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Takeuchi repair of anomalous left coronary artery from the pulmonary artery. J Cardiovasc Comput Tomogr 2015;9(5):457-8

Date

04/07/2015

Pubmed ID

25843240

DOI

10.1016/j.jcct.2015.02.002

Scopus ID

2-s2.0-84941743498 (requires institutional sign-in at Scopus site)   5 Citations

Abstract

Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare form of congenital heart disease that has been successfully palliated for decades. Prior to coronary reimplantation, the Takeuchi repair was the most common operative palliation. The Takeuchi repair is still seen today at less experienced congenital centers or when reimplantation is not possible. Patients who have had the Takeuchi repair are at risk of having subsequent complications related to this repair. Unfortunately, due to the surgical rarity, the post surgical anatomy is often poorly understood by cardiologists leading to inadequate risk factor assessment and compromised patient care. Coronary computed tomography angiography is a useful imaging modality to follow patients who have had the Takeuchi repair.

Author List

Cramer JW, Cinquegrani M, Cohen SB

Authors

Michael P. Cinquegrani MD Director, Professor in the Medicine department at Medical College of Wisconsin
Scott B. Cohen MD Associate Professor in the Medicine department at Medical College of Wisconsin




MESH terms used to index this publication - Major topics in bold

Adult
Bland White Garland Syndrome
Cineangiography
Coronary Angiography
Coronary Vessels
Humans
Male
Palliative Care
Pulmonary Artery
Tomography, X-Ray Computed
Treatment Outcome