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Treatment of Platelet Products with Riboflavin and UV Light: Effectiveness Against High Titer Bacterial Contamination
Published on: August 24, 2015
Observational study of corrected count increments after transfusion of platelets treated with riboflavin pathogen
Sarah M Drawz1, Susanne Marschner2, Martha Yañez3
1Department of Lab Medicine and Pathology, University of Minnesota, Minneapolis, Minnesota.
Background:
Mirasol pathogen reduction technology (PRT) treatment inactivates bacteria, viruses, and parasites in plasma products and platelets (PLTs) suspended in plasma and PLT additive solutions (PAS). Few clinical studies exist documenting transfusions with PAS. This study objective was to evaluate the count increments of PRT-treated PAS-C and PAS-E buffy coat (BC) PLTs in routine use observational settings.
Study Design And Methods:
PLT pools of five or six BCs were collected, processed, and suspended in PAS-C or PAS-E, respectively. Products were exposed to ultraviolet light in the presence of riboflavin and then transfused into 19 patients with hematologic diseases. Patients were monitored for PLT corrected count increment (CCI) at 1 and 24 hours and for any adverse events in the 72 hours after transfusion. Sterility monitoring was performed with a microbial detection system (BacT/ALERT, bioMérieux).
Results:
The PAS-E products had significantly higher PLT concentrations and counts than the PAS-C products. The mean CCIs of per-protocol (PP) units at 1 and 24 hours were 11,900 (n=27) and 5500 (n=30), respectively. Seventy-eight percent of PP transfusions classify as successful with CCIs at 1 hour of higher than 7500, and 63% higher than 4500 at 24 hours. One patient was excluded from all analyses as she was refractory to Mirasol-treated PLT transfusions and follow-up untreated transfusion products. No adverse events were observed and no contaminated products were detected by BacT/ALERT.
Conclusion:
PRT-treated BC PLTs in PAS-C or PAS-E demonstrate PLT transfusion success rates in hematology patients with thrombocytopenia that are comparable to previous studies examining PLTs stored in plasma.
Insights
Mirasol pathogen reduction technology effectively treats buffy coat platelets in additive solutions, showing comparable transfusion success rates to plasma-stored platelets in hematology patients. This technology offers a safe and viable option for platelet transfusions.
Area of Science:
- Transfusion Medicine
- Hematology
- Biotechnology
Background:
- Mirasol pathogen reduction technology (PRT) inactivates pathogens in plasma products and platelets (PLTs).
- Limited clinical data exists for PRT-treated PLTs in Platelet-Additive Solutions (PAS).
- This study evaluated PRT-treated buffy coat (BC) PLTs in PAS-C and PAS-E.
Purpose of the Study:
- To assess the efficacy of PRT-treated buffy coat PLTs in PAS-C and PAS-E.
- To evaluate platelet count increments (CCI) in patients receiving these transfusions.
- To monitor for adverse events and product contamination.
Main Methods:
- Platelet pools were processed and suspended in PAS-C or PAS-E.
- Products underwent PRT treatment using ultraviolet light and riboflavin.
- Transfusions were administered to 19 hematology patients, with monitoring for CCI and adverse events.
Main Results:
- PAS-E products showed higher platelet concentrations than PAS-C.
- Mean corrected count increments (CCI) at 1 and 24 hours were 11,900 and 5500, respectively.
- 78% of transfusions were successful at 1 hour (CCI > 7500), and 63% at 24 hours (CCI > 4500). No adverse events or contamination were reported.
Conclusions:
- PRT-treated buffy coat PLTs in PAS-C or PAS-E demonstrate effective platelet transfusion outcomes.
- Success rates are comparable to historical data for platelets stored in plasma.
- This technology presents a viable alternative for platelet transfusion in hematology patients.
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