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Kawasaki Disease from a Single-Referral Center in Morocco with Emphasis on Diagnosis Delay and Treatment Onset
Bouayed Kenza1,2, Jalal Maryam1, Sakhi Asmaa1,2
1Department of Pediatric Rheumatology, A Harouchi Mother and Child Hospital, CHU Ibn Rochd, Casablanca, Morocco.
Insights
Kawasaki disease (KD) affects children, causing heart issues. Early diagnosis and treatment, especially in infants and older children, are crucial to prevent coronary artery problems. Awareness among physicians is key.
Area of Science:
- Pediatrics
- Cardiology
- Rheumatology
Background:
- Kawasaki disease (KD) is a leading cause of acquired heart disease in children.
- Understanding its epidemiology and cardiac involvement is vital for early intervention.
Purpose of the Study:
- To describe the epidemiological features of Kawasaki disease in Morocco.
- To emphasize the cardiac involvement and associated risk factors in pediatric patients.
Main Methods:
- A cross-sectional observational study of 69 pediatric patients diagnosed with KD between 2019 and 2023.
- Diagnosis followed the 2017 American Heart Association criteria.
- Statistical analyses included chi-square, Mann-Whitney U, and Fisher's exact tests.
Main Results:
- The mean age was 36 months, with a male:female ratio of 1.6.
- Coronary dilatations and aneurysms occurred in 20.3% and 10.1% of patients, respectively.
- Risk factors for coronary involvement included age ≤ 12 months or ≥ 60 months and delayed intravenous immunoglobulin (IVIG) infusion (>10 days).
Conclusions:
- Raising physician awareness of KD is essential, particularly regarding delayed referrals and extreme age groups.
- Prompt recognition and treatment are critical to mitigate cardiac complications in Kawasaki disease.
Abstract:
Objective: Kawasaki disease (KD) is one of the most common systemic vasculitides and a cause of acquired heart disease in children. The aim was to provide an epidemiological picture of KD with an emphasis on cardiac involvement in Morocco. Materials and Methods: This is a cross-sectional observational study recruiting patients with KD between January 2019 and December 2023. Diagnosis was based on 2017 American Heart Association criteria under the supervision of an expert. Statistical analysis was carried out using the chi-square, Mann-Whitney U, and Fisher's exact tests. Results: Sixty-nine patients were admitted; the mean age was 36 months, the sex ratio was 1.6 (male:female), and the mean days to the first consultation was 10.1. Thirty-nine cases met the criteria for complete forms and 30 for incomplete forms. Coronary dilatations and aneurysms were found in 20 and 7 patients respectively, including 3 giant aneurysms. All patients were treated with intravenous immunoglobulin (IVIG) except 1 and acetylsalicylic acid (ASA), and 23.1% received corticosteroids. Fourteen patients (20.3%) were resistant and 4.3% could benefit from a rescue treatment including second IVIG, Anakinra, and corticosteroids. Six predictive factors of coronary involvement were analyzed and were significant for age ≤ 12 months and ≥ 60 months and delay in IVIG infusion of more than 10 days (P= .045/P = .017). Conclusion: This study demonstrates the importance of raising awareness of KD among primary care physicians, given that a significant proportion of patients were referred from day 10 of fever onward, and paying more attention to extreme ages where coronary involvement is more common.
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