نتایج جستجو برای: secundum type atrial septal defect asd

تعداد نتایج: 1514125  

2014
Zine el abidine Benali Hatim Abdedaim

Atrial septal defect (ASD) is characterized by a defect in the interatrial septum allowing pulmonary venous return from the left atrium to pass directly to the right atrium. ASD account for 10% of all congenital heart disease, and as much as 30 % of congenital heart disease presenting in adulthood. There are four types of ASD that can be recognized as the seat of the port: ostium secundum, the ...

Journal: :the journal of tehran university heart center 0
mohammad sahebjam tehran heart center, tehran university of medical sciences, tehran, iran. reyhaneh zavar tehran heart center, tehran university of medical sciences, tehran, iran. masoumeh lotfi-tokaldany tehran heart center, tehran university of medical sciences, tehran, iran. hakimeh sadeghian tehran heart center, tehran university of medical sciences, tehran, iran. arezou zoroufian tehran heart center, tehran university of medical sciences, tehran, iran.

background: given the dearth of data in the existing literature on the size and morphologic variability of secundum-type atrial-septal defect (asd-ii) in adult patients, we aimed to address this issue in a series of consecutive adult patients evaluated by transesophageal echocardiography (tee). methods: a total of 50 patients (68.0% female) with isolated asd-ii underwent tee for the evaluation ...

Journal: :the journal of tehran university heart center 0
maryam esmaeilzadeh shaheed rajaei cardiovascular medical and research center, tehran, iran. azadeh sadatnaseri sina general hospital, tehran university of medical sciences, tehran, iran. feridoun noohi shaheed rajaei cardiovascular medical and research center, tehran, iran. majid maleki shaheed rajaei cardiovascular medical and research center, tehran, iran. anita sadeghpour shaheed rajaei cardiovascular medical and research center, tehran, iran. ahmad mohebbi shaheed rajaei cardiovascular medical and research center, tehran, iran.

background: there is some evidence indicating improvement in myocardial performance after atrial septal defect closure, either device closure or surgical, but ventricular dyssynchrony has not been evaluated before and after surgical closure. the aim of this study was to evaluate ventricular mechanical dyssynchrony in patients with atrial septal defect before and after surgical closure. methods:...

Journal: :Acta Cardiologica Sinica 2013
Kuan-Miao Lin Chi-Di Liang Shao-Ju Chien Ying-Jui Lin I-Chun Lin Mao-Hung Lo Ting-Hsin Wu Chien-Fu Huang

PUPOSE To determine predictive factors of spontaneous closure or size reduction in large secundum-type atrial septal defects (ASD) diagnosed in infancy prior to catheterization or surgical intervention. METHODS From June 2003 to October 2009, 59 infants diagnosed with secundum-type ASDs measuring ≥ 8 mm in the first year of life were retrospectively enrolled. We reviewed medical records, as w...

Journal: :Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia 2001
S Aoyagi H Kawano H Tomoeda R Hiratsuka T Kawara

A 9-year-old girl who had ostium secundum atrial septal defect (ASD) and hereditary spherocytosis (HS) is described. The patient had a history of splenectomy for HS and underwent repair of the ASD under cardiopulmonary bypass (CPB), however, no significant or persistent hemolysis was observed during and after CPB. Only 10 patients with HS who underwent cardiac operations using CPB have been rep...

Journal: :Turk Kardiyoloji Dernegi arsivi : Turk Kardiyoloji Derneginin yayin organidir 2010
Selçuk Pala Göksel Açar Kürşat Tigen Cevat Kırma

Percutaneous closure of secundum atrial septal defects (ASD) may be complicated by immediate embolization. We report on a 35-year-old woman who underwent percutaneous device closure for a secundum ASD. The diameter of the defect was measured as 4 mm by two-dimensional transesophageal echocardiography and a 7-mm Figulla ASD occluder device was implanted without prior balloon sizing of the defect...

2011
Eun Kyoung Kim Sang Chol Lee Sung Bum Park Silvia Park Sunha Bahng Yeon Hyeon Choe Kiick Sung

We report a case of a 46-year-old woman who presented with subacute exertional dyspnea and severe hypoxia. A large cystic mass compressing the right side of the heart along with right-to-left atrial shunt flow through an alleged atrial septal defect (ASD) were detected on echocardiography. CT scan of the chest and MRI of the heart revealed a loculated cystic mediastinal mass with hemorrhage mea...

Journal: :Journal of the Formosan Medical Association = Taiwan yi zhi 2007
Shan-Miao Lin Haw-Kwei Hwang Ming-Ren Chen

Percutaneous transcatheter atrial septal defect (ASD) closure is a widely used technique that has replaced open-heart surgical closure in many centers. The most common implant is the Amplatzer septal occluder which seems to be a highly effective and safe device. However, there are reports of complications associated with its implantation. We report a 9-year-old boy who presented with complete a...

2011
Mi Jin Cho Jinyoung Song Soo Jin Kim Eun Young Choi Sang Yoon Lee Woo Seup Shim

Percutaneous device occlusion of secundum atrial septal defect (ASD) has become an accepted alternative to surgical repair. A variety of devices have been used successfully. However, all of them have limitations. We report our experience with two devices used to close multiple ASDs.

2017
Shunsuke Tatebe Koichiro Sugimura Tatsuo Aoki Saori Yamamoto Nobuhiro Yaoita Hideaki Suzuki Haruka Sato Katsuya Kozu Ryo Konno Kimio Satoh Koji Fukuda Osamu Adachi Ryoko Saito Norifumi Nakanishi Hiroko Morisaki Kotaro Oyama Yoshikatsu Saiki Yoshinori Okada Hiroaki Shimokawa

Severe pulmonary arterial hypertension (PAH) rarely develops in children with an atrial septal defect (ASD), even those with a large defect. We herein report the case of a 27-year-old man with a moderate-sized secundum ASD and right ventricular failure due to severe PAH, which developed in his early teens. He was diagnosed as having a genetic mutation of the bone morphogenetic protein receptor-...

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