A better approach for left ventricular training in transposition of the great arteries and intact interventricular septum: Bidirectional cavopulmonary anastomosis and pulmonary artery banding.

Abstract:

OBJECTIVE:Management of the patients with transposition of the great arteries and intact ventricular septum may be challenging beyond the newborn period. Herein, we would like to present our alternative strategy for training the left ventricle in these patients. METHODS:Six patients with transposition of the great arteries and intact ventricular septum were evaluated in our clinic. Two of them were palliated with Glenn procedure and pulmonary banding as a definitive treatment strategy at other centers. Four patients were operated on and a bidirectional cavopulmonary anastomosis in combination with pulmonary artery banding was performed (stage-1: palliation and ventricular training) in our center. In four out of these six patients, arterial switch operation was performed with takedown and direct re-anastomosis of the superior vena cava to right atrium after an interstage period of 21-30 months (stage-2: anatomical repair). RESULTS:Any mortality was not encountered. The left ventricular mass indices increased from 18-32 to 44-74 g/m2 in patients undergoing the anatomical repair. All of the patients were uneventfully discharged following the second stage. The mean follow-up period was 20 months (9-32 months) following stage 2. All of the patients are doing well with trivial neoaortic regurgitation and normal biventricular function. CONCLUSIONS:Bidirectional cavopulmonary anastomosis with pulmonary artery banding may be a promising left ventricle training approach in ventriculoarterial discordance when compared to the traditional pulmonary artery banding with concomitant systemic-to-pulmonary artery shunt procedures which still carry a significant interstage morbidity and mortality.

journal_name

Congenit Heart Dis

journal_title

Congenital heart disease

authors

Bilal MS,Özyüksel A,Kemal Avşar M,Demiroluk Ş,Küçükosmanoğlu O,Yalçın Y

doi

10.1111/chd.12749

subject

Has Abstract

pub_date

2019-05-01 00:00:00

pages

464-469

issue

3

eissn

1747-079X

issn

1747-0803

journal_volume

14

pub_type

杂志文章
  • Thrombus in right ventricular outflow tract: unique cause of refractory cyanotic spell.

    abstract::Iron deficiency state in patients with cyanotic congenital heart disease can mimic as well as aggravate hyperviscosity symptoms. Correction of iron deficiency in these cases is expected to improve symptoms. We report an unexpected occurrence of refractory cyanotic spell in a child with tetralogy of Fallot due to throm...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2011.00608.x

    authors: Gupta SK,Saxena A,Anil OM,Bisoi AK

    更新日期:2012-07-01 00:00:00

  • Outcomes of tracheostomy following congenital heart surgery: a contemporary experience.

    abstract:INTRODUCTION:Following congenital heart surgery, pediatric patients may experience persistent respiratory failure that requires tracheostomy placement. Currently, definitive knowledge of the optimal timing for tracheostomy placement in this patient population is lacking. METHODS:An 8-year retrospective review of 17 pe...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12192

    authors: Costello JP,Emerson DA,Shu MK,Peer SM,Zurakowski D,Reilly BK,Klugman D,Jonas RA,Nath DS

    更新日期:2015-01-01 00:00:00

  • Midgestation fetal pulmonary annulus size is predictive of outcome in tetralogy of fallot.

    abstract:BACKGROUND:Surgical management of tetralogy of Fallot (TOF) is increasingly moving toward valve-sparing approaches rather than transannular patch (TAP). We evaluate whether fetal pulmonary valve (PV) size is predictive of postnatal course and surgical approach in TOF. METHODS:In this retrospective study, fetal and pos...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12120

    authors: Friedman K,Balasubramanian S,Tworetzky W

    更新日期:2014-05-01 00:00:00

  • Determinants of intensive care unit length of stay for infants undergoing cardiac surgery.

