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Published on: December 9, 2015
Epidemiological data of national Kawasaki disease registry in Iran, 2007-2019
Leila Shahbaznejad1, Ali Hosseininasab2, Leila Mahboobi3
1Pediatric Infectious Diseases Research Center, Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Insights
This study established the first national registry for Kawasaki disease (KD) in Iran, revealing a high incidence of incomplete KD presentations. Increased healthcare worker awareness is crucial for timely diagnosis and management of this childhood vasculitis.
Area of Science:
- Pediatrics
- Rheumatology
- Epidemiology
Background:
- Kawasaki disease (KD) is a critical childhood vasculitis affecting coronary arteries.
- There is a lack of national prevalence data for KD in Iran.
Purpose of the Study:
- To establish a national registry for Kawasaki disease in Iran over a 13-year period.
- To analyze the epidemiological characteristics and clinical presentations of KD in Iran.
Main Methods:
- A retrospective analysis of medical records from patients under 19 years old admitted to tertiary hospitals in Iran (2007-2019).
- Data collected included demographics, clinical criteria, laboratory findings, echocardiography, and treatment modalities.
- Patients were classified as complete or incomplete KD based on clinical criteria.
Main Results:
- The registry included 1,682 KD patients (59.39% male), with a mean age of 3.08 years.
- Incomplete KD (78.54%) and abnormal echocardiography (36.80%) were common.
- Key laboratory findings included leukocytosis, anemia, thrombocytosis, elevated ESR, and CRP. No deaths were reported.
Conclusions:
- Atypical presentations of Kawasaki disease are prevalent in Iran.
- Enhancing primary healthcare worker awareness through education is vital for early diagnosis and effective management of KD.
Introduction:
Kawasaki disease(KD) is a vasculitis of childhood that tends to influence the coronary arteries. There is no national data about the prevalence of KD in Iran. This study aimed to perform a national registry in Iran for 13 years.
Methods:
In this retrospective study, the data for KD extracted from medical records of <19 year-old patients admitted to tertiary hospitals in Iran between 2007 and 2019 were recorded in the national KD registry system. Age, admission date, gender, location, and presence of KD criteria, laboratory and echocardiography findings, and treatment modalities were evaluated. Complete KD was considered if ≥4 clinical criteria of the KD existed and otherwise, incomplete KD was considered.
Results:
Data from 1,682 KD patients including 999(59.39%) boys and 683(40.61%) girls and male/female ratio of 1.46 were evaluated. The mean age was 3.08 ± 2.49 years and 1465(87%) were living in urban regions. The yearly incidence of the disease was between 2.62 to 3.03 from 2015 to 2019. The highest age-specific incidence was observed in children <1-year-old. Incomplete and resistant KD included 1,321(78.54%) and 9(0.54%) patients, respectively. Abnormal echocardiography was detected in 619(36.80%) patients. Leukocytosis, with dominancy of neutrophils, anemia, thrombocytosis and increased ESR and CRP were the most noticeable laboratory findings. No death due to KD disease was reported.
Conclusion:
Based on this study, most of the KD cases are presented with atypical presentation in Iran. So, increasing awareness of primary healthcare workers by educating and updating their data is very important in timely diagnosis and management of the disease.
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