Modern management of adult coarctation: transcatheter and surgical options
Heiko Schneider1, Anselm Uebing, Darryl F Shore
1Adult Congenital Heart Centre and Centre for Pulmonary Hypertension, Royal Brompton Hospital, London, UK - a.uebing@rbht.nhs.uk.
Insights
Transcatheter interventions are now the primary choice for adult coarctation of the aorta (CoA) treatment. Complex cases may still require surgical repair, with ongoing advancements in both approaches.
Area of Science:
- Cardiovascular Medicine
- Interventional Cardiology
- Thoracic Surgery
Background:
- Coarctation of the aorta (CoA) is a congenital heart defect affecting 5-8% of patients with congenital heart disease.
- Surgical and transcatheter treatments for CoA have evolved significantly since the 1950s.
Purpose of the Study:
- To review current endovascular and surgical practices for coarctation of the aorta.
- To highlight modern developments and limitations in CoA treatment.
Main Methods:
- Review of current endovascular techniques for native and recurrent coarctation of the aorta.
- Analysis of surgical approaches for complex aortic arch anatomy and aneurysms.
- Discussion of treatment strategies for recurrent coarctation and associated aneurysms.
Main Results:
- Transcatheter options are the preferred initial treatment for adult patients with native or recurrent CoA.
- Surgical techniques remain essential for complex cases, including extensive arch hypoplasia, stenosis, or para-CoA aneurysms.
- Stent implantation for aneurysms may necessitate preparatory vascular surgery; bypass conduits are used for complex re-CoA.
Conclusions:
- Transcatheter interventions represent the current standard of care for most adult CoA cases.
- Surgical management is reserved for intricate anatomical presentations of coarctation of the aorta.
- Ongoing advancements continue to refine both endovascular and surgical treatment paradigms for CoA.
Abstract:
Coarctation of the aorta (CoA), a juxtaductal obstructive lesion in the descending aorta and commonly associated with hypoplasia of the aortic arch occurs in 5-8% of patients with congenital heart disease. Since the initial surgical corrections in the 1950, surgical and transcatheter options have constantly evolved. Nowadays, transcatheter options are widely accepted as the initial treatment of choice in adults presenting with native or recurrent CoA. Surgical techniques are mainly reserved for patients with complex aortic arch anatomy such as extended arch hypoplasia or stenosis or para-CoA aneurysm formation. Extended aneurysms can be covered by conformable stents but stent implantation may require preparative vascular surgery. Complex re-CoA my best be treated by an ascending to descending bypass conduit. The following review aims to describe current endovascular and surgical practice pointing out modern developments and their limitations.
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