Multicenter clinical trial using an accelerated streptokinase regimen in patients with acute myocardial infarction

Chin Med J (Engl). 2000 Aug;113(8):733-6.

Abstract

Objective: To observe the clinical efficacy and safety of intravenous thrombolytic therapy using an accelerated streptokinase (SK) regimen in acute myocardial infarction (AMI).

Methods: Data were collected from 40 hospitals during April 1996 to July 1997. Clinical therapeutic efficacy, five-week mortality, and adverse events were analyzed in 527 patients with AMI treated with an accelerated SK regimen (1.5 million IU within 30 min).

Results: The reperfusion rate of infarct-related arteries (IRAs) was 79.7% (421/528) assessed by clinical signs. The total mortality in the first 5 weeks was 6.6% (35/527). The incidence of allergic reactions and hypotension was 3.8% (20/528) and 4.2% (22/528), respectively. The incidence of bleeding was 2.7% (14/528), including cerebral bleeding 0.8% (4/528) and other major bleeding 0.8% (4/528).

Conclusion: Intravenous accelerated SK therapy can markedly improve reperfusion rate without increasing adverse events such as bleeding, allergic reactions and hypotension.

Publication types

  • Clinical Trial
  • Multicenter Study

MeSH terms

  • Aged
  • Drug Administration Schedule
  • Female
  • Fibrinolytic Agents / therapeutic use*
  • Humans
  • Male
  • Middle Aged
  • Myocardial Infarction / drug therapy*
  • Prospective Studies
  • Streptokinase / therapeutic use*
  • Thrombolytic Therapy*

Substances

  • Fibrinolytic Agents
  • Streptokinase