What is the recommended dose of Streptokinase (fibrinolytic agent) for acute ischemic stroke, pulmonary embolism, or myocardial infarction?

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Streptokinase Dosing for Cardiovascular Emergencies

For acute myocardial infarction, streptokinase should be administered as 1.5 million units intravenously over 30-60 minutes. 1

Dosing by Indication

Acute Myocardial Infarction

  • Recommended dose: 1.5 million units administered intravenously over 30-60 minutes 1
  • Streptokinase should be considered when primary PCI cannot be performed by an experienced team within 120 minutes of first medical contact 1
  • Administration may be associated with hypotension, but severe allergic reactions are rare 1
  • Re-administration of streptokinase should be avoided due to antibodies that can impair its activity and increase risk of allergic reactions 1

Pulmonary Embolism

  • The recommended dose is 1.5 million units administered intravenously over one hour 2
  • This regimen has been shown to reverse acute pulmonary arterial hypertension and improve pulmonary perfusion without increasing hemorrhagic complications 2

Acute Ischemic Stroke

  • Streptokinase is NOT recommended for acute ischemic stroke due to increased mortality primarily from hemorrhagic transformation of ischemic cerebral infarcts 3
  • Studies have shown that 1.5 million units over one hour resulted in significantly higher mortality at 10 days (34.0% vs. 18.2%) compared to placebo 3

Adjunctive Therapy with Streptokinase

Antiplatelet Therapy

  • Aspirin should be administered with streptokinase (150-500 mg orally or 250 mg IV if oral ingestion is not possible) 1
  • Clopidogrel should be added to aspirin (loading dose of 300 mg orally if aged ≤75 years, followed by maintenance dose of 75 mg/day) 1
  • The benefits of aspirin and streptokinase are additive 1

Anticoagulation

  • Anticoagulation is recommended until revascularization (if performed) or for the duration of hospital stay up to 8 days 1
  • Options include:
    • Unfractionated heparin: 60 U/kg IV bolus (maximum 4000 U) followed by IV infusion of 12 U/kg/hr (maximum 1000 U/hr) for 24-48 hours, targeting aPTT 50-70 seconds or 1.5-2.0 times control 1
    • Enoxaparin: For patients <75 years, 30 mg IV bolus followed by 1 mg/kg SC every 12 hours; for patients >75 years, no IV bolus with first SC dose of 0.75 mg/kg 1
    • Fondaparinux: 2.5 mg IV bolus followed by 2.5 mg SC once daily (preferred with streptokinase) 1

Monitoring and Post-Administration Care

  • Monitor for reperfusion: relief of symptoms, maintenance of hemodynamic/electrical stability, and reduction of ST-segment elevation by at least 50% at 60-90 minutes 1
  • Transfer to a PCI-capable center following fibrinolysis is indicated in all patients 1
  • Angiography with a view to revascularization is recommended after successful fibrinolysis, optimally between 3-24 hours 1
  • Monitor for bleeding complications, which occur in 4-13% of patients 1
  • Watch for hypotension, which commonly occurs with streptokinase administration 1

Special Considerations and Contraindications

  • Streptokinase should not be re-administered due to antibody formation 1
  • Intracranial hemorrhage occurs in 0.9-1.0% of patients 1
  • Risk factors for intracranial hemorrhage include lower weight, female sex, previous cerebrovascular disease, and systolic/diastolic hypertension on admission 1
  • Fibrin-specific agents (tenecteplase, alteplase, reteplase) are generally preferred over streptokinase due to better safety profile 1

Comparative Efficacy

  • Accelerated streptokinase administration (1.5 million units over 20 minutes) has been associated with higher rates of coronary reperfusion (80%) compared to standard protocol over 60 minutes (58%) 4
  • However, fibrin-specific agents are generally preferred over streptokinase due to reduced risk of non-cerebral bleeding and blood transfusion 1

References

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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