Fetal echocardiography: new grounds to explore during fetal cardiac intervention.

Abstract:

:Over the past decade, revolutionary advances in ultrasound imaging technology have allowed the study of the evolution of congenital heart disease during fetal life. The frustration arising from watching the prenatal progression of severe semilunar valve obstructions and therapy-refractory fetal arrhythmias has prompted the interest in developing procedures for fetal cardiac intervention. Ultrasound techniques as the primary diagnostic and monitoring modalities in fetal medicine will play a key role in defining patient groups, peri-interventional assessment of fetal hemodynamics, and monitoring during these procedures. The purpose of this article is to provide pediatric cardiologists and perinatal medicine specialists an overview over the various technical approaches at fetal cardiac intervention and the special tasks that fetal echocardiography will have to accomplish. It also aims at illustrating the potential of fetal echocardiography for fetal selection.

journal_name

Pediatr Cardiol

journal_title

Pediatric cardiology

authors

Kohl T

doi

10.1007/s00246-001-0197-6

subject

Has Abstract

pub_date

2002-05-01 00:00:00

pages

334-46

issue

3

eissn

0172-0643

issn

1432-1971

journal_volume

23

pub_type

杂志文章,评审
  • Surgical Timing and Outcomes of Unilateral Versus Bilateral Superior Cavopulmonary Anastomosis: An Analysis of Pediatric Heart Network Public Databases.

    abstract::Requiring bilateral superior cavopulmonary anastomosis (bSCPA) instead of unilateral superior cavopulmonary anastomosis (uSCPA) could influence surgical timing and outcomes. We compared surgical timing and outcomes for patients who underwent uSCPA to those who underwent bSCPA through use of the Pediatric Heart Network...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-020-02527-4

    authors: Shuler JM,Statile C,Heydarian H,Lehenbauer DG,Hill GD

    更新日期:2021-01-08 00:00:00

  • Prevalence of asymptomatic cardiac valve anomalies in idiopathic scoliosis.

    abstract::The prevalence of asymptomatic cardiac valve anomalies was determined in 82 patients (69 females and 13 males) diagnosed as having idiopathic scoliosis and scheduled for corrective surgery (mean age at surgery 16.3 years). The preoperative study in each patient included echocardiography and ultrasound Doppler. Twenty-...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-002-1443-2

    authors: Colomina MJ,Puig L,Godet C,Villanueva C,Bago J

    更新日期:2002-07-01 00:00:00

  • Pulse-oximetry screening to detect critical congenital heart disease in the neonatal intensive care unit.

    abstract::The current pulse-oximetry screening (POS) protocol for detection of critical congenital heart defects (CCHDs) is recommended only for newborns in well-infant and intermediate care nurseries, and there is no evidence-based protocol for infants discharged from the neonatal intensive care unit (NICU). The objectives of ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-013-0793-2

    authors: Iyengar H,Kumar P,Kumar P

    更新日期:2014-03-01 00:00:00

  • Anterosuperior diverticula of the right ventricle: morphological spectrum and long-term outcome of a distinct cardiac anomaly.

    abstract::Right-ventricular diverticula (RVD), although rare, have particular characteristics. Our study describes the morphology of anterosuperior diverticula of the right ventricle (RV) and patient outcome for this anomaly. Retrospective analysis was performed on all patients with anterosuperior RVD diagnosed in two tertiary ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-014-0885-7

    authors: Wiegand G,Rauch R,Singer H,Koch A,Hofbeck M

    更新日期:2014-08-01 00:00:00

  • Intrauterine closure of membranous ventricular septal defects: mechanism of closure in two autopsy specimens.

    abstract::Anatomic evidence of intrauterine closure of ventricular septal defects (VSDs) has been reported rarely. Between 1985 and 1990, 112 autopsies were performed at the Mayo Clinic on third trimester stillborns and infants who died during the first week of life. There were 21 (19%) cases of congenital heart disease. VSD wa...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF00797004

    authors: Nir A,Driscoll DJ,Edwards WD

    更新日期:1994-01-01 00:00:00

  • Isolated left-sided scimitar vein connecting all left pulmonary veins to the right inferior vena cava.

