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Updated: Jan 30, 2026

Procoagulant Platelet Characterization by Measuring Phosphatidylserine Exposure and Microvesicle Release from Human Purified Platelets
Published on: November 29, 2024
Adding to platelet safety and life: Platelet additive solutions.
Ankit Mathur1, Narasimha Swamy1, Samrat Thapa1
1Department of Transfusion Medicine, Rotary Bangalore TTK Blood Bank, Bangalore Medical Services Trust, Bengaluru, Karnataka, India.
Platelet additive solutions (PAS) significantly reduce ABO antibody titers in single donor platelets (SDP), enabling ABO-incompatible transfusions. This improves platelet inventory management and reduces allergic transfusion reactions.
Area of Science:
- Transfusion Medicine
- Hematology
- Blood Component Therapy
Background:
- Platelet additive solutions (PAS) are used for platelet storage, replacing a significant portion of plasma.
- PAS reduces the volume of storage plasma in platelet components.
- Platelets stored in PAS are associated with a lower risk of allergic transfusion reactions and maintain clinical efficacy.
Purpose of the Study:
- To evaluate the clinical and laboratory efficacy of platelets stored in PAS (PAS-platelets).
Main Methods:
- Collected 1674 single donor platelets (SDP) in PAS from June to September 2016.
- Performed quality control on 356 units, analyzing ABO antibody titers, volume, platelet count, pH, and bacterial contamination.
- Utilized Amicus, Trima Accel, and MCS+ apheresis systems for SDP processing.
Main Results:
- Significantly reduced Anti-A and Anti-B titers (≤1:32) in PAS-SDP.
- All tested units were negative for bacterial contamination.
- No adverse transfusion reactions were reported for transfused PAS-SDP units.
- Other quality parameters for platelets remained satisfactory.
Conclusions:
- PAS addition significantly reduces ABO antibody titers, facilitating ABO-incompatible SDP transfusions.
- Reduced plasma volume in PAS-SDP units lowers the risk of allergic transfusion reactions.
- PAS-SDP improves platelet inventory management without compromising clinical or laboratory efficacy.
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