Ferrari Irene, Shehu Nerejda, Stern Heiko, Meierhofer Christian
Congenital Heart Disease and Pediatric Cardiology, German Heart Center Munich, Technical University of Munich, Lazarettstrasse 36, Munich 80636, Germany.
Pediatric Cardiology and Congenital Heart Disease, Borgo Trento Hospital, University of Verona, Verona, Italy.
Eur Heart J Case Rep. 2023 Mar 15;7(3):ytad126. doi: 10.1093/ehjcr/ytad126. eCollection 2023 Mar.
Arrhythmias after palliation of congenital malformations with functional monoventricle by different Fontan modifications are very common. Sinus node dysfunction and junctional rhythm are known to have a high prevalence and a detrimental impact on the optimal functioning of Fontan circulations. Maintaining sinus node function has high prognostic significance, and some cases have even been described where atrial pacing with restoring of atrioventricular synchrony was able to reverse protein-losing enteropathy with overt failure of the Fontan.
A 12-year-old boy with a complex congenital malformation (double outlet right ventricle, transposition of the great arteries, pulmonary stenosis, and straddling atrioventricular valve) palliated through a modified Fontan (total cavopulmonary connection with a fenestrated extracardiac 18 mm Gore-Tex conduit) presented for cardiac magnetic resonance evaluation for mild asthenia and worsening of exercise tolerance. Flow profiles in all the regions of the Fontan (both caval veins and right and left pulmonary arteries) showed a small amount of retrograde flow; a four-chamber cine sequence clearly showed contraction of the atria against closed atrioventricular valve; this haemodynamic condition can be caused either by retro-conducted junctional rhythm (previously demonstrated in our patient) or by isorhythmic dissociation of sinus rhythm.
Our finding directly demonstrates the profound impact of retro-conducted junctional rhythm on the haemodynamic of a Fontan circulation in which, with each cardiac beat, the pressure rise in the atria and pulmonary veins due to atrial contraction with closed atrioventricular valves is able to stop and invert the passive flow of the systemic venous return towards the lungs.
通过不同的Fontan术式对功能性单心室先天性畸形进行姑息治疗后,心律失常非常常见。已知窦房结功能障碍和交界性心律患病率很高,并且对Fontan循环的最佳功能有不利影响。维持窦房结功能具有很高的预后意义,甚至有一些病例描述了通过恢复房室同步的心房起搏能够逆转Fontan明显衰竭伴有的蛋白丢失性肠病。
一名12岁男孩患有复杂先天性畸形(右心室双出口、大动脉转位、肺动脉狭窄和跨骑式房室瓣),通过改良Fontan术(经心外带孔18 mm Gore-Tex导管的全腔肺连接)进行姑息治疗,因轻度乏力和运动耐量恶化前来进行心脏磁共振评估。Fontan所有区域(腔静脉以及左右肺动脉)的血流情况显示有少量逆流;四腔电影序列清晰显示心房在关闭的房室瓣时收缩;这种血流动力学状况可能是由逆向传导的交界性心律(此前在我们的患者中已证实)或窦性心律的等律分离引起的。
我们的发现直接证明了逆向传导的交界性心律对Fontan循环血流动力学的深远影响,在这种情况下,每一次心跳时,由于心房在房室瓣关闭时收缩,心房和肺静脉内压力升高,能够阻止并逆转体静脉血向肺部的被动流动。