Full Text Journal Articles about
Tetralogy of Fallot With Absent Pulmonary Valve

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Unusually abnormal vessels in tetralogy of Fallot with absent pulmonary valve.

M Saito, T Ishii, Y Hamamichi,

Ultrasound Obstet Gynecol (Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology)
[2020, 55(3):417-419]

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The role of primary surgical repair technique on late outcomes of Tetralogy of Fallot: a multicentre study.

Massimo A Padalino, Nicola Pradegan, Danila Azzolina, Lorenzo Galletti, Carlo Pace Napoleone, Salvatore Agati, Gaetano Palma, Stefano Maria Marianeschi, Francesco Seddio, Maria Teresa Cascarano, Cristina Carro, Dario Gregori, Vladimiro Lorenzo Vida, Giovanni Stellin,

OBJECTIVES:Repair of Tetralogy of Fallot (TOF) has currently excellent results with either transventricular or transatrial approach. However, it is unclear as to which has better late outcomes and what role of residual pulmonary valve (PV) regurgitation in the long term is. We report on late clinical outcomes after repair in ... Read more >>

Eur J Cardiothorac Surg (European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery)
[2020, 57(3):565-573]

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Quantification of Initial Right Ventricular Dimensions by Computed Tomography in Infants with Congenital Heart Disease and a Hypoplastic Right Ventricle.

Hyun Woo Goo,

OBJECTIVE:To demonstrate the feasibility of using cardiothoracic CT for quantification of the initial right ventricle (RV) dimensions in infants with congenital heart disease (CHD) and a hypoplastic RV and to compare these measurements with those obtained in a control group with CHD without a hypoplastic RV. MATERIALS AND METHODS:Initial RV ... Read more >>

Korean J Radiol (Korean journal of radiology)
[2020, 21(2):203-209]

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Iron-deficiency anaemia in children with congenital heart diseases at a teaching hospital in Ghana.

Inna Ossei, Kwame Ohene Buabeng, Paul Poku Sampene Ossei, Samuel Blay Nguah, William Gilbert Ayibor, Berko Panyin Anto, Agyemang-Duah Eric, Mahama Duwiejua,

Background:Uncorrected congenital heart lesions in children keep them in a state of constant hypoxia with compromised quality of life and reduced life expectancy. This requires early diagnosis and interventions including prevention and treatment of the resultant anaemia. Unfortunately, congenital heart disease (CHD) often goes unrecognized and thus untreated. Objectives:We determined ... Read more >>

Heliyon (Heliyon)
[2020, 6(2):e03408]

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Long-term follow-up after transatrial-transpulmonary repair of tetralogy of Fallot: influence of timing on outcome.

Eva van den Bosch, Ad J J C Bogers, Jolien W Roos-Hesselink, Arie P J van Dijk, Marie H E J van Wijngaarden, Eric Boersma, Aagje Nijveld, Linda W G Luijten, Ronald Tanke, Laurens P Koopman, Willem A Helbing,

OBJECTIVES:Our goal was to report the long-term serial follow-up after transatrial-transpulmonary repair of tetralogy of Fallot (TOF) and to describe the influence of the timing of the repair on outcome. METHODS:We included all patients with TOF who had undergone transatrial-transpulmonary repair between 1970 and 2012. Records were reviewed for patient ... Read more >>

Eur J Cardiothorac Surg (European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery)
[2020, 57(4):635-643]

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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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Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing.

Xin Shi, Li Zhang, Kai Bai, Huilin Xie, Tieliu Shi, Ruilin Zhang, Qihua Fu, Sun Chen, Yanan Lu, Yu Yu, Kun Sun,

Pulmonary atresia (PA) is a rare congenital heart defect (CHD) with complex manifestations and a high mortality rate. Since the genetic determinants in the pathogenesis of PA remain elusive, a thorough identification of the genetic factors through whole exome sequencing (WES) will provide novel insights into underlying mechanisms of PA. ... Read more >>

Comput Struct Biotechnol J (Computational and structural biotechnology journal)
[2020, 18:381-392]

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Long-Term Comparison Between Pulmonary Homograft Versus Bioprosthesis for Pulmonary Valve Replacement in Tetralogy of Fallot.

