Related Experiment Video
Updated: Jul 17, 2026

O-Ring Aortic Banding Versus Traditional Transverse Aortic Constriction for Modeling Pressure Overload-Induced Cardiac Hypertrophy
Published on: October 6, 2022
Aortic coarctation: an overview
Pietro Angelo Abbruzzese1, Enrico Aidala
1Division of Cardiac Surgery, Regina Margherita Children's Hospital, Turin, Italy. pa.abbruzzese@virgilio.it
Insights
Surgical repair is essential for severe aortic coarctation in newborns. A median sternotomy approach without extracorporeal circulation shows satisfactory results for aortic coarctation with a hypoplastic aortic arch.
Area of Science:
- Cardiology
- Pediatric Surgery
- Thoracic Surgery
Background:
- Severe aortic coarctation necessitates prompt surgical intervention in neonates.
- Optimal timing for elective repair of isolated aortic coarctation is typically 3-6 months or upon diagnosis.
- Aortic arch hypoplasia affects up to 70% of neonatal and infant coarctations, often requiring surgical treatment.
Purpose of the Study:
- To evaluate the efficacy of a median sternotomy approach without extracorporeal circulation for treating aortic coarctation with a hypoplastic aortic arch.
- To assess the short-term outcomes of this surgical technique in pediatric patients.
Main Methods:
- A cohort of 11 patients with aortic coarctation and a hypoplastic aortic arch underwent surgical repair.
- The surgical approach utilized was median sternotomy without extracorporeal circulation.
- Patients were followed up for an average of 40 months.
Main Results:
- The median sternotomy approach without extracorporeal circulation yielded satisfactory results in the treated patients.
- No major complications were reported during the follow-up period.
- The technique appears effective for managing aortic coarctation, particularly with associated hypoplastic aortic arch.
Conclusions:
- Median sternotomy without extracorporeal circulation is a viable and effective treatment option for aortic coarctation with a hypoplastic aortic arch.
- This approach offers a promising alternative, especially in cases where cardiopulmonary bypass may pose additional risks.
- Further research with larger cohorts is warranted to confirm long-term outcomes and compare with other surgical techniques.
Abstract:
In severe aortic coarctation in the neonatal period, surgical repair is required soon after clinical stabilization. Elective repair of isolated aortic coarctation is nowadays indicated at 3-6 months of life or at the time of diagnosis. At present, no single operation appears to have a clear superiority. However, during the first months of life, an extended end-to-end anastomosis is considered the best option by most authors, even though weight at operation and anatomy of the aortic arch are also significant determinants of late recoarctation. In cases of aortic arch hypoplasia, which occurs in up to 70% of neonatal and infant coarctations, especially when associated anomalies are present, surgery seems the treatment of choice. After 3 months of age and in the adult population, balloon angioplasty and stent placement are considered a suitable option. Recently, we adopted a median sternotomy approach without the use of extracorporeal circulation for the treatment of aortic coarctation with a hypoplastic aortic arch. We treated 11 patients with satisfactory results at an average follow-up of 40 months.
Related Concept Videos
Aneurysm I: Introduction
Aortic Regurgitation I: Introduction
Aortic Regurgitation II: Clinical Features and Diagnostic Tests
Aneurysm II: Clinical Manifestations and Diagnostic Studies
Aneurysm III: Interprofessional Care
Aortic Regurgitation III: Medical Management

