1997
DOI: 10.1016/s0735-1097(97)00370-7
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Sixty-Minute Alteplase Protocol: A New Accelerated Recombinant Tissue-Type Plasminogen Activator Regimen for Thrombolysis in Acute Myocardial Infarction

Abstract: The 60-min alteplase thrombolysis in AMI protocol achieved a TIMI grade 3 patency rate of 81.1% at 90 min with no indication of an increased bleeding hazard; it was associated with a 1.2% overall mortality rate. These results are substantially better than those reported from all currently utilized regimens. Head to head comparison with established thrombolytic regimens in a large-scale randomized trial is warranted.

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Cited by 28 publications
(8 citation statements)
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“…27 Mortality and intracranial hemorrhage tended to be higher with the double-bolus approach, leading investigators to conclude that this modification could not be recommended for general use. Gulba et al 28 have recently demonstrated that a 60-minute rt-PA infusion in an open-labeled, nonrandomized study yielded an 81% TIMI 3 patency at 90 minutes. Further study of this regimen has not been undertaken.…”
Section: Fibrin-specific Agentsmentioning
confidence: 99%
“…27 Mortality and intracranial hemorrhage tended to be higher with the double-bolus approach, leading investigators to conclude that this modification could not be recommended for general use. Gulba et al 28 have recently demonstrated that a 60-minute rt-PA infusion in an open-labeled, nonrandomized study yielded an 81% TIMI 3 patency at 90 minutes. Further study of this regimen has not been undertaken.…”
Section: Fibrin-specific Agentsmentioning
confidence: 99%
“…However, its beneficial effect is limited to only about half the patients exposed to thrombolytic agents. The success rate, defined as TIMI-3 flow (TIMI=thrombolysis in myocardial infarction) at 90 min after the start of treatment, varies between 32% [2] and 80% [3] . Furthermore, thrombolysis exposes the patient to the risk of bleeding: 0·5-1% risk of intracranial haemorrhage and 3-6% risk of other major bleeding complications.…”
Section: Introductionmentioning
confidence: 99%
“…Pharmacological regimen: After providing informed consent, patients in FT group assigned to weight-adjusted intravenous UH received a bolus of 60 U/Kg [15] (maximum 4,000 U) and then a bolus of 15 mg ([65 years) or 20 mg (\65 years) of alteplase followed by 75 or 80 mg over 1-h infusion [16,17] by peripheral vein. After FT a constant heparin infusion (12 U/Kg per hour, maximum 1,000 U/h) adjusted to maintain an activated partial thromboplastin time of 50-70 s for 24-48 h was started.…”
Section: Trial Designmentioning
confidence: 99%
“…The main advantage of current FT regimens is to achieve a rapid ''pharmacological embolectomy'' to improve right ventricle dysfunction and consequently the cardiopulmonary and systemic hemodynamic. Considering our previous experiences with 1-h streptokinase regimen [4,6] that has been used in STelevation myocardial infarction successfully, we decided to assess the efficacy and safety profile of 1-h alteplase infusion [16,17], based on the following advantages: (a) the highest TIMI-3 flow in ST-elevation myocardial infarction (81%) [16] in the history of pharmacological reperfusion, (b) in México it was an effective and safe option [17] and (c) low incidence of bleeding complications [16,17]. In addition, 1-h alteplase regimen known as the ''Jerjes PE lysis regimen'' was decided by consensus considering previous results with streptokinase regimen in 1-h [4,6], the pharmacologic alteplase advantages [16] and the strong experience obtained with this regimen in STelevation myocardial infarction in Mexico [17,23].…”
Section: Adjunctive Treatmentmentioning
confidence: 99%
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