Literature DB >> 18701026

Surgical treatment of anomalous origin of coronary artery from the pulmonary artery.

Qing-yu Wu1, Zhong-hua Xu.   

Abstract

BACKGROUND: Anomalous origin of coronary artery from the pulmonary artery is a rare congenital cardiac malformation with a mortality rate of up to 90% within the first year of life without surgical intervention. Direct implantation of the anomalous coronary artery (ACA) into the aorta is successful in early life, but it may have increased surgical difficulty and risk with age. This retrospective study summarized our operative experience in direct implantation for treatment of this coronary anomaly in pediatric and adult patients.
METHODS: From August 2000 to January 2003, 4 consecutive patients aged from 9 months to 41 years underwent dual coronary repair. Among them, two children and one infant with anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) and one adult was anomalous origin of right coronary artery from the pulmonary artery (ARCAPA). Coronary arteries were directly implanted into the ascending aorta in 4 patients. In a boy with ALCAPA associated with moderate mitral insufficiency (MI), whose ACA arose remotely from the ascending aorta, we created a tube-shaped graft using part of the pulmonary arterial wall in continuity with the origin of the left coronary artery (LCA). Concomitant moderate MI was repaired in 2 patients, including this boy, after a dual-coronary repair.
RESULTS: All patients survived. There were no hospital or late deaths and no major complications as well. Echocardiography revealed that the left ventricular (LV) function including LV end-diastolic dimension (EDD) and ejection fraction (EF) was markedly improved at hospital discharge. At 3 - 6 years follow-up after surgery all patients were asymptomatic and currently in NYHA class I.
CONCLUSIONS: The best results are achieved with direct implantation of the ACA into the ascending aorta and simultaneous mitral valve repair if needed. Direct implantation is feasible in pediatric and adult patients with ALCAPA or ARCAPA including the coronary artery in a location remote from the ascending aorta. It is a good procedure to lengthen the ACA by creating a tube-shape graft using part of the pulmonary arterial wall in continuity with the origin of ACA.

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Year:  2008        PMID: 18701026

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN: 0366-6999            Impact factor:   2.628


  4 in total

1.  Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery: Diagnoses and Surgical Results in 12 Pediatric Patients.

Authors:  Moises Rodriguez-Gonzalez; Antonio Moruno Tirado; Reza Hosseinpour; Jose Santos de Soto
Journal:  Tex Heart Inst J       Date:  2015-08-01

2.  Anomalous origin of the right coronary artery from the main pulmonary artery treated surgically in a 6-week-old infant. A case report and review of the literature.

Authors:  Krzysztof Grabowski; Maciej Aleksander Karolczak; Ewa Zacharska-Kokot; Wojciech Mądry; Jacek Pająk
Journal:  J Ultrason       Date:  2018-03-30

3.  A rare case of anomalous origin of the left main coronary artery in an adult patient.

Authors:  Pierre O Dionne; Nancy Poirier; Jessica Forcillo; Louis M Stevens; Carl Chartrand-Lefebvre; Samer Mansour; Nicolas Noiseux
Journal:  J Cardiothorac Surg       Date:  2013-01-22       Impact factor: 1.637

4.  Midterm outcome after surgical correction of anomalous left coronary artery from the pulmonary artery.

Authors:  Yunfei Ling; Sandeep Bhushan; Qiang Fan; Menglin Tang
Journal:  J Cardiothorac Surg       Date:  2016-08-26       Impact factor: 1.637

  4 in total

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