نتایج جستجو برای: long qt سندرم

تعداد نتایج: 790950  

2011
Ji Hun Ahn Sang-Ho Park Won Yong Shin Se Whan Lee Seung Jin Lee Dong Kyu Jin Han Min Lee Jun Young Eun

Prolongation of QTc interval associated with Takotsubo cardiomyopathy (TC) has previously been reported in published case series. We report an unusual case of a patient who presented with TC associated with long-QT syndrome and developed cardiac arrest secondary to torsade de pointes. Since QT prolongation and bradycardia persisted after the resolution of TC, the patient received permanent pace...

Journal: :Circulation. Arrhythmia and electrophysiology 2012
Andrew D Krahn Jeffrey S Healey Vijay S Chauhan David H Birnie Jean Champagne Shubhayan Sanatani Kamran Ahmad Emily Ballantyne Brenda Gerull Raymond Yee Allan C Skanes Lorne J Gula Peter Leong-Sit George J Klein Michael H Gollob Christopher S Simpson Mario Talajic Martin Gardner

BACKGROUND Epinephrine infusion may unmask latent genetic conditions associated with cardiac arrest, including long-QT syndrome and catecholaminergic polymorphic ventricular tachycardia (VT). METHODS AND RESULTS Patients with unexplained cardiac arrest (normal left ventricular function and QT interval) and selected family members from the Cardiac Arrest Survivors with Preserved Ejection Fract...

Journal: :Circulation 1998
E J Rashba W Zareba A J Moss W J Hall J Robinson E H Locati P J Schwartz M Andrews

BACKGROUND The effects of pregnancy on women with the hereditary long QT syndrome are currently unknown. The appropriate medical management of pregnant patients with the long QT syndrome has not been established. METHODS AND RESULTS The study was a retrospective analysis of the 422 women (111 probands affected with the long QT syndrome and 311 first-degree relatives) enrolled in the long QT s...

Journal: :Archives of disease in childhood 1979
D P Southall W A Arrowsmith J R Oakley G McEnery R H Anderson E A Shinebourne

Two neonates with arrhythmias and the long QT syndrome are described. The arrhythmias were detected in utero and both infants were apparently well after birth. The first infant, although well, had a bradycardia for the first 9 days of life. A normal heart rate was documented at 10 days but a prolonged QT interval was not appreciated on the ECG. He was discharged from hospital but died suddenly ...

Journal: :emergency journal 0
majid zamani mehrdad esmailian isfahan university of medical sciences zahra yoosefian

introduction: prolongation of qt interval might result in dangerous cardiac arrhythmias, including torsades de pointes (tdp), consequently leading to syncope or death. a limited number of studies carried out in this respect to date have shown that qt interval might increase during pregnancy. on the other hand, it has been shown that each pregnancy might result in an increase in the risk of card...

Journal: :Journal of the American College of Cardiology 2007
Andrew J Sauer Arthur J Moss Scott McNitt Derick R Peterson Wojciech Zareba Jennifer L Robinson Ming Qi Ilan Goldenberg Jenny B Hobbs Michael J Ackerman Jesaia Benhorin W Jackson Hall Elizabeth S Kaufman Emanuela H Locati Carlo Napolitano Silvia G Priori Peter J Schwartz Jeffrey A Towbin G Michael Vincent Li Zhang

OBJECTIVES The aims of this study were: 1) to evaluate risk factors influencing the clinical course of mutation-confirmed adult patients with long QT syndrome (LQTS), 2) to study life-threatening cardiac events as a specific end point in adults, and 3) to examine the protective effect of beta-blocker therapy on cardiac events in adult LQTS patients with known cardiac channel mutations. BACKGR...

2007

he advent of genetic testing and the implantable ardioverter-defibrillator (ICD) have so revolutionized the utlook for patients with long QT that the cardiac commuity needs to revise its thinking about long QT syndrome LQTS). This is the underlying message of a report by theridge et al. (1) in this issue of the Journal. Etheridge et al. (1) studied 128 children with LQTS. bout one-half of their...

2016
Myriam Berthet Nawal Benammar

OBJECTIVES We hypothesized that neonatal long QT syndrome (LQTS) with 2:1 atrioventricular block (AVB) could be related to HERG mutations. BACKGROUND Early onset of LQTS is rare but carries a high risk of life-threatening events such as ventricular arrhythmias and conduction disorders. There are no data on possible gene specificity. METHODS We analyzed the characteristics and outcomes of 23 neo...

Journal: :Journal of the American College of Cardiology 1984

Journal: :The Korean Journal of Pain 2018

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