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Pharmacology

Fibrinolytic agents and the pharmacology of stroke thrombolysis

The plasminogen-plasmin system, why tenecteplase is a single bolus and alteplase an infusion, fibrin specificity and PAI-1 resistance, dosing pitfalls, bleeding and angioedema mechanisms and reversal, and time-dependent NNTs from the trial data.

Tier 2Medical sciences concept

Written with AI assistance and fact-checked against the sources below. For exam study, not clinical decisions. How notes are made

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At a glance

  • Fibrinolytics convert plasminogen to plasmin, which breaks down fibrin in the clot. The benefit is restoring flow to the ischaemic penumbra before it infarcts; the main harm is bleeding, especially intracranial.
  • Tenecteplase 0.25 mg/kg (maximum 25 mg) as a single bolus is now standard in Australian stroke services and is TGA-registered for stroke within 4.5 hours. Alteplase 0.9 mg/kg is the historical comparator.
  • Benefit is strongly time dependent: about 1.9 million neurons are lost each minute of a large vessel occlusion.

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Last updated
14 November 2026
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