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Clinical characteristics of Kawasaki disease in Polish children: A retrospective study
Anna Smorczewska-Kiljan1, Magdalena Marszał1, Joanna Friedman-Gruszczyńska2
1Department of Pediatrics, Nutrition and Metabolic Diseases, The Children's Memorial Health Institute, Warszawa, Poland.
Insights
Kawasaki disease (KD) can lead to coronary artery aneurysms (CAA). Late diagnosis, low hemoglobin, and high platelets are key predictors of CAA in children with KD.
Area of Science:
- Pediatric Cardiology
- Rheumatology
- Vasculitis Research
Background:
- Kawasaki disease (KD) is a leading cause of acquired heart disease in children.
- KD is an acute, generalized vasculitis with increasing global incidence.
- It is associated with a significant risk of developing coronary heart disease.
Purpose of the Study:
- To analyze the clinical course of Kawasaki disease in pediatric patients.
- To identify risk factors for persistent coronary vessel changes post-treatment.
- To evaluate predictors of coronary artery aneurysms (CAA) in children with KD.
Main Methods:
- Retrospective analysis of 140 pediatric patients diagnosed with KD (2006-2019).
- Evaluation of clinical course, laboratory parameters, treatment response, and cardiac complications.
- Analysis stratified by age groups and compared outcomes based on specific clinical and laboratory findings.
Main Results:
- Coronary artery aneurysms (CAA) were detected in 16% of patients at 6-8 weeks.
- Boys and infants showed a higher likelihood of developing CAA.
- Predictors of CAA included atypical KD course, late diagnosis, pre-existing coronary changes, immunoglobulin resistance, low hemoglobin, and high platelet count.
Conclusions:
- Late diagnosis, low hemoglobin, high platelet count, and early coronary changes predict CAA development.
- Atypical KD course and resistance to intravenous immunoglobulin are significant risk factors for CAA.
- These findings aid in early identification and management of children at risk for KD complications.
Background:
Kawasaki disease (KD), an acute, generalized vasculitis, is associated with an increased risk of coronary heart disease and is the most common cause of acquired heart disease in childhood. The incidence of KD is increasing worldwide.
Aims:
Our study aims to analyze KD's clinical course in children and to evaluate risk factors for persistent changes in coronary vessels after 6-8 weeks of treatment.
Methods:
The retrospective analysis included patients with KD hospitalized in a single tertiary carehospital. The diagnosis, as well as treatment, were based on the current worldwide treatment standards. The clinical course, selected laboratory parameters, the treatment effect, and following cardiac complications were analyzed in different age groups.
Results:
In the years 2006-2019, 140 patients aged from two months to 16 years: 52 girls and 88 boys, were diagnosed with KD. Coronary artery aneurysms (CAA) at weeks 6-8 of disease were found in 16% of patients. Boys and infants were more likely to develop aneurysms at weeks 6-8 of the disease (P = 0.045; P = 0.03; respectively). The CAA frequency was related to the atypical course (P = 0.02), late diagnosis (P = 0.04), presence of changes in the coronary arteries at the time of diag nosis (P<0.001), immunoglobulin resistance (P = 0.002), a lower hemoglobin concentraction (P<0.001), and a higher platelet count (P = 0.02). There were 28% of patients resistant to first-line time treatment. In this group, we found CAA in 31% of children.
Conclusions:
We found that late diagnosis, low hemoglobin level, high platelet count, CAA presence at diagnosis, atypical course of KD, and resistance to intravenous immunoglobulins are predictors of CAA after 6-8 weeks in KD patients.
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