Randomized Trial of Adjunctive Prednisolone for Kawasaki Disease

N Engl J Med. 2026 Apr 16;394(15):1480-1490. doi: 10.1056/NEJMoa2511478.

Abstract

Background: The effect of adjunctive glucocorticoids in the primary treatment of Kawasaki disease in unselected patients remains unknown.

Methods: In this multicenter, open-label, randomized, controlled trial in China, we assigned participants with newly diagnosed Kawasaki disease in a 1:1 ratio to receive prednisolone plus standard treatment or standard treatment alone. The primary outcome was the occurrence of coronary-artery lesions at 1 month after illness onset. Prespecified key secondary outcomes, for which analyses were not controlled for multiplicity, included receipt of rescue therapy, duration of fever, change in the C-reactive protein (CRP) level, and changes in coronary-artery z scores.

Results: A total of 3208 participants underwent randomization, with coronary-artery lesions detected at baseline in 870 of 3184 participants (27.3%). At 1 month, coronary-artery lesions were detected in 16.0% of the participants receiving prednisolone plus standard treatment and in 13.8% of those receiving standard treatment alone (adjusted risk difference, 1.1 percentage points; 95% confidence interval, -1.0 to 3.4; P = 0.31). Rescue therapy was used in 4.6% of the participants receiving prednisolone plus standard therapy and in 10.1% of those receiving standard treatment alone; the median duration of fever was 8.4 hours and 13.2 hours, respectively, and the reductions in the C-reactive protein level at 72 hours were 67.5 mg per liter and 59.8 mg per liter. Decreases in coronary-artery z scores were similar in the two groups. At 3 months, the incidence of coronary-artery lesions was 12.6% with prednisolone plus standard therapy and 10.5% with standard treatment alone; the percentage of participants with progression of coronary-artery lesions was 28.6% and 28.9%, respectively, and the incidence of medium-to-giant coronary-artery aneurysms was 1.9% and 1.1%. The overall incidence of adverse events did not differ significantly between the two groups.

Conclusions: The addition of prednisolone to standard primary treatment for Kawasaki disease did not reduce the incidence of coronary-artery lesions at 1 month after illness onset. (Funded by the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences and the National Natural Science Foundation of China; ClinicalTrials.gov number, NCT04078568.).

Publication types

  • Clinical Trial, Phase III
  • Multicenter Study
  • Randomized Controlled Trial

MeSH terms

  • C-Reactive Protein / analysis
  • Child, Preschool
  • China / epidemiology
  • Coronary Aneurysm* / diagnosis
  • Coronary Aneurysm* / epidemiology
  • Coronary Aneurysm* / etiology
  • Coronary Aneurysm* / prevention & control
  • Coronary Artery Disease* / diagnosis
  • Coronary Artery Disease* / epidemiology
  • Coronary Artery Disease* / etiology
  • Coronary Artery Disease* / prevention & control
  • Coronary Vessels / diagnostic imaging
  • Drug Therapy, Combination / adverse effects
  • Drug Therapy, Combination / methods
  • Echocardiography
  • Female
  • Glucocorticoids* / administration & dosage
  • Glucocorticoids* / adverse effects
  • Humans
  • Incidence
  • Infant
  • Male
  • Mucocutaneous Lymph Node Syndrome* / blood
  • Mucocutaneous Lymph Node Syndrome* / complications
  • Mucocutaneous Lymph Node Syndrome* / drug therapy
  • Prednisolone* / administration & dosage
  • Prednisolone* / adverse effects
  • Treatment Outcome

Substances

  • C-Reactive Protein
  • Glucocorticoids
  • Prednisolone

Associated data

  • ClinicalTrials.gov/NCT04078568