Reliability of Peak Exercise Stroke Volume Assessment by Impedance Cardiography in Patients with Residual Right Outflow Tract Lesions After Congenital Heart Disease Repair.

Abstract:

:Global ventricular response to exercise may be useful in follow-up of patients with residual right outflow tract lesions after congenital heart disease repair. In this context, impedance cardiography is considered accurate for stroke volume (SV) measurement during exercise testing, however, to date, only partial assessment of its reliability has been reported. We retrospectively evaluated relative and absolute reliability of peak SV by impedance cardiography during exercise using intraclass correlation (ICC) and standard error of measurement (SEM) in this population. Peak SV was measured in 30 young patients (mean age 14.4 years ± 2.1) with right ventricular outflow tract reconstruction who underwent two cardiopulmonary exercise tests at a mean one-year interval. SV was measured using a signal morphology impedance cardiography analysis device (PhysioFlow®) and was indexed to body surface area. ICC of peak indexed SV measurement was 0.80 and SEM was 10.5%. High heterogeneity was seen when comparing patients according to peak indexed SV; in patients with peak SV < 50 ml/m2 (15 patients), ICC rose to 0.95 and SEM dropped to 2.7%, while in patients with a peak SV > 50 ml/m2 relative and absolute reliability decreased (ICC = 0.45, SEM = 12.2%). Peak exercise SV assessment by a PhysioFlow® device represents a highly reliable method in patients with residual right outflow tract lesions after congenital heart disease repair, especially in patients with peak SV < 50 ml/m2. In this latter group, a peak SV decrease > 7.3% (corresponding to the minimum "true" difference) should be considered a clinically-relevant decrease in global ventricular performance and taken into account when deciding whether to perform residual lesion removal.

journal_name

Pediatr Cardiol

journal_title

Pediatric cardiology

authors

Legendre A,Bonnet D,Bosquet L

doi

10.1007/s00246-017-1725-3

subject

Has Abstract

pub_date

2018-01-01 00:00:00

pages

45-50

issue

1

eissn

0172-0643

issn

1432-1971

pii

10.1007/s00246-017-1725-3

journal_volume

39

pub_type

杂志文章
  • Decision-Making in the Catheter Laboratory: The Most Important Variable in Successful Outcomes.

    abstract::Increasingly the importance of how and why we make decisions in the medical arena has been questioned. Traditionally the aeronautical and business worlds have shed a light on this complex area of human decision-making. In this review we reflect on what we already know about the complexity of decision-making in additio...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-020-02295-1

    authors: Duignan S,Walsh KP,McMahon CJ

    更新日期:2020-03-01 00:00:00

  • Recurrent Kawasaki disease.

    abstract::This case report describes a boy who had Kawasaki disease (KD) at age 12 months and had a recurrence one year later. The coronary arteries were normal following the initial episode; however, during the second episode he developed coronary aneurysms. Gallium-67 radionuclide imaging, echocardiography, and angiography we...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02310998

    authors: Vargo TA,Huhta JC,Moore WH,Person DA,Edwards MS

    更新日期:1986-01-01 00:00:00

  • Prevalence, treatment, and outcome of heart disease in live-born children: a prospective analysis of 91,823 live-born children.

    abstract::All 91,823 children born in 1980 in Bohemia (population 6.314 million; area 52,478 square kilometers) were examined at least four times during infancy and at the age of three and four years. All children who died were autopsied and those with heart disease were selected. A total of 779 children (8.223/1000 live births...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/BF02083294

    authors: Samánek M,Slavík Z,Zborilová B,Hrobonová V,Vorísková M,Skovránek J

    更新日期:1989-10-01 00:00:00

  • Rho-kinase in development and heart failure: insights from genetic models.

    abstract::Rho-kinase (ROCK) belongs to the AGC (protein kinase A/protein kinase G/protein kinase C, PKA/PKG/PKC) family of serine/threonine kinases and is a major downstream effector of small GTPase RhoA. Rho-kinase is involved in a wide range of fundamental cellular functions such as contraction, adhesion, migration, and proli...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-011-9920-0

    authors: Shi J,Zhang L,Wei L

    更新日期:2011-03-01 00:00:00

  • Complex transposition with interrupted right aortic arch and partial Di George syndrome: successful palliation with combined medical and surgical therapy.

    abstract::A five-day-old infant with transposition of the great arteries, ventricular septal defect, and an interrupted right aortic arch underwent successful balloon septostomy, pulmonary artery banding, and aortic arch repair. The infant also had abnormal facies with severe refractory hypocalcemia and depressed T-lymphocyte n...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02427049

    authors: Duncan WJ,Tyrrell MJ,Bharadwaj B,Rosenberg AM,Schroeder ML,Bingham WT

    更新日期:1984-07-01 00:00:00

  • Isolated junctional tachycardia in a patient with pheochromocytoma: an unusual presentation of an uncommon disease.

