Tenecteplase Dosing for ST-Elevation Myocardial Infarction
For patients with ST-elevation myocardial infarction (STEMI), tenecteplase should be administered as a single IV weight-based bolus according to the following dosing regimen: 30 mg for weight <60 kg, 35 mg for 60-69 kg, 40 mg for 70-79 kg, 45 mg for 80-89 kg, and 50 mg for ≥90 kg. 1, 2
Dosing Details and Administration
The weight-based dosing of tenecteplase for STEMI is as follows:
| Patient Weight (kg) | TNKase (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 |
- Tenecteplase should be administered as a single IV bolus over 5 seconds 2
- Treatment should be initiated as soon as possible after symptom onset, with greatest benefit within the first 12 hours 1
- Tenecteplase is preferred over non-fibrin specific agents due to superior patency rates and less immunogenicity 1
Adjunctive Therapy
When administering tenecteplase for STEMI, the following adjunctive therapies should be given:
Antiplatelet therapy:
Anticoagulation:
Special Considerations
- Elderly patients (>75 years): Consider half-dose tenecteplase to reduce the risk of intracranial hemorrhage 3
- Timing: Fibrinolysis should be considered if time from first medical contact to balloon inflation is >90 minutes for early presenters (<2 hours) with large infarcts and low bleeding risk, or >120 minutes for other patients 1
- Post-fibrinolysis care: Transfer to a PCI-capable center immediately after fibrinolysis is recommended 1
- Rescue PCI: Should be performed immediately if fibrinolysis fails (<50% ST-segment resolution at 60 minutes) 1
Contraindications
Absolute Contraindications 1:
- Any prior intracranial hemorrhage
- Known structural cerebral vascular lesion
- Known malignant intracranial neoplasm
- Ischemic stroke within 3 months
- Suspected aortic dissection
- Active bleeding or bleeding diathesis
- Significant closed-head or facial trauma within 3 months
- Intracranial or intraspinal surgery within 2 months
- Severe uncontrolled hypertension (SBP >180 mm Hg or DBP >110 mm Hg)
Relative Contraindications 1:
- History of chronic, severe, poorly controlled hypertension
- Significant hypertension on presentation
- History of prior ischemic stroke >3 months
- Dementia
- Traumatic or prolonged CPR
- Major surgery (<3 weeks)
- Recent internal bleeding
- Noncompressible vascular punctures
- Pregnancy
- Active peptic ulcer
- Oral anticoagulant therapy
Clinical Efficacy
Tenecteplase has demonstrated equivalent efficacy to alteplase in mortality reduction but with fewer non-cerebral bleeding complications 4, 5. The ASSENT-2 trial showed similar 30-day mortality rates (approximately 6.2%) between tenecteplase and alteplase, with reduced bleeding complications in the tenecteplase group 5.