TY - JOUR TI - Haemostatic profile of riboflavin-treated apheresis platelet concentrates. AU - Petrou, Eleni AU - Nikolopoulos, Georgios K. AU - Kriebardis, Anastasios G. AU - Pantavou, Katerina AU - Loukopoulou, Electra AU - Tsantes, Andreas G. AU - Georgatzakou, Hara T. AU - Maratou, Eirini AU - Rapti, Evdoxia AU - Mellou, Sofia AU - Kokoris, Styliani AU - Gialeraki, Argyri AU - Tsantes, Argirios E. JO - Blood transfusion = Trasfusione del sangue PY - 2021 VL - null TODO - null SP - null PB - SN - null TODO - 10.2450/2021.0089-21 TODO - null TODO - BACKGROUND: The haemostatic activity of platelet concentrates (PCs) treated with pathogen reduction technology (PRT) remains a subject of debate. Our aim was to investigate the effect of Mirasol PRT on the haemostatic properties of PCs stored in plasma. MATERIAL AND METHODS: Untreated and Mirasol-treated platelets stored in plasma and derived from ten split double-dose apheresis PCs were evaluated in vitro on days 1, 3 and 5 post collection for functionality, microparticle procoagulation activity (MPA), endogenous thrombin potential (ETP), and haemostatic profile using rotational thromboelastometry (ROTEM). RESULTS: P-selectin expression was significantly higher in Mirasol-treated platelets compared with untreated counterparts on days 3 and 5 (p=0.003 and p=0.002, respectively). Clot strength, as shown by EXTEM maximum clot firmness (MCF), was significantly lower in the Mirasol-treated platelets at all time points (days 1, 3, 5) than in untreated platelets (p=0.009, p<0.001, p<0.001, respectively). There was a considerable increase in MPA over time (p<0.001) and this was significantly higher in the Mirasol-treated platelets on day 5 (p=0.015). A notable acceleration of decrease in ETP values was observed for Mirasol-treated PCs over time (p<0.001), with significant differences between PRT-treated and untreated PCs on days 3 and 5 (p=0.038 and p=0.019, respectively). Clot strength attenuation was significantly associated with pH reduction (p<0.001, Spearman’s rho: 0.84), increased microparticle procoagulant activity (p<0.001, Spearman’s rho: -0.75), and with decreased ETP (p<0.032, Spearman’s rho: 0.41). DISCUSSION: Increased platelet activation induced by PRT treatment leads to a decrease in in vitro haemostatic capacity as seen by reduced clot strength and thrombin generation capacity over time. The clinical relevance of this needs to be investigated. ER -