Manz M, Mletzko R, Jung W, Lüderitz B
Department of Cardiology, University of Bonn, Germany.
Eur Heart J. 1992 Aug;13(8):1123-8. doi: 10.1093/oxfordjournals.eurheartj.a060324.
The electrophysiological and haemodynamic effects of lidocaine (100 mg) and ajmaline (50 mg) were evaluated while attempting to interrupt sustained ventricular tachycardia. The study was performed as a prospective, non-blinded, randomized investigation in 61 patients. Lidocaine terminated ventricular tachycardia in four of 31 patients, ajmaline in 19 of 30 patients (P less than 0.001). QRS and RR intervals during ventricular tachycardia were prolonged by ajmaline from 164 +/- 28 ms to 214 +/- 49 ms and from 371 +/- 86 ms to 479 +/- 137 ms (P less than 0.001), respectively; lidocaine did not influence these parameters. The duration of the return cycles after termination of ventricular tachycardia did not differ between the two groups. Lidocaine did not change cardiac output during ventricular tachycardia whereas cardiac output increased significantly under ajmaline from 3.5 +/- 1.21.min-1 to 5.5 +/- 1.91.min-1 (P less than 0.001). It is concluded that anti-arrhythmic agents such as ajmaline, which slow conduction velocity and prolong refractoriness, are more effective than lidocaine in the medical treatment of haemodynamically stable, sustained ventricular tachycardia.
在试图终止持续性室性心动过速时,评估了利多卡因(100毫克)和阿吗灵(50毫克)的电生理和血流动力学效应。该研究作为一项前瞻性、非盲法、随机调查,纳入了61例患者。利多卡因使31例患者中的4例室性心动过速终止,阿吗灵使30例患者中的19例终止(P<0.001)。阿吗灵使室性心动过速时的QRS和RR间期分别从164±28毫秒延长至214±49毫秒和从371±86毫秒延长至479±137毫秒(P<0.001);利多卡因未影响这些参数。两组在室性心动过速终止后的折返周期持续时间无差异。利多卡因在室性心动过速期间未改变心输出量,而阿吗灵使心输出量从3.5±1.2升/分钟显著增加至5.5±1.9升/分钟(P<0.001)。得出的结论是,像阿吗灵这样能减慢传导速度并延长不应期的抗心律失常药物,在血流动力学稳定的持续性室性心动过速的药物治疗中比利多卡因更有效。