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      Recent outcomes of the extracardiac Fontan procedure in patients with hypoplastic left heart syndrome

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          Abstract

          Objective:

          To investigate patient-related factors, echocardiographic, and anatomic variables associated with immediate and long-term clinical outcomes after extracardiac Fontan procedure at our institution.

          Materials and Methods:

          Retrospective review of preoperative cardiac catheterizations and echocardiograms as well as medical records of all children with hypoplastic left heart syndrome (HLHS) who underwent Fontan between June 2002 and December 2018.

          Results:

          Seventy-seven patients with HLHS were included (age 4 years [1.5–11.7]). Seventy patients (91%) received a nonfenestrated Fontan and 57 patients (74%) underwent Fontan without cardiopulmonary bypass (CPB). Presence of a Fontan fenestration ( P = 0.69) and use of CPB ( P = 0.79) did not differ between those with <2 weeks compared to those with ≥2 weeks of chest tube drainage. There were no differences in either pre- or intra-operative hemodynamics between patients who weighed <15 kg compared to those who weighed ≥15 kg at time of surgery; incidence of death, transplant, and transplant listing were similar between weight groups. Inferior vena cava (IVC) diameter z-score did not differ among patients with and without chylous chest tube drainage ( P = 0.78), with and without development of protein losing enteropathy ( P = 0.23), or death/heart transplant/transplant listing compared to survivors without transplant ( P = 0.26).

          Conclusion:

          In HLHS patients undergoing Fontan, preoperative weight and IVC diameter appeared to have no influence on immediate postoperative outcomes. Performing the Fontan off CPB and with a fenestration also conferred no added clinical benefit. These observations should be considered when deciding optimal timing for Fontan completion.

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          Most cited references24

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          Guidelines and standards for performance of a pediatric echocardiogram: a report from the Task Force of the Pediatric Council of the American Society of Echocardiography.

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            Evaluation and Management of the Child and Adult With Fontan Circulation: A Scientific Statement From the American Heart Association

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              Fontan operation in five hundred consecutive patients: factors influencing early and late outcome.

              The purpose of this study was to review a large, evolving, single-center experience with the Fontan operation and to determine risk factors influencing early and late outcome. The first 500 patients undergoing modifications of the Fontan operation at our institution were identified. Perioperative variables were recorded and a cross-sectional review of survivors was undertaken. The incidence of early failure decreased from 27.1% in the first quartile of the experience to 7.5% in the last quartile. In a multivariate model, the following variables were associated with an increased probability of early failure: a mean preoperative pulmonary artery pressure of 19 mm Hg or more (p < 0.001), younger age at operation (p = 0.001), heterotaxy syndrome (p = 0.03), a right-sided tricuspid valve as the only systemic atrioventricular valve (p = 0.001), pulmonary artery distortion (p = 0.04), an atriopulmonary connection originating at the right atrial body or appendage (p = 0.001), the absence of a baffle fenestration (p = 0.002), and longer cardiopulmonary bypass time (p = 0.001). An increased probability of late failure was associated with the presence of a pacemaker before the Fontan operation (p < 0.001). A morphologically left ventricle with normally related great arteries or a single right ventricle (excluding heterotaxy syndrome and hypoplastic left heart syndrome) were associated with a decreased probability of late failure (p = 0.003). These analyses indicate that early failure has declined over the study period and that this decline is related in part to procedural modifications. A continuing late hazard phase is associated with few patient-related variables and does not appear related to procedural variables.
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                Author and article information

                Journal
                Ann Pediatr Cardiol
                Ann Pediatr Cardiol
                APC
                Annals of Pediatric Cardiology
                Wolters Kluwer - Medknow (India )
                0974-2069
                0974-5149
                Jul-Sep 2020
                29 June 2020
                : 13
                : 3
                : 186-193
                Affiliations
                [1 ]Department of Pediatrics, Division of Pediatric Cardiology, Stanford University School of Medicine, Stanford, CA, USA
                [2 ]Department of Pediatrics, Division of Critical Care Medicine, Stanford University School of Medicine, Stanford, CA, USA
                [3 ]Department of Cardiothoracic Surgery, Division of Pediatric Cardiac Surgery, Stanford University School of Medicine, Stanford, CA, USA
                Author notes
                Address for correspondence: Dr. Alisa Arunamata, 750 Welch Road, Suite 325, Palo Alto, CA 94304, USA. E-mail: alisa.arunamata@ 123456stanford.edu
                Article
                APC-13-186
                10.4103/apc.APC_5_20
                7437630
                32863652
                6020f2fc-9680-4213-b67c-9963d596d60a
                Copyright: © 2020 Annals of Pediatric Cardiology

                This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.

                History
                : 12 January 2020
                : 17 April 2020
                : 05 November 2020
                Categories
                Original Article

                Cardiovascular Medicine
                fontan procedure,hypoplastic left heart syndrome,clinical outcomes,congenital heart disease

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