Mavroudis Constantine, Deal Barbara J
Johns Hopkins Children's Heart Surgery, Florida Hospital for Children, Johns Hopkins University School of Medicine, Orlando, FL, USA
Division of Pediatric Cardiology, Department of Pediatrics, Ann & Robert H Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
World J Pediatr Congenit Heart Surg. 2016 Mar;7(2):192-8. doi: 10.1177/2150135115623960.
Early survival after the Fontan operation has improved significantly leading to a lifetime of Fontan circulation for patients. There is a natural progression of pulmonary artery pressure during the human lifetime that is easily tolerated in two-ventricle physiology but is deleterious for single-ventricle physiology. Obstructions in the venous to pulmonary artery pathway and pulmonary venous return or ventricular outflow, atrioventricular valve dysfunction (regurgitation), pulmonary arteriovenous malformations, venous thrombosis, and the development of atrial arrhythmias can lead to reduced functional status. These complications have been demonstrated in older patients with largely atriopulmonary connections owing to time accrual and unfavorable flow characteristics. Various surgical and catheter interventions aimed at reducing morbidity and mortality have been attempted to treat these identifiable abnormalities. The purpose of this article is to review the extant literature on Fontan Conversion and to assess the lessons learned over 20 years.
Fontan手术后的早期生存率已显著提高,使患者能够终身维持Fontan循环。在人的一生中,肺动脉压力会自然升高,这在双心室生理状态下很容易耐受,但对单心室生理状态是有害的。静脉至肺动脉通路、肺静脉回流或心室流出道的梗阻、房室瓣功能障碍(反流)、肺动静脉畸形、静脉血栓形成以及房性心律失常的发生,都可能导致功能状态下降。由于时间累积和不利的血流特性,这些并发症在接受大部分心房-肺连接的老年患者中已得到证实。为了治疗这些可识别的异常情况,人们尝试了各种旨在降低发病率和死亡率的手术和导管干预措施。本文的目的是回顾关于Fontan转换的现有文献,并评估20年来所吸取的经验教训。