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Abstract

Coarctation of the aorta (CoA) is the sixth most common congenital heart disease (CHD). It consists of a narrowing in the proximal descending aorta that encompasses a variety of severity, from a mild discrete stenosis to severe tubular hypoplasia. CoA results from abnormal ductal tissue surrounding the descending aorta and altered fetal blood flow patterns. It was one of the first successfully treated forms of CHD. There are currently several surgical and transcatheter techniques available to treat coarctation. Management strategy depends on several factors including patient age, morphology of the CoA, presence of coexisting defects, and confounding risk factors. Despite adequate relief of the stenosis, patients with CoA remain with significant long-term morbidity related to an altered blood pressure phenotype as vascular dysfunction, which underline that CoA is not a mere focal stenosis but a challenging systemic arterial disease.

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Abbreviations

AAO:

Ascending aorta

ABPM:

Ambulatory blood pressure monitoring

BD:

Balloon dilation

BMI:

Body mass index

BP:

Blood pressure

CHD:

Congenital heart disease

CMR:

Cardiovascular magnetic resonance

CoA:

Coarctation of the aorta

CT:

Computed tomography

CV:

Cardiovascular

CVD:

Cardiovascular disease

ECG:

Electrocardiogram

HR:

Heart rate

HTN:

Hypertension

LV:

Left ventricle

RAA:

Renin-angiotensin-aldosterone

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Martins, J.D., Prakash, A., Trigo, C., Fragata, J., Geva, T. (2021). Coarctation of the Aorta. In: da Cruz, E.M., Ivy, D., Hraska, V., Jaggers, J. (eds) Pediatric and Congenital Cardiology, Cardiac Surgery and Intensive Care. Springer, London. https://doi.org/10.1007/978-1-4471-4999-6_27-2

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