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Pediatric Valvar Aortic Stenosis

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Surgical Management of Aorto-Ventricular Tunnel. A Multicenter Study.

Eleftherios M Protopapas, Robert H Anderson, Carl L Backer, José Fragata, Nicolas Hakim, Vladimiro L Vida, George E Sarris, , David J Barron, Håkan Berggren, Mark G Hazekamp, Vladimir Ilyin, Oleg J Kornoukhov, Martin Kostolny, Stojan Lazarov, Mauro Lo Rito, Michael C Monge, Yaroslav Mykychak, Matej Nosal, René Prêtre, Anastasios C Polimenakos, Vladimir Sojak, Giovanni Stellin, Altin Veshti, Illya Yemets,

Aorto-ventricular tunnel (AoVT), a rare congenital anomaly, is a channel originating in the ascending aorta just above the sinotubular junction and leading to the cavity of the left ventricle (AoLVT), or, rarely, the right (AoRVT). This study reviews our collective 30-year experience with the surgical treatment of AoVT. Data were ... Read more >>

Semin. Thorac. Cardiovasc. Surg. (Seminars in thoracic and cardiovascular surgery)
[2020, :]

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Caught-off guard: Unguarded mitral valve orifice in usual atrial arrangement with discordant atrioventricular connections and pulmonary atresia.

Nayan Banerji, Mani Ram Krishna, Raman Krishna Kumar, Robert H Anderson,

Unguarding of an atrioventricular valvar orifice is a rare form of congenital heart disease that requires staged functionally univentricular palliation. Unguarding of the mitral valvar orifice has previously been reported in the setting of mirror-imaged atrial arrangement. We report a neonate with unguarding of the mitral valvar orifice in the ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2020, 13(1):84-86]

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Rare Association of Absent Pulmonary Valve Syndrome with Double Outlet Right Ventricle and Hypoplastic Left Heart Complex.

Erik L Frandsen, Arpan R Doshi, Sujatha Buddhe, Bhawna Arya, Sathish M Chikkabyrappa,

Kans J Med (Kansas journal of medicine)
[2020, 13:21-22]

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Double-Outlet Left Ventricle: The Importance of Echocardiographic and Computed Tomographic Assessment.

Ezequiel Sagray, M Yasir Qureshi, Thomas A Foley, Donald J Hagler, Patrick W O'Leary, Frank Cetta,

CASE (Phila) (CASE (Philadelphia, Pa.))
[2019, 3(4):141-144]

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Prevalence of Noonan spectrum disorders in a pediatric population with valvar pulmonary stenosis.

Kailyn Anderson, James Cnota, Jeanne James, Erin M Miller, Ashley Parrott, Valentina Pilipenko, Kathryn Nicole Weaver, Amy Shikany,

OBJECTIVE:To evaluate the prevalence of Noonan spectrum disorders (NSD) in a pediatric population with valvar pulmonary stenosis (vPS) and identify the clinical characteristics that differentiate those with NSD from those without NSD. DESIGN:A retrospective chart review of 204 patients diagnosed with vPS between 9/1/2012 and 12/1/2016 at a pediatric medical ... Read more >>

Congenit Heart Dis (Congenital heart disease)
[2019, 14(2):264-273]

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Balloon valvuloplasty in a dog with congenital bicuspid aortic valve and supravalvar aortic stenosis (atypical Shone's complex).

R L Winter, D K Newhard, A R Taylor, J A Johnson, E D Baravik-Munsell,

An 8-month-old intact female pug was presented for evaluation and possible balloon valvuloplasty (BV) for severe aortic stenosis. A bicuspid, severely stenotic aortic valve of type 3 morphology with a supravalvar stenosis component was diagnosed, consistent with the diagnosis of atypical Shone's complex. There was severe concentric hypertrophy of the ... Read more >>

J Vet Cardiol (Journal of veterinary cardiology : the official journal of the European Society of Veterinary Cardiology)
[2019, 23:88-95]

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Management of Congenital Heart Disease: State of the Art; Part I-ACYANOTIC Heart Defects.

