AN INTERNATIONAL RANDOMIZED TRIAL COMPARING 4 THROMBOLYTIC STRATEGIES FOR ACUTE MYOCARDIAL-INFARCTION

被引:3257
作者
TOPOL, E
CALIFF, R
VANDEWERF, F
ARMSTRONG, PW
AYLWARD, P
BARBASH, G
BATES, E
BETRIU, A
BOISSEL, JP
CHESEBRO, J
COL, J
DEBONO, D
GORE, J
GUERCI, A
HAMPTON, J
HIRSH, J
HOLMES, D
HORGAN, J
KLEIMAN, N
MARDER, V
MORRIS, D
OHMAN, M
PFISTERER, M
ROSS, A
RUTSCH, W
SADOWSKI, Z
SIMOONS, M
VAHANIAN, A
WEAVER, WD
WHITE, H
WILCOX, R
机构
[1] DUKE UNIV, MED CTR, COORDINATING CTR, DURHAM, NC 27710 USA
[2] CATHOLIC UNIV LEUVEN, INTERMEDIATE COORDINATING CTR, B-3000 LOUVAIN, BELGIUM
关键词
D O I
10.1056/nejm199309023291001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. The relative efficacy of streptokinase and tissue plasminogen activator and the roles of intravenous as compared with subcutaneous heparin as adjunctive therapy in acute myocardial infarction are unresolved questions. The current trial was designed to compare new, aggressive thrombolytic strategies with standard thrombolytic regimens in the treatment of acute myocardial infarction. Our hypothesis was that newer thrombolytic strategies that produce earlier and sustained reperfusion would improve survival. Methods. In 15 countries and 1081 hospitals, 41,021 patients with evolving myocardial infarction were randomly assigned to four different thrombolytic strategies, consisting of the use of streptokinase and subcutaneous heparin, streptokinase and intravenous heparin, accelerated tissue plasminogen activator (t-PA) and intravenous heparin, or a combination of streptokinase plus t-PA with intravenous heparin. (''Accelerated'' refers to the administration of t-PA over a period of 1 1/2 hours - with two thirds of the dose given in the first 30 minutes - rather than the conventional period of 3 hours.) The primary end point was 30-day mortality. Results. The mortality rates in the four treatment groups were as follows: streptokinase and subcutaneous heparin, 7.2 percent; streptokinase and intravenous heparin, 7.4 percent; accelerated t-PA and intravenous heparin, 6.3 percent; and the combination of both thrombolytic agents with intravenous heparin, 7.0 percent. This represented a 14 percent reduction (95 percent confidence interval, 5.9 to 21.3 percent) in mortality for accelerated t-PA as compared with the two streptokinase-only strategies (P = 0.001). The rates of hemorrhagic stroke were 0.49 percent, 0.54 percent, 0.72 percent, and 0.94 percent in the four groups, respectively, which represented a significant excess of hemorrhagic strokes for accelerated t-PA (P = 0.03) and for the combination strategy (P<0.001), as compared with streptokinase only. A combined end point of death or disabling stroke was significantly lower in the accelerated-t-PA group than in the streptokinase-only groups (6.9 percent vs. 7.8 percent, P = 0.006). Conclusions. The findings of this large-scale trial indicate that accelerated t-PA given with intravenous heparin provides a survival benefit over previous standard thrombolytic regimens.
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收藏
页码:673 / 682
页数:10
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