基于 181 例手术标本的主动脉粥样硬化新分类法

IF 2.3 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
P.-E. Seguela , C. Guidon , X. Iriart , Z. Jalal , J.B. Thambo , F. Roubertie
{"title":"基于 181 例手术标本的主动脉粥样硬化新分类法","authors":"P.-E. Seguela ,&nbsp;C. Guidon ,&nbsp;X. Iriart ,&nbsp;Z. Jalal ,&nbsp;J.B. Thambo ,&nbsp;F. Roubertie","doi":"10.1016/j.acvd.2024.07.038","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><p>The term coarctation of the aorta (CoA) stands for a narrowing of the thoracic aorta with heterogeneous morphologic phenotypes resulting in different treatment strategies. Its origin remains controversial (hemodynamical versus ductal tissue theory), some types being detected prenatally, while others are diagnosed later in life.</p></div><div><h3>Objective</h3><p>We attempted to establish a classification system based on a 10-year data collection of surgical specimens.</p></div><div><h3>Methods</h3><p>It was a monocentric retrospective study: using precise descriptions of aortic morphology obtained from operative reports (2010–2020) of 181 patients with CoA, we analyzed different characteristics to generate a classification system.</p></div><div><h3>Results</h3><p>Four types of isthmic CoA were depicted: narrowing (1) associated with aortic hypoplasia (33%), (2) due to a posterior shelf (64%), (3) due to intraluminal membrane (1%) and (4) aortic kinking (2%). Age at surgery ranged from 7 days to 51 years. Prenatal diagnosis rate and associated cardiac anomalies were more frequent in type 1. Distinction of localized (types 2, 3 and 4) and diffuse narrowing (type 1) revealed a significant difference for age at surgery, prenatal diagnosis, and associated anomaly. The presence of a bicuspid aortic valve (48.6%) did not differ according to the types. A left superior vena cava (7.7%) was equally encountered in all the subtypes (<span><span>Fig. 1</span></span>).</p></div><div><h3>Conclusion</h3><p>A new classification system for CoA is presented. According to our data, all the types could be prenatally diagnosed. This classification might be advantageous to better understand pathophysiology of CoA and facilitate scientific communication.</p></div>","PeriodicalId":55472,"journal":{"name":"Archives of Cardiovascular Diseases","volume":"117 8","pages":"Page S237"},"PeriodicalIF":2.3000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"New classification of aortic coarctation based on 181 surgical specimens\",\"authors\":\"P.-E. Seguela ,&nbsp;C. Guidon ,&nbsp;X. Iriart ,&nbsp;Z. Jalal ,&nbsp;J.B. Thambo ,&nbsp;F. Roubertie\",\"doi\":\"10.1016/j.acvd.2024.07.038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Introduction</h3><p>The term coarctation of the aorta (CoA) stands for a narrowing of the thoracic aorta with heterogeneous morphologic phenotypes resulting in different treatment strategies. Its origin remains controversial (hemodynamical versus ductal tissue theory), some types being detected prenatally, while others are diagnosed later in life.</p></div><div><h3>Objective</h3><p>We attempted to establish a classification system based on a 10-year data collection of surgical specimens.</p></div><div><h3>Methods</h3><p>It was a monocentric retrospective study: using precise descriptions of aortic morphology obtained from operative reports (2010–2020) of 181 patients with CoA, we analyzed different characteristics to generate a classification system.</p></div><div><h3>Results</h3><p>Four types of isthmic CoA were depicted: narrowing (1) associated with aortic hypoplasia (33%), (2) due to a posterior shelf (64%), (3) due to intraluminal membrane (1%) and (4) aortic kinking (2%). Age at surgery ranged from 7 days to 51 years. Prenatal diagnosis rate and associated cardiac anomalies were more frequent in type 1. Distinction of localized (types 2, 3 and 4) and diffuse narrowing (type 1) revealed a significant difference for age at surgery, prenatal diagnosis, and associated anomaly. The presence of a bicuspid aortic valve (48.6%) did not differ according to the types. A left superior vena cava (7.7%) was equally encountered in all the subtypes (<span><span>Fig. 1</span></span>).</p></div><div><h3>Conclusion</h3><p>A new classification system for CoA is presented. According to our data, all the types could be prenatally diagnosed. This classification might be advantageous to better understand pathophysiology of CoA and facilitate scientific communication.</p></div>\",\"PeriodicalId\":55472,\"journal\":{\"name\":\"Archives of Cardiovascular Diseases\",\"volume\":\"117 8\",\"pages\":\"Page S237\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of Cardiovascular Diseases\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1875213624002596\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Cardiovascular Diseases","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1875213624002596","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0