P Syamasundar Rao,

Since the description of surgery for patent ductus arteriosus in late 1930s, an innumerable number of advances have taken place in the management of congenital heart defects (CHDs). In this review the current status of treatment of seven of the most common acyanotic CHDs was reviewed. The discussion included indications ... Read more >>

Children (Basel) (Children)
[2019, 6(3):]

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Successful balloon valvuloplasty of a subpulmonic membrane associated with cor triatriatum dexter: a case report.

Meryem Haboub, Abdenasser Drighil,

BACKGROUND:Subpulmonic membrane as a cause of right ventricular outflow tract obstruction in patients with concordant ventriculoarterial connection and intact ventricular septum is considered to be rare. Association with cor triatriatum dexter and success of subpulmonic balloon valvuloplasty have never been reported, at least to the best of our knowledge. CASE ... Read more >>

J Med Case Rep (Journal of medical case reports)
[2019, 13(1):291]

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The Effect of Multidisciplinary Approach on the Birth Rate of Fetuses with Prenatally Diagnosed Congenital Heart Disease.

Susan Taejung Kim, Jinyoung Song, June Huh, I Seok Kang, Ji Hyuk Yang, Tae Gook Jun, Soo Young Oh, Suk Joo Choi, Cheong Rae Roh,

BACKGROUND:This study aimed to determine the effect of a multidisciplinary approach on the birth rate of fetuses with prenatally diagnosed congenital heart diseases (CHDs). METHODS:Among the fetuses of 724 gravidas who underwent fetal echocardiography in Samsung Medical Center from January 2013 to June 2017, 463 fetuses with normal cardiac structure, ... Read more >>

J. Korean Med. Sci. (Journal of Korean medical science)
[2019, 34(24):e170]

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Double whammy: A case of bilateral bicuspid arterial valves in transposition, with a review of the literature.

Pushpa Shivaram, Kavisha Shah, Amy Dossey, Brian Reemtsen, Robert H Anderson,

Bicuspidity of both the semilunar valves is rarely reported. We report the first ever case of bilateral bicuspid semilunar valves in a case of transposition. ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2019, 12(1):56-59]

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Abnormally increased carotid intima media-thickness and elasticity in patients with Morquio A disease.

Raymond Y Wang, Kyle D Rudser, Donald R Dengel, Nicholas Evanoff, Julia Steinberger, Nina Movsesyan, Robert Garrett, Katherine Christensen, Deborah Boylan, Stephen R Braddock, Marwan Shinawi, Qi Gan, Adriana M Montaño,

BACKGROUND:Cardiovascular disease frequently causes morbidity and mortality in mucopolysaccharidoses (MPS); however, cardiovascular anatomy and dysfunction in MPS IVA (Morquio A disease) is not well described. Consequently, the study aimed to compare carotid artery structure and elasticity of MPS IVA patients with other MPS patients and healthy control subjects, and quantitate ... Read more >>

Orphanet J Rare Dis (Orphanet journal of rare diseases)
[2020, 15(1):73]

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The science and art of aortic and/or pulmonary root translocation.

Supreet P Marathe, Sachin Talwar,

This review aims to present and compare different surgical techniques of root translocation of the great arteries except the Ross procedure. The historical aspects, technical considerations, and results are briefly elucidated. ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2020, 13(1):56-66]

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Hypoplastic Left Heart Syndrome: A New Paradigm for an Old Disease?

Paul Grossfeld, Shuyi Nie, Lizhu Lin, Lu Wang, Robert H Anderson,

Hypoplastic left heart syndrome occurs in up to 3% of all infants born with congenital heart disease and is a leading cause of death in this population. Although there is strong evidence for a genetic component, a specific genetic cause is only known in a small subset of patients, consistent ... Read more >>

J Cardiovasc Dev Dis (Journal of cardiovascular development and disease)
[2019, 6(1):]

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A novel, data-driven conceptualization for critical left heart obstruction.

