of exposures result in clusters of cases of Kawasaki disease that share a similar response pattern. Analyzing cases within clusters or cases who share demographic and clinical features may lead to new insights into the etiology of Kawasaki disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Linfonodos Mucocutâneos Tipo de estudo: Health_economic_evaluation / Observational_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: America do norte Idioma: En Revista: J Pediatr Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Linfonodos Mucocutâneos Tipo de estudo: Health_economic_evaluation / Observational_studies / Risk_factors_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male País/Região como assunto: America do norte Idioma: En Revista: J Pediatr Ano de publicação: 2021 Tipo de documento: Article