    abstract:OBJECTIVE:The purpose of this study was to identify factors that influence postoperative intensive care unit length of stay (ICULOS) in infants less than 6 months of age undergoing congenital heart surgery. METHODS:Records from a single institution, from January 2000 to December 2000, were reviewed. For analysis, surg...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2006.00027.x

    authors: Gillespie M,Kuijpers M,Van Rossem M,Ravishankar C,Gaynor JW,Spray T,Clark B 3rd

    更新日期:2006-07-01 00:00:00

  • A different therapeutic strategy for severe tetralogy of Fallot with origin of the left pulmonary artery from the ascending aorta: stenting of the right ventricular outflow tract before complete repair.

    abstract::The origin of pulmonary artery branches (particularly the left pulmonary artery) from the ascending aorta is a rare condition. We detected prominent hypoplasia of the main and right pulmonary arteries in a 3.5-month-old 3.7 kg female infant who had tetralogy of Fallot with origin of the left pulmonary artery in the as...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2011.00542.x

    authors: Saritas T,Erdem A,Karaci AR,Demir F,Celebi A

    更新日期:2012-05-01 00:00:00

  • Surveillance and screening practices of New England congenital cardiologists for patients after the Fontan operation.

    abstract:INTRODUCTION:Surveillance and management guidelines for Fontan patients are lacking due to the paucity of evidence in the literature of screening efficacy on outcome measures. METHODS:The Fontan Working Group within the New England Congenital Cardiology Association designed an electronic survey to assess surveillance ...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12854

    authors: Davey BT,Toro-Salazar OH,Gauthier N,Valente AM,Elder RW,Wu FM,Berman N,Pollack P,Lee JH,Rathod RH

    更新日期:2019-11-01 00:00:00

  • Pulmonary vein stenosis with Down syndrome: a rare and frequently fatal cause of pulmonary hypertension in infants and children.

    abstract::Down syndrome (DS) patients are prone to pulmonary hypertension (PHTN) due to various cardiopulmonary causes. However, the association of DS with pulmonary vein stenosis (PVS) is not adequately described. We illustrate three cases from our center and an additional 13 cases from an extensive review of the literature of...

    journal_title:Congenital heart disease

    pub_type: 杂志文章,评审

    doi:10.1111/chd.12088

    authors: Gowda S,Bhat D,Feng Z,Chang CH,Ross RD

    更新日期:2014-05-01 00:00:00

  • Fontan operation and the single ventricle.

    abstract::The Fontan operation has gone through multiple incarnations since Fontan and Baudet's initial description in 1971. Through the medical dossier of a patient with a single ventricle, we plot the history of medical, surgical, and percutaneous interventions over the past 40 years, specifically focusing on the Fontan proce...

    journal_title:Congenital heart disease

    pub_type: 历史文章,杂志文章,评审

    doi:10.1111/j.1747-0803.2007.00065.x

    authors: AboulHosn JA,Shavelle DM,Castellon Y,Criley JM,Plunkett M,Pelikan P,Dinh H,Child JS

    更新日期:2007-01-01 00:00:00

  • Racial disparities in clinic follow-up early in life among survivors of congenital heart disease.

    abstract:OBJECTIVE:The current study aims to identify the rates of lapses in care and loss to follow-up before age one through age five for white and nonwhite congenital heart disease (CHD) survivors. Nonwhite CHD survivors were hypothesized to experience an earlier lapse in care and be lost to follow-up than whites. DESIGN:Pa...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12732

    authors: Jackson JL,Morack J,Harris M,DeSalvo J,Daniels CJ,Chisolm DJ

    更新日期:2019-03-01 00:00:00

  • Congenital heart disease patients' and parents' perception of disease-specific knowledge: Health and impairments in everyday life.

    abstract:BACKGROUND:Children and adolescents with congenital heart disease (CHD) and their families require qualified combined medical and psychosocial information, care, and counseling. This study aimed to analyze CHD patients' and parents' perception of disease-specific knowledge, state of health, and impairments experienced ...