James M Meza, Martijn Slieker, Eugene H Blackstone, Luc Mertens, William M DeCampli, James K Kirklin, Mohsen Karimi, Pirooz Eghtesady, Kamal Pourmoghadam, Richard W Kim, Phillip T Burch, Marshall L Jacobs, Tara Karamlou, Brian W McCrindle, ,

BACKGROUND:Qualitative features of aortic and mitral valvar pathology have traditionally been used to classify congenital cardiac anomalies for which the left heart structures are unable to sustain adequate systemic cardiac output. We aimed to determine if novel groups of patients with greater clinical relevance could be defined within this population ... Read more >>

Comput Methods Programs Biomed (Computer methods and programs in biomedicine)
[2018, 165:107-116]

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Isolation of the left brachiocephalic artery revisited: A 52-year literature review and introduction of a novel anatomic-clinical-prognostic classification.

Elaheh Malakan Rad, Hamid Reza Pouraliakbar,

Isolation of the left brachiocephalic artery (ILBA) is an extremely rare anomaly of aortic arch with diverse manifestations in the neurologic system, heart, and left upper arm. This anomaly is defined as the absence of connection of the left brachiocephalic artery (LBA) to aortic arch and connection of LBA to ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2019, 12(2):117-129]

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Progression of aortic root dilatation and aortic valve regurgitation after the arterial switch operation.

Roel L F van der Palen, Teun van der Bom, Annika Dekker, Roula Tsonaka, Nan van Geloven, Irene M Kuipers, Thelma C Konings, Lukas A J Rammeloo, Arend D J Ten Harkel, Monique R M Jongbloed, Dave R Koolbergen, Barbara J M Mulder, Mark G Hazekamp, Nico A Blom,

OBJECTIVE:To study neo-aortic growth and the evolution of neo-aortic valve regurgitation (AR) in patients with transposition of the great arteries (TGA) after arterial switch operation (ASO) from newborn to adulthood and to identify patients at risk. METHODS:Neo-aortic dimensions (annulus/root/sinotubular junction) and neo-aortic valve regurgitation were assessed serially in 345 patients ... Read more >>

Heart (Heart (British Cardiac Society))
[2019, 105(22):1732-1740]

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EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: Congenital left-sided heart obstruction.

Michelle Carr, Stephanie Curtis, Jan Marek,

Congenital obstruction of the left ventricular outflow tract remains a significant problem and multilevel obstruction can often coexist. Obstruction can take several morphological forms and may involve the subvalvar, valvar or supravalvar portion of the aortic valve complex. Congenital valvar stenosis presenting in the neonatal period represents a spectrum of ... Read more >>

Echo Res Pract (Echo research and practice)
[2018, 5(2):R23-R36]

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Anomalous Origin of Left Coronary Artery - an unusual case.

U Abbas, W Cossor,

Anomalies of the coronary arteries are rare but are an important cause of sudden cardiac arrest in young athletes. Sudden cardiac arrest has been reported in patients with congenital anomalies of the coronary arteries. We present a rare case of sudden cardiac arrest caused by anomalous left main coronary artery ... Read more >>

Images Paediatr Cardiol (Images in paediatric cardiology)
[2018, 20(2):1-4]

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Anomalous Fusion of Right Pulmonary Artery to Aortic Arch: Case Report of a Rare and Fatal Congenital Malformation in a Newborn and a Literature Review.

Cristian D'Ovidio, Lidia Decembrino, Mauro Stronati, Aldo Carnevale, Rossano Lattanzio,

BACKGROUND We present a report of a rare cardiac malformation case as well as a review of the literature. In addition, the diagnostic features are discussed. CASE REPORT The case of a female newborn who died on her third day of life was studied at the Institute of Legal Medicine, ... Read more >>

Am J Case Rep (The American journal of case reports)
[2018, 19:1416-1421]

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Position Statement on Indications of Echocardiography in Adults - 2019.

