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Antithrombotic drugs for carotid artery dissection
1Neurology, University Hospital Basel, Petersgraben 4, Basel, Switzerland.
The Cochrane Database of Systematic Reviews
|August 15, 2003
Summary
No randomized trials exist for extracranial internal carotid artery dissection treatment. Evidence does not support routine use of anticoagulants or antiplatelet drugs, and further research is needed.
Area of Science:
- Neurology
- Vascular Medicine
- Clinical Trials
Background:
- Extracranial internal carotid artery dissection is a cause of ischemic stroke, particularly in younger adults.
- It accounts for approximately 2.5% of all strokes.
- Antithrombotic treatments carry risks of bleeding, necessitating careful evaluation of their benefits and safety.
Purpose of the Study:
- To evaluate the efficacy and safety of antithrombotic drugs (antiplatelet and anticoagulation) for treating extracranial internal carotid artery dissection.
- To determine the optimal antithrombotic treatment strategy.
Main Methods:
- Searched multiple databases including Cochrane Stroke Group Trials Register, Cochrane Central Register of Controlled Trials, MEDLINE, and EMBASE.
- Included randomized controlled trials, controlled clinical trials, and non-randomized studies (case series) with at least 4 patients.
- Extracted data on primary outcomes (death, death or disability) and secondary outcomes (stroke, hemorrhage).
Main Results:
- No randomized trials were identified, thus no reliable comparisons with control groups.
- Twenty-six non-randomized studies with 327 patients were analyzed.
- No significant difference in mortality or death/disability was found between antiplatelet drugs and anticoagulants. Few intracranial hemorrhages were reported with anticoagulants.
Conclusions:
- Lack of randomized trials means no evidence supports routine use of anticoagulants or antiplatelet drugs for extracranial internal carotid artery dissection.
- Non-randomized studies did not demonstrate a significant difference between these treatments.
- A large-scale randomized trial with at least 1400 patients per arm is recommended.