    journal_title:Congenital heart disease

    pub_type: 杂志文章,多中心研究

    doi:10.1111/chd.12581

    authors: Helm PC,Kempert S,Körten MA,Lesch W,Specht K,Bauer UMM

    更新日期:2018-05-01 00:00:00

  • Effect of Left Cardiac Sympathetic Denervation on the Electromechanical Window in Patients with either Type 1 or Type 2 Long QT Syndrome: A Pilot Study.

    abstract:BACKGROUND:Left cardiac sympathetic denervation (LCSD) exerts significant antifibrillatory effects in patients with long QT syndrome (LQTS). Recently, electromechanical window (EMW) has emerged as a novel torsadogenic marker in LQTS, superior to QT interval (QTc) in distinguishing symptomatic from asymptomatic patients...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12332

    authors: Schneider AE,Bos JM,Ackerman MJ

    更新日期:2016-09-01 00:00:00

  • Complete heart block due to Lyme carditis in two pediatric patients and a review of the literature.

    abstract::Carditis is a common manifestation of adult patients with Lyme disease affecting 4-10% of Lyme patients in the United States. However, children with Lyme disease rarely present with acute carditis. The management of pediatric patients with complete heart block (CHB) secondary to Lyme carditis has not been well describ...

    journal_title:Congenital heart disease

    pub_type: 杂志文章,评审

    doi:10.1111/j.1747-0803.2007.00122.x

    authors: Silver E,Pass RH,Kaufman S,Hordof AJ,Liberman L

    更新日期:2007-09-01 00:00:00

  • Scimitar syndrome with right hemianomalous pulmonary venous drainage into superior vena cava/right atrium junction.

    abstract::Scimitar syndrome is characterized by anomalous pulmonary venous drainage of a part or the whole of the right lung into the inferior vena cava (IVC). It is extremely uncommon in scimitar syndrome for the pulmonary veins to drain anomalously to a site other than the IVC. The following case report describes an otherwise...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2011.00513.x

    authors: Kotecha MK,Krishnamanohar SR,Kumar RS

    更新日期:2012-01-01 00:00:00

  • Endovascular stenting for native coarctation of the aorta is an effective alternative to surgical intervention in older children.

    abstract:OBJECTIVE:Assess the early and intermediate results with respect to blood pressure control in older children undergoing endovascular stenting for native coarctation of the aorta. DESIGN:Eleven hypertensive patients (10 +/- 3 years of age) underwent endovascular stenting via standard techniques for native coarctation o...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2007.00148.x

    authors: Weber HS,Cyran SE

    更新日期:2008-01-01 00:00:00

  • Adverse effects of amiodarone therapy in adults with congenital heart disease.

    abstract:OBJECTIVE:Amiodarone is a highly effective antiarrhythmic therapy, however its toxicity profile often limits treatment. This is particularly relevant in adults with congenital heart disease (CHD), who are often young and in whom other antiarrhythmic agents commonly fail or are contraindicated. We sought to determine in...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12657

    authors: Moore BM,Cordina RL,McGuire MA,Celermajer DS

    更新日期:2018-11-01 00:00:00

  • Clinical Experience of Transcatheter Closure for Residual Ventricular Septal Defect in Pediatric Patients.

    abstract:BACKGROUND:Open cardiac surgery has traditionally been the gold standard for repair of ventricular septal defect (VSD). The inherent risks and complications associated with open surgery and the incidence of postoperative residual VSD are significant disadvantages of the open surgical approach. OBJECTIVE:To evaluate th...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12357

    authors: Zhou W,Li F,Fu L,Gao W,Guo Y,Liu T,Huang M,Zhang Y

    更新日期:2016-07-01 00:00:00

  • Fetal heart size measurements as new predictors of homozygous α-thalassemia-1 in mid-pregnancy.