    abstract::Pheochromocytoma is a rare disease, which often presents a diagnostic challenge due to a variable symptom presentation complex. We report the case of a child who presented with isolated symptoms of palpitations and was found to have junctional tachycardia with subsequent development of cardiomyopathy. Further evaluati...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-007-9134-7

    authors: Kim JJ,Valdes SO,Kertesz NJ,Cannon BC

    更新日期:2008-09-01 00:00:00

  • Large anomalous systemic arterial supply to the left lung without pulmonary sequestration: a rare cause of heart failure in a child.

    abstract::A 10-month-old boy was referred for tachypnea and heart murmur. An echocardiogram showed unexplained left heart dilation without evidence of an intracardiac shunt. A 64-slice computed tomographic contrast-enhanced angiography showed a large tortuous anomalous artery arising from the descending thoracic aorta and suppl...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-008-9287-z

    authors: Wong MN,Joshi P,Sim KH

    更新日期:2009-01-01 00:00:00

  • Diagnostic and Prognostic Value of Plasma Levels of Cardiac Myosin Binding Protein-C as a Novel Biomarker in Heart Failure.

    abstract::Heart failure (HF) has high morbidity and mortality in children. This study aimed to investigate the value of cardiac myosin binding protein-C (cMyBP-C) as a diagnostic and prognostic biomarker in children with heart failure. This study was a prospective case-control study that involved 50 children with acute HF and 2...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-016-1532-2

    authors: El Amrousy D,Hodeib H,Suliman G,Hablas N,Salama ER,Esam A

    更新日期:2017-02-01 00:00:00

  • Effects of circuit residual volume salvage reinfusion on the postoperative clinical outcome for pediatric patients undergoing cardiac surgery.

    abstract::This study aimed to evaluate the effects of washed cardiopulmonary (CPB) circuit residual blood reinfusion on the postoperative clinical outcome for pediatric patients undergoing cardiac surgery. A total of 309 consecutive Chinese cardiac patients receiving CPB between October 2010 and April 2011 were prospectively an...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0606-z

    authors: Ye L,Lin R,Fan Y,Yang L,Hu J,Shu Q

    更新日期:2013-06-01 00:00:00

  • Isolated innominate artery as a cause of subclavian steal and cerebral hemisphere atrophy.

    abstract::A rare case of isolated innominate artery arising from a left persistent arterial duct with a right aortic arch is presented. Of interest in this case is the retrograde flow in the left carotid system, the history of developmental delay, and the magnetic resonance image (MRI) brain findings suggestive of asymmetric vo...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-010-9739-0

    authors: Reeves BM,Colen TM,Sheridan BJ,Ward C

    更新日期:2010-10-01 00:00:00

  • Two cases of warfarin-induced tracheobronchial calcification after Fontan surgery.

    abstract::This study identified tracheobronchial cartilage calcification in children with congenital heart disease. Calcification of the tracheobronchial airways has been found previously in adults receiving warfarin and in children receiving warfarin after mitral valve replacement. A 9-year-old girl who had received a Fontan r...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-014-0880-z

    authors: Eckersley L,Stirling J,Occleshaw C,Wilson N

    更新日期:2014-08-01 00:00:00

  • Acute pulmonary vasodilator testing with inhaled treprostinil in children with pulmonary arterial hypertension.

    abstract::Acute pulmonary vasodilator testing (AVT) is essential to determining the initial therapy for children with pulmonary arterial hypertension (PAH). This study aimed to report the initial experience with inhaled treprostinil used for AVT in children with PAH and to evaluate the hemodynamic change after inhaled treprosti...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0597-9

    authors: Takatsuki S,Parker DK,Doran AK,Friesen RH,Ivy DD

    更新日期:2013-04-01 00:00:00

  • Neonatal pulmonary artery thrombosis presenting as persistent pulmonary hypertension of the newborn.

    abstract::Pulmonary artery thrombosis in neonates occurs rarely. This report describes the case of a term infant with a pulmonary artery thrombosis presenting as persistent pulmonary hypertension of the newborn. The risk factors identified in the case included maternal diabetes and heterozygous factor V Leiden deficiency. The p...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-008-9349-2

    authors: Sawyer T,Antle A,Studer M,Thompson M,Perry S,Mahnke CB

    更新日期:2009-05-01 00:00:00

  • Radiofrequency catheter ablation of tachycardia in patients with congenital heart disease.

