Abstract

Parallel advancements in surgical technique, preoperative and postoperative care, as well as a better understanding of physiology in patients with duct-dependent pulmonary or systemic circulation and a functional single ventricle, have led to superb results in staged palliation of most complex congenital heart disease (CHD) [1]. The Fontan procedure and its technical modifications have resulted in markedly improved outcomes of patients with single ventricle anatomy [2,3,4]. The improved early survival has led to an exponential increase of the proportion of Fontan patients surviving long into adolescence and young adulthood [5]. Improved early and late survival has not yet abolished late mortality secondary to myocardial failure, therefore increasing the referrals for cardiac transplantation [6]. Interstage attrition [7] is moreover expected in staged palliation towards completion of a Fontan-type circulation, while Fontan failure represents a growing indication for heart transplantation [8]. Heart transplantation has therefore become the potential “fourth stage” [9] or a possible alternative to a high-risk Fontan operation [10] in a strategy of staged palliation for single ventricle physiology. Heart transplant barely accounts for 16% of pediatric solid organ transplants [11]. The thirteenth official pediatric heart transplantation report- 2010 [11] indicates that pediatric recipients received only 12.5% of the total reported heart transplants worldwide. Congenital heart disease is not only the most common recipient diagnosis, but also the most powerful predictor of 1-year mortality after OHT. Results of orthotopic heart transplantations (OHT) for failing single ventricle physiology are mixed. Some authors advocate excellent early and mid-term survival after OHT for failing Fontan [9], while others suggest that rescue-OHT after failing Fontan seems unwarranted [10]. Moreover, OHT outcome appears to be different according to the surgical staging towards the Fontan operation and surgical technique of Fontan completion [12].The focus of this report is a complete review of the recent literature on OHT for failing single ventricles, outlining the clinical issues affecting Fontan failure, OHT listing and OHT outcome. These data are endorsed reporting our experience with OHT for failing single ventricle physiology in recent years.

Highlights

  • Neonatal palliation and staged reconstruction towards a Fontan-type circulation is currently feasible in most patients with complex congenital heart disease (CHD) and single ventricle physiology

  • A number of endothelium-derived vasoactive factors have been implicated in the pathophysiology of the endothelial dysfunction characteristic of diseases such as pulmonary arterial hypertension [32] and their role has been investigated as a potential mechanism of increased PVR after Fontan completion

  • This is demonstrated by an increased mesenteric vascular impedance measured by Doppler echocardiography in patients with Fontan circulation compared with age-matched normal controls

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Summary

BACKGROUND

Neonatal palliation and staged reconstruction towards a Fontan-type circulation is currently feasible in most patients with complex CHD and single ventricle physiology. Single ventricle circulation appears to have a limited durability per se and myocardial dysfunction or failure/intolerance of Fontan physiology represent a growing indication for heart transplantation. CHD still represents the leading independent predictor of 1year mortality after pediatric heart transplantation, doubling the risk of death of OHT for non-congenital diagnosis. This occurs while 63% of OHT in infancy are accomplished on patients with CHD. The efficacy of OHT as a therapeutic option for failing single ventricles should consider two important points: modality of Fontan failure as an indication for OHT and optimal surgical staging of single ventricles towards Fontan completion versus heart transplantation

MODALITIES OF FONTAN FAILURE
Orthotopic Heart Transplantation in Univentricular Heart
Findings
LISTING AND OHT OUTCOME
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