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Isolated aortic coarctation: experience in 100 consecutive patients
Ana Peres1, José Diogo Ferreira Martins, Filipa Paramés
1Serviço de Cardiologia Pediátrica, Hospital de Santa Marta, Lisboa, Portugal.
Insights
Coarctation of the aorta (CoA) is a complex condition with excellent short-term outcomes but significant long-term risks. Careful follow-up is crucial for managing hypertension and other complications in pediatric cardiology patients.
Area of Science:
- Pediatric Cardiology
- Congenital Heart Disease
- Vascular Surgery
Background:
- Coarctation of the aorta (CoA) is a congenital narrowing of the descending aorta.
- While immediate treatment results are good, long-term complications are common.
Purpose of the Study:
- To analyze the presentation, treatment, and long-term outcomes of 100 patients with isolated CoA.
- To highlight the importance of early diagnosis and ongoing management.
Main Methods:
- Retrospective analysis of 100 isolated CoA patients treated between 1987 and 2008.
- Evaluation of clinical presentation, treatment modalities (surgical vs. percutaneous), and follow-up data.
Main Results:
- Patients diagnosed younger than one year presented with heart failure; older patients often had hypertension.
- Surgical repair was more common in younger patients; immediate mortality was 2% (surgical group).
- Recoarctation occurred in 8 patients; 46 patients developed hypertension during follow-up.
Conclusions:
- Isolated CoA requires lifelong monitoring due to significant long-term morbidity, including hypertension.
- Early detection through physical examination and prompt treatment are vital.
- Treatment choice depends on patient age, associated conditions, and surgical team expertise.
Introduction:
Coarctation of the aorta (CoA) is a stenosis usually located in the descending aorta. Treatment consists of surgical or percutaneous removal of the obstruction and presents excellent immediate results but significant residual problems often persist.
Objectives:
To describe the presentation, treatment and long-term evolution of a population of 100 unselected consecutive patients with isolated CoA in a single pediatric cardiology center.
Methods:
This was a retrospective study of all patients with isolated CoA treated during4 the last 21 years (1987-2008).
Results:
The patients (n=100, 68.3% male) were diagnosed at a median age of 94 days (1 day to 16 years). The clinical presentation differed between patients aged less or more than one year, the former presenting with heart failure and the latter being asymptomatic with evidence of hypertension (88 and 63%, respectively; p < 0.01). Treatment, a median of 8 days after diagnosis, was surgical in 79 cases (20 end-to-end anastomosis, 31 subclavian flap, 28 patch) and percutaneous in the remaining 21 (15 balloon angioplasty, 6 with stenting). The mean age of surgical patients was younger than in those treated percutaneously (3.4 vs. 7.5 years; p < 0.01). Immediate mortality was 2% and occurred in the surgical group. There was no late mortality, in a mean follow-up of 7.2 +/- 5.4 years. Recoarctation occurred in 8 patients (6 surgical, 2 percutaneous). There are 46 patients who currently have hypertension (19 at rest, 27 with effort), their median age at diagnosis being older than the others (23 vs. 995 days; p < 0.01).
Conclusions:
Isolated CoA has an excellent short-term prognosis but a significant incidence of long-term complications, and should thus no longer be seen as a simple obstruction in the descending aorta, but rather as a complex pathology that requires careful follow-up after treatment. Its potentially insidious presentation requires a high level of clinical suspicion, femoral pulse palpation during physical examination of newborns and older children being particularly important. Delay in treatment has an impact on late morbidity and mortality. Taking into account the data currently available on late and immediate results, the final choice of therapeutic technique depends on the patient's age, associated lesions and the experience of the medical-surgical team. Hypertension should be closely monitored in the follow-up of these patients, as well as its risk factors and complications.
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