What is the recommended dose of tenectiplase (TNK-tPA) for acute myocardial infarction (AMI)?

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Tenecteplase Dosing for Acute Myocardial Infarction

The recommended dose of tenecteplase (TNK-tPA) for acute myocardial infarction is administered as a single intravenous bolus based on patient weight: 30 mg if <60 kg, 35 mg if 60 to <70 kg, 40 mg if 70 to <80 kg, 45 mg if 80 to <90 kg, and 50 mg if ≥90 kg. 1, 2, 3, 4

Administration Protocol

  • Tenecteplase should be administered as a single intravenous bolus over 5-10 seconds 3, 4
  • The drug exhibits a biphasic elimination with an initial half-life of 17-24 minutes and a terminal half-life of 65-132 minutes 5
  • This prolonged half-life (compared to alteplase's 3.5 minutes) allows for the single bolus administration rather than an infusion 5, 6
  • Tenecteplase has higher fibrin specificity and resistance to plasminogen activator inhibitor-1 compared to alteplase 6

Weight-Based Dosing Table

Patient Weight (kg) Tenecteplase Dose (mg) Volume to Administer (mL)
< 60 30 6
60 to < 70 35 7
70 to < 80 40 8
80 to < 90 45 9
≥ 90 50 10

1, 2, 3, 4

Required Adjunctive Therapy

  • Aspirin: 150-300 mg orally or 80-150 mg IV if oral ingestion is not possible, followed by maintenance dose of 75-100 mg/day 1, 2, 3
  • Clopidogrel: Loading dose of 300 mg orally if aged ≤75 years, followed by maintenance dose of 75 mg/day 1, 2, 3
  • Anticoagulation is required until revascularization or for the duration of hospital stay (up to 8 days) 2, 3
    • Enoxaparin (preferred): 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
    • 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 1

Post-Administration Management

  • Monitor for signs of successful reperfusion: relief of symptoms, maintenance of hemodynamic/electrical stability, and reduction of ST-segment elevation by at least 50% at 60-90 minutes 2
  • Transfer to a PCI-capable center following fibrinolysis is indicated in all patients 2, 3
  • Consider rescue PCI immediately if fibrinolysis has failed (<50% ST-segment resolution at 60 minutes) 2
  • Angiography with a view to revascularization is recommended after successful fibrinolysis, optimally between 3-24 hours 1, 2

Clinical Efficacy and Safety

  • Tenecteplase has demonstrated equivalent efficacy to alteplase in the ASSENT-2 trial with 30-day mortality rates of approximately 6.2% for both agents 4, 6
  • The rate of non-cerebral bleeding was lower with tenecteplase than with alteplase (26.43% vs 28.95%) 6
  • Intracranial hemorrhage rates were similar between tenecteplase and alteplase (0.9% for both) 4

Special Considerations and Contraindications

  • Avoid tenecteplase in patients >75 years when using low molecular weight heparin as ancillary therapy 2
  • Avoid low molecular weight heparin in patients with significant renal dysfunction (serum creatinine >2.5 mg/dL in men or >2.0 mg/dL in women) 2
  • The combination of tenecteplase, aspirin, enoxaparin, and clopidogrel has been extensively studied as part of a pharmacoinvasive strategy 1, 2
  • Absolute contraindications include any prior intracranial hemorrhage, known structural cerebral vascular lesion, ischemic stroke within 3 months, suspected aortic dissection, active bleeding, significant closed-head trauma within 3 months, and severe uncontrolled hypertension 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Administration Protocol for Tenecteplase in Myocardial Infarction

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Tenecteplase Administration for STEMI

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Tenecteplase: a review of its pharmacology and therapeutic efficacy in patients with acute myocardial infarction.

American journal of cardiovascular drugs : drugs, devices, and other interventions, 2001

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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