Lucia Cocomello, Marco Meloni, Filippo Rapetto, Mai Baquedano, Maria Victoria Ordoñez, Giovanni Biglino, Chiara Bucciarelli-Ducci, Andrew Parry, Serban Stoica, Massimo Caputo,

Background Tetralogy of Fallot repair results in late occurrence of pulmonary regurgitation, which requires pulmonary valve replacement in a large proportion of patients. Both homografts and bioprostheses are used for pulmonary valve replacement as uncertainty remains on which prosthesis should be considered superior. We performed a long-term imaging and clinical ... Read more >>

J Am Heart Assoc (Journal of the American Heart Association)
[2019, 8(24):e013654]

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Functional characterisation of a novel PBX1 de novo missense variant identified in a patient with syndromic congenital heart disease.

Dimuthu Alankarage, Justin O Szot, Nick Pachter, Anne Slavotinek, Licia Selleri, Joseph T Shieh, David Winlaw, Eleni Giannoulatou, Gavin Chapman, Sally L Dunwoodie,

PBX1 is an essential developmental transcription factor, mutations in which have recently been associated with CAKUTHED syndrome, characterised by multiple congenital defects including congenital heart disease. During analysis of a whole-exome-sequenced cohort of heterogeneous CHD patients, we identified a de novo missense variant, PBX1:c.551G>C p.R184P, in a patient with tetralogy ... Read more >>

Hum. Mol. Genet. (Human molecular genetics)
[2019, :]

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Multi-detector computed tomography angiographic evaluation of right ventricular outflow tract obstruction and other associated cardiovascular anomalies in tetralogy of Fallot patients.

Rani Kunti R Singh, Neeraj Jain, Sunil Kumar, Naveen Garg,

Purpose:To evaluate various types of right ventricular outflow tract obstruction associated with tetralogy of Fallot (TOF) with emphasis on the abnormality of pulmonary arterial system and other associated cardiovascular anomalies using computed tomography (CT) angiography. Material and methods:We retrospectively evaluated 184 consecutive previously diagnosed TOF patients who underwent CT angiography ... Read more >>

Pol J Radiol (Polish journal of radiology)
[2019, 84:e511-e516]

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Current era outcomes of pulmonary atresia with ventricular septal defect: A single center cohort in Thailand.

Kanthalas Lertsakulpiriya, Chodchanok Vijarnsorn, Prakul Chanthong, Paweena Chungsomprasong, Supaluck Kanjanauthai, Kritvikrom Durongpisitkul, Jarupim Soongswang, Thaworn Subtaweesin, Somchai Sriyoschati,

Pulmonary atresia with ventricular septal defect (PA/VSD) is a complex cyanotic congenital heart disease with a wide-range of presentations and treatment strategies, depending on the source of pulmonary circulation, anatomy of pulmonary arteries (PAs), and major aortopulmonary collateral arteries (MAPCAs). Data about the outcomes in developing countries is scarce. We ... Read more >>

Sci Rep (Scientific Reports)
[2020, 10(1):5165]

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Diagnosis and treatment of abnormal left coronary artery originating from the pulmonary artery: A single-center experience.

Kahraman Yakut, Niyazi Kursad Tokel, Murat Ozkan, Birgul Varan, Ilkay Erdogan, Mehmet Sait Aslamaci,

OBJECTIVE:We aimed to review symptoms, findings, surgical treatment options, short- and mid-term outcomes, and reoperation rate of patients diagnosed with of left coronary artery from the pulmonary artery (ALCAPA) of an anomalous origin in our institution. METHODS:From May 2000 to March 2018, 33 patients who had left coronary artery originating ... Read more >>

Anatol J Cardiol (Anatolian journal of cardiology)
[2019, 22(6):325-331]

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Genetics of Congenital Heart Disease.

