Pediatric rheumatology

Effect of additional intravenous immunoglobulin for infliximab-refractory Kawasaki disease: a cohort study

Pediatr Rheumatol Online JPublished Cohort study

Main finding · Time until fever resolutionResult — go to the resultHR for fever resolution 1.00 95% CI 0.58–1.70

Authors' conclusion

Additional IVIG for IFX-refractory KD may have a therapeutic effect comparable to that of the second IVIG for IVIG-resistant KD and be a hopeful therapeutic option for IFX-refractory KD.

Study context

Population
Patients with Kawasaki disease refractory to infliximab, single centre
Participants
27 vs 38
Exposure
Additional intravenous immunoglobulin (IVIG) after infliximab (IFX) for IFX-refractory Kawasaki disease (KD) vs second IVIG for IVIG-resistant KD
  • IVIG-after-IFXn = 27
  • second-IVIGn = 38reference
Outcome
Time from initiation of treatment to resolution of fever
Methodological detailssingle-centre, descriptive statistics and survival analysis
  • Single-centre
  • Descriptive statistics and survival analysis

Main finding

Time until fever resolution

HR for fever resolution

1.00

95% CI 0.58–1.70

P = 0.783

By group

IVIG-after-IFXvs Second-IVIG
HR for fever resolution 1.00 (95% CI 0.58–1.70); P = 0.783

As reported in the abstract

Observational data: associations, not effects.

Further findings

Fever resolved within 2.0 days after therapy initiation

Coronary artery lesions (CALs) before initiating IVIG-after-IFX

CALs identified before initiating IVIG-after-IFX
26% (7/27)

New CALs after IVIG after IFX

New CALs after IVIG after IFX
7% (2/27)

Persistent CALs · 12 months after diagnosis

Persistent CALs after 12 months after diagnosis
19% (5/27)

Original publication

Effect of additional intravenous immunoglobulin for infliximab-refractory Kawasaki disease: a cohort study. Pediatr Rheumatol Online J. Published 13 May 2025. doi:10.1186/s12969-025-01108-0

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