Volume 1, Issue 1 (1-2013)                   JPR 2013, 1(1): 44-52 | Back to browse issues page

XML Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Navaeifar M R, Rezai M S. Intravenous Immunoglobulin Resistant Kawasaki Disease. JPR. 2013; 1 (1) :44-52
URL: http://jpr.mazums.ac.ir/article-1-34-en.html
1- Pediatrics Nosocomial Infection Research Center
2- Subspecialist of pediatrics infectious diseases Department of Pediatric Infectious Disease , drmsrezaeii@yahoo.com
Abstract:   (7351 Views)
ABSTRACT Kawasaki disease is a systemic vasculitis that mainly affects younger children. Although the definite cause still remains unknown but the clinical and epidemiologic findings discuss an infectious cause. The prevalence of incomplete Kawasaki disease reported 15 to 36.2%, and it is more frequent in the extremes of the age spectrum. Non delayed treatment of disease should be initiated because of critical cardiac vascular complications. Up to 15% - 25% of patients with Kawasaki disease who remain febrile after administration of first dose of intravenous immunoglobin plus aspirin are classified as refractory disease. These intravenous immunoglobin resistant cases are at increasing risk for coronary artery complications. The strategy on prediction of potentially non responder and treatment of intravenous immunoglobin resistant patients is now controversial but some useful points were recommended.
Full-Text [PDF 272 kb]   (3012 Downloads)    
Type of Study: Narrative Review |
Received: 2013/01/6 | Accepted: 2013/08/17 | Published: 2013/08/17

Add your comments about this article : Your username or Email:
CAPTCHA code

Send email to the article author


© 2018 All Rights Reserved | Journal of Pediatrics Review

Designed & Developed by : Yektaweb