The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review

Background Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiovascular defect that occurs in approximately 1/300 000 live births or 0.5% of children with congenital heart disease. There are two types of ALCAPA syndrome: the infant type and the adult type. Th...

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Main Authors: Aliasghar Moeinipour, Mohammad Abbassi Teshnisi, Hassan Mottaghi Moghadam, Nahid Zirak, Reihaneh Hassanzadeh, Hamid Hoseinikhah, Abbas Bahreini
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2016-02-01
Series:International Journal of Pediatrics
Subjects:
LAD
Online Access:http://ijp.mums.ac.ir/pdf_6438_741d794dda856cdd9993195c0509344f.html
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spelling doaj-49d2dd96ea07468aaac80529cf8d291e2020-11-25T01:49:12ZengMashhad University of Medical SciencesInternational Journal of Pediatrics2345-50472345-50552016-02-0142139714056438The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief ReviewAliasghar Moeinipour0Mohammad Abbassi Teshnisi1Hassan Mottaghi Moghadam2Nahid Zirak3Reihaneh Hassanzadeh4Hamid Hoseinikhah5Abbas Bahreini6Assistant professor, Department of cardiac surgery, Atherosclerosis Prevention Research Center Faculty of medical science, Mashhad University of Medical Sciences, IranAssociated Professor, Department of cardiac surgery, Atherosclerosis Prevention Research Center, Faculty of medical science, Imam Reza Hospital, Mashhad University of Medical Sciences, IranAssociated professor of pediatric cardiology,. Mashhad University of Medical Sciences, Mashhad, IranAssociated Professor, Department of anesthesiology, Imam Reza Hospital, Mashhad University of Medical Sciences, IranResident of Anesthesiology, Department of anesthesiology, Mashhad University of Medical Sciences, Mashhad, IranAssistant professor, Department of cardiac surgery, Atherosclerosis Prevention Research Center Faculty of medical science, Mashhad University of Medical Sciences, IranResident of Neurosurgery, Faculty of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.Background Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiovascular defect that occurs in approximately 1/300 000 live births or 0.5% of children with congenital heart disease. There are two types of ALCAPA syndrome: the infant type and the adult type. The most infants experience myocardial infarction and congestive heart failure, and approximately 90% die within the first year of life; also, without early surgical intervention they have a dismal prognosis. Materials and Methods We report 3- year experiences from January 2013 to January 2016 of Imam Reza Hospital center (a tertiary referral hospital North East of Iran) that consist of all patients with ALCAPA syndrome. Results The Takeuchi procedure, were successfully performed in five children with anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA). There was no death and significant mitral regurgitation postoperative (n=0) in this short study. All of patients (n=5) had evidence of improving ischemic myocardium status by increasing of ejection fraction and regional wall motion of left ventricular in follow up echocardiography. Conclusion The only cure treatment for ALCAPA syndrome is surgical intervention that needs to be performed immediately after diagnosis to prevent myocardial infarction and chronic heart failure. Today, establishing a system with two coronary arteries is the goal in definitive surgical repair. The Takeuchi procedure is a prefer method to establish a two-coronary repair for ALCAPA.http://ijp.mums.ac.ir/pdf_6438_741d794dda856cdd9993195c0509344f.htmlALCAPAchildrenCoronary arteryHeart surgeryLADTakeuchi procedure
collection DOAJ
language English
format Article
sources DOAJ
author Aliasghar Moeinipour
Mohammad Abbassi Teshnisi
Hassan Mottaghi Moghadam
Nahid Zirak
Reihaneh Hassanzadeh
Hamid Hoseinikhah
Abbas Bahreini
spellingShingle Aliasghar Moeinipour
Mohammad Abbassi Teshnisi
Hassan Mottaghi Moghadam
Nahid Zirak
Reihaneh Hassanzadeh
Hamid Hoseinikhah
Abbas Bahreini
The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review
International Journal of Pediatrics
ALCAPA
children
Coronary artery
Heart surgery
LAD
Takeuchi procedure
author_facet Aliasghar Moeinipour
Mohammad Abbassi Teshnisi
Hassan Mottaghi Moghadam
Nahid Zirak
Reihaneh Hassanzadeh
Hamid Hoseinikhah
Abbas Bahreini
author_sort Aliasghar Moeinipour
title The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review
title_short The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review
title_full The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review
title_fullStr The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review
title_full_unstemmed The Anomalous Origin of the Left Coronary Artery from the Pulmonary Artery (ALCAPA): a Case Series and Brief Review
title_sort anomalous origin of the left coronary artery from the pulmonary artery (alcapa): a case series and brief review
publisher Mashhad University of Medical Sciences
series International Journal of Pediatrics
issn 2345-5047
2345-5055
publishDate 2016-02-01
description Background Anomalous left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital cardiovascular defect that occurs in approximately 1/300 000 live births or 0.5% of children with congenital heart disease. There are two types of ALCAPA syndrome: the infant type and the adult type. The most infants experience myocardial infarction and congestive heart failure, and approximately 90% die within the first year of life; also, without early surgical intervention they have a dismal prognosis. Materials and Methods We report 3- year experiences from January 2013 to January 2016 of Imam Reza Hospital center (a tertiary referral hospital North East of Iran) that consist of all patients with ALCAPA syndrome. Results The Takeuchi procedure, were successfully performed in five children with anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA). There was no death and significant mitral regurgitation postoperative (n=0) in this short study. All of patients (n=5) had evidence of improving ischemic myocardium status by increasing of ejection fraction and regional wall motion of left ventricular in follow up echocardiography. Conclusion The only cure treatment for ALCAPA syndrome is surgical intervention that needs to be performed immediately after diagnosis to prevent myocardial infarction and chronic heart failure. Today, establishing a system with two coronary arteries is the goal in definitive surgical repair. The Takeuchi procedure is a prefer method to establish a two-coronary repair for ALCAPA.
topic ALCAPA
children
Coronary artery
Heart surgery
LAD
Takeuchi procedure
url http://ijp.mums.ac.ir/pdf_6438_741d794dda856cdd9993195c0509344f.html
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