What is the dose of Tenecteplase for a patient with suspected acute myocardial infarction?

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Tenecteplase Dosing for Acute Myocardial Infarction

Tenecteplase (TNK) is administered as a single weight-based intravenous bolus over 5 seconds for patients with suspected acute myocardial infarction with ST-segment elevation. 1

Weight-Based Dosing Regimen

The dose is determined by patient weight as follows: 1, 2

  • <60 kg: 30 mg (6 mL)
  • 60-69 kg: 35 mg (7 mL)
  • 70-79 kg: 40 mg (8 mL)
  • 80-89 kg: 45 mg (9 mL)
  • ≥90 kg: 50 mg (10 mL)

This weight-tiered dosing was developed based on exploratory analyses showing that 0.5-0.6 mg/kg optimizes the patency-to-bleeding relationship across patient weights. 3

Administration Details

  • Route: Single intravenous bolus 1, 2
  • Duration: Administer over 5 seconds 2, 3
  • Timing: Greatest benefit occurs within first 12 hours of symptom onset, with maximal benefit within 2 hours 2
  • Preparation: Reconstitute 50 mg vial with 10 mL Sterile Water for Injection 3

Mandatory Adjunctive Therapy

All patients receiving tenecteplase must receive: 2

Antiplatelet therapy:

  • Aspirin 150-325 mg loading dose (or 80-150 mg IV if oral not possible), then 75-100 mg daily 2
  • Clopidogrel 300 mg loading dose (if age ≤75 years), then 75 mg daily 2
  • For patients >75 years: No clopidogrel loading dose, start 75 mg daily 2

Anticoagulation (choose one):

  • Enoxaparin (preferred): 2
    • Age <75 years: 30 mg IV bolus, then 1 mg/kg subcutaneous every 12 hours
    • Age ≥75 years: No IV bolus, 0.75 mg/kg subcutaneous every 12 hours
  • Unfractionated heparin: 60 U/kg IV bolus (max 4000 U), then 12 U/kg/hour infusion (max 1000 U/hour) for 24-48 hours 2

Absolute Contraindications

Do not administer tenecteplase if any of the following are present: 1, 2

  • Any prior intracranial hemorrhage
  • Known structural cerebral vascular lesion or malignant intracranial neoplasm
  • Ischemic stroke within 3 months (except acute ischemic stroke)
  • Suspected aortic dissection
  • Active bleeding or bleeding diathesis (excluding menses)
  • Significant closed-head or facial trauma within 3 months
  • Intracranial or intraspinal surgery within 2 months
  • Severe uncontrolled hypertension (SBP >180 mmHg or DBP >110 mmHg unresponsive to therapy)

Post-Administration Management

All patients must be transferred to a PCI-capable center following fibrinolysis. 2 The timing of angiography depends on reperfusion success:

  • Successful fibrinolysis: Routine angiography 3-24 hours post-administration in stable patients 2
  • Failed fibrinolysis: Emergency angiography immediately if <50% ST-segment resolution at 60-90 minutes 2

Clinical Context

Tenecteplase is indicated when primary PCI cannot be performed within 120 minutes of first medical contact. 2 In the ASSENT-2 trial of 16,949 patients, tenecteplase demonstrated equivalent 30-day mortality to alteplase (approximately 6.2%) with reduced noncerebral bleeding (26.43% vs 28.95%). 4 The single-bolus administration offers significant workflow advantages over alteplase's 90-minute infusion. 1, 5

Critical pitfall: Do not use tenecteplase as facilitated therapy before planned primary PCI, as the ASSENT-4 PCI trial showed increased mortality (6.7% vs 4.9%) and worse composite outcomes when tenecteplase was given prior to PCI. 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Fibrinolytic Therapy Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

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

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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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