White H D
Cardiovascular Research Unit, Green Lane Hospital, Auckland, New Zealand.
Am J Cardiol. 1991 Dec 5;68(16):30E-37E. doi: 10.1016/0002-9149(91)90303-3.
Three available thrombolytic agents, streptokinase, alteplase, and anistreplase, have been shown to have similar effects on preservation of left ventricular function and mortality reduction after acute myocardial infarction (AMI). The agents are, however, quite different with respect to their safety profiles. Clinical trials to date suggest that alteplase (tissue plasminogen activator) or anistreplase administration is associated with a high incidence of cerebral hemorrhage. In contrast, streptokinase is associated with a low rate of cerebral hemorrhage. Streptokinase and anistreplase are associated with a higher risk of allergic reaction when compared with alteplase. Hypotension is also more common with streptokinase and anistreplase, but occurs significantly with alteplase as well. Alteplase is associated with a lower reinfarction rate when compared with streptokinase and anistreplase. The Third International Study of Infarct Survival (ISIS-3), a direct comparison of 3 thrombolytic agents (streptokinase, anistreplase, and duteplase), may provide some insight regarding the safety of these agents. Because these agents have been shown to be equally effective, selection of an appropriate agent for an individual patient may depend more on assessment of the likelihood of an adverse event or other factors, such as cost or convenience of administration, rather than assessment of the probability of greater benefit with a particular agent.
三种可用的溶栓剂,即链激酶、阿替普酶和茴香酰化纤溶酶原链激酶激活剂复合物,已被证明在急性心肌梗死(AMI)后对左心室功能的保护和死亡率降低方面具有相似的效果。然而,这些药物在安全性方面有很大差异。迄今为止的临床试验表明,使用阿替普酶(组织型纤溶酶原激活剂)或茴香酰化纤溶酶原链激酶激活剂复合物与脑出血的高发生率相关。相比之下,链激酶与脑出血的发生率较低相关。与阿替普酶相比,链激酶和茴香酰化纤溶酶原链激酶激活剂复合物发生过敏反应的风险更高。低血压在链激酶和茴香酰化纤溶酶原链激酶激活剂复合物使用时也更常见,但阿替普酶使用时也会显著发生。与链激酶和茴香酰化纤溶酶原链激酶激活剂复合物相比,阿替普酶与再梗死率较低相关。第三次国际梗死生存研究(ISIS-3),对三种溶栓剂(链激酶、茴香酰化纤溶酶原链激酶激活剂复合物和 duteplase)的直接比较,可能会为这些药物的安全性提供一些见解。由于这些药物已被证明具有同等疗效,为个体患者选择合适的药物可能更多地取决于对不良事件可能性或其他因素(如成本或给药便利性)的评估,而不是对特定药物更大获益概率的评估。