    abstract::When the common pulmonary vein fails to develop, the embryonic connections of the pulmonary veins to one or more of the systemic veins almost always persist. Anomalous pulmonary venous connections to the inferior vena cava (IVC) are typically characterized by hypoplasia of the involved pulmonary veins and pulmonary ar...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-005-0920-9

    authors: Juraszek AL,Cohn H,Van Praagh R,Van Praagh S

    更新日期:2005-11-01 00:00:00

  • Is routine cardiac catheterization necessary in the management of patients with single ventricles across staged Fontan reconstruction? No!

    abstract::With the advent of cardiac magnetic resonance imaging and high-resolution echocardiography, cardiac catheterization is unnecessary in clinical protocols in the "routine" single ventricle patient. Catheterization adds little to clinical care in these cases, and there are significant risks and costs associated with it. ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s00246-004-0960-6

    authors: Fogel MA

    更新日期:2005-03-01 00:00:00

  • Pseudohypertension in a child with Williams syndrome.

    abstract::Pseudohypertension has often been reported in elderly subjects, but is an unusual phenomenon in children. We report the case of a 5-year-old child who presented with features of Williams syndrome (characterized by elfin facies, supravalvar aortic stenosis, and peripheral pulmonary artery stenosis). Repeated blood pres...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF00796994

    authors: Narasimhan C,Alexander T,Krishnaswami S

    更新日期:1993-03-01 00:00:00

  • Magnetic resonance imaging of unroofed coronary sinus: three cases.

    abstract::Unroofed coronary sinus is a rare cardiac anomaly in which communication occurs between the coronary sinus and the left atrium due to the partial or complete absence of the roof of the coronary sinus. It is usually associated with other cardiovascular anomalies, especially persistent left superior vena cava. It is oft...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s002460010087

    authors: Hahm JK,Park YW,Lee JK,Choi JY,Sul JH,Lee SK,Cho BK,Choe KO

    更新日期:2000-07-01 00:00:00

  • Contractility reserve in children undergoing dialysis by dobutamine stress echocardiography.

    abstract::Left ventricular hypertrophy is an adaptive mechanism in children undergoing chronic dialysis to improve contractility at rest. The aim of this study was to determine the left ventricular performance and contractility reserve by "dobutamine stress echocardiography" in children undergoing chronic dialysis. Thirty-five ...

    journal_title:Pediatric cardiology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s00246-010-9721-x

    authors: Mese T,Guven B,Yilmazer MM,Serdaroglu E,Tavli V,Haydar A,Bak M

    更新日期:2010-10-01 00:00:00

  • Fenestration in extracardiac conduits in children after modified Fontan operation by implantation of stent grafts.

    abstract::Three patients (ages 3, 5, and 8 years) with various forms of functionally univentricular heart lesions received a total cavopulmonary connection with an extracardiac conduit as a final reconstructive procedure. Failure of the Fontan circulation occurred immediately after surgery because of spontaneous closure of surg...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-004-0693-6

    authors: Michel-Behnke I,Luedemann M,Bauer J,Hagel KJ,Akintuerk H,Schranz D

    更新日期:2005-01-01 00:00:00

  • Transient third-degree atrioventricular block in a 4-year-old child with familial dysautonomia.

    abstract::The case of a transient third degree atrioventricular block in a 4-year-old patient with familial dysautonomia is reported. A review of the literature follows with analysis of the significance of arrhythmias in the natural history of the patient with familial dysautonomia. ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF00793955

    authors: Rutkowski M,Axelrod FB,Danilowicz D

    更新日期:1992-07-01 00:00:00

  • Prognosis in fetal tetralogy of Fallot.

    abstract::The outcome in a series of 23 cases of tetralogy of Fallot diagnosed prenatally was compared to published figures for this condition when (a) identified postnatally or (b) treated surgically. There was a marked difference in the survival between these groups, with the highest mortality (75%) occurring when the diagnos...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF00788220

    authors: Allan LD,Sharland GK

    更新日期:1992-01-01 00:00:00

  • PTPN11 mutation associated with aortic dilation and hypertrophic cardiomyopathy in a pediatric patient with Noonan syndrome.

