O. Werner , M. Pouzenc , S. Guillaumont , M. Vincenti , G. De La Villeon
{"title":"Neonatal coarctation of the aorta: A 10 years observational study to identify influencing factor of the technique of surgery","authors":"O. Werner , M. Pouzenc , S. Guillaumont , M. Vincenti , G. De La Villeon","doi":"10.1016/j.acvdsp.2023.07.002","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p><span><span>Coarctation of the aorta is one of the most common </span>congenital heart diseases<span> (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 </span></span>anatomy<span><span> of the aortic arch and whether or not it is hypoplastic, the associated heart defect and the </span>patient's characteristics<span>. 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<span><span> 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 </span>coarctation.</span></span></span></p></div><div><h3>Methods</h3><p>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.</p></div><div><h3>Results/Expected results</h3><p><span>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. </span>Prostaglandin<span><span> perfusion was necessary in 58% of cases. In echocardiography<span>, 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 </span></span>antenatal screening<span>, cardiac malformations<span> associated, use of prostin, the horizontal aortic size, mitral hypoplasia. Standard deviation was not significant.</span></span></span></p></div><div><h3>Conclusion/Perspectives</h3><p>These preliminary results give an interesting view of the epidemiology of coarctation in France. Further extended data will be presented.</p></div>","PeriodicalId":8140,"journal":{"name":"Archives of Cardiovascular Diseases Supplements","volume":"15 4","pages":"Page 273"},"PeriodicalIF":18.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Cardiovascular Diseases Supplements","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878648023002239","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
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.
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.