About this item:

636 Views | 592 Downloads

Author Notes:

Corresponding author: Ryan A. Maddox, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, MS A-30, Atlanta, GA 30333; Tel: 404-639-1170; Email: rmaddox@cdc.gov

The authors do not declare any financial support or relationships that would pose conflicts of interest.

The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the funding agencies.

Subjects:

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Pediatrics
  • epidemiology
  • Kawasaki disease
  • Kawasaki syndrome
  • mucocutaneous lymph node syndrome
  • recurrence
  • CORONARY-ARTERY ABNORMALITIES
  • AMERICAN-HEART-ASSOCIATION
  • UNITED-STATES
  • RISK-FACTORS
  • NATIONWIDE SURVEYS
  • HOSPITALIZATIONS
  • CRITERIA

Recurrent Kawasaki disease: USA and Japan

Tools:

Journal Title:

Pediatrics International

Volume:

Volume 57, Number 6

Publisher:

, Pages 1116-1120

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Background Descriptive epidemiologic studies of recurrent and non-recurrent Kawasaki disease (KD) may identify other potentially important differences between these illnesses. Methods Data from the USA and Japan, the Centers for Disease Control and Prevention (CDC) national KD surveillance(1984-2008) and the 17th Japanese nationwide survey (2001-2002), respectively, were analyzed to examine recurrent KD patients <18 years of age meeting the CDC KD case or atypical KD case definition. These patients were compared with non-recurrent KD patients. Results Of the 5557 US KD patients <18 years of age during 1984-2008, 97 (1.7%) were identified as having had recurrent KD. Among the US Asian/Pacific Islander KD patients, 3.5% had recurrent KD, which was similar to the percentage identified among KD patients (3.5%) in the Japanese survey. Compared with non-recurrent KD patients, KD patients [with recurrent KD] were more likely to be older, fulfill the atypical KD case definition, and have coronary artery abnormalities (CAA) despite i.v. immunoglobulin (IVIG) treatment. Conclusions Differences in the age, race, and frequency of CAA exist between recurrent and non-recurrent KD patients. The increased association of CAA with recurrent KD suggests that more aggressive treatment strategies in conjunction with IVIG may be indicated for the second episode of KD.

Copyright information:

© 2015 Japan Pediatric Society.

Export to EndNote