Proposed diagnostic criteria for short QT syndrome are badly founded.
نویسنده
چکیده
account for the increase in both VF and acute HF risk in patients presenting with STE in lead V4R. The interventricular septum is nown to play an important role in arrhythmias after myocardial nfarction (1). Morita et al. (2) demonstrated that acute ischemia f the interventricular septum in canine cardiac wedge preparations roduced asymmetric suppression of conduction velocity in the eptum, and they suggested that such changes could contribute to he initiation of arrhythmia in patients with septal infarction. ore recently, Sicouri et al. (3) demonstrated that dispersion of epolarization across the interventricular septum in canine wedge reparations is twice that of the left ventricular free wall, predisosing to development of Torsades de Pointes arrhythmias. The elatively low incidence of the combined end point (primary VF, cute HF, or both) calls for caution in the interpretation of the esults, especially with regard to the multivariate analysis. Should ur findings be confirmed in a larger cohort, we would recommend hat right precordial leads be a routine part of the initial electroardiographic study in all patients with anterior STEMI.
منابع مشابه
Evaluation of QT interval duration and dispersion and proposed clinical criteria in diagnosis of long QT syndrome in patients with a genetically uniform type of LQT1.
OBJECTIVES This study investigated the ability of QT duration, QT dispersion (QTD) and clinical diagnostic criteria to correctly identify genetically documented LQT1 type long QT syndrome (LQTS) patients, and to separate symptomatic and asymptomatic LQT1 patients. BACKGROUND Ventricular repolarization has played an essential role both in diagnosis and risk assessment of LQTS. Today, molecular...
متن کاملThe Evolutionary Approach for Diagnostic Criteria of Polycystic Ovary Syndrome in Adolescents: a Review
p.p1 {margin: 0.0px 0.0px 0.0px 0.0px; text-align: justify; font: 12.0px 'Times New Roman'} span.s1 {text-decoration: underline} span.s2 {font: 11.0px Helvetica} Introduction: Polycystic ovary syndrome (PCOS) in adults is diagnosed based on clinical, biochemical, and radiological criteria, although in adolescents, some of these criteria may overlap with the normal process of puberty, which ...
متن کاملDiagnostic criteria for the long QT syndrome. An update.
T he idiopathic long QT syndrome (LQTS) is a congenital disease with frequent familial transmission, characterized primarily by prolongation of the QT interval and by the occurrence of life-threatening tachyarrhythmias, particularly in association with emotional or physical stress.1-5 Among untreated symptomatic patients, lethality is high, with 20% mortality in the first year after the initial...
متن کاملگزارش یک مورد سندرم ژرول- لانژنلسون
Long QT syndrome, which is defined by corrected QT interval longer than 0.45 seconds in men and o. 47 sec in women , could be divided into idiopathic (congenital ) and acquired forms. The idiopathic form is a familial disorder that can be associated with sensorineural deafness (Jervell and Lange- Neelson syndrome), which is transmitted with an autosomal recessive pattern. Although this syndrome...
متن کاملCongenital long QT syndrome
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias. Disease prevalence is estimated at close to 1 in 2,500 live births. The two cardinal manifestations of LQTS are syncopal episodes, that may lead to cardiac arrest and sudden cardiac death, and electrocardiographic ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Journal of the American College of Cardiology
دوره 58 5 شماره
صفحات -
تاریخ انتشار 2011