What is the recommended dose of tenectiplase (tissue plasminogen activator) for a patient with impaired renal function and a history of ischemic stroke or myocardial infarction?

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Tenecteplase Dosing

For acute myocardial infarction, tenecteplase is dosed based on body weight using a tiered regimen: 30 mg for patients <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, administered as a single IV bolus over 5 seconds. 1, 2, 3

Standard Weight-Based Dosing for STEMI

The weight-tiered dosing regimen is straightforward and does not require dose adjustment for renal impairment:

  • <60 kg: 30 mg (6 mL) 1, 2, 3
  • 60 to <70 kg: 35 mg (7 mL) 1, 2, 3
  • 70 to <80 kg: 40 mg (8 mL) 1, 2, 3
  • 80 to <90 kg: 45 mg (9 mL) 1, 2, 3
  • ≥90 kg: 50 mg (10 mL) 1, 2, 3

The dose is administered as a single intravenous bolus over 5-10 seconds. 2, 3

Critical Consideration for Renal Impairment

Tenecteplase dosing does NOT require adjustment for impaired renal function. 3, 4 The drug exhibits primarily hepatic metabolism with a clearance of 99-119 mL/min that is independent of renal function. 3, 4 Body weight accounts for only 19% of clearance variability, and renal function does not significantly impact tenecteplase pharmacokinetics. 4

This contrasts sharply with adjunctive anticoagulation, where dose modifications are mandatory for renal impairment. For example, enoxaparin requires dose reduction in patients with creatinine clearance <30 mL/min. 1

Dosing for Ischemic Stroke

For acute ischemic stroke with large vessel occlusion, the recommended dose is 0.25 mg/kg (maximum 25 mg) administered as a single IV bolus. 2, 5, 6 This lower dose has demonstrated superior recanalization compared to alteplase without increased bleeding risk. 5, 6

A higher dose of 0.40 mg/kg was tested but showed no advantage over 0.25 mg/kg in achieving reperfusion before thrombectomy and was associated with numerically higher symptomatic intracranial hemorrhage (4.7% vs 1.3%). 7, 8

Age-Related Considerations

For patients >75 years with STEMI, use the standard weight-based dose without reduction. 1 The 2024 European Society of Cardiology guidelines note that half-dosing should be considered in elderly patients only in the context of increased bleeding risk, but this is not a blanket recommendation. 1

For stroke patients >75 years, the 0.25 mg/kg dose remains appropriate without age-based reduction. 5, 6

Obesity Considerations

In patients with class ≥2 obesity (BMI ≥35) or body weight >90 kg, the maximum dose is capped at 50 mg for STEMI. 1, 2, 3 For stroke, the maximum is 25 mg when using the 0.25 mg/kg regimen. 5, 6

The 2024 ESC consensus statement emphasizes measuring actual body weight to avoid underdosing in obese patients, as higher body weight is associated with worse artery patency if underdosed. 1

History of Prior Stroke or MI

Prior ischemic stroke or myocardial infarction does NOT require dose adjustment of tenecteplase. 1, 3 However, recent ischemic stroke within 3-6 months is an absolute contraindication to fibrinolytic therapy. 2

Unlike streptokinase, tenecteplase can be re-administered if clinically indicated, as it does not induce antibody formation. 2

Common Pitfalls to Avoid

Do not reduce the tenecteplase dose for renal impairment – this is a critical error that would lead to underdosing and treatment failure. 3, 4 The confusion likely arises because adjunctive enoxaparin DOES require dose reduction in renal dysfunction (no IV bolus and 0.75 mg/kg subcutaneous every 12 hours in patients ≥75 years; dose reduction for creatinine clearance <30 mL/min). 1, 2

Do not use the 0.5 mg/kg dose approved for STEMI in stroke patients – stroke trials consistently used lower doses (0.25 mg/kg), and higher doses showed no benefit with potential harm. 7, 5, 8

Do not delay administration to calculate precise weight – estimated weight is acceptable for the weight-tiered regimen, as the dose bands provide a margin of safety. 3

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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