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Kawasaki disease in Thai infants compared with older children
Rekwan Sittiwangkul1, Yupada Pongprot, Wanathorn Thongsongkrit
1Division of Cardiology, Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand. rsittiwa@med.cmu.ac.th
Insights
Infants with Kawasaki disease (KD) present with more non-classical symptoms and delayed treatment, increasing their risk for coronary artery abnormalities (CAA). Early recognition and intervention are crucial for better outcomes in infant KD patients.
Area of Science:
- Pediatrics
- Cardiology
- Infectious Diseases
Background:
- Kawasaki disease (KD) poses a significant risk of coronary artery abnormalities (CAA) in infants.
- Understanding infant-specific clinical features is vital for timely diagnosis and management.
Purpose of the Study:
- To evaluate clinical features of KD in infants.
- To compare infant KD cases with older children.
- To identify risk factors for CAA in infants with KD.
Main Methods:
- Retrospective study of 51 children with KD admitted to a tertiary care hospital (1993-2003).
- Analysis of clinical manifestations, treatment delays, and CAA development.
- Comparison between infants (<1 year) and older children.
Main Results:
- Infants (43% of cohort) showed more non-classical symptoms like diarrhea (68% vs 38%).
- Infants received intravenous immunoglobulin (IVIG) treatment 2 days later on average.
- Predictors of CAA in infants included IVIG resistance and prolonged fever duration.
Conclusions:
- Infants with KD often present with atypical symptoms, potentially delaying diagnosis and treatment.
- Delayed treatment and atypical presentations in infants are linked to increased risk of CAA.
- Further research into early diagnostic markers and treatment strategies for infant KD is warranted.
Abstract:
Infants with Kawasaki disease (KD) are at increased risk of having coronary artery abnormalities (CAA). The purpose of this study was to evaluate the clinical features of KD in infants and compare these with findings in older children to determine the risk factors for CAA in infants. All children with KD admitted to a tertiary care hospital between January 1993 and April 2003 were studied retrospectively. Of a total of 51 patients included in the study, 22 (43%) were <1 year of age (mean 8 months, range 2-12 months). All had classical clinical manifestations such as fever, skin rash and mucositis; extremity change occurred in 95%, conjunctivitis in 81% and cervical lymphadenopathy in 27%. Infants had significantly more non-classical symptoms, e.g. diarrhoea (68%), than older children (38%) (p=0.04). The mean number of days before intravenous immunoglobulin (IVIG) treatment was given to infants was 2 days later than in older children. The predictors of CAA in infants were resistance to IVIG treatment (p=0.02) and long duration of fever (p=0.009). Compared with older children, the less typical presentations and delay in diagnosis and treatment in infants might be important factors in CAA in KD.
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