Di Pasquale P, Barone G, Paterna S, Cannizzaro S, Bucca V, Licata G
Divisione di Cardiologia, Ospedale GF Ingrassia, Palermo.
Cardiologia. 1993 Jul;38(7):463-9.
Several experimental studies, carried out on animals and on isolated heart, showed that captopril can reduce the post-ischemic reperfusion injury. Our study was aimed at checking the effects of captopril before thrombolysis in acute myocardial infarction (AMI) and included 204 patients, hospitalized within 4 hours from the onset of symptoms. Patients were randomly subdivided into 2 groups: the first group (105 patients, Group A: pretreatment) received 6.25 mg captopril orally about 15 min before iv administration of urokinase (2 million), the second group (99 patients, Group B: late-treatment) received captopril about 3 days after thrombolytic treatment. Captopril doses were later increased in both groups according to blood pressure. All patients were subdivided according to the localization of infarction. One hundred and thirty-seven patients showed anterior AMI (70 from Group A and 67 from Group B); 67 patients showed inferior AMI (35 from Group A and 32 from Group B). Ventricular hyperkinetic arrhythmias (VHA) due to reperfusion were evaluated during the first 2 hours. Ventricular hyperkinetic arrhythmias occurred in 11.4% of patients with anterior AMI in Group A versus 38.8% in Group B (p < 0.001). CK peak normalization time in the group with anterior AMI was achieved after 58 +/- 2 hours in Group A versus 72 +/- 2 hours in Group B (p < 0.01). Late arrhythmias, > Lown's class 2 was found to occur in 15.7% of patients with anterior AMI of Group A versus 32.8% in Group B (p < 0.05), at predischarge Holter test. One hundred and nineteen patients underwent a hemodynamic test about 3 weeks after AMI.(ABSTRACT TRUNCATED AT 250 WORDS)
多项在动物和离体心脏上进行的实验研究表明,卡托普利可减轻缺血后再灌注损伤。我们的研究旨在检验卡托普利在急性心肌梗死(AMI)溶栓治疗前的效果,纳入了204例在症状发作后4小时内入院的患者。患者被随机分为两组:第一组(105例患者,A组:预处理组)在静脉注射尿激酶(200万单位)前约15分钟口服6.25毫克卡托普利,第二组(99例患者,B组:延迟治疗组)在溶栓治疗约3天后服用卡托普利。两组随后均根据血压增加卡托普利剂量。所有患者根据梗死部位进行细分。137例患者表现为前壁AMI(A组70例,B组67例);67例患者表现为下壁AMI(A组35例,B组32例)。在最初2小时内评估再灌注导致的心室运动过度性心律失常(VHA)。A组前壁AMI患者中11.4%发生VHA,而B组为38.8%(p<0.001)。前壁AMI组中,A组肌酸激酶(CK)峰值恢复正常时间为58±2小时,B组为72±2小时(p<0.01)。出院前动态心电图检查发现,A组前壁AMI患者中15.7%发生晚期心律失常(>洛恩2级),B组为32.8%(p<0.05)。119例患者在AMI约3周后接受了血流动力学检查。(摘要截断于250字)