Langer A, Krucoff M W, Klootwijk P, Veldkamp R, Simoons M L, Granger C, Califf R M, Armstrong P W
Division of Cardiology, St. Michael's Hospital, Toronto, Ontario, Canada.
J Am Coll Cardiol. 1995 Jun;25(7):1552-7. doi: 10.1016/0735-1097(95)00110-p.
The ST segment monitoring substudy of the Global Utilization of Streptokinase and Tissue Plasminogen Activator for Occluded Coronary Arteries (GUSTO-I) trial compared the speed and stability of ST segment recovery among four thrombolytic strategies for acute myocardial infarction.
Rapid resolution of ST segment elevation has been suggested as a noninvasive marker of infarct-related artery patency. We expected that patients treated with accelerated recombinant tissue-type plasminogen activator (rt-PA) would show a quicker recovery than that of other patients but that those treated with streptokinase would show greater stability of recovery.
ST segment monitoring was initiated in 1,067 patients within 30 min of the start of thrombolysis and continued for > 18 h with the use of a three-channel continuous vectorcardiographic monitor, a 12-lead continuous electrocardiographic (ECG) monitor or a three-channel (V2, V5, aVF) Holter ambulatory ECG monitor.
Time to 50% recovery could be assessed in 618 patients and was similar in the four treatment groups: median 45 min with streptokinase/subcutaneous heparin, 45 min with streptokinse/intravenous heparin, 42 min with accelerated rt-PA and 47 min with combination therapy (p = 0.7). No significant difference among the thrombolytic regimens was shown with the three monitors used. Time to initiation of ST segment analysis was directly related to time to 50% recovery (p = 0.0001) and was its best predictor in a multiple regression model. ST segment elevation recurred equally in each treatment group (approximately 36%, p = 0.9) but was significantly more common in patients with a patent infarct-related artery (p = 0.033) or a low ejection fraction (p = 0.001).
The greater 90-min patency seen with accelerated rt-PA in the angiographic substudy did not correlate with a shorter time to 50% ST segment recovery, possibly because of technical limitations and study design. The similar rates of recurrent ischemia (as assessed by ST elevation) among the regimens support the similar infarction and reocclusion rates seen in the main trial and angiographic substudy.
全球急性冠状动脉闭塞应用链激酶和组织型纤溶酶原激活剂研究(GUSTO-I)试验的ST段监测子研究比较了急性心肌梗死四种溶栓策略中ST段恢复的速度和稳定性。
ST段抬高的快速消退被认为是梗死相关动脉通畅的无创标志物。我们预期接受加速重组组织型纤溶酶原激活剂(rt-PA)治疗的患者恢复速度比其他患者更快,但接受链激酶治疗的患者恢复稳定性更高。
1067例患者在溶栓开始后30分钟内开始ST段监测,并使用三通道连续心电向量图监测仪、12导联连续心电图(ECG)监测仪或三通道(V2、V5、aVF)动态心电图监测仪持续监测超过18小时。
618例患者可评估达到50%恢复的时间,四个治疗组相似:链激酶/皮下肝素组中位数为45分钟,链激酶/静脉肝素组为45分钟,加速rt-PA组为42分钟,联合治疗组为47分钟(p = 0.7)。使用的三种监测仪显示溶栓方案之间无显著差异。ST段分析开始时间与达到50%恢复的时间直接相关(p = 0.0001),并且在多元回归模型中是其最佳预测指标。每个治疗组ST段抬高复发率相同(约36%,p = 0.9),但在梗死相关动脉通畅的患者(p = 0.033)或射血分数低的患者(p = 0.001)中显著更常见。
血管造影子研究中加速rt-PA观察到的90分钟时更高的通畅率与达到50% ST段恢复的较短时间不相关,可能是由于技术限制和研究设计。各方案中复发性缺血(通过ST段抬高评估)的相似发生率支持了主要试验和血管造影子研究中观察到的相似梗死和再闭塞率。