Long-Term Outcome of the Anomalous Origin of the Left Coronary Artery From the Pulmonary Artery (ALCAPA) in Children After Cardiac Surgery: A Single-Center Experience

被引:6
作者
Ismail, Muna [1 ]
Jijeh, Abdulraouf [2 ]
Alhuwaymil, Rathath M. [3 ]
Alahmari, Raneem [3 ]
Alshahrani, Rawan [3 ]
Almutairi, Reem [3 ]
Habshan, Fahad [4 ]
Shaath, Ghassan A. [5 ]
机构
[1] Minist Natl Guard Hlth Affairs, King Abdulaziz Cardiac Ctr, Cardiac Sci Dept, Pediat Cardiol, Riyadh, Saudi Arabia
[2] Minist Natl Guard Hlth Affairs, Pediat Cardiac Intens Care Unit, Cardiac Sci Dept, Riyadh, Saudi Arabia
[3] King Saud bin Abdulaziz Univ Hlth Sci, Echocardiog Technol, Coll Appl Med Sci, Riyadh, Saudi Arabia
[4] King Abdulaziz Med City Riyadh, King Abdulaziz Cardiac Ctr, Pediat Cardiol, Riyadh, Saudi Arabia
[5] Minist Natl Guard Hlth Affairs, Cardiac Sci Dept, Pediat Cardiac Intens Care Unit, King Abdulaziz Cardiac Ctr, Riyadh, Saudi Arabia
关键词
anomalous origin of the left coronary artery from pulmonary artery; children; ejection fraction; fractional shortening; echocardiography; WHITE-GARLAND SYNDROME; SURGICAL INTERVENTION; REPAIR; INFANTS;
D O I
10.7759/cureus.11829
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background The anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital coronary artery anomaly. It induces left ventricular (LV) dysfunction and mitral valve regurgitation (MR). If untreated, survival beyond infancy is rare. The aim of our study was to analyze the outcome in children with ALCAPA after cardiac surgery. Methods We retrospectively reviewed all patients who were diagnosed at our institution with ALCAPA and underwent surgical repair from 1999 to the end of 2018 (for 20 years). We followed LV dimensions, function, the progress of MV regurgitation, and the somatic growth of children after surgical repair. Results Twenty-nine patients underwent ALCAPA repair while 15 (52%) patients were male. The median age at surgical repair was 5.3 (IQR: 3.8-7.4) months and the mean weight was 5.5 +/- 2 kg. Surgical repair was performed in form of coronary reimplantation in 26 (90%) patients and Takeuchi repair in three (10%) patients. Intensive care unit (ICU) stay was eight (IQR: 6-17) days and hospital stay was 15 (IQR: 12-21) days. The follow-up duration was 5 +/- 3.6 years. Echocardiographic parameters started to improve by six weeks after the repair, and they normalized by one year. At the time of surgery ejection fraction (EF) was 34 +/- 17%, fractional shortening (FS) was 15 +/- 10%, and LV inner diameter in diastole (LVIDD) z score was 5.7 +/- 2.8. These parameters improved by one year after surgery to 66 +/- 7%, 34 +/- 6%, and 0 +/- 1.3, respectively. However, somatic growth started to improve six months after surgical repair. MR was moderate to severe in seven (24%) patients at the time of surgery and regressed to no more moderate nor severe MR at the last follow-up. None of the 29 patients died. Conclusions LV systolic function and dimensions start to improve by six weeks after surgery and reach normal values by one year. MR regresses without intervention in correspondence with the regression of LV dimensional parameters. The somatic growth of children improves six months after repair.
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相关论文
共 24 条
[1]   An aneurysm of the left heart ventricle with an abnormal outlet of the left coronory artery of the pulmonalis in a five-month old child. [J].
Abrikossoff, A .
VIRCHOWS ARCHIV FUR PATHOLOGISCHE ANATOMIE UND PHYSIOLOGIE UND FUR KLINISCHE MEDIZIN, 1911, 203 (03) :413-420
[2]  
Al Umairi Rashid Saif, 2016, Oman Med J, V31, P387, DOI 10.5001/omj.2016.77
[3]   Repair of anomalous origin of the left coronary artery from the pulmonary artery in infants and children [J].
Alexi-Meskishvili, Vladimir ;
Nasseri, Boris A. ;
Nordmeyer, Sarah ;
Schmitt, Boris ;
Weng, Yu-Guo ;
Boettcher, Wolfgang ;
Huebler, Michael ;
Berger, Felix ;
Hetzer, Roland .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2011, 142 (04) :868-874
[4]   Anatomic repair of anomalous left coronary artery from the pulmonary artery by aortic reimplantation: Early survival, patterns of ventricular recovery and late outcome [J].
Azakie, A ;
Russell, JL ;
McCrindle, BW ;
Van Arsdell, GS ;
Benson, LN ;
Coles, JG ;
Williams, WG .
ANNALS OF THORACIC SURGERY, 2003, 75 (05) :1535-1541
[5]  
Backer Carl L., 2000, Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu, V3, P165
[6]   Anomalous origin of the left coronary artery from the pulmonary artery: late results with special attention to the mitral valve [J].
Ben Ali, Walid ;
Metton, Olivier ;
Roubertie, Francois ;
Pouard, Philippe ;
Sidi, Daniel ;
Raisky, Olivier ;
Vouhe, Pascal R. .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2009, 36 (02) :244-249
[7]  
Birk E, 2000, ISRAEL MED ASSOC J, V2, P111
[8]   Outcomes of Anomalous Left Coronary Artery From Pulmonary Artery Repair: Beyond Normal Function [J].
Cabrera, Antonio G. ;
Chen, Diane W. ;
Pignatelli, Ricardo H. ;
Khan, Muhammad S. ;
Jeewa, Aamir ;
Mery, Carlos M. ;
McKenzie, E. Dean ;
Fraser, Charles D., Jr. .
ANNALS OF THORACIC SURGERY, 2015, 99 (04) :1342-1347
[9]   Excellent long-term functional outcome after an operation for anomalous left coronary artery from the pulmonary artery [J].
Cochrane, AD ;
Coleman, DM ;
Davis, AM ;
Brizard, CP ;
Wolfe, R ;
Karl, TR .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1999, 117 (02) :332-340
[10]   Bland-White-Garland syndrome of anomalous left coronary artery arising from the pulmonary artery (ALCAPA): a historical review [J].
Cowles, Robert A. ;
Berdon, Walter E. .
PEDIATRIC RADIOLOGY, 2007, 37 (09) :890-895