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Aspirin Dose and Treatment Outcomes in Kawasaki Disease: A Historical Control Study in Japan
Yu Ito1, Takuya Matsui2, Kota Abe1
1Department of Pediatrics, Tokyo Women's Medical University Yachiyo Medical Center, Chiba, Japan.
Insights
High-dose aspirin (50 mg/kg/day) for Kawasaki disease (KD) showed no significant difference in coronary artery abnormalities (CAAs) compared to lower doses. However, the higher dose may reduce the need for further treatment.
Area of Science:
- Pediatrics
- Cardiology
- Rheumatology
Background:
- Kawasaki disease (KD) treatment involves aspirin, with ongoing debate about optimal dosing during the acute phase.
- Coronary artery abnormalities (CAAs) are a significant complication of KD, necessitating effective treatment strategies.
Purpose of the Study:
- To compare the incidence of CAAs and the need for further treatment between high-dose (50 mg/kg/day) and low-dose (30 mg/kg/day) aspirin in KD patients.
- To evaluate the antipyretic effect and safety of different aspirin dosages in KD management.
Main Methods:
- A retrospective, single-center, historical cohort study involving 587 KD patients.
- Patients were divided into two groups: 50 mg/kg/day aspirin (2007-2014) and 30 mg/kg/day aspirin (2014-2016), both receiving intravenous immunoglobulin (IVIG).
- Primary endpoint: incidence of CAAs (Z score ≥2.5) at week 4. Secondary endpoint: incidence of further treatment. Analysis used inverse probability weighting.
Main Results:
- No significant difference in the incidence of CAAs was observed between the 30 mg/kg/day and 50 mg/kg/day aspirin groups (OR 0.769, 95% CI: 0.537-1.101, p=0.151).
- The risk of requiring further treatment after initial IVIG was significantly higher in the 30 mg/kg/day group compared to the 50 mg/kg/day group (OR 1.379, 95% CI: 1.051-1.811, p=0.021).
Conclusions:
- Aspirin 50 mg/kg/day does not significantly increase the risk of CAAs compared to 30 mg/kg/day in KD patients.
- Higher-dose aspirin (50 mg/kg/day) may be associated with a reduced need for further treatment in KD management.
Abstract:
Aspirin has been used as a concomitant drug in the treatment of Kawasaki disease (KD). In recent years, there has been discussion concerning whether high-dose aspirin is appropriate for treatment in the acute phase of KD. We retrospectively investigated the incidence of coronary artery abnormalities (CAAs) and the antipyretic effect of 30 to 50 mg/kg/day aspirin, the minimum and the maximum approved doses in Japan. This was a single-center, non-randomized, retrospective, historical cohort study. Patients were routinely treated with 50 mg/kg/day aspirin (50-mg Group) between 2007 and April 2014, and with 30 mg/kg/day aspirin (30-mg Group) between May 2014 and 2016. All patients were given initial and, if necessary, subsequent intravenous immunoglobulin (IVIG) 2.0 g/kg. The primary endpoint was incidence of CAAs defined as a CA diameter with a Z score ≥2.5 at treatment week 4. The secondary endpoint was incidence of further treatment. Incidences were compared using inverse probability weighting analysis adjusting for age, sex, and risk scores. In 587 patients, there was no significant difference in incidence of CAAs (odds ratio in 30-mg Group 0.769, 95% confidence interval (CI): 0.537-1.101, p = 0.151). Risk of further treatment after the first IVIG in the 30-mg Group was significantly higher than that in the 50-mg Group (odds ratio 1.379, 95% CI: 1.051-1.811, p = 0.021). Although this study has some limitations, the findings suggest that aspirin 50 mg/kg/day may have no significant effect on improving incidence of CAAs compared with 30 mg/kg/day but may have a lower rate of further treatment.
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