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A Murine Model of Subarachnoid Hemorrhage
Published on: November 21, 2013
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Platelet activation and aggregation after aneurysmal subarachnoid hemorrhage
Pauline Perez1, Anne-Claire Lukaszewicz2,3, Stephanie Lenck4
1Anesthesiology and Critical Care Department, Lariboisière Hospital, Paris, France.
BMC Neurology
|April 30, 2018
Summary
Platelets in patients with aneurysmal subarachnoid hemorrhage (aSAH) show prolonged activation and aggregation. Targeting the ADP pathway may reduce clotting and ischemic events after endovascular treatment.
Area of Science:
- Neuroscience
- Hematology
- Vascular Surgery
Background:
- Endovascular treatment for aneurysmal subarachnoid hemorrhage (aSAH) carries risks like arterial clotting and dissection.
- Platelet activation and hemostatic alterations may underlie these complications.
- Investigating platelet behavior is crucial for managing aSAH patients undergoing endovascular procedures.
Purpose of the Study:
- To investigate platelet activation and aggregation pathways in patients with aSAH undergoing endovascular treatment.
- To compare platelet behavior in aSAH patients with orthopedic postoperative patients (POSTOP).
Main Methods:
- Collected blood samples from aSAH patients early after bleeding and during vasospasm risk period.
- Assessed platelet activation via GpIIbIIIa and P-selectin expression.
- Measured platelet aggregation rates with agonists and compared with POSTOP patients.
Main Results:
- Platelets in aSAH patients exhibited spontaneous and sustained activation.
- aSAH platelets showed rapid aggregation in response to agonists, particularly ADP.
- Platelet aggregation in aSAH patients was comparable to POSTOP patients.
Conclusions:
- aSAH platelets demonstrate prolonged activation and aggregation.
- Targeting the adenosine diphosphate (ADP) pathway could mitigate clotting and ischemic risks.
- Further research into ADP pathway inhibition may benefit aSAH patients undergoing endovascular interventions.
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