Mid-term outcomes of surgical repair for anomalous origin of the left coronary artery from the pulmonary artery: In infants, children and adults

Background: Anomalous origin of left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital malformation. We sought to evaluate in-hospital and mid-term outcomes of patients with a diagnosis of ALCAPA who underwent surgical repair. Objectives: The objective of this study is to evalu...

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Main Authors: Maziar Gholampour Dehaki (Author), Alwaleed Al-Dairy (Author), Yousef Rezaei (Author), Alireza Alizadeh Ghavidel (Author), Gholamreza Omrani (Author), Nader Givtaj (Author), Reza Sadat Afjehi (Author), Hassan Tatari (Author), Amir Hossein Jalali (Author), Mohammad Mahdavi (Author)
Format: Book
Published: Wolters Kluwer Medknow Publications, 2017-01-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Maziar Gholampour Dehaki  |e author 
700 1 0 |a Alwaleed Al-Dairy  |e author 
700 1 0 |a Yousef Rezaei  |e author 
700 1 0 |a Alireza Alizadeh Ghavidel  |e author 
700 1 0 |a Gholamreza Omrani  |e author 
700 1 0 |a Nader Givtaj  |e author 
700 1 0 |a Reza Sadat Afjehi  |e author 
700 1 0 |a Hassan Tatari  |e author 
700 1 0 |a Amir Hossein Jalali  |e author 
700 1 0 |a Mohammad Mahdavi  |e author 
245 0 0 |a Mid-term outcomes of surgical repair for anomalous origin of the left coronary artery from the pulmonary artery: In infants, children and adults 
260 |b Wolters Kluwer Medknow Publications,   |c 2017-01-01T00:00:00Z. 
500 |a 0974-2069 
500 |a 10.4103/0974-2069.205140 
520 |a Background: Anomalous origin of left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital malformation. We sought to evaluate in-hospital and mid-term outcomes of patients with a diagnosis of ALCAPA who underwent surgical repair. Objectives: The objective of this study is to evaluate the mid-term outcomes of surgical repair of ALCAPA at our center and to analyze the surgical techniques used. Materials and Methods: In a retrospective study, we analyzed early and mid-term clinical and echocardiographic data to determine the outcomes of patients who underwent surgical repair of ALCAPA in our institution between 2005 and 2015. Results: Twenty-one patients underwent surgical repair for ALCAPA using aortic reimplantation (n = 10, 47.6%), ostial closure. (n = 8, 38.1%), or ligation. (n = 3, 14.3%). The median age of patients was 24. months. (range 22 days to 51 years). There were 2 (9.5%) in-hospital mortalities in infants undergoing the reimplantation technique. All patients were followed up for a median of 21 months. (range 1-60 months). No patients required reoperation, and there was no mortality from discharge to mid-term follow-up. Severe early postoperative mitral regurgitation. (MR) was associated with composite end-point, defined as a combination of mortality after surgery, moderate to severe MR, and moderate to severe left ventricular dysfunction at late follow-up. (P = 0.019) while mitral valve repair was not. (P = 0.469). Conclusion: The surgical management of ALCAPA can be associated with good in-hospital and mid-term outcomes regardless of the age, at which the patient has been operated. 
546 |a EN 
690 |a Anomalous origin of left coronary artery from the pulmonary artery 
690 |a ligation 
690 |a mitral regurgitation 
690 |a mitral valve repair 
690 |a ostial closure 
690 |a reimplantation 
690 |a Medicine 
690 |a R 
690 |a Pediatrics 
690 |a RJ1-570 
690 |a Diseases of the circulatory (Cardiovascular) system 
690 |a RC666-701 
655 7 |a article  |2 local 
786 0 |n Annals of Pediatric Cardiology, Vol 10, Iss 2, Pp 137-143 (2017) 
787 0 |n http://www.annalspc.com/article.asp?issn=0974-2069;year=2017;volume=10;issue=2;spage=137;epage=143;aulast=Dehaki 
787 0 |n https://doaj.org/toc/0974-2069 
856 4 1 |u https://doaj.org/article/8f1a2c990adb4f248a56eee5b0b76d4b  |z Connect to this object online.