4.6 Article Proceedings Paper

Patients with anomalous aortic origin of the coronary artery remain at risk after surgical repair

Journal

JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY
Volume 155, Issue 6, Pages 2554-2562

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.jtcvs.2017.12.134

Keywords

anomalous coronary artery; congenital heart disease; congenital heart surgery; sudden death; pediatrics

Funding

  1. Division of Cardiac, Thoracic and Vascular Surgery at Columbia University
  2. National Institutes of Health [NCATS KL2 TR001874, NHLBI K23 HL33454]
  3. National Institute of Health [5T32 HL007854-22]

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Objectives: Anomalous aortic origin of a coronary artery (AAOCA) from the opposite sinus of Valsalva is a rare cardiac anomaly associated with sudden cardiac death (SCD). Single-center studies describe surgical repair as safe, although medium-and long-term effects on symptoms and risk of SCD remain unknown. We sought to describe outcomes of surgical repair of AAOCA. Methods: We reviewed institutional records for patients who underwent AAOCA repair, from 2001 to 2016, at 2 affiliated institutions. Patients with associated heart disease were excluded. Results: In total, 60 patients underwent AAOCA repair. Half of the patients (n = 30) had an anomalous left coronary artery arising from the right sinus of Valsalva and half had an anomalous right. Median age at surgery was 15.4 years (interquartile range, 11.9-17.9 years; range, 4 months to 68 years). The most common presenting symptoms were chest pain (n = 38; 63%) and shortness of breath (n = 17; 28%); aborted SCD was the presenting symptom in 4 patients (7%). Follow-up data were available for 54 patients (90%) over a median of 1.6 years. Of 53 patients with symptoms at presentation, 34 (64%) had complete resolution postoperatively. Postoperative mild or greater aortic insufficiency was present in 8 patients (17%) and moderate supravalvar aortic stenosis in 1 (2%). One patient required aortic valve replacement for aortic insufficiency. Two patients required reoperation for coronary stenosis at 3 months and 6 years postoperatively. Conclusions: Surgical repair of AAOCA is generally safe and adverse events are rare. Restenosis, and even sudden cardiac events, can occur and long-term surveillance is critical. Multi-institutional collaboration is vital to identify at-risk subpopulations and refine current recommendations for long-term management.

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