Kylia Williams, Jason Carson, Cecilia Lo,

Congenital heart disease (CHD) is one of the most common birth defects. Studies in animal models and humans have indicated a genetic etiology for CHD. About 400 genes have been implicated in CHD, encompassing transcription factors, cell signaling molecules, and structural proteins that are important for heart development. Recent studies ... Read more >>

Biomolecules (Biomolecules)
[2019, 9(12):]

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Counseling for Prenatal Congenital Heart Disease-Recommendations Based on Empirical Assessment of Counseling Success.

Alexander Kovacevic, Andreas Simmelbauer, Sebastian Starystach, Michael Elsässer, Andreas Müller, Stefan Bär, Matthias Gorenflo,

Objectives: Empirical assessment of parental needs and affecting factors for counseling success after prenatal diagnosis of congenital heart disease (CHD). Methods:Counseling success after fetal diagnosis of CHD was assessed by a validated standardized questionnaire. The dependent variable "Effective Counseling" was measured in five created analytical dimensions (1. "Transfer of Medical ... Read more >>

Front Pediatr (Frontiers in Pediatrics)
[2020, 8:26]

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Pregnancy outcomes among 31 patients with tetralogy of Fallot, a retrospective study.

Kana Wang, Junguo Xin, Xiaodong Wang, Haiyan Yu, Xinghui Liu,

BACKGROUND:Tetralogy of Fallot (TOF) is a severe type of congenital heart disease (CHD) and it confers substantial risk to mother and fetus for pregnant women. However, the outcome of pregnancy in women with TOF has not been well studied. METHODS:Women with TOF who have been seen and/or delivered at our ... Read more >>

BMC Pregnancy Childbirth (BMC pregnancy and childbirth)
[2019, 19(1):486]

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Pregnancy in Women with Complex Congenital Heart Disease. A Constant Challenge.

Walkiria Samuel Avila, Veronica Martins Ribeiro, Eduardo Giusti Rossi, Maria Angelica Binotto, Maria Rita Bortolotto, Carolina Testa, Rossana Francisco, Ludhmilla Abraão Hajjar, Nana Miura,

BACKGROUND:The improvement in surgical techniques has contributed to an increasing number of childbearing women with complex congenital heart disease (CCC). However, adequate counseling about pregnancy in this situation is uncertain, due to a wide variety of residual cardiac lesions. OBJECTIVES:To evaluate fetal and maternal outcomes in pregnant women with CCC ... Read more >>

Arq. Bras. Cardiol. (Arquivos brasileiros de cardiologia)
[2019, 113(6):1062-1069]

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A PTPN11 mutation in a woman with Noonan syndrome and protein-losing enteropathy.

Na Wang, Wen Shi, Yang Jiao,

BACKGROUND:Noonan syndrome is an autosomal dominant, variably expressed multisystem disorder characterized by specific facial and cardiac defects, delayed growth, ectodermal abnormalities, and lymphatic dysplasias. Lymphedema and chylous pleural effusions are common in Noonan syndrome, but protein-losing enteropathy (PLE) has only rarely been described in the condition and little is known ... Read more >>

BMC Gastroenterol (BMC gastroenterology)
[2020, 20(1):34]

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Diagnosis and management of congenital absence of pericardium: a case report.

Melissa Bouchard, A Hoschtitzky, M Gatzoulis,

Background:Absence of the pericardium is a rare congenital defect with an approximate incidence of <1/10 000. We review a case of complete pericardial agenesis in a symptomatic patient with gross cardiac mobility, for which pericardial reconstruction was undertaken successfully. Case summary:A 24-year-old otherwise fit and well patient, with debilitating exertional chest ... Read more >>

Eur Heart J Case Rep (European Heart Journal: Case Reports)
[2019, 3(4):1-5]

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Guidelines for Cardiovascular Magnetic Resonance Imaging from the Korean Society of Cardiovascular Imaging-Part 2: Interpretation of Cine, Flow, and Angiography Data.

Jae Wook Lee, Jee Hye Hur, Dong Hyun Yang, Bae Young Lee, Dong Jin Im, Su Jin Hong, Eun Young Kim, Eun Ah Park, Yeseul Jo, JeongJae Kim, Chul Hwan Park, Hwan Seok Yong,

Cardiovascular magnetic resonance imaging (CMR) is expected to be increasingly used in Korea due to technological advances and the expanded national insurance coverage of CMR assessments. For improved patient care, proper acquisition of CMR images as well as their accurate interpretation by well-trained personnel are equally important. In response to ... Read more >>

Korean J Radiol (Korean journal of radiology)
[2019, 20(11):1477-1490]

Cited: 1 time

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Pulmonary artery aneurysm: a review.

