Unexpectedly high incidence of Kawasaki Disease in a Canadian Atlantic Province- an 11-year retrospective descriptive study

• Published in: Pediatric Rheumatology Vol. 21; no. 1; p. 30
• Main Authors: Alkanhal, Abdulrahman, Saunders, Joseph, Altammar, Fajer, Huber, Adam M, Lynk, Andrew, MacLeod, Alison, Ortiz-Alvarez, Oliva, Adams, Meighan, Ramsey, Suzanne, Stringer, Elizabeth, Warren, Andrew, Lang, Bianca
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 03.04.2023; BioMed Central; BMC
• Subjects: Adolescent; Age groups; Aneurysms; Canada; Cardiology; Censuses; Child; Child, Preschool; Coronary Aneurysm - diagnosis; Coronary Aneurysm - epidemiology; Coronary Aneurysm - etiology; Coronary artery aneurysm; Coronary vessels; Diseases; Epidemiology; Female; Heart attacks; Heart diseases; Humans; Immunoglobulins, Intravenous - therapeutic use; Incidence; Infant; Infant, Newborn; Kawasaki disease; Lymphatic system; Male; Medical records; Mucocutaneous lymph node syndrome; Mucocutaneous Lymph Node Syndrome - complications; Mucocutaneous Lymph Node Syndrome - diagnosis; Mucocutaneous Lymph Node Syndrome - drug therapy; Mucocutaneous Lymph Node Syndrome - epidemiology; Nova Scotia; Nova Scotia - epidemiology; Patients; Pediatric cardiology; Pediatrics; Population; Provinces; Research ethics; Retrospective Studies; Variables; Vasculitis; Veins & arteries; Nova Scotia; Canada; United States > US; Kawasaki disease; Vasculitis; Mucocutaneous lymph node syndrome; Epidemiology; Coronary artery aneurysm
• ISSN: 1546-0096; 1546-0096
• DOI: 10.1186/s12969-023-00805-y

Kawasaki Disease (KD) is the leading cause of acquired heart disease in children in developed countries with a variable incidence worldwide. Previous studies reported an unexpectedly high incidence of KD in the Canadian Atlantic Provinces. The goals of our study were to validate this finding in the province of Nova Scotia and to carefully review patients' characteristics and disease outcomes. This was a retrospective review of all children < 16 years old from Nova Scotia diagnosed with KD between 2007-2018. Cases were identified using a combination of administrative and clinical databases. Clinical information was collected retrospectively by health record review using a standardized form. Between 2007-2018, 220 patients were diagnosed with KD; 61.4% and 23.2% met the criteria for complete and incomplete disease, respectively. The annual incidence was 29.6 per 100,000 children < 5 years. The male to female ratio was 1.3:1 and the median age was 3.6 years. All patients diagnosed with KD in the acute phase received intravenous immunoglobulin (IVIG); 23 (12%) were refractory to the first dose. Coronary artery aneurysms were found in 13 (6%) patients and one patient died with multiple giant aneurysms. We have confirmed an incidence of KD in our population which is higher than that reported in Europe and other regions of North America despite our small Asian population. The comprehensive method to capture patients may have contributed to the detection of the higher incidence. The role of local environmental and genetic factors also deserves further study. Increased attention to regional differences in the epidemiology of KD may improve our understanding of this important childhood vasculitis.