Key result
Tenecteplase 0.25 mg/kg proves safe and effective for acute ischemic stroke within 4.5 hours.
Why the study?
Does tenecteplase improve outcomes in patients with acute ischemic stroke?
Does tenecteplase improve outcomes in patients with acute ischemic stroke?
Answers are grounded in this paper and cite their sources.
Tenecteplase at 0.25 mg/kg within 4.5 hours of symptom onset is an effective and safe thrombolytic option for acute ischemic stroke.
Tenecteplase (TNK) is a genetically engineered variant of alteplase, showing promise for acute ischemic stroke treatment. With a longer half-life and higher fibrin specificity, TNK enables more targeted and efficient clot dissolution. Clinical trials demonstrate potential advantages, including improved reperfusion rates and functional outcomes with lower systemic bleeding. Though not officially approved for this purpose by all regulatory agencies, TNK is used off-label and in acute stroke guidelines due to its ease of administration and effectiveness. The 0.25 mg/kg dosage within 4.5 hours of symptom onset was shown to be consistently effective and safe. Further trials are expected to identify patient subgroups that benefit most from TNK treatment. The present narrative review assesses the existing literature and evidence regarding the use of tenecteplase for the treatment of acute ischemic stroke.
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Silva et al. (2025) conducted a review in Acute ischemic stroke. Tenecteplase was evaluated. Tenecteplase administered at 0.25 mg/kg within 4.5 hours of symptom onset is consistently effective and safe for acute ischemic stroke, offering potential advantages in reperfusion.
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