نتایج جستجو برای: asd secundum

تعداد نتایج: 10741  

Journal: :Egyptian Journal of Radiology and Nuclear Medicine 2023

Abstract Background The coexisting of transposition the great arteries (TGA) with total anomalous pulmonary venous connection (TAPVC) is one rare anomalies. incidence TAPVC and TGA unknown very few cases ever reported. Case presentation We reported a case 13-month-old female toddler history cyanosis. Echocardiography revealed atrioventricular ambiguity atresia, all PVs drain into innominate vei...

Journal: :Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography 2001
M Saric R M Applebaum C K Phoon E S Katz S A Goldstein P A Tunick I Kronzon

BACKGROUND The pulmonary venous flow velocity pattern (PVFVP) in atrial septal defect (ASD) has not been previously studied in detail. Normally, PVFVP is primarily determined by the left heart performance. We hypothesized that the impact of left-sided heart dynamics on PVFVP is diminished in patients with ASD because of the presence of a left-to-right shunt into the low-resistance right side of...

2017
Sigurdur S Stephensen Katarina Steding-Ehrenborg Ulf Thilén Johan Holm Peter Hochbergs Hakan Arheden Marcus Carlsson

Background The purpose of this study was to determine the effect of stress on left-to-right shunting in patients with atrial septal defect (ASD) and to investigate if the degree of shunting, cardiac output (CO), and right ventricular (RV) volumes are related to exercise capacity. Methods Twenty-six patients with a secundum ASD and 16 healthy volunteers were studied with rest/stress cardiac ma...

2011
Mostafa Behjati Sayed-Jalil Mirhosseini Saiyed-Habibollah Hosseini Shahrokh Rajaei

OBJECTIVE Transcatheter closure of secundum atrial septal defect (ASD) with Amplatzer device is an alternative procedure to surgical repair, with some limitations. The aim of this study was to assess the initial and mid-term results of the treatment of ASD with Amplatzer septal occluder in children and adolescents. METHODS From May 2003 to January 2008 sixty three consecutive children and ado...

Journal: :RA journal of applied research 2021

ASD and more frequently the ostium secundum type is a relatively common adult congenital heart disease. Sjogren’s syndrome on other side second most frequent auto immune disease, Involving lungs in 9–20% of patients. We report case 69 years old woman, complaining long-standing dyspnea was diagnosed with syndrom. Her CT scan pulmonary function tests were normal. That lead to investigate for hype...

Journal: :Journal of the American College of Cardiology 2004
Alessandro Giardini Andrea Donti Roberto Formigari Salvatore Specchia Daniela Prandstraller Gabriele Bronzetti Marco Bonvicini Fernando M Picchio

OBJECTIVES We sought to evaluate the course of cardiopulmonary function after transcatheter atrial septal defect (ASD) closure and to identify the physiopathologic mechanisms leading to this change. BACKGROUND Conflicting reports exist on cardiopulmonary functional improvement in asymptomatic adults after transcatheter closure of a secundum ASD. METHODS Thirty-two consecutive adults (13 mal...

2004
Ta-Cheng Huang Cheng-Liang Lee Chu-Chun Lin Kai-Sheng Hsieh

Objective: To assess the short-term outcome following transcatheter closure of secundum atrial septal defect (ASD) in our hospital. Patients and Methods: Between June 2000 and November 2001, 20 patients diagnosed as secundum atrial septal defects underwent transcatheter closure of their defects using the Amplatzer septal occluder (ASO) device. Indications for 18 patients were larger atrial sept...

2014
Bijun Zhao Yuan Lin Jing Xu Bixian Ni Min Da Chenyue Ding Yuanli Hu Kai Zhang Shiwei Yang Xiaowei Wang Shiqiang Yu Yijiang Chen Xuming Mo Jiayin Liu Hongbing Shen Jiahao Sha Hongxia Ma

Congenital heart disease (CHD) is the most common form of congenital human birth anomalies and a leading cause of perinatal and infant mortality. Some studies including our published genome-wide association study (GWAS) of CHD have indicated that genetic variants may contribute to the risk of CHD. Recently, Cordell et al. published a GWAS of multiple CHD phenotypes in European Caucasians and id...

2016
Doff B. McElhinney Elizabeth Geiger Elizabeth Goldmuntz

OBJECTIVES The purpose of this study was to estimate the frequency of NKX2.5 mutations in specific cardiovascular anomalies and investigate genotype-phenotype correlations in individuals with NKX2.5 mutations. BACKGROUND Recent reports have implicated mutations in the transcription factor NKX2.5 as a cause of various congenital heart defects (CHD). METHODS We tested genomic deoxyribonucleic aci...

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