The surgical outcome of anomalous origin of the left coronary artery from the pulmonary artery.

IF 0.2 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Tasneem Muzaffar, Farooq Ahmad Ganie, Sunil Gpoal Swamy, Nasir-Ud-Din Wani
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引用次数: 0

Abstract

Background: Anomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) is a rare congenital anomaly which represents one of the most common causes of myocardial ischemia and infarction in children. This anomaly, if left untreated, results in a very high mortality rate within the first year of life. Yet, immediate surgical correction can lead to excellent results.

Objectives: The present study aimed to determine the surgical outcome of ALCAPA.

Methods: This study was conducted on 53 patients with ALCAPA operated from January 2005 to December 2012. Surgical repair was carried out as soon as the diagnosis was made. Surgery was thus undertaken on an urgent basis (within 48 hours) in the patients with congestive heart failure or critical clinical status and on a semi- elective basis (within a few days) in the remaining children. Operations for all the patients were performed through a median sternotomy using established standard cardiopulmonary bypass technique. Grouped variables were compared using chi-square test with Yates' correction. Besides, McNemar's test was used to assess the relationship between preoperative ejection fraction and mitral incompetence. All the analyses were performed using the SPSS statistical software, version 11.5 (SPSS Inc., Chicago, IL).

Results: The patients' median age at presentation was 4 months. The mean preoperative ejection fraction was 36.5%. The results showed a significant relationship between age at presentation and impairment of ejection fraction (P < 0.001). At first, 23% of our patients presented with ejection fraction < 35%. However, 6 months after the operation, the ejection fraction improved to a mean of 53.07% (SD = 8.5) ranging from 38 - 66%. There were 5 postoperative hospital deaths with an overall mortality rate of 9.6%.

Conclusions: Excellent results with desirable long-term outcomes can be achieved in the infants with ALCAPA using coronary artery implantation techniques. The best potential for recovery of the left ventricular function is in younger symptomatic infants despite the worst initial presentation. Normalization of cardiac function is expected within the first year in all operative survivors with a patent dual coronary system.

左冠状动脉起源于肺动脉异常的手术结果。
背景:左冠状动脉起源于肺动脉异常(ALCAPA)是一种罕见的先天性异常,是儿童心肌缺血和梗死的最常见原因之一。这种异常,如果不加以治疗,会导致在出生后第一年的死亡率非常高。然而,立即进行手术矫正可以取得良好的效果。目的:本研究旨在确定ALCAPA的手术效果。方法:对2005年1月至2012年12月行ALCAPA手术的53例患者进行分析。确诊后立即进行手术修复。因此,对于充血性心力衰竭或临床状态危急的患者,手术是紧急的(48小时内),而对于其余的儿童,手术是半选择性的(几天内)。所有患者的手术均采用已建立的标准体外循环技术进行胸骨正中切开术。分组变量比较采用卡方检验和Yates校正。此外,采用McNemar试验评估术前射血分数与二尖瓣功能不全的关系。所有分析均使用SPSS统计软件11.5版(SPSS Inc., Chicago, IL)进行。结果:患者就诊时中位年龄为4个月。术前平均射血分数为36.5%。结果显示,发病年龄与射血分数损伤有显著相关性(P < 0.001)。起初,23%的患者表现为射血分数< 35%。然而,术后6个月,射血分数改善至平均53.07% (SD = 8.5),范围为38 - 66%。术后住院死亡5例,总死亡率9.6%。结论:应用冠状动脉植入术治疗ALCAPA患儿可获得良好的疗效和理想的远期预后。尽管最初表现最糟糕,但最可能恢复左心室功能的是年龄较小的有症状婴儿。在所有双冠状动脉系统通畅的手术幸存者中,心功能有望在一年内恢复正常。
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来源期刊
International Cardiovascular Research Journal
International Cardiovascular Research Journal CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
0.40
自引率
50.00%
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0
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