Background Despite the widespread use of intravenous thrombolytictherapy and of immediate percutaneous transluminal coronaryangioplasty for the treatment of acute myocardial infarction,randomized comparisons of the two approaches to reperfusionare lacking. We report the results of a prospective, randomizedtrial comparing immediate coronary angioplasty (without previousthrombolytic therapy) with intravenous streptokinase treatment.
Methods A total of 142 patients with acute myocardial infarctionwere randomly assigned to receive one of the two treatments.The left ventricular ejection fraction was measured by radionuclidescanning before hospital discharge. Quantitative coronary angiographywas performed to assess the degree of residual stenosis in theinfarct-related arteries.
Results A total of 72 patients were assigned to receive streptokinaseand 70 patients to undergo immediate angioplasty. Angioplastywas technically successful in 64 of the 65 patients who underwentthe procedure. Infarction recurred in nine patients assignedto receive streptokinase, but in none of those assigned to receiveangioplasty (P = 0.003 ). Fourteen patients in the streptokinasegroup had unstable angina after their infarction, but only fourin the angioplasty group (P = 0.02). The mean (±SD) leftventricular ejection fraction as measured before discharge was45 ±12 percent in the streptokinase group and 51 ±11percent in the angioplasty group (P = 0.004). The infarct-relatedartery was patent in 68 percent of the patients in the streptokinasegroup and 91 percent of those in the angioplasty group (P =0.001). Quantitative coronary angiography revealed stenosisof 36 ±20 percent of the luminal diameter in the angioplastygroup, as compared with 76 ±19 percent in the streptokinasegroup (P<0.001).
Conclusions Immediate angioplasty after acute myocardial infarctionwas associated with a higher rate of patency of the infarct-relatedartery, a less severe residual stenotic lesion, better leftventricular function, and less recurrent myocardial ischemiaand infarction than was intravenous streptokinase. .
Source Information
From the Departments of Cardiology (F.Z., M.J.B., J.C.A.H., H.S.) and Nuclear Medicine (S.R.), Ziekenhuis de Weezenlanden, Zwolle; and the Laboratory for Clinical and Experimental Image Processing, Department of Diagnostic Radiology and Nuclear Medicine, University Hospital, Leiden (J.H.C.R.) -- both in the Netherlands.
Address reprint requests to Dr. Zijlstra at Z.H. de Weezenlanden, Department of Cardiology, Groot Wezenland 20, 8011 JW Zwolle, the Netherlands.
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