Is tenecteplase administered as an intravenous infusion or as a weight‑based bolus for acute ST‑segment‑elevation myocardial infarction?

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Tenecteplase Administration for STEMI

Tenecteplase is administered as a single intravenous weight-based bolus over 5–10 seconds, not as an infusion, for acute ST-segment-elevation myocardial infarction. 1, 2

Administration Method

  • Tenecteplase is given as a rapid single bolus injection over 5–10 seconds, contrasting sharply with alteplase which requires a 90-minute infusion regimen. 1, 2, 3

  • The entire dose is delivered as one rapid push; no infusion pump is required and the drug must not be diluted for infusion over time. 2

  • This single-bolus approach eliminates infusion-related delays, reduces medication administration errors, and provides significant workflow advantages, particularly in centers planning patient transfer or endovascular therapy. 2

Weight-Based Dosing Regimen

The weight-tiered dosing for STEMI is standardized across major guidelines: 1, 4

Patient Weight Tenecteplase Dose Volume (mL)
<60 kg 30 mg 6
60–69 kg 35 mg 7
70–79 kg 40 mg 8
80–89 kg 45 mg 9
≥90 kg 50 mg 10
  • This corresponds to approximately 0.5 mg/kg (maximum 50 mg) for STEMI patients. 2, 3

  • Precise weight measurement is not mandatory; estimated weight can be used to avoid treatment delays, as the tiered dosing system accommodates reasonable estimates. 2

Pharmacokinetic Rationale

  • Tenecteplase exhibits a fourfold slower plasma clearance (105 mL/min) compared to alteplase, with a mean initial half-life of 17–24 minutes and terminal half-life of 65–132 minutes. 5, 6

  • The drug's 80-fold reduced binding to PAI-1 and 6-fold prolonged plasma half-life (22 minutes vs 3.5 minutes for alteplase) enable single-bolus administration. 5

  • Systemic exposure to tenecteplase at all times after bolus administration is higher than for alteplase 100 mg infusion, allowing more rapid restoration of coronary patency. 5

Timing and Clinical Context

  • Administer immediately after STEMI diagnosis when primary PCI cannot be performed within 120 minutes of first medical contact. 1, 4

  • Treatment is recommended within 12 hours of symptom onset, with greatest benefit occurring with earlier administration. 4

  • For patients presenting very early (<2 hours) with large infarct and low bleeding risk, consider fibrinolysis if time to balloon inflation exceeds 90 minutes. 4

Critical Distinction: STEMI vs Stroke Dosing

The STEMI dose (0.5 mg/kg, maximum 50 mg) must never be used for acute ischemic stroke. 2

  • For stroke, the dose is 0.25 mg/kg (maximum 25 mg) administered as a bolus over 5–10 seconds. 2

  • Using the higher STEMI dose for stroke is not supported by evidence and may increase bleeding risk. 2

Common Pitfalls to Avoid

  • Do not observe after administration to assess clinical response before proceeding to mechanical thrombectomy—this delays definitive treatment and worsens outcomes. 1

  • Do not administer as an infusion; the entire therapeutic advantage of tenecteplase over alteplase is lost if given over time rather than as a rapid bolus. 2, 3

  • Do not use tenecteplase as facilitated PCI (administering thrombolytic before planned primary PCI with anticipated delay of 1–3 hours)—the ASSENT-4 PCI trial showed increased mortality (6.7% vs 4.9%) and worse composite outcomes with this strategy. 3

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Tenectepline Administration Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Administration Protocol for Tenecteplase in Myocardial Infarction

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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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