A 22-year-old female suffering from idiopathic long-QT syndrome complicated by frequent syncope, torsade-de-pointes-type ventricular tachycardia, and asthma, was successfully treated by video-assisted extensive left second and third thoracic sympathetic ganglionectomy, instead of left stellate and first thoracic ganglio-nectomy, to avoid postoperative Horner’s syndrome. The QT interval was significantly shortened from 0.6 to 0.43 seconds four days after the surgery. It remained at 0.43 seconds during a 3-month follow-up with no recurrence of tachycardia or syncope. (Asian Cardiovasc Thorac Ann 2000;8:52–3
Background - The management of long-QT syndrome (LQTS) patients who continue to have cardiac events ...
Sindroma pemanjangan QT (Long QT syndrome) diakibatkan oleh defek genetik, merupakan kasus jarang, ...
OBJECTIVES: We sought to compare the arrhythmic risk and sensitivity to sympathetic stimulation of m...
The feasibility, safety, and effectiveness of video-assisted thoracoscopic sympathectomy (VATS) for ...
To assess the feasibility, safety and effectiveness of video-assisted thoracoscopic sympathectomy (V...
Background. The purpose of this study was to assess the feasibility and long-term effect of video-as...
The primary aim of the present study was to investigate the short-term effects of surgical left card...
Congenital long QT syndrome (LQTS) is a rare genetic disorder that has been associated with various ...
Long QT syndrome (LQTS) is a potentially fatal cardiac disorder caused by channelopathies. Such arrh...
Background A significant shortening of the corrected QT interval (QTc) in addition to parasympatheti...
Congenital long QT syndrome (LQTS) is a disorder of prolonged cardiac repolarisation, manifest by a ...
BackgroundWe reported the outcomes of a single-institution experience using video-assisted thoracosc...
BACKGROUND Thoracoscopic sympathicotomy was, at first, thought to be a simple and safe method for tr...
ABSTRACT During the past 4 years 196 patients with the idiopathic long QT syndrome were enrolled in ...
Long QT syndrome (LQTS) is a rare congenital and inherited or acquired heart condition in which dela...
Background - The management of long-QT syndrome (LQTS) patients who continue to have cardiac events ...
Sindroma pemanjangan QT (Long QT syndrome) diakibatkan oleh defek genetik, merupakan kasus jarang, ...
OBJECTIVES: We sought to compare the arrhythmic risk and sensitivity to sympathetic stimulation of m...
The feasibility, safety, and effectiveness of video-assisted thoracoscopic sympathectomy (VATS) for ...
To assess the feasibility, safety and effectiveness of video-assisted thoracoscopic sympathectomy (V...
Background. The purpose of this study was to assess the feasibility and long-term effect of video-as...
The primary aim of the present study was to investigate the short-term effects of surgical left card...
Congenital long QT syndrome (LQTS) is a rare genetic disorder that has been associated with various ...
Long QT syndrome (LQTS) is a potentially fatal cardiac disorder caused by channelopathies. Such arrh...
Background A significant shortening of the corrected QT interval (QTc) in addition to parasympatheti...
Congenital long QT syndrome (LQTS) is a disorder of prolonged cardiac repolarisation, manifest by a ...
BackgroundWe reported the outcomes of a single-institution experience using video-assisted thoracosc...
BACKGROUND Thoracoscopic sympathicotomy was, at first, thought to be a simple and safe method for tr...
ABSTRACT During the past 4 years 196 patients with the idiopathic long QT syndrome were enrolled in ...
Long QT syndrome (LQTS) is a rare congenital and inherited or acquired heart condition in which dela...
Background - The management of long-QT syndrome (LQTS) patients who continue to have cardiac events ...
Sindroma pemanjangan QT (Long QT syndrome) diakibatkan oleh defek genetik, merupakan kasus jarang, ...
OBJECTIVES: We sought to compare the arrhythmic risk and sensitivity to sympathetic stimulation of m...