    abstract:OBJECTIVE:To evaluate the efficacy of using fetal heart size measurements derived from axial echocardiography to predict homozygous α-thalassemia-1. DESIGN:Prospective diagnostic study. SETTING:The carrier rate of α-thalassemia-1 (-/αα) in China's Guangxi Zhuang Autonomous Region is approximately 15%. If both parents...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12568

    authors: Li X,Qiu X,Huang H,Zhao Y,Li X,Li M,Tian X

    更新日期:2018-03-01 00:00:00

  • Recurrent exacerbations of protein-losing enteropathy after initiation of growth hormone therapy in a Fontan patient controlled with spironolactone.

    abstract::Protein-losing enteropathy (PLE) is a rare, but serious complication in single ventricle patients after Fontan palliation, and is associated with a 5-year mortality of 46%. We describe a patient with PLE after Fontan palliation who achieved remission with high-dose spironolactone (an aldosterone antagonist), but had t...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2009.00320.x

    authors: Grattan MJ,McCrindle BW

    更新日期:2010-03-01 00:00:00

  • Rasmussen's aneurysm in childhood: a case report.

    abstract::In medical literature, few cases of Rasmussen's aneurysm have been reported until now, and to the best of our knowledge, there has been no description of a case of Rasmussen's aneurysm in childhood. The child described in the case report had a restrictive cardiomyopathy, complicated by pulmonary hypertension, in assoc...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2011.00609.x

    authors: Gesuete V,Corzani A,Bronzetti G,Lovato L,Picchio FM

    更新日期:2013-03-01 00:00:00

  • Protein-losing enteropathy after the Fontan operation: associations and predictors of clinical outcome.

    abstract:OBJECTIVE:We sought to define what clinical parameters were related to the ultimate outcome in Fontan patients who had developed protein-losing enteropathy (PLE). BACKGROUND:PLE is a serious complication of the Fontan operation. Several preoperative and perioperative findings are associated with later PLE. However, th...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2008.00200.x

    authors: Silvilairat S,Cabalka AK,Cetta F,Grogan M,Hagler DJ,O'Leary PW

    更新日期:2008-07-01 00:00:00

  • Circulating biomarkers of left ventricular hypertrophy in pediatric coarctation of the aorta.

    abstract:OBJECTIVE:Patients undergoing surgical repair of aortic coarctation have a 50% risk of pathologic left ventricular remodeling (increased left ventricular mass or relative wall thickness). Endothelin 1, ST2, galectin 3, norepinephrine and B-natriuretic peptide are biomarkers that have been associated with pathologic LV ...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12744

    authors: Frank BS,Urban TT,Lewis K,Tong S,Cassidy C,Mitchell MB,Nichols CS,Davidson JA

    更新日期:2019-05-01 00:00:00

  • Stress echocardiography: An overview for use in pediatric and congenital cardiology.

    abstract::Currently, the role of stress echocardiography primarily resides in diagnosing acquired coronary artery disease (CAD) in adults. Besides an increasing concern for traditional CAD in young patients due to obesity and other chronic pediatric diseases, there is also a growing population of adolescents and young adults wi...

    journal_title:Congenital heart disease

    pub_type: 杂志文章,评审

    doi:10.1111/chd.12495

    authors: Ermis P

    更新日期:2017-09-01 00:00:00

  • Building a comprehensive team for the longitudinal care of single ventricle heart defects: Building blocks and initial results.

    abstract:INTRODUCTION:With increasing survival of children with HLHS and other single ventricle lesions, the complexity of medical care for these patients is substantial. Establishing and adhering to best practice models may improve outcome, but requires careful coordination and monitoring. METHODS:In 2013 our Heart Center beg...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12459

    authors: Texter K,Davis JAM,Phelps C,Cheatham S,Cheatham J,Galantowicz M,Feltes TF

    更新日期:2017-07-01 00:00:00

  • Acute and long-term effects of endovascular debanding of pulmonary arteries in a swine model.

