“…Nevertheless, the rate of complications differ widely depending on factors such as the time of diagnosis, the age at repair, or the severity of aortic narrowing, and it has been shown that fetal diagnosis [31], the need to repair in the neonatal period [32,33,34], and long segment aortic arch hypoplasia [6,32,33] adversely affect the outcome. Specifically, recoarctation of the aorta, which usually implies the need for reintervention, has been reported in 2-25% of patients after native CoAo repair [7,31,35,36]. This wide interval may be attributed, at least partially, to the characteristics of the population, with the highest rates being observed in patients diagnosed in fetal life [31], and in those that need be repaired in the neonatal period [32,33,34].…”