摘要

导言主动脉共动脉症(CoA)是指胸主动脉狭窄,其形态表型各不相同,因此治疗策略也不尽相同。其起源仍存在争议(血液动力学理论与导管组织理论),有些类型在出生前就能发现,而有些类型则在出生后才被诊断出来。方法这是一项单中心回顾性研究:利用从181例CoA患者的手术报告(2010-2020年)中获得的主动脉形态学精确描述,我们分析了不同的特征,从而建立了一个分类系统。结果描述了四种类型的峡部CoA:狭窄(1)与主动脉发育不良有关(33%),(2)由于后架(64%),(3)由于腔内膜(1%)和(4)主动脉扭转(2%)。手术年龄从 7 天到 51 岁不等。产前诊断率和相关心脏畸形在1型中更为常见。局部狭窄(2、3、4 型)和弥漫性狭窄(1 型)在手术年龄、产前诊断和相关畸形方面存在显著差异。主动脉瓣双瓣(48.6%)在不同类型中没有差异。左上腔静脉(7.7%)在所有亚型中的出现率相同(图 1)。根据我们的数据,所有类型均可在产前确诊。这种分类方法可能有助于更好地理解 CoA 的病理生理学,并促进科学交流。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New classification of aortic coarctation based on 181 surgical specimens

Introduction

The term coarctation of the aorta (CoA) stands for a narrowing of the thoracic aorta with heterogeneous morphologic phenotypes resulting in different treatment strategies. Its origin remains controversial (hemodynamical versus ductal tissue theory), some types being detected prenatally, while others are diagnosed later in life.

Objective

We attempted to establish a classification system based on a 10-year data collection of surgical specimens.

Methods

It was a monocentric retrospective study: using precise descriptions of aortic morphology obtained from operative reports (2010–2020) of 181 patients with CoA, we analyzed different characteristics to generate a classification system.

Results

Four types of isthmic CoA were depicted: narrowing (1) associated with aortic hypoplasia (33%), (2) due to a posterior shelf (64%), (3) due to intraluminal membrane (1%) and (4) aortic kinking (2%). Age at surgery ranged from 7 days to 51 years. Prenatal diagnosis rate and associated cardiac anomalies were more frequent in type 1. Distinction of localized (types 2, 3 and 4) and diffuse narrowing (type 1) revealed a significant difference for age at surgery, prenatal diagnosis, and associated anomaly. The presence of a bicuspid aortic valve (48.6%) did not differ according to the types. A left superior vena cava (7.7%) was equally encountered in all the subtypes (Fig. 1).

Conclusion

A new classification system for CoA is presented. According to our data, all the types could be prenatally diagnosed. This classification might be advantageous to better understand pathophysiology of CoA and facilitate scientific communication.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Archives of Cardiovascular Diseases
Archives of Cardiovascular Diseases 医学-心血管系统
CiteScore
4.40
自引率
6.70%
发文量
87
审稿时长
34 days
期刊介绍: The Journal publishes original peer-reviewed clinical and research articles, epidemiological studies, new methodological clinical approaches, review articles and editorials. 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. 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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信