Sotalol testing unmasks altered repolarization in patients with suspected acquired long-QT-syndrome -: a case-control pilot study using i.v. sotalol

被引:87
作者
Kääb, S [1 ]
Hinterseer, M [1 ]
Näbauer, M [1 ]
Steinbeck, G [1 ]
机构
[1] Univ Munich, Klinikum Grosshadern, Dept Med 1, D-81366 Munich, Germany
关键词
long-QT syndrome; repolarization; Torsades de Pointes; risk factors; d; l-sotalol;
D O I
10.1016/S0195-668X(02)00806-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims The aim of this pilot study was to evaluate provocative sotalol testing to unmask abnormal repolarization due to altered myocardial electrical properties as the key feature in acquired Long-QT-Syndrome. Reliable diagnosis and risk stratification for the individual patient are complicated by the multitude of mechanisms involved in acquired QT-prolongation. The combined influence of all components determines susceptibility to arrhythmias related to QT-prolongation. Methods Twenty consecutive patients who had experienced torsades de pointes in association with QT-prolonging drugs were tested with i.v. d,l-sotatot (2 mg/kg) with 24-h intensive care monitoring to evaluate the repolarization process by determining QT- and QTc-prolongations. Results were compared to age and sex matched controls. Results At baseline, no differences between control and study population with regard to QT and QTc were detected. After sotalol infusion, QTc increased from 422 17 to 450+/-22 ms in controls and from 434+/-20 to 541+/-37 ms in the study population. Torsades de pointes occurred in three out of 20 patients (15%) in the study population but in none of the control patients following i.v. sotalol testing. Conclusions Controlled exposure to sotalol successfully identifies patients with normal QTc intervals but altered myocardial repolarization. This may be useful for clarifying diagnosis and pathogenesis of acquired Long-QT-Syndrome. (C) 2003 The European Society of Cardiology. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:649 / 657
页数:9
相关论文
共 34 条
[1]   MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia [J].
Abbott, GW ;
Sesti, F ;
Splawski, I ;
Buck, ME ;
Lehmann, WH ;
Timothy, KW ;
Keating, MT ;
Goldstein, SAN .
CELL, 1999, 97 (02) :175-187
[2]  
Bazett HC, 1920, HEART-J STUD CIRC, V7, P353
[3]   CANINE LEFT-VENTRICULAR HYPERTROPHY PREDISPOSES TO VENTRICULAR-TACHYCARDIA INDUCTION BY PHASE-2 EARLY AFTERDEPOLARIZATIONS AFTER ADMINISTRATION OF BAY-K-8644 [J].
BENDAVID, J ;
ZIPES, DP ;
AYERS, GM ;
PRIDE, HP .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1992, 20 (07) :1576-1584
[4]   BRADYCARDIA-DEPENDENT TRIGGERED ACTIVITY - RELEVANCE TO DRUG-INDUCED MULTIFORM VENTRICULAR-TACHYCARDIA [J].
BRACHMANN, J ;
SCHERLAG, BJ ;
ROSENSHTRAUKH, LV ;
LAZZARA, R .
CIRCULATION, 1983, 68 (04) :846-856
[5]   Congenital and acquired long QT syndrome [J].
Camm, AJ ;
Janse, MJ ;
Roden, DM ;
Rosen, MR ;
Cinca, J ;
Cobbe, SM .
EUROPEAN HEART JOURNAL, 2000, 21 (15) :1232-1237
[6]   Non-invasive testing of acquired long QT syndrome:: Evidence for multiple arrhythmogenic substrates [J].
Chevalier, P ;
Rodriguez, C ;
Bontemps, L ;
Miquel, M ;
Kirkorian, G ;
Rousson, R ;
Potet, F ;
Schott, JJ ;
Baró, I ;
Touboul, P .
CARDIOVASCULAR RESEARCH, 2001, 50 (02) :386-398
[7]  
Choy AM, 1997, CIRCULATION, V96, P2149
[8]   TIME FOR YET ANOTHER QT CORRECTION ALGORITHM - BAZETT AND BEYOND [J].
FRANZ, MR .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1994, 23 (07) :1554-1556
[9]  
Fridericia LS., 1920, Acta Med Scand, V53, P469, DOI DOI 10.1111/J.0954-6820.1920.TB18266.X
[10]   Safety and effectiveness of dofetilide for conversion of atrial fibrillation and nesiritide for acute decompensation of heart failure - A report from the Cardiovascular and Renal Advisory Panel of the Food and Drug Administration [J].
Grines, CL .
CIRCULATION, 2000, 101 (21) :E200-E201