    abstract::Noonan syndrome is an autosomal dominant disease that manifests a wide variety of clinical characteristics. The syndrome is also associated with some cardiac defects. Half of all Noonan syndrome cases are caused by mutations in the PTPN11 gene, but only limited data are available regarding aortic involvement in these ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-009-9537-8

    authors: Jefferies JL,Belmont JW,Pignatelli R,Towbin JA,Craigen WJ

    更新日期:2010-01-01 00:00:00

  • Interatrial groove tear: an unusual complication of balloon atrial septostomy.

    abstract::The authors present an unusual complication of the balloon atrial septostomy procedure performed in a neonate with D-transposition of the great arteries. Cardiac tamponade developed shortly after the balloon atrial septostomy procedure and the infant was found to have a tear in the superior aspect of the left atrium, ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02076340

    authors: Blanchard WB,Knauf DG,Victorica BE

    更新日期:1983-04-01 00:00:00

  • Noninvasive measurement of cardiac output in critically ill children.

    abstract::This study was performed to evaluate the hemodynamic status of children admitted to the intensive care unit, using suprasternal and transesophageal Doppler ultrasound, and to establish a suitable noninvasive technique to monitor trends in cardiac output in critically ill children. Twenty children were studied over a p...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-001-0014-2

    authors: Mohan UR,Britto J,Habibi P,de MC,Nadel S

    更新日期:2002-01-01 00:00:00

  • Cor triatiratum dexter: a rare cause of isolated right atrial enlargement.

    abstract::Cor triatriatum sinistrum (division of the left atrium) is a recognized clinical and surgical entity. Division of the right atrium, also known as cor triatriatum dexter, is an extremely rare congenital abnormality in which persistence of the right valve of the embryonic systemic sinus venosus divides the right atrium ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0443-0

    authors: Choudhary D,Sivasankaran S,Venkateshwaran S,Sasidharan B

    更新日期:2013-01-01 00:00:00

  • Use of a novel hybrid approach to salvage an attempted transcatheter pulmonary valve implant.

    abstract::Transcatheter pulmonary valve implantation in the setting of right ventricle-to-pulmonary artery conduit dysfunction is a relatively new procedure with encouraging early and midterm results. Malpositioning of the valve during implantation is a potentially serious complication. This report describes a case in which val...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0224-9

    authors: Berman DP,Burke R,Zahn EM

    更新日期:2012-06-01 00:00:00

  • Absent right atrioventricular connection and double-inlet ventricle due to an unbalanced familial 8:13 chromosome translocation: a cautionary tale.

    abstract::A two-year-old child who had had palliative surgery as a neonate for an absent right atrioventricular connection and double-inlet ventricle was shown to be developmentally retarded. Trisomy for the short arm of chromosome 8 was demonstrated, resulting from a familial 8:13 translocation, with a high risk of recurrence....

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02306750

    authors: Burn J,Baraitser M,Hughes DT,Saldana-Garcia P,Taylor JF

    更新日期:1984-01-01 00:00:00

  • Relationship of Right Ventricular Size and Function with Respiratory Status in Duchenne Muscular Dystrophy.

    abstract::The relationship between pulmonary function and right ventricle (RV) in Duchenne muscular dystrophy (DMD) has not been evaluated. Using cardiac magnetic resonance (CMR), we describe the relationship of RV size and function with spirometry in a DMD cohort. Fifty-seven boys undergoing CMR and pulmonary function testing ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-016-1362-2

    authors: Mehmood M,Ambach SA,Taylor MD,Jefferies JL,Raman SV,Taylor RJ,Sawani H,Mathew J,Mazur W,Hor KN,Al-Khalidi HR

    更新日期:2016-06-01 00:00:00

  • Successful modified Fontan procedure in an adolescent after left pneumonectomy.

    abstract::We performed a Waterston's anastomosis on a patient with complicated tricuspid atresia when she was two months of age. At age 14 years she required left pneumonectomy for massive, idiopathic hemoptysis. Four months after the pneumonectomy we substituted a modified Fontan anastomosis for the Waterston anastomosis. Rest...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/BF02238530

    authors: Danilowicz D,Langsner A,Colvin SB

    更新日期:1991-07-01 00:00:00

  • Paradoxical relationship between B-type natriuretic peptide and pulmonary vascular resistance in patients with ventricular septal defect and concomitant severe pulmonary hypertension.

