Coarctation of the aorta is a narrowing of the aorta, classically (but not always) just distal to the origin of the left subclavian artery. Here are ten key facts about coarctation of the aorta to be aware of in your cardiology clinic.
|MR aortogram showing coarctation of the aorta plus collaterals|
- Coarctation of the aorta accounts for 5-8% of congenital heart defects, with a prevalence of around 0.03% of live births
- The location of coarctation of the aorta is most commonly at the insertion point of the ductus arteriosus (just distal to the origin of the left subclavian artery)
- Ectopic coarctation can sometimes occur in the ascending aorta, the descending aorta or even the abdominal aorta
- The region of coarctation is most commonly discrete, but it can sometimes extend over a long segment of the aorta. There is often some dilatation of the aorta immediately beyond the coarctation
- Mild cases of coarctation of the aorta may not present until adulthood. Common presentations include incidental hypertension (affecting the upper body) or a murmur
- A blood pressure gradient >20mmHg between upper and lower limbs indicates significant coarctation of the aorta
- Chest X-ray findings include rib notching (caused by collaterals) and a double contour of the descending aorta ('figure 3 sign')
- Both MRI (see image above) and cardiac CT are useful non-invasive methods for imaging the anatomy of coarctation of the aorta, and the presence of collateral vessels
- Treatment options include stenting, resection with end-to-end anastomosis, and resection with interposition of a graft
After primary repair of coarctation of the aorta, long-term survival remains below that of normal controls, and the need for re-operation is relatively common. Patients should therefore remain under lifelong surveillance after surgical repair.
For further reading about the importance of ongoing surveillance after surgical repair, read the following reference: