Early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery

Introduction/Objective. The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is rare congenital disease, which causes myocardial ischemia and subsequent heart failure in infants. The aim is early and mid-term follow up evaluation of the heart function after surgical re...

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Main Authors: Prijić Sergej, Krasić Staša, Košutić Jovan, Stajević Mila, Ninić Sanja, Popović Saša, Bjelaković Bojko, Mahmutović Meho, Vukomanović Vladislav
Format: Article
Language:English
Published: Serbian Medical Society 2019-01-01
Series:Srpski Arhiv za Celokupno Lekarstvo
Subjects:
Online Access:http://www.doiserbia.nb.rs/img/doi/0370-8179/2019/0370-81791900032P.pdf
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spelling doaj-5295467b1ca14b5697f87a7711f4303c2021-01-02T10:59:15ZengSerbian Medical SocietySrpski Arhiv za Celokupno Lekarstvo0370-81792019-01-011479-1056757010.2298/SARH180730032P0370-81791900032PEarly and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary arteryPrijić Sergej0Krasić Staša1Košutić Jovan2Stajević Mila3Ninić Sanja4Popović Saša5Bjelaković Bojko6Mahmutović Meho7Vukomanović Vladislav8Mother and Child Health Institute of Serbia, Belgrade + Faculty of Medicine, Belgrade, SerbiaMother and Child Health Institute of Serbia, Belgrade, SerbiaMother and Child Health Institute of Serbia, Belgrade, Serbia + Faculty of Medicine, Belgrade, SerbiaMother and Child Health Institute of Serbia, Belgrade, Serbia + Faculty of Medicine, Belgrade, SerbiaMother and Child Health Institute of Serbia, Belgrade, SerbiaMother and Child Health Institute of Serbia, Belgrade, SerbiaFaculty of Medicine, Niš Clinical Centre, Clinic of Pediatrics, Niš, SerbiaNovi Pazar General Hospital, Novi Pazar, SerbiaMother and Child Health Institute of Serbia, Belgrade, Serbia + Faculty of Medicine, Belgrade, SerbiaIntroduction/Objective. The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is rare congenital disease, which causes myocardial ischemia and subsequent heart failure in infants. The aim is early and mid-term follow up evaluation of the heart function after surgical repair of ALCAPA. Methods. Investigation was retrospective and included medical records of the ALCAPA patients treated surgically, between 2009 and 2017, at the tertiary referent heart center. Results. Five patients (four girls) with coronary anomaly were included in the study. All patients had significantly increased left ventricular end diastolic diameter (z-score 6.6 ± 2.43) and left atria size (z-score 3.09 ± 0.37), along with decreased systolic function (ejection fraction 34.8 ± 7.4% and fractional shortening 15.5 ± 3.4%). The surgery was performed on average at the age of 8.2 ± 7.8 months. Operative treatment was associated with early improvement in echocardiographic parameters (except the size of the left atria). Patients were followed for 4.5 ± 2.6 years. Improvement in echocardiographic parameters was age-related. Patients under four months had recovery early after surgery, those treated at 5.5–6 months of age had normalization after 12 months, and patient who was recognized in the second year of life had late recovery (after ≥ 24 months). Conclusion. Operative treatment in the first 3–4 months of life is related with the most favorable prognosis and rapid normalization of the echocardiographic parameters.http://www.doiserbia.nb.rs/img/doi/0370-8179/2019/0370-81791900032P.pdfalcapacardiomyopathyechocardiography
collection DOAJ
language English
format Article
sources DOAJ
author Prijić Sergej
Krasić Staša
Košutić Jovan
Stajević Mila
Ninić Sanja
Popović Saša
Bjelaković Bojko
Mahmutović Meho
Vukomanović Vladislav
spellingShingle Prijić Sergej
Krasić Staša
Košutić Jovan
Stajević Mila
Ninić Sanja
Popović Saša
Bjelaković Bojko
Mahmutović Meho
Vukomanović Vladislav
Early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery
Srpski Arhiv za Celokupno Lekarstvo
alcapa
cardiomyopathy
echocardiography
author_facet Prijić Sergej
Krasić Staša
Košutić Jovan
Stajević Mila
Ninić Sanja
Popović Saša
Bjelaković Bojko
Mahmutović Meho
Vukomanović Vladislav
author_sort Prijić Sergej
title Early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery
title_short Early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery
title_full Early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery
title_fullStr Early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery
title_full_unstemmed Early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery
title_sort early and midterm results after surgical repair of anomalous origin of the left coronary artery from the pulmonary artery
publisher Serbian Medical Society
series Srpski Arhiv za Celokupno Lekarstvo
issn 0370-8179
publishDate 2019-01-01
description Introduction/Objective. The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is rare congenital disease, which causes myocardial ischemia and subsequent heart failure in infants. The aim is early and mid-term follow up evaluation of the heart function after surgical repair of ALCAPA. Methods. Investigation was retrospective and included medical records of the ALCAPA patients treated surgically, between 2009 and 2017, at the tertiary referent heart center. Results. Five patients (four girls) with coronary anomaly were included in the study. All patients had significantly increased left ventricular end diastolic diameter (z-score 6.6 ± 2.43) and left atria size (z-score 3.09 ± 0.37), along with decreased systolic function (ejection fraction 34.8 ± 7.4% and fractional shortening 15.5 ± 3.4%). The surgery was performed on average at the age of 8.2 ± 7.8 months. Operative treatment was associated with early improvement in echocardiographic parameters (except the size of the left atria). Patients were followed for 4.5 ± 2.6 years. Improvement in echocardiographic parameters was age-related. Patients under four months had recovery early after surgery, those treated at 5.5–6 months of age had normalization after 12 months, and patient who was recognized in the second year of life had late recovery (after ≥ 24 months). Conclusion. Operative treatment in the first 3–4 months of life is related with the most favorable prognosis and rapid normalization of the echocardiographic parameters.
topic alcapa
cardiomyopathy
echocardiography
url http://www.doiserbia.nb.rs/img/doi/0370-8179/2019/0370-81791900032P.pdf
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