Silvio Henrique Barberato, Minna Moreira Dias Romano, Adenalva Lima de Souza Beck, Ana Clara Tude Rodrigues, André Luiz Cerqueira de Almeida, Bruna Morhy Borges Leal Assunção, Eliza de Almeida Gripp, Fabio Villaça Guimarães Filho, Henry Abensur, José Maria Del Castillo, Marcelo Haertel Miglioranza, Marcelo Luiz Campos Vieira, Márcio Vinicius Lins de Barros, Maria do Carmo Pereira Nunes, Maria Estefania Bosco Otto, Renato de Aguiar Hortegal, Rodrigo Bellio de Mattos Barretto, Thais Harada Campos, Vicente Nicoliello de Siqueira, Samira Saady Morhy,

Arq. Bras. Cardiol. (Arquivos brasileiros de cardiologia)
[2019, 113(1):135-181]

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Magnetic resonance imaging of the papillary muscles of the left ventricle: normal anatomy, variants, and abnormalities.

Prabhakar Rajiah, Nicholas Lim Fulton, Michael Bolen,

Left ventricular papillary muscles are small myocardial structures that play an important role in the functioning of mitral valve and left ventricle. Typically, there are two groups of papillary muscles, namely the anterolateral and the posteromedial groups. Cardiovascular magnetic resonance (CMR) is a valuable imaging modality in the evaluation of ... Read more >>

Insights Imaging (Insights into imaging)
[2019, 10(1):83]

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mDixon ECG-gated 3-dimensional cardiovascular magnetic resonance angiography in patients with congenital cardiovascular disease.

Soultana Kourtidou, Marty R Jones, Ryan A Moore, Justin T Tretter, Nicholas J Ollberding, Eric J Crotty, Mantosh S Rattan, Robert J Fleck, Michael D Taylor,

BACKGROUND:Cardiovascular magnetic resonance (CMR) angiography (CMRA) is an important non-invasive imaging tool for congenital heart disease (CHD) and aortopathy patients. The conventional 3D balanced steady-state free precession (bSSFP) sequence is often confounded by imaging artifacts. We sought to compare the respiratory navigated and electrocardiogram (ECG) gated modified Dixon (mDixon) CMRA ... Read more >>

J Cardiovasc Magn Reson (Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance)
[2019, 21(1):52]

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Congenital aortic stenosis: treatment outcomes in a nationwide survey.

Merja Kallio, Otto Rahkonen, Ilkka Mattila, Jaana Pihkala,

To evaluate treatment outcomes of pediatric valvar aortic stenosis (AS) in a nationwide follow-up.Balloon aortic valvuloplasty (BAV) has been the preferred treatment for congenital AS in Finland since the year 2000. All children treated due to isolated AS during 2000-2014 were included in this retrospective study. Treatment outcomes were categorized ... Read more >>

Scand. Cardiovasc. J. (Scandinavian cardiovascular journal : SCJ)
[2017, 51(5):277-283]

Cited: 2 times

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Congenital Pulmonary Artery Anomalies: A Review and Approach to Classification.

Leslie E Hirsig, Priya G Sharma, Nupur Verma, Dhanashree A Rajderkar,

Congenital pulmonary artery anomalies are infrequent but given improved prenatal diagnosis and care, and neonatal surgical advances, over the past two decades are not uncommonly encountered by cardiothoracic imagers. An understanding of their etiology, classifications, associated anomalies, and surgical management can be helpful to avoid under or overdiagnosis. Timely diagnosis ... Read more >>

J Clin Imaging Sci (Journal of clinical imaging science)
[2018, 8:29]

Cited: 1 time

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Estimating pressure gradients by auscultation: How technology (echocardiography) can help improve clinical skills.

Rohini L Kadle, Colin K L Phoon,

To extend our previously-published experience in estimating pressure gradients (PG) via physical examination in a large patient cohort.From January 1, 1997 through December 31, 2009, an attending pediatric cardiologist compared clinical examination (EXAM) with Doppler-echo (ECHO), in 1193 patients with pulmonic stenosis (PS, including tetralogy of Fallot), aortic stenosis (AS), ... Read more >>

World J Cardiol (World journal of cardiology)
[2017, 9(8):693-701]

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