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The effects of additive solutions on the development of storage lesions in stored canine platelet concentrates
Author(s) -
Haines Jillian M.,
Hwang Julianