Milne J R, Hellestrand K J, Bexton R S, Burnett P J, Debbas N M, Camm A J
Eur Heart J. 1984 Feb;5(2):99-107. doi: 10.1093/oxfordjournals.eurheartj.a061633.
Class 1 antiarrhythmic drugs have been subdivided into 1a, 1b and 1c according to their effect on the action potential duration. The effects on the surface electrocardiogram of one drug from each subgroup were investigated in nine patients. Electrocardiographic recordings were taken during sinus rhythm and at identical atrial and ventricular paced rates. Disopyramide (1a) significantly prolonged the QT interval during sinus rhythm and at the identical paced rates, by increasing both the QRS duration and JT interval. Lignocaine (1b) significantly reduced the QT interval during sinus rhythm and at the identical paced rates, by reducing the JT interval. Lignocaine had no effect on the QRS duration. Flecainide (1c) significantly prolonged the QRS duration during sinus rhythm, but not the QTc. However the QT interval at the paced rates prolonged significantly, due entirely to an increase of the QRS duration. Flecainide had no effect on the JT interval. These characteristic electrocardiographic differences support the differentiation of class 1 drugs into three separate subgroups.
Ⅰ类抗心律失常药物根据其对动作电位时程的影响已被细分为1a、1b和1c类。在9例患者中研究了每个亚组中一种药物对体表心电图的影响。在窦性心律以及相同的心房和心室起搏频率下进行心电图记录。丙吡胺(1a类)在窦性心律和相同起搏频率下显著延长QT间期,这是通过增加QRS时限和JT间期实现的。利多卡因(1b类)在窦性心律和相同起搏频率下显著缩短QT间期,这是通过缩短JT间期实现的。利多卡因对QRS时限无影响。氟卡尼(1c类)在窦性心律时显著延长QRS时限,但不延长QTc。然而,在起搏频率下QT间期显著延长,这完全是由于QRS时限增加所致。氟卡尼对JT间期无影响。这些特征性的心电图差异支持将Ⅰ类药物分为三个独立的亚组。