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Published on: August 9, 2024
Long-term outcome of coronary artery dilatation in Kawasaki disease
Najib Advani1, Sudigdo Sastroasmoro1, Teddy Ontoseno2
1Department of Child Health, Faculty of Medicine, Universitas Indonesia-Cipto Mangunkusumo Hospital, Jakarta, Indonesia.
Insights
Most Kawasaki disease (KD) coronary artery dilatations regress within two years, especially smaller ones. Giant aneurysms often persist, with outcomes depending on diameter, not location.
Area of Science:
- Pediatric Cardiology
- Systemic Vasculitis Research
- Medical Imaging in Pediatrics
Background:
- Kawasaki disease (KD) is a significant cause of acquired heart disease in children, characterized by systemic vasculitis.
- Coronary artery aneurysms are a common complication of KD, but many regress spontaneously over time.
- Understanding the natural history of coronary artery dilatation in KD is crucial for patient management.
Purpose of the Study:
- To investigate the long-term course and resolution of coronary artery dilatation in children diagnosed with Kawasaki disease.
- To evaluate the factors influencing the regression of coronary artery aneurysms, including size and location.
- To compare outcomes across different coronary artery branches affected by dilatation.
Main Methods:
- Retrospective cohort study analyzing midterm follow-up data of KD patients with coronary dilatation.
- Serial echocardiography utilized for monitoring coronary artery dimensions over 1-10.5 years.
- Kaplan-Meier survival analysis applied to assess regression rates and time to resolution.
Main Results:
- Out of 154 patients, 33.3% had coronary dilatation in the acute phase, decreasing to 7.9% by 6-8 weeks.
- A total of 245 dilatations were observed, with a median regression time of 2.6 months (mean 10.5 months) over a median follow-up of 41 months.
- Small and medium dilatations showed significantly better regression outcomes than giant aneurysms; location did not impact the outcome.
Conclusions:
- The majority of small-to-medium coronary dilatations in KD regress within two years, while giant aneurysms are more likely to persist.
- Coronary artery dilatation outcomes are primarily dictated by aneurysm diameter, not anatomical location.
- Regression rates are inversely correlated with dilatation size, with smaller lesions resolving faster.
Background:
Kawasaki disease (KD) is an acute systemic vasculitis syndrome with a high incidence of coronary aneurysms in untreated children. The majority of aneurysms resulting from KD are known to regress with time.
Aims:
This study aimed to determine the course and outcome of coronary artery dilatation in patients with KD and ascertain whether there are any differences in the outcomes in the different branches.
Setting And Design:
This is a retrospective cohort study of patients diagnosed with KD with midterm follow-up data.
Methods:
Serial echocardiography was performed in all KD patients with coronary dilatation for 1-10½ years. The Kaplan-Meier curve was used for statistical analysis.
Results:
There were 154 patients with coronary dilatation studied. The frequency of coronary dilatation in acute phase was 33.3% and decreased to 7.9% 6-8 weeks later. Each patient could have dilatations at more than one branch, so the total number of dilatations was 245. The median time needed for regression was 2.6 months (mean: 10.5 months) while the median of follow-up duration was 41 months (mean: 23 months). Small- and medium-sized dilatations had more favorable outcomes compared to the giant ones. Location of dilatation did not influence the outcome.
Conclusions:
The majority (77.4%) of small- and medium-sized dilatations regress within 2 years, but giant aneurysms tend to persist. The outcome of coronary dilatation is determined by the diameter and not by the location. Regression rate is faster in smaller dilatations. Left main coronary artery is the most frequent location for dilatation.
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