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2013 ACR/ARHP Annual Meeting: Diagnostic,Treatment Approaches Evolve for Kawasaki Disease

Mary Beth Nierengarten  |  Issue: February 2014  |  February 1, 2014

Based on what is currently known from the Adult KD Collaborative study, Dr. Burns feels strongly that all patients with any coronary artery abnormality should be followed for life by a cardiologist with knowledge of KD vasculopathy. More controversial, she said, is whether patients with normal echocardiograms throughout their initial course of KD need follow up by a cardiologist.

Finding the right therapy to give children with early coronary artery abnormalities to prevent progression to aneurysm formation remains a key challenge in treating KD, she said.

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Mary Beth Nierengarten is a freelance medical journalist based in St. Paul, Minn.

References

  1. Newburger JW, Takahashi M, Gerber, MA, et al. Diagnosis, treatment, and long-term management of Kawasaki Disease. Circulation. 2004;110:2747-2771.
  2. Koren G, Silverman E, Sundel R, et al. Decreased protein binding of salicylates in Kawasaki disease. J Pediatr. 1991;118:456-459.
  3. Kahn AM, Budoff MJ, Daniels LB, et al. Calcium scoring in patients with a history of Kawasaki disease. JACC Imaging. 2012;5:264-272.

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Filed under:Career DevelopmentEducation & TrainingMeeting ReportsProfessional TopicsResearch Rheum Tagged with:ACR/ARHP Annual MeetingCardiacDiagnosisdrugimaginginfliximabKawasaki diseasepatient carePediatricsResearchrheumatologistTreatment

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