    abstract:OBJECTIVES:The primary objective of this study was to demonstrate that pulmonary artery (PA) debanding via cardiac catheterization using balloon angioplasty is feasible and safe in swine. The secondary objectives were to determine the acute and long-term effects of this therapy. DESIGN:This is a chronic survival exper...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12449

    authors: Perez M,Kumar TS,Hoskoppal D,Akkhawattanangkul Y,Allen K,Knott-Craig CJ,Waller BR,Sathanandam S

    更新日期:2017-05-01 00:00:00

  • The impact of obesity on early postoperative outcomes in adults with congenital heart disease.

    abstract:BACKGROUND:As the prevalence of obesity continues to increase, it now includes the growing number of patients with congenital heart disease (CHD). This particular obese patient population may pose additional intraoperative as well as postoperative challenges that may contribute to poor outcomes. Our aims were to determ...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/j.1747-0803.2011.00522.x

    authors: Zaidi AN,Bauer JA,Michalsky MP,Olshove V,Boettner B,Phillips A,Cook SC

    更新日期:2011-05-01 00:00:00

  • Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.

    abstract:OBJECTIVE:Atrial septal defect (ASD) is the second most common congenital heart defect (CHD) and is observed in families as an autosomal dominant trait as well as in nonfamilial CHD. Mutations in the NKX2-5 gene, located on chromosome 5, are associated with ASD, often combined with conduction disturbances, cardiomyopat...

    journal_title:Congenital heart disease

    pub_type: 杂志文章,评审

    doi:10.1111/chd.12317

    authors: Ellesøe SG,Johansen MM,Bjerre JV,Hjortdal VE,Brunak S,Larsen LA

    更新日期:2016-05-01 00:00:00

  • Twin pregnancy in a patient after the Fontan operation: report of a case.

    abstract::Singleton pregnancy in patients with single ventricle after the Fontan operation has been reported with significant offspring and maternal complications. We report a twin pregnancy and premature delivery, in a patient following the Fontan operation. ...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12054

    authors: Nir A,Elchalal U,Hammerman C,Rein AJ

    更新日期:2013-11-01 00:00:00

  • Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the Young.

    abstract:INTRODUCTION:Perturbations in the CACNA1C-encoded L-type calcium channel α-subunit have been linked recently to heritable arrhythmia syndromes, including Timothy syndrome, Brugada syndrome, early repolarization syndrome, and long QT syndrome. These heritable arrhythmia syndromes may serve as a pathogenic basis for auto...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12371

    authors: Sutphin BS,Boczek NJ,Barajas-Martínez H,Hu D,Ye D,Tester DJ,Antzelevitch C,Ackerman MJ

    更新日期:2016-12-01 00:00:00

  • "Frontiers in Fontan failure: A summary of conference proceedings".

    abstract::"Frontiers in Fontan Failure" was the title of a 2015 conference sponsored by Children's Healthcare of Atlanta and Emory University School of Medicine. In what is hoped to be the first of many such gatherings, speakers and attendees gathered to discuss the problem of long-term clinical deterioration in these patients....

    journal_title:Congenital heart disease

    pub_type:

    doi:10.1111/chd.12407

    authors: Hebson C,Book W,Elder RW,Ford R,Jokhadar M,Kanter K,Kogon B,Kovacs AH,Levit RD,Lloyd M,Maher K,Reshamwala P,Rodriguez F,Romero R,Tejada T,Marie Valente A,Veldtman G,McConnell M

    更新日期:2017-01-01 00:00:00

  • Spontaneous closure of a symptomatic coronary artery fistula just within a few days of newborn period.

    abstract::We present a rare case of spontaneous closure of a fistula between the left coronary artery and the right ventricle (RV) within a few days of newborn period. A 14-day-old male newborn was referred to our clinic for investigation of tachypnea and cardiac murmur. A color flow Doppler echocardiography revealed turbulent ...

    journal_title:Congenital heart disease

    pub_type: 杂志文章

    doi:10.1111/chd.12060

    authors: Yilmazer MM,Demir F,Yolbaş I,Bilici M

    更新日期:2014-01-01 00:00:00