textabstractAn intravenous infusion of 40 mg of recombinant tissue-type plasminogen activator (rt-PA) was given intravenously over 90 minutes to 123 patients with acute myocardial infarction (AMI) of less than 4 hours' duration. A coronary angiogram was recorded at the end of the infusion in 119 patients. Central assessment of the angiograms revealed a patent infarct-related artery in 78 patients (patency rate 66%, 95% confidence limits 57 to 74%). Patients with a patent infarct-related artery at the first angiogram were randomized in a double-blind manner to receive a subsequent 6-hour infusion of either 30 mg of rt-PA or placebo. All patients had received an initial bolus of 5,000 IU of heparin and then 1,000 IU/hour until a second angiog...
Summary A randomised trial of 367 patients with acute myocardial infarction was performed to determi...
In a double-blind, placebo-controlled, randomized trial the long-term (± 3 months) effects of intrav...
BACKGROUND. The European Cooperative Study Group conducted two randomized trials in patients with su...
AbstractThe relation between coronary patency after infusion of recombinant tissue-type plasminogen ...
The initial studies in Europe with tissue-type plasminogen activator (rt-PA) have been coordinated b...
AbstractThe effects of recombinant tissue plasminogen activator (rt-PA) and urokinase on patency and...
In a double-blind, placebo-controlled, randomized trial the long-term (± 3 months) effects of intrav...
AbstractObjectives. The present study was designed to test the efficacy and safety of a sequential c...
AbstractClot dissolution with restoration of infarct-related artery blood flow is the likely mechani...
AbstractThe relation between coronary patency after infusion of recombinant tissue-type plasminogen ...
Coronary recanalization rates and changes in plasma proteins of the fibrinolytic system were evaluat...
This study assesses whether administration of recombinant tissue-type plasminogen activator (rt-PA) ...
This study assesses whether administration of recombinant tissue-type plasminogen activator (rt-PA) ...
AbstractThe safety and efficacy of a new regimen of intravenous recombinant tissue-type plasminogen ...
This study assesses whether administration of recombinant tissue-type plasminogen activator (rt-PA) ...
Summary A randomised trial of 367 patients with acute myocardial infarction was performed to determi...
In a double-blind, placebo-controlled, randomized trial the long-term (± 3 months) effects of intrav...
BACKGROUND. The European Cooperative Study Group conducted two randomized trials in patients with su...
AbstractThe relation between coronary patency after infusion of recombinant tissue-type plasminogen ...
The initial studies in Europe with tissue-type plasminogen activator (rt-PA) have been coordinated b...
AbstractThe effects of recombinant tissue plasminogen activator (rt-PA) and urokinase on patency and...
In a double-blind, placebo-controlled, randomized trial the long-term (± 3 months) effects of intrav...
AbstractObjectives. The present study was designed to test the efficacy and safety of a sequential c...
AbstractClot dissolution with restoration of infarct-related artery blood flow is the likely mechani...
AbstractThe relation between coronary patency after infusion of recombinant tissue-type plasminogen ...
Coronary recanalization rates and changes in plasma proteins of the fibrinolytic system were evaluat...
This study assesses whether administration of recombinant tissue-type plasminogen activator (rt-PA) ...
This study assesses whether administration of recombinant tissue-type plasminogen activator (rt-PA) ...
AbstractThe safety and efficacy of a new regimen of intravenous recombinant tissue-type plasminogen ...
This study assesses whether administration of recombinant tissue-type plasminogen activator (rt-PA) ...
Summary A randomised trial of 367 patients with acute myocardial infarction was performed to determi...
In a double-blind, placebo-controlled, randomized trial the long-term (± 3 months) effects of intrav...
BACKGROUND. The European Cooperative Study Group conducted two randomized trials in patients with su...