    abstract::B-type natriuretic peptide (BNP) reflects volume overload on left ventricle and pulmonary hypertension (PH) in patients with ventricular septal defect (VSD). Pulmonary vascular resistance (PVR) has been reported to correlate positively with BNP in VSD patients with various degrees of PH. We aimed to investigate the re...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-007-9037-7

    authors: Toyono M,Harada K,Tamura M,Aoki-Okazaki M,Shimada S,Oyamada J,Takada G

    更新日期:2008-01-01 00:00:00

  • Pain management after surgery for single-ventricle palliation using the hybrid approach.

    abstract::The hybrid pathway for the management of patients with hypoplastic left heart syndrome was pioneered at our institution and is the preferred approach compared with the traditional Norwood pathway. Patients undergoing this surgery are generally <6 months of age, and pain management in this age group after surgery for c...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0233-8

    authors: Naguib AN,Dewhirst E,Winch PD,Simsic J,Galantowicz M,Tobias JD

    更新日期:2012-10-01 00:00:00

  • 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

  • Epidemiology, etiology, and management of Kawasaki disease: state of the art.

    abstract::Since its first description in Japan 30 years ago, Kawasaki disease has been reported worldwide. Although an infectious etiology is suspected based on the epidemiology and clinical features, a causative agent has not been identified. The majority of the morbidity and mortality associated with this condition is attribu...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章,评审

    doi:10.1007/s002469900436

    authors: Laupland KB,Dele Davies H

    更新日期:1999-05-01 00:00:00

  • Percutaneous device closure of a bifurcated inferior vena cava and completion of the Kawashima procedure for the "difficult" univentricular heart.

    abstract::Azygos continuation of inferior venacava (IVC) is well known in association with interrupted IVC. We report azygos connection of uninterrupted IVC in a young child with complex univentricular heart. This peculiar anatomy was made suitable for univentricular repair by combining percutaneous device closure of prehepatic...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-010-9802-x

    authors: Chaudhuri M,Shivanna D,Jayranganath M,Chandra S

    更新日期:2011-01-01 00:00:00

  • Functional echocardiographic assessment of myocardial performance in anemic premature infants: a pilot study.

    abstract::This prospective observational study conducted in a neonatal intensive care unit aimed to evaluate echocardiographic changes provoked by anemia and transfusion of packed red blood cells (pRBCs) in premature infants. In this study, 32 anemic premature infants had serial echocardiographic assessment of left ventricular ...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-012-0154-6

    authors: Radicioni M,Troiani S,Mezzetti D

    更新日期:2012-04-01 00:00:00

  • Fenestration of the Fontan circuit as treatment for plastic bronchitis.

    abstract::Plastic bronchitis is a rare, potentially life-threatening condition in which protein casts form within and occlude the bronchus, resulting in pulmonary failure, and has been identified as a complication after the Fontan procedure. We present a case of a 5-year-old girl who had undergone an extracardiac fenestrated Fo...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-005-0913-8

    authors: Wilson J,Russell J,Williams W,Benson L

    更新日期:2005-09-01 00:00:00

  • Long-term outcome after surgical closure of atrial septal defect in childhood with extensive assessment including MRI measurement of the ventricles.

    abstract::Surgical closure of the secundum type of atrial septal defect (ASD) in childhood leads to excellent survival. However, relevant morbidity has been reported. Transcatheter closure of these defects has now become an alternative approach. To compare the results of the two different interventions, reliable data are needed...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s00246-005-0838-2

    authors: Bolz D,Lacina T,Buser P,Buser M,Guenthard J

    更新日期:2005-09-01 00:00:00

  • Congenital subclavian artery to subclavian vein fistula presenting with congestive heart failure in an infant.

    abstract::Contrary to acquired arteriovenous fistulas, the congenital malformations are very rare. Here we report a case of congenital arteriovenous fistula forming a communication between the right subclavian artery to subclavian vein. To our knowledge, there is no similar case in which an infant has been successfully operated...

    journal_title:Pediatric cardiology

    pub_type: 杂志文章

    doi:10.1007/s002460010056

    authors: Dogan R,Yilmaz M,Ozkutlu S,Elsharshari H

    更新日期:2000-05-01 00:00:00