    abstract::Patients with anomalies of the heart frequently suffer from arrhythmias that either are associated with a congenital heart defect or result from the course of the disease. For most of the bradyarrhythmias, appropriate timing of the initiation of treatment is more challenging than its eventual execution. In the case of...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s002460010134

    authors: Hebe J,Hansen P,Ouyang F,Volkmer M,Kuck KH

    更新日期:2000-11-01 00:00:00

  • Assessing ST Segment Changes and Ischemia During Exercise Stress Testing in Patients with Hypoplastic Left Heart Syndrome and Fontan Palliation.

    abstract::While exercise stress testing (EST) is an important tool, little is known about its use for determining ischemia in patients with hypoplastic left heart syndrome (HLHS) and Fontan palliation. We sought to determine the frequency of ST segment changes during EST in HLHS patients after Fontan and examine results of furt...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-015-1312-4

    authors: Kyle WB,Denfield SW,Valdes SO,Penny DJ,Bolin EH,Lopez KN

    更新日期:2016-03-01 00:00:00

  • Relationship Between Pulmonary Arterial Resistance and Compliance in Patients with Down Syndrome.

    abstract::This study aimed to clarify the characteristics of pulmonary arterial resistance (Rp)-compliance (Cp) coupling in individuals with Down syndrome (DS), who have increased risks of pulmonary arterial hypertension (PAH). We performed cardiac catheterization before and after corrective surgery in 85 DS infants and 85 cont...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-019-02080-9

    authors: Iwaya Y,Muneuchi J,Inoue Y,Watanabe M,Okada S,Ochiai Y

    更新日期:2019-04-01 00:00:00

  • Kearns-Sayre syndrome presenting as complete heart block.

    abstract::Kearns-Sayre syndrome (KSS) is a rare mitochondrial disorder characterized by large-scale deletions of mitochondrial DNA. Neuromuscular and cardiac conduction systems are most commonly involved in these patients. Here, we discuss a 10-year-old patient with diabetes mellitus who presented in complete heart block leadin...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-007-9040-z

    authors: Chawla S,Coku J,Forbes T,Kannan S

    更新日期:2008-05-01 00:00:00

  • Epicardial Pacemaker in Neonates and Infants: Is There a Relationship Between Patient Size, Device Size, and Wound Complicatıon?

    abstract::We aimed to investigate the complications after epicardial pacemaker (PM) implantation in neonates and infants and their relationship with factors such as device size and patient size. Between May 2010 and July 2018, 55 patients under 1 year of age who underwent epicardial PM placement were retrospectively evaluated. ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-020-02306-1

    authors: Ergün S,Kafalı HC,Genç SB,Yildiz O,Güneş M,Onan İS,Ergül Y,Güzeltaş A,Haydin S

    更新日期:2020-04-01 00:00:00

  • Myocardial perfusion abnormalities in patients occurring more than 1 year after successful univentricular (Fontan surgery) and biventricular repair (complete repair of tetralogy of Fallot).

    abstract::The outcome of children born with cyanotic congenital heart disease has markedly improved over the years. Follow up is recommended for most post-operated cases as complications may occur over long term. One of the complications is the development of ventricular dysfunction, often seen after a successful Fontan surgery...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0531-1

    authors: Priyadarshini A,Saxena A,Patel C,Paul VK,Lodha R,Airan B

    更新日期:2013-04-01 00:00:00

  • A triple challenge: thrombocytopenia in a 7-year-old girl with unrepaired d-transposition of the great arteries, ventricular septal defect, and pulmonary hypertension.

    abstract::Thrombocytopenia can be a real challenge during cardiac surgery in children with cyanotic congenital heart disease. This report describes a 7-year-old girl with d-transposition of the great arteries, ventricular septal defect, pulmonary hypertension, chronic thrombocytopenia, polycythemia, and chronic renal impairment...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0570-7

    authors: Al-Biltagi M,Ismail MF,Al-Radi OO,Baho H

    更新日期:2013-01-01 00:00:00

  • Comparison of the effectiveness of oral sildenafil versus oxygen administration as a test for feasibility of operation for patients with secondary pulmonary arterial hypertension.

    abstract::It is shown that phosphodiesterase type 5 (PDE5) inhibitors such as sildenafil can modulate pulmonary arterial hypertension (PAH) via increasing the level of guanosine-3,5-cyclic monophosphate (cGMP) and decreases pulmonary artery pressure (PAP). In this study we determined the effectiveness of sildenafil and compared...

    journal_title:Pediatric cardiology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s00246-007-9139-2

    authors: Ajami GH,Borzoee M,Radvar M,Amoozgar H

    更新日期:2008-05-01 00:00:00

  • Delayed contrast enhancement magnetic resonance imaging in congenital aortic stenosis.

