What is the recommended dose and administration protocol for Urokinase (urokinase) in acute myocardial infarction (MI)?

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Urokinase Administration Protocol for Acute Myocardial Infarction

For patients with acute myocardial infarction requiring urokinase thrombolytic therapy, administer urokinase as an intravenous bolus of 1 million units followed by a second bolus of 1 million units after 60 minutes, along with heparin (10,000 U bolus followed by 1,000 IU/hour for 48 hours). 1

Dosing Protocol

Initial Administration

  • Give urokinase as an IV bolus of 1 million units
  • Follow with a second bolus of 1 million units after 60 minutes
  • Total dose: 2 million units

Concurrent Anticoagulation

  • Administer heparin as a 10,000 U IV bolus
  • Continue with heparin infusion at 1,000 IU/hour for 48 hours
  • Adjust heparin to maintain aPTT at 1.5 to 2.0 times control (approximately 50-70 seconds) 2

Timing Considerations

  • Administer urokinase within the first 6 hours of symptom onset for optimal efficacy 3
  • Earlier administration (within 2 hours) is associated with better outcomes and improved wall motion at the infarct site 4
  • Administration after 6 hours from symptom onset shows limited benefit in limiting necrotic focus or reducing mortality 3

Patient Selection

  • Urokinase should be given to patients with nonselective fibrinolytic agents who are at high risk for systemic emboli, including:
    • Large or anterior MI
    • Atrial fibrillation
    • Previous embolus
    • Known LV thrombus 2

Monitoring During Administration

  • Monitor for reperfusion signs within 60-180 minutes after initiation of therapy:
    • Relief of symptoms
    • Restoration of hemodynamic and electrical stability
    • Reduction of at least 50% of initial ST-segment elevation on follow-up ECG 2
  • Monitor daily platelet counts in patients receiving heparin 2
  • Monitor fibrinogen levels (significant decrease expected with effective therapy) 5

Precautions and Contraindications

  • Exercise caution in patients with:

    • Severe uncontrolled hypertension
    • History of cerebrovascular events
    • Recent trauma or major surgery
    • Noncompressible vascular punctures
    • Recent internal bleeding
    • Pregnancy
    • Active peptic ulcer 6
  • Absolute contraindications include:

    • Previous hemorrhagic stroke
    • Other strokes or cerebrovascular events within 1 year
    • Known intracranial neoplasm
    • Active internal bleeding
    • Suspected aortic dissection 6

Expected Outcomes and Efficacy

  • Reperfusion rates of approximately 60-70% can be expected 1, 7
  • Peak serum creatine kinase levels are typically lower in patients achieving reperfusion 4
  • Anterior infarction patients may show greater mortality benefit (10.3% vs 13.9% with heparin alone) 1
  • Bleeding complications are relatively rare (approximately 0.4%) 1

Alternative Approaches

  • For patients with hepatic impairment, consider dose reduction as urokinase is rapidly cleared by the liver with an elimination half-life of approximately 12.6 minutes 8
  • Combined therapy with defibrinogenase may enhance thrombolytic efficacy and accelerate coronary thrombus lysis 7

Remember that primary PCI is preferred over thrombolysis when it can be performed in a timely fashion (within 120 minutes of first medical contact) by skilled operators in high-volume centers 6.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Intravenous urokinase in acute myocardial infarction.

The American journal of cardiology, 1985

Guideline

Acute Myocardial Infarction Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

[Study on defibrinogenasing enhancing the thrombolytic effect of urokinase on acute myocardial infarction].

Zhongguo wei zhong bing ji jiu yi xue = Chinese critical care medicine = Zhongguo weizhongbing jijiuyixue, 2003

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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