Related Experiment Video
Updated: May 11, 2026

Prehospital Thrombolysis: A Manual from Berlin
Published on: November 26, 2013
Reducing haemorrhagic transformation after thrombolysis for stroke: a strategy utilising minocycline
David J Blacker1, David Prentice, Anthony Alvaro
1Department of Neurology and Clinical Neurophysiology, Sir Charles Gairdner Hospital, Nedlands, Western Australia and School of Medicine and Pharmacology, University of Western Australia, Nedlands, WA 6009, Australia.
Abstract:
Haemorrhagic transformation (HT) of recently ischaemic brain is a feared complication of thrombolytic therapy that may be caused or compounded by ischaemia-induced activation of matrix metalloproteinases (MMPs). The tetracycline antibiotic minocycline inhibits matrix MMPs and reduces macroscopic HT in rodents with stroke treated with tissue plasminogen activator (tPA). The West Australian Intravenous Minocycline and TPA Stroke Study (WAIMATSS) aims to determine the safety and efficacy of adding minocycline to tPA in acute ischaemic stroke. The WAIMATSS is a multicentre, prospective, and randomised pilot study of intravenous minocycline, 200 mg 12 hourly for 5 doses, compared with standard care, in patients with ischaemic stroke treated with intravenous tPA. The primary endpoint is HT diagnosed by brain CT and MRI. Secondary endpoints include clinical outcome measures. Some illustrative cases from the early recruitment phase of this study will be presented, and future perspectives will be discussed.
Insights
Minocycline may reduce haemorrhagic transformation (HT) after ischemic stroke treatment with tissue plasminogen activator (tPA). This pilot study assesses the safety and efficacy of adding minocycline to tPA for acute stroke patients.
Area of Science:
- Neurology
- Pharmacology
- Stroke Research
Background:
- Haemorrhagic transformation (HT) is a serious complication of acute ischemic stroke treated with thrombolytics like tissue plasminogen activator (tPA).
- Ischemia-induced matrix metalloproteinases (MMPs) activation is implicated in causing or worsening HT.
- Minocycline, a tetracycline antibiotic, is known to inhibit MMPs and has shown potential in reducing HT in animal models.
Purpose of the Study:
- To evaluate the safety and efficacy of combining intravenous minocycline with intravenous tPA for acute ischemic stroke.
- To determine if minocycline reduces the incidence or severity of haemorrhagic transformation in stroke patients receiving tPA.
Main Methods:
- The West Australian Intravenous Minocycline and TPA Stroke Study (WAIMATSS) is a multicenter, prospective, randomized pilot trial.
- Patients with acute ischemic stroke treated with tPA received either intravenous minocycline (200 mg every 12 hours for 5 doses) or standard care.
- Primary endpoint: diagnosis of HT via brain CT and MRI. Secondary endpoints: clinical outcome measures.
Main Results:
- Illustrative cases from the early recruitment phase will be presented.
- Data on the primary endpoint (HT) and secondary clinical outcomes are being collected and analyzed.
Conclusions:
- The study aims to provide preliminary data on the safety and efficacy of minocycline as an adjunct therapy in acute ischemic stroke.
- Findings will inform future larger trials investigating minocycline for stroke treatment and HT prevention.
Related Concept Videos
Venous Thrombosis III: Interprofessional Care
Anticoagulant Drugs: Low-Molecular-Weight Heparins
Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
Clot Retraction and Fibrinolysis
Atherosclerosis III: Management