Mridul Gupta, Abhinav Agrawal, Annamaria Iakovou, Stuart Cohen, Rakesh Shah, Arunabh Talwar,

Pulmonary artery aneurysm is a rare but important entity in the spectrum of pulmonary vascular diseases. The etiologies can be varied and patients can present with non-specific symptoms with the diagnosis being incidental. There is limited consensus regarding the diagnostic criteria and follow-up imaging for patients diagnosed with this entity. ... Read more >>

Pulm Circ (Pulmonary Circulation)
[2020, 10(1):2045894020908780]

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Severe thrombocytopenia in tetralogy of Fallot patients: A contraindication for corrective surgery?

Suraj Patil, Jay Relan, Milind Hote, Shyam Sunder Kothari,

A 3-year-old boy with tetralogy of Fallot and recurrent cyanotic spells was found to have severe thrombocytopenia with platelet counts in the range of 11-30,000/mm3. There was a hesitation to operate in view of the high bleeding risk due to profound thrombocytopenia. However, the total correction was done after excluding ... Read more >>

Ann Pediatr Cardiol (Annals of pediatric cardiology)
[2019, 12(3):305-307]

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Pregnancy in non-palliated functionally single ventricle: challenges of management in resource-poor settings.

Desrie Delsol-Gyan, Ernest Aniteye, Samuel Oppong, Ernest Ofosu-Appiah, Frank Edwin,

Women with complex functionally univentricular hearts rarely survive into adulthood without corrective or palliative surgery. Reports of pregnancy outcome in this group of patients in resource-poor settings are sparse. We report a case of unrepaired pulmonary atresia ventricular septal defect (VSD) with major aorto-pulmonary collateral arteries (MAPCA) who survived into ... Read more >>

Pan Afr Med J (The Pan African medical journal)
[2020, 35:6]

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A rare case of adult congenital heart disease: single ventricular chamber with anomalous right coronary artery in an octogenarian.

Muhammad Shabbir Rawala, Amna Saleem Ahmed, Syed Bilal Rizvi,

Patients with single-ventricle physiology encompass a wide array of anatomic subtypes, including but not limited to: tricuspid atresia, hypoplastic left heart syndrome, double-outlet or double-inlet ventricles. The outcomes for patients with single ventricle born before 1990 are relatively poor. An 81-year-old female presented to the hospital as non-ST elevation myocardial ... Read more >>

J Community Hosp Intern Med Perspect (Journal of community hospital internal medicine perspectives)
[2019, 9(5):446-448]

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A unique variant of a right persistent hypoglossal artery arising from the common carotid artery with complex cardiovascular anomalies in a female neonatal patient.

Paul A Miller, Kerby C Oberg, Alex Sun, Adina Achiriloaie,

Persistent primitive hypoglossal artery is a carotid-vertebrobasilar anastomosis, which commonly arises from the internal carotid artery at the level of the C (cervical) 1-3 vertebrae. We describe a unique case of a female infant patient with this anomaly that has an unusually low origin from the distal common carotid artery ... Read more >>

J Radiol Case Rep (Journal of radiology case reports)
[2019, 13(9):28-35]

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A Rare Case of Isolated Unilateral Atresia of Pulmonary Artery in an Elderly Female.

Qurat Ul Ain, Omair A Khan, Mahnoor Sherazi, Mirza Faris Ali Baig, Fakeha Siddiqui,

Isolated unilateral agenesis/atresia of pulmonary artery (IUAPA) is a rare congenital disorder, an uncommon variant of unilateral agenesis of pulmonary artery (UAPA). Patients with IUAPA may remain asymptomatic and undiagnosed till late adulthood as they present with vague symptoms which may be overlooked. We report a case of IUAPA of ... Read more >>

Cureus (Cureus)
[2019, 11(10):e5869]

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