新生儿主动脉缩窄:手术技术影响因素的10年观察研究

O. Werner , M. Pouzenc , S. Guillaumont , M. Vincenti , G. De La Villeon
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引用次数: 0

摘要

主动脉缩窄是最常见的先天性心脏病之一(5-8%),临床表现多样(新生儿与儿童,伴或不伴心功能不全)。从外科的角度来看,有许多不同的技术将考虑到主动脉弓的解剖结构以及它是否发育不良,相关的心脏缺陷和患者的特征。这种手术技术的选择是未来预后(再狭窄,动脉高血压)的主要因素之一。然而,外科医生是否对主动脉弓进行延长成形术的选择并不是很明确,因为发育不全的定义本身可以讨论。此外,有必要评估不同成像技术对决策过程的贡献。本回顾性多中心研究旨在评估手术类型的潜在影响因素,并对新生儿缩窄进行流行病学描述。方法回顾性多中心观察研究,纳入2011年至2021年在法国南部4个外科中心进行的1岁以下主动脉缩窄手术患者。结果/预期结果共纳入686例患者。产前诊断率43%;性别比率M/F: 68/32%;6%的人基因检测呈阳性;全球死亡率为3%。23%的患者在诊断时出现心功能不全。58%的病例需要前列腺素灌注。在超声心动图中,53-57%的病例被描述为主动脉弓发育不全,这取决于分析方法。19%的患者进行了CT血管造影,58%的患者描述了发育不全。在手术方面,只有18%的患者进行了主动脉弓成形术。手术技术的主要预测因素是产前筛查,心脏畸形相关,前列腺素的使用,主动脉水平大小,二尖瓣发育不全。标准差不显著。结论/观点这些初步结果提供了一个有趣的观点在法国的缩窄的流行病学。将提供进一步的扩展数据。
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Neonatal coarctation of the aorta: A 10 years observational study to identify influencing factor of the technique of surgery

Introduction

Coarctation of the aorta is one of the most common congenital heart diseases (5–8%) with various clinical presentations (neonatal vs. pediatric, with or without cardiac insufficiency). On a surgical point of view, there are many different techniques that will take into account the anatomy of the aortic arch and whether or not it is hypoplastic, the associated heart defect and the patient's characteristics. The choice of this surgical technique is one of the predominant elements of the future prognosis (recoarctation, arterial hypertension). However, the choice of the surgeon whether to treat or not the aortic arch with an extended plasty is not very codified as the definition of hypoplasia itself can be discussed. Moreover there is a need to evaluate the contribution of different imaging techniques into the decision making process. This retrospective multicentric study intends to assess the potential influencing factors of the type of surgery and to make an epidemiological description of neonatal coarctation.

Methods

Retrospective multicentric observational study including patients of less than 1 years-old operated of coarctation of the aorta between 2011 and 2021 in four surgical centers in south France.

Results/Expected results

In total, 686 patients included. 43% of antenatal diagnosis; Sex ratio M/F: 68/32%; 6% of genetic test positive; the global mortality rate was 3%. 23% of patients presented cardiac insufficiency at diagnosis. Prostaglandin perfusion was necessary in 58% of cases. In echocardiography, an aortic arch hypoplasia was described between 53–57% of cases, depending of analysis method. A CT angiography was performed in 19% of patients with 58% of hypoplasia described. Concerning surgery, an aortic arch plasty was performed in only 18% of patients. The main predictors of surgical technique was antenatal screening, cardiac malformations associated, use of prostin, the horizontal aortic size, mitral hypoplasia. Standard deviation was not significant.

Conclusion/Perspectives

These preliminary results give an interesting view of the epidemiology of coarctation in France. Further extended data will be presented.

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来源期刊
Archives of Cardiovascular Diseases Supplements
Archives of Cardiovascular Diseases Supplements CARDIAC & CARDIOVASCULAR SYSTEMS-
自引率
0.00%
发文量
508
期刊介绍: Archives of Cardiovascular Diseases Supplements is the official journal of the French Society of Cardiology. The journal publishes original peer-reviewed clinical and research articles, epidemiological studies, new methodological clinical approaches, review articles, editorials, and Images in cardiovascular medicine. The topics covered include coronary artery and valve diseases, interventional and pediatric cardiology, cardiovascular surgery, cardiomyopathy and heart failure, arrhythmias and stimulation, cardiovascular imaging, vascular medicine and hypertension, epidemiology and risk factors, and large multicenter studies. Additionally, Archives of Cardiovascular Diseases also publishes abstracts of papers presented at the annual sessions of the Journées Européennes de la Société Française de Cardiologie and the guidelines edited by the French Society of Cardiology.
期刊最新文献
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