Pulmonary Atresia and Ventricular Septal Defect: Definitions, Nomenclature, and Classification.

Christo I Tchervenkov, Richard Tang, Giles J Peek, Mark S Bleiweis, Jeffrey P Jacobs
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Abstract

This manuscript will provide information about pulmonary atresia + ventricular septal defect, including definitions, nomenclature, and classification, based on the 2021 International Paediatric and Congenital Cardiac Code (IPCCC) and the Eleventh Revision of the International Classification of Diseases (ICD-11). The 2021 IPCCC and ICD-11 provide the following definition for Tetralogy of Fallot with pulmonary atresia: Tetralogy of Fallot with pulmonary atresia is defined as "A congenital cardiovascular malformation that is a variant of tetralogy of Fallot in which there is no direct communication between the right ventricle and the pulmonary arterial tree." The 2021 IPCCC and ICD-11 provide the following definition for Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral arteries: Tetralogy of Fallot with pulmonary atresia and systemic-to-pulmonary collateral arteries is defined as "A congenital cardiovascular malformation that is a variant of tetralogy of Fallot in which there is no direct communication between the right ventricle and the pulmonary arterial tree and there are collateral blood vessels between the systemic and pulmonary arteries." "Tetralogy of Fallot + pulmonary atresia" is a specific type of "pulmonary atresia + ventricular septal defect" where the intracardiac malformation is more accurately defined. The presence or absence of major aortopulmonary collateral arteries (MAPCA[s]) does not change these definitions. Therefore, "tetralogy of Fallot + pulmonary atresia + MAPCA(s)" is a specific type of "pulmonary atresia + ventricular septal defect + MAPCA(s)" where the intracardiac malformation is more accurately defined. In the universe of patients with pulmonary atresia + ventricular septal defect, the anatomy and morphology of the pulmonary circulation to a large extent determines the surgical approach and overall outcome, with the intracardiac anatomy playing a secondary role. Based on the characterization of the pulmonary circulation, patients with pulmonary atresia + ventricular septal defect can be classified into three groups: In type A, pulmonary blood flow is provided by native pulmonary arteries (NPAs). In type B, pulmonary blood flow is provided by both NPA and MAPCA(s). In type C, pulmonary blood flow is provided only by MAPCA(s).

肺闭锁和室间隔缺损:定义、命名和分类。
本文将根据2021年国际儿科和先天性心脏法典(IPCCC)和第十一次修订的国际疾病分类(ICD-11),提供肺闭锁+室间隔缺损的信息,包括定义、命名和分类。2021 IPCCC和ICD-11为法洛四联症合并肺闭锁提供了以下定义:法洛四联症合并肺闭锁被定义为“先天性心血管畸形,是法洛四联症的一种变体,右心室和肺动脉树之间没有直接联系。”2021年IPCCC和ICD-11对法洛四联症合并肺闭锁和全身到肺侧支动脉的定义如下:法洛四联症合并肺闭锁和全身到肺侧支动脉被定义为“一种先天性心血管畸形,是法洛四联症的一种变体,右心室和肺动脉树之间没有直接的联系,全身动脉和肺动脉之间有侧支血管。”“法洛四联症+肺闭锁”是“肺闭锁+室间隔缺损”的一种特殊类型,其对心内畸形的定义更为准确。主动脉肺动脉侧支(MAPCA[s])的存在与否并不改变这些定义。因此,“法洛四联症+肺闭锁+ MAPCA(s)”是“肺闭锁+室间隔缺损+ MAPCA(s)”的一种特殊类型,对心内畸形的定义更为准确。在肺闭锁+室间隔缺损患者中,肺循环的解剖形态在很大程度上决定了手术入路和整体预后,心内解剖结构起次要作用。根据肺循环特征,肺闭锁+室间隔缺损患者可分为三组:A型肺血流由原生肺动脉(NPAs)提供;在B型肺中,肺血流由NPA和MAPCA提供。在C型中,肺血流仅由MAPCA(s)提供。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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