Key result
Late diagnosis of Kawasaki disease linked to a 68% rate of coronary anomalies.
Why the study?
Kawasaki disease is the leading cause of acquired heart disease in children, but clinical features and low physician awareness can make diagnosis difficult.
Observational (n=19)
No
Late diagnosis of Kawasaki disease and delayed administration of intravenous immunoglobulin are associated with a high incidence of coronary anomalies, highlighting the need for increased awareness among primary care physicians.
Answers are grounded in this paper and cite their sources.
Supports heightened primary care awareness for Kawasaki disease; leaves open optimal strategies to reduce residual coronary anomalies in larger cohorts.
Introduction. Kawasaki disease (KD) is the most common cause of acquired heart disease in children. Diagnosis of CD is based on the clinical manifestations of the disease, however, a number of its features and low awareness of doctors can make diagnosis difficult. Aim. To study epidemiological indicators, patient routing and clinical and laboratory features of the course of Kawasaki disease in children hospitalized at the City Children’s Hospital No. 1 of Kazan with this diagnosis in the period 2015–2022. Materials and methods. An empirical description of a patient case series was conducted on a group of 19 children hospitalized with a diagnosis of full-blown CD. Results and discussion. Late periods of diagnosis were identified (14.4 ± 7.3 days) and administration of intravenous immunoglobulin at a dose of 2 g/kg body weight (16.1 ± 7.9 days, the mode of the indicator was the 13th day), as well as a large percentage detection of coronary anomalies in the study group (68%, n = 13) and residual coronary anomalies at discharge (32%, n = 6). The referral diagnosis was correct only in 21% of cases; most often, the diagnosis of an infectious disease was made at the prehospital stage and in 79% of cases antimicrobial drugs were prescribed. At the prehospital stage, patients were diagnosed with rash syndrome (84%), changes in the oral mucosa (74%) and conjunctivitis (63%). Laboratory abnormalities in all patients before hospitalization were typical for Kawasaki disease: accelerated erythrocyte sedimentation rate (41.4 ± 14.3 mm/ hour), increased C-reactive protein (98.2 ± 47.6 mg/l), leukocytosis (23.0 ± 8.4 x 109/l), decreased hemoglobin (100.0 ± 8.9 g/l) and thrombocytosis (630.6 ± 215.5 x 109/l). Conclusions. The study included only children with the full form of CD; therefore, the most likely reason for the late diagnosis is the low level of awareness of the disease criteria among non-rheumatological doctors. It is required to conduct educational activities among pediatricians, infectious disease specialists, and general practitioners to increase alertness for the purpose of early diagnosis of CD.
No takes yet. Share an insight, caveat, or question.
Lutfullin et al. (2025) conducted an observational in Kawasaki disease (n=19). Late diagnosis was evaluated on Coronary anomalies. Late diagnosis of Kawasaki disease in 19 children was associated with a 68% rate of coronary anomalies and a 32% rate of residual coronary anomalies at discharge.
Synapse has enriched 10 related papers. Consider them for comparative context: