Surgical approach to complicated cervical aortic arch: anatomic, developmental, and surgical considerations

D B McElhinney1, L D Thompson, P M Weinberg

  • 1Division of Cardiothoracic Surgery, University of California, San Francisco, USA.

Insights

Patients with a cervical aortic arch often have associated brachiocephalic arterial and arch abnormalities. Surgical repair of these complex congenital heart defects is successful, with no long-term complications observed in this study.

Area of Science:

  • Cardiovascular Surgery
  • Congenital Heart Disease
  • Vascular Anomalies

Background:

  • Cervical aortic arch is frequently associated with abnormal brachiocephalic arterial branching and arch laterality.
  • Structural anomalies, including obstruction, aneurysms, and tortuosity, are common in cervical aortic arch cases.

Purpose of the Study:

  • To evaluate surgical outcomes for patients with obstructed right cervical aortic arch and associated anomalies.
  • To analyze the spectrum of anatomical variations and surgical strategies in this patient cohort.

Main Methods:

  • Retrospective review of 6 patients with obstructed right cervical arch between 1990 and 1998.
  • Surgical repair techniques included patch augmentation aortoplasty, tube grafting, and direct anastomosis.
  • Detailed analysis of vascular ring presence, vessel origin abnormalities, and descending aorta laterality.

Main Results:

  • All 6 patients underwent successful surgical repair without perioperative complications.
  • Follow-up (1-9 years) showed all patients alive and well, with no recurrence of obstruction.
  • One patient had a 22q11 microdeletion; associated anomalies included aneurysms, tortuosity, and vascular rings.

Conclusions:

  • Structural anomalies are common in cervical aortic arch patients, potentially due to hemodynamic factors or abnormal vascular tissue.
  • Surgical approaches must be tailored to the highly variable anatomy of complicated cervical aortic arches.
  • Successful surgical management is achievable for these complex congenital vascular anomalies.
Abstract

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