What is the recommended dose of teneactplase (tnk-tPA) for a 43-year-old patient weighing 96 kg with acute ischemic stroke?

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Tenecteplase Dosing for Acute Ischemic Stroke

For a 43-year-old patient weighing 96 kg with acute ischemic stroke, administer 24 mg of tenecteplase as a single intravenous bolus (calculated as 0.25 mg/kg, with a maximum dose of 25 mg). 1, 2, 3

Weight-Based Dosing Calculation

  • The recommended dose of tenecteplase for acute ischemic stroke is 0.25 mg/kg administered as a single intravenous bolus with a maximum dose of 25 mg. 1, 2, 3

  • For this 96 kg patient: 96 kg × 0.25 mg/kg = 24 mg, which is below the 25 mg maximum. 2

  • This dose is specifically validated for stroke treatment and differs critically from the myocardial infarction dosing of 0.5 mg/kg—clinicians must not confuse these protocols. 1

Critical Distinction from MI Dosing

  • The FDA-approved myocardial infarction dosing uses a weight-tiered approach (30 mg for <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), but this is NOT appropriate for stroke. 4

  • The stroke dose of 0.25 mg/kg (maximum 25 mg) is approximately half the MI dose and was established through trials demonstrating superior recanalization and improved 3-month outcomes in large vessel occlusions. 2, 5

Evidence Supporting 0.25 mg/kg Dose

  • Meta-analysis demonstrates that tenecteplase 0.25 mg/kg produces significant improvements in early neurological improvement (OR = 1.52), excellent functional outcome at 90 days (mRS 0-1: OR = 1.19), good functional outcome (mRS 0-2: OR = 1.21), and reduced mortality (OR = 0.78). 5

  • The 0.25 mg/kg dose achieves superior reperfusion rates (22% vs 10% substantial reperfusion) compared to alteplase when used prior to mechanical thrombectomy. 1

  • Higher doses are unsafe: tenecteplase 0.4 mg/kg significantly increases symptomatic intracranial hemorrhage risk (OR = 2.35) and mortality, particularly in moderate to severe strokes. 5, 6

Administration Guidelines

  • Administer as a single intravenous bolus over 5-10 seconds, which offers substantial workflow advantages over alteplase's 1-hour infusion. 1, 2, 3

  • Treatment should be initiated as soon as possible after CT scan, with a target door-to-needle time of less than 60 minutes in 90% of treated patients. 1

  • The longer half-life of tenecteplase (90-130 minutes) eliminates the need for continuous infusion and reduces nursing time and potential medication errors. 2, 3, 4

Guideline Status and Patient Selection

  • The American Heart Association/American Stroke Association suggests tenecteplase might be considered as an alternative to alteplase in patients with minor neurological impairment and no major intracranial occlusion (Class IIb, Level of Evidence B-R). 1, 2, 3

  • Patients eligible for IV thrombolysis should receive it even if endovascular therapies are being considered (Class I, Level of Evidence A). 1, 3

  • Both tenecteplase and alteplase share similar contraindications including intracranial hemorrhage, recent significant trauma or surgery, and uncontrolled hypertension. 2, 3

Safety Profile

  • The absolute increase in symptomatic intracranial hemorrhage risk with thrombolysis is approximately 6% (7% with thrombolysis vs 1% without), yielding a number needed to harm of 17. 1, 3

  • The number needed to treat for favorable outcomes is 8-14, which should be discussed with patients and families during shared decision-making. 1, 3

References

Guideline

Tenecteplase vs Alteplase for Acute Ischemic Stroke Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Tenecteplase Dosage and Administration for Acute Ischemic Stroke

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Tenecteplase in Acute Ischemic Stroke and Pulmonary Embolism

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

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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