    abstract::We report a case of a 12-year-old boy with severe congenital aortic stenosis in whom magnetic resonance imaging (MRI) with delayed contrast enhancement demonstrated extensive subendocardial hyperenhancement within the left ventricle. The hyperenhancement was confirmed to be subendocardial infarct and fibrosis by histo...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-005-5891-3

    authors: La Salvia EA,Gilkeson RC,Dahms BB,Siwik E

    更新日期:2006-05-01 00:00:00

  • Diagnostic Effect of the Single BP Cut-Offs for Identifying Elevated BP and Hypertension in Adolescents Aged 13-17 Years.

    abstract::In contrast to the percentile-based definitions of elevated blood pressure (BP) and hypertension for children and adolescents of all ages in the 2004 fourth report, the 2017 American Academy of Pediatrics (AAP) BP guideline recommends a change to single BP cut-offs for clinical diagnosis (120/< 80-129/< 80 mmHg for el...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-019-02058-7

    authors: Liu Q,Hou Y,Yang L,Zhao M,Li S,Xi B

    更新日期:2019-04-01 00:00:00

  • Early and mid-term results of the arterial switch operation in patients with intramural coronary artery.

    abstract::Intramural coronary artery is known to be a risk factor for early death after an arterial switch operation (ASO). We evaluated the early and mid-term results of ASO for patients with intramural coronary artery. From September 2008 to March 2012, seven patients with an intramural coronary artery underwent ASO at our ho...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-014-0968-5

    authors: Chen X,Cui H,Chen W,Yang S,Cui Y,Xia Y,Ma L

    更新日期:2015-01-01 00:00:00

  • Prospective assessment of novice learners in a simulation-based extracorporeal membrane oxygenation (ECMO) education program.

    abstract::This study aimed to assess the impact of integrating a simulation-based education module into an extracorporeal membrane oxygenation (ECMO) curriculum on novice learners and to test the duration of time that skills obtained during this training exercise were retained. The authors hypothesized that multidisciplinary, s...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0490-6

    authors: Chan SY,Figueroa M,Spentzas T,Powell A,Holloway R,Shah S

    更新日期:2013-03-01 00:00:00

  • Lack of association of the 3'-UTR polymorphism (rs1017) in the ISL1 gene and risk of congenital heart disease in the white population.

    abstract::Congenital heart defects (CHDs) are the most prevalent of all birth defects and the leading cause of death in the first year of life. The molecular causes of most CHDs remain largely unknown. The LIM homeodomain transcriptor factor ISL1 is a marker for undifferentiated cardiac progenitor cells that give rise to both t...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0578-z

    authors: Cresci M,Vecoli C,Foffa I,Pulignani S,Ait-Ali L,Andreassi MG

    更新日期:2013-04-01 00:00:00

  • Supracardiac total anomalous pulmonary venous connection with a descending vertical vein.

    abstract::The commonly used Darling classification for total anomalous pulmonary venous connection (TAPVC) consists of supracardiac, cardiac, infracardiac, and mixed types (Craig et al., Lab Invest 6:44-64, 1967). In supracardiac TAPVC, the common pulmonary vein drains superiorly into the left innominate vein, the superior vena...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-009-9509-z

    authors: Shah S,Singh M,John C,Maheshwari S

    更新日期:2009-10-01 00:00:00

  • Progressive congenital valvar aortic stenosis during infancy: five cases.

    abstract::We report our experience with asymptomatic valvar aortic stenosis diagnosed during infancy. During the period between November 1, 1986 and October 31, 1992 a total of 13 infants were diagnosed with asymptomatic aortic stenosis, 5 of whom showed rapid progression over the first 2 years of life. Two of these asymptomati...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s002469900105

    authors: Anand R,Mehta AV

    更新日期:1997-01-01 00:00:00

  • Late pulmonary venous obstruction after surgical repair of infradiaphragmatic total anomalous pulmonary venous return.

    abstract::Twelve years after an apparently successful surgical correction of infradiaphragmatic (obstructed) total anomalous pulmonary venous drainage, a 12-year-old boy developed evidence of pulmonary artery hypertension secondary to pulmonary venous obstruction due to an apparent lack of growth at the anastomotic site. ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02080561

    authors: Kveselis DA,Chameides L,Diana DJ,Ellison L,Rowland T

    更新日期:1988-01-01 00:00:00

  • Right-ventricular global longitudinal strain may predict neo-aortic arch obstruction after Norwood/Sano procedure in children with hypoplastic left heart syndrome.

    abstract::Neo-aortic arch obstruction (NAAO) is a common complication following the Norwood/Sano procedure (NP) for hypoplastic left heart syndrome (HLHS) and is associated with increased morbidity and mortality. However, there is currently no objective method for predicting which patients will develop NAAO. This study was desi...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-013-0713-5

    authors: Raucci FJ Jr,Seckeler MD,Saunders C,Gangemi JJ,Peeler BB,Jayakumar KA

    更新日期:2013-01-01 00:00:00