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Two decades of aortic coarctation treatment in children; evaluating techniques
E J Dijkema1, L Dik2, J M P Breur2
1Department of Pediatric Cardiology, Wilhelmina Children's Hospital (WKZ), University Medical Center Utrecht, Utrecht, The Netherlands. ellesdijkema@gmail.com.
Insights
Surgical repair is preferred for complex pediatric aortic coarctation, while catheter interventions suit simpler cases. Reintervention is common, especially after catheter procedures and early surgery, with one-fifth of patients developing hypertension.
Area of Science:
- Pediatric Cardiology
- Congenital Heart Disease
- Surgical Innovation
Background:
- Aortic coarctation is a critical congenital heart defect requiring timely intervention.
- Treatment strategies have evolved, necessitating an evaluation of long-term outcomes.
- Understanding treatment trends and their impact on morbidity is crucial for pediatric cardiac care.
Purpose of the Study:
- To analyze the evolution of treatment techniques for pediatric aortic coarctation.
- To assess the long-term morbidity associated with different treatment modalities.
- To identify factors influencing reintervention rates and long-term outcomes.
Main Methods:
- Retrospective cohort study of 206 patients with native aortic coarctation.
- Inclusion of patients with a minimum of 7 years of follow-up.
- Categorization into three eras based on the year of primary intervention to track changes over time.
Main Results:
- Surgical repair, particularly with simultaneous aortic arch repair, increased in recent eras.
- Reintervention rates were significantly higher for catheter-based interventions (HR 1.8) and surgery under 3 months of age (HR 2.1).
- Hypertension was observed in 20% of patients, highlighting a significant long-term morbidity.
Conclusions:
- Current practice favors surgical intervention for complex aortic coarctation with associated defects.
- Catheter-based interventions are increasingly used for less complex cases.
- High reintervention rates, particularly in specific patient groups, underscore the need for ongoing monitoring and potential improvements in treatment strategies.
Objective:
This study focuses on the evolution of treatment techniques for aortic coarctation in children and assesses long-term morbidity.
Methods:
This retrospective cohort study evaluates patients treated for native aortic coarctation, with at least 7 years of follow-up. To assess time-related changes, three time periods were distinguished according to year of primary intervention (era 1, 2 and 3). Operative and long-term follow-up data were collected by patient record reviews.
Results:
The study population consisted of 206 patients (177 surgical and 29 catheter-based interventions), with a median follow-up of 151 months. Anterior approach with simultaneous repair of aortic arch and associated cardiac lesions was more common in the most recent era. Median age at intervention did not change over time. Reintervention was necessary in one third of the cohort with an event-free survival of 74% at 5‑year and 68% at 10-year follow-up. Reintervention rates were significantly higher after catheter-based interventions compared with surgical interventions (hazard ratio [HR] 1.8, 95% confidence interval [CI] 1.04-3.00, p = 0.04) and in patients treated before 3 months of age (HR 2.1, 95% CI 1.27-3.55, p = 0.003). Hypertension was present in one out of five patients.
Conclusion:
Nowadays, complex patients with associated cardiac defects and arch hypoplasia are being treated surgically on bypass, whereas catheter-based intervention is introduced for non-complex patients. Reintervention is common and more frequent after catheter-based intervention and in surgery under 3 months of age. One fifth of the 206 patients remained hypertensive.
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