Touboul P, Moleur P, Mathieu M P, Vrancea F, Ferry S, Kirkorian G, Atallah G, Marchand A, Stahl C, Zoheir F
Hôpital Cardiovasculaire et Pneumologique Louis Pradel, Lyon, France.
Eur Heart J. 1988 Nov;9(11):1188-93. doi: 10.1093/oxfordjournals.eurheartj.a062428.
A double-blind, placebo-controlled trial comparing the antiarrhythmic effects of lidocaine (given intravenously as a bolus injection of 100 mg followed by an infusion of 2 mg min-1) and propafenone (given as a bolus of 105 mg followed by 300 mg orally every 8 h) was conducted in the first 24 h following acute myocardial infarction. Analysis of ventricular arrhythmias was carried out by Holter recordings. The three treatment groups, propafenone (36 patients), lidocaine (28 patients), and placebo (25 patients), did not differ with respect to age, gender, prevalence of previous infarction, delay from the onset of pain to hospitalization, clinical features on entry (the patients with heart failure or malignant arrhythmias were excluded), site of acute myocardial infarction, or CPK peak. A decrease in the number of ventricular premature beats was noted with lidocaine, but was not statistically significant. The analysis of the first 8 h showed trends suggesting that only lidocaine could suppress complex arrhythmias, couplets and ventricular tachycardia. The drugs were well tolerated. Mean plasma concentrations of propafenone and lidocaine were 517 +/- 464 ng ml-1 and 3.84 +/- 1.10 mg l-1, respectively. In conclusion, this study does not favour the use of propafenone as an alternative to lidocaine therapy during the acute phase of myocardial infarction.
在急性心肌梗死后的头24小时内,进行了一项双盲、安慰剂对照试验,比较利多卡因(静脉推注100毫克,随后以每分钟2毫克的速度输注)和普罗帕酮(推注105毫克,随后每8小时口服300毫克)的抗心律失常作用。通过动态心电图记录对室性心律失常进行分析。三个治疗组,即普罗帕酮组(36例患者)、利多卡因组(28例患者)和安慰剂组(25例患者),在年龄、性别、既往梗死患病率、从疼痛发作到住院的延迟时间、入院时的临床特征(排除心力衰竭或恶性心律失常患者)、急性心肌梗死部位或肌酸磷酸激酶峰值方面无差异。利多卡因使室性早搏数量减少,但无统计学意义。对前8小时的分析显示,有趋势表明只有利多卡因能抑制复杂心律失常、成对早搏和室性心动过速。这些药物耐受性良好。普罗帕酮和利多卡因的平均血浆浓度分别为517±464纳克/毫升和3.84±1.10毫克/升。总之,本研究不支持在心肌梗死急性期使用普罗帕酮替代利多卡因治疗。