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Published on: June 18, 2021
Major ABO-Incompatible Platelet Transfusions Are Associated With Brain Ischemia After Intracerebral Hemorrhage
Fernanda Carvalho Poyraz1,2, Mohamed Ridha1,3, Marialaura Simonetto1
1Department of Neurology (F.C.P., M.R., M.S., A.K., S.G., S.A., S.P., J.C., D.J.R.), Vagelos College of Physicians and Surgeons, Columbia University, New York.
Major ABO-incompatible platelet transfusions increase the risk of brain MRI ischemic lesions in patients with intracerebral hemorrhage (ICH). These findings suggest a link between ABO-incompatible transfusions and secondary brain injury after ICH.
Area of Science:
- Neurology
- Hematology
- Transfusion Medicine
Background:
- Major ABO-incompatible platelet transfusions are linked to poor outcomes in intracerebral hemorrhage (ICH).
- Ischemic lesions on brain MRI are indicators of secondary brain injury and predict poor outcomes after ICH.
- ABO-incompatible transfusions may promote thrombo-inflammation and endothelial damage, potentially worsening cerebral ischemia.
Purpose of the Study:
- To investigate if major ABO-incompatible platelet transfusions are a risk factor for developing ischemic lesions on brain MRI in ICH patients.
Main Methods:
- Analysis of adult ICH patients receiving platelet transfusions within 24 hours of admission.
- Inclusion criteria: available ABO data and brain MRI during hospitalization.
- Adjusted regression models were used to assess the association between ABO-incompatible platelet units and MRI ischemic lesions.
Main Results:
- A total of 40 patients were analyzed; 20% received major ABO-incompatible platelet units.
- Major ABO-incompatible platelet transfusions were significantly associated with increased odds of MRI ischemic lesions (aOR, 9.2).
- This association remained after adjusting for ICH severity.
Conclusions:
- Exploratory findings suggest ABO-incompatible platelet transfusions may contribute to secondary brain injury post-ICH.
- Further research is warranted to determine if avoiding these transfusions can mitigate secondary brain injury and improve ICH outcomes.
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