Seabra-Gomes R, Aniceto Silva J, Aleixo A, Real T, Freire I, Torres I, Freitas R, Crespo F
Hospital de Santa Cruz, Carnaxide.
Drugs. 1987;33 Suppl 3:169-74. doi: 10.2165/00003495-198700333-00028.
Ten patients with symptoms of acute myocardial infarction of less than 6 hours duration were randomised to receive either anisoylated plasminogen streptokinase activator complex [APSAC] (30U) or streptokinase (1,500,000U) intravenously. The aims of the study were to compare the angiographic patency of the infarct-related coronary arteries and to monitor drug safety and tolerance for up to 24 hours. The left anterior descending artery was occluded in 3, the left circumflex in 3 and right coronary artery in 4 patients. Time between onset of pain and treatment ranged from 150 to 330 minutes. At 90 minutes, 8 patients, 3 of 5 (60%) of the APSAC group and all of the streptokinase group, had patent arteries. No significant differences were found in measurements of coagulation. There were no haemorrhagic complications. One patient of the APSAC group had reinfarction 6 hours after treatment and died in cardiogenic shock. APSAC seems safe and is easier to use than streptokinase, and both agents result in patency in the majority of patients, although too few patients were included to allow a valid comparison. However, thrombolysis should be considered only a temporary solution in acute myocardial infarction, associated mainly with 3-vessel disease.
10名急性心肌梗死症状持续时间少于6小时的患者被随机分组,分别静脉注射茴香酰化纤溶酶原链激酶激活剂复合物APSAC或链激酶(1,500,000U)。该研究的目的是比较梗死相关冠状动脉的血管造影通畅情况,并监测长达24小时的药物安全性和耐受性。3例患者左前降支闭塞,3例患者左旋支闭塞,4例患者右冠状动脉闭塞。疼痛发作至治疗的时间为150至330分钟。90分钟时,8例患者血管通畅,其中APSAC组5例中的3例(60%),链激酶组全部患者。凝血指标未发现显著差异。无出血并发症。APSAC组1例患者治疗6小时后再发心肌梗死,死于心源性休克。APSAC似乎安全,且比链激酶更容易使用,两种药物在大多数患者中都能使血管通畅,尽管纳入患者数量过少无法进行有效比较。然而,溶栓治疗在急性心肌梗死中应仅被视为一种临时解决方案,主要适用于三支血管病变。