TY - JOUR
T1 - A new thrombolytic regimen for acute myocardial infarction using combination half dose tissue-type plasminogen activator with full dose streptokinase
T2 - A pilot study
AU - Grines, Cindy L.
AU - Nissen, Steven E.
AU - Booth, David C.
AU - Branco, Marcelo C.
AU - Gurley, John C.
AU - Bennett, Kim A.
AU - Demaria, Anthony N.
N1 - Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 1989/9
Y1 - 1989/9
N2 - Because a previous study utilizing a combination of recombinant tissue-type plasminogen activator (rt-PA) and urokinase demonstrated reduced reocclusion rates compared with rates obtained with rt-PA alone, this study was conducted to determine whether the combination of rt-PA and streptokinase might achieve similar results at reduced cost. Forty patients with acute myocardial infarction were treated with a I h infusion of rt-PA (50 mg) and streptokinase (1.5 million U) administered within 6 h (mean 3.6 ± 1.2) of symptom onset. Emergency coronary arteriography revealed patency of the infarct-related artery in 30 (75%) of 40 patients. With the addition of coronary angioplasty in those who had unsuccessful thrombolytic reperfusion, the early patency rate was increased to 98%. In-hospital mortality rate (2.5%) and the incidence of significant bleeding requiring transfusion (15%) were low. Angiographically documented reocclusion of the infarct vessel occurred in 3 (8%) of 37 patients by day 7. Regional wall motion of the infarct zone improved by 0.9 ± 0.9 SD/chord (p < 0.0005), and ejection fraction increased 3.68% units (p < 0.05) between immediate and day 7 studies. In contrast to the price of full dose rt-PA ($2,300) or rt-PA with urokinase ($3,500), the cost of this regimen was $1,230. This pilot study demonstrates that at half the cost, a combination of half dose rt-PA with full dose streptokinase offers high infarct vessel patency, recovery of ventricular function, a low rate of reocclusion and few bleeding complications. To assess the precise comparability of this combined regimen with other thrombolytic approaches will require a large randomized prospective trial, which is ongoing.
AB - Because a previous study utilizing a combination of recombinant tissue-type plasminogen activator (rt-PA) and urokinase demonstrated reduced reocclusion rates compared with rates obtained with rt-PA alone, this study was conducted to determine whether the combination of rt-PA and streptokinase might achieve similar results at reduced cost. Forty patients with acute myocardial infarction were treated with a I h infusion of rt-PA (50 mg) and streptokinase (1.5 million U) administered within 6 h (mean 3.6 ± 1.2) of symptom onset. Emergency coronary arteriography revealed patency of the infarct-related artery in 30 (75%) of 40 patients. With the addition of coronary angioplasty in those who had unsuccessful thrombolytic reperfusion, the early patency rate was increased to 98%. In-hospital mortality rate (2.5%) and the incidence of significant bleeding requiring transfusion (15%) were low. Angiographically documented reocclusion of the infarct vessel occurred in 3 (8%) of 37 patients by day 7. Regional wall motion of the infarct zone improved by 0.9 ± 0.9 SD/chord (p < 0.0005), and ejection fraction increased 3.68% units (p < 0.05) between immediate and day 7 studies. In contrast to the price of full dose rt-PA ($2,300) or rt-PA with urokinase ($3,500), the cost of this regimen was $1,230. This pilot study demonstrates that at half the cost, a combination of half dose rt-PA with full dose streptokinase offers high infarct vessel patency, recovery of ventricular function, a low rate of reocclusion and few bleeding complications. To assess the precise comparability of this combined regimen with other thrombolytic approaches will require a large randomized prospective trial, which is ongoing.
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U2 - 10.1016/0735-1097(89)90095-8
DO - 10.1016/0735-1097(89)90095-8
M3 - Article
C2 - 2504797
AN - SCOPUS:0024418525
SN - 0735-1097
VL - 14
SP - 573
EP - 580
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 3
ER -