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Anomalous Aortic Origin of a Coronary Artery.
Stephens, Elizabeth H; Jegatheeswaran, Anusha; Brothers, Julie A; Ghobrial, Joanna; Karamlou, Tara; Francois, Christopher J; Krishnamurthy, Rajesh; Dearani, Joseph A; Binsalamah, Ziyad; Molossi, Silvana; Mery, Carlos M.
Affiliation
  • Stephens EH; Department of Cardiovascular Surgery, Mayo Clinic, Rochester, Minnesota. Electronic address: stephens.elizabeth@mayo.edu.
  • Jegatheeswaran A; Department of Cardiothoracic Surgery, Great Ormond Street Hospital, London, United Kingdom; Department of Children's Cardiovascular Disease, Institute of Cardiovascular Science, University College London, London, United Kingdom.
  • Brothers JA; Division of Cardiology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
  • Ghobrial J; Department of Cardiology, Cleveland Clinic, Cleveland, Ohio.
  • Karamlou T; Division of Pediatric and Congenital Cardiac Surgery, Department of Thoracic and Cardiovascular Surgery, Cleveland Clinic, Cleveland, Ohio.
  • Francois CJ; Department of Radiology, Mayo Clinic, Rochester, Minnesota.
  • Krishnamurthy R; Division of Cardiovascular Imaging, Department of Radiology, Nationwide Children's Hospital, Columbus, Ohio.
  • Dearani JA; Department of Cardiovascular Surgery, Mayo Clinic, Rochester, Minnesota.
  • Binsalamah Z; Division of Congenital Heart Surgery, Department of Surgery, Texas Children's Hospital, Houston, Texas.
  • Molossi S; Division of Cardiology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas.
  • Mery CM; Department of Surgery and Perioperative Care, Dell Medical School at The University of Texas at Austin, Dell Children's Medical Center, Austin, Texas.
Ann Thorac Surg ; 117(6): 1074-1086, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38302054
ABSTRACT

BACKGROUND:

Although anomalous aortic origin of a coronary artery (AAOCA) is associated with risk of sudden cardiac arrest (SCA), there is a spectrum of disease, with the appropriate management for many remaining unclear. Increasing data warrant review for an updated perspective on management.

METHODS:

A panel of congenital cardiac surgeons, cardiologists, and imaging practitioners reviewed the current literature related to AAOCA and its management. Survey of relevant publications from 2010 to the present in PubMed was performed.

RESULTS:

The prevalence of AAOCA is 0.4% to 0.8%. Anomalous left coronary artery is 3 to 8 times less common than anomalous right coronary, but carries a much higher risk of SCA. Nevertheless, anomalous right coronary is not completely benign; 10% demonstrate ischemia, and it remains an important cause of SCA. Decision-making regarding which patients should be recommended for surgical intervention includes determining anatomic features associated with ischemia, evidence of ischemia on provocative testing, and concerning cardiovascular symptoms. Ischemia testing continues to prove challenging with low sensitivity and specificity, but the utility of new modalities is an active area of research. Surgical interventions focus on creating an unobstructed path for blood flow and choosing the appropriate surgical technique given the anatomy to accomplish this. Nontrivial morbidity has been reported with surgery, including new-onset ischemia.

CONCLUSIONS:

A proportion of patients with AAOCA demonstrate features and ischemia that warrant surgical intervention. Continued work remains to improve the ability to detect inducible ischemia, to risk stratify these patients, and to provide guidance in terms of which patients warrant surgical intervention.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Coronary Vessel Anomalies Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Ann Thorac Surg Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Coronary Vessel Anomalies Type of study: Risk_factors_studies Limits: Humans Language: En Journal: Ann Thorac Surg Year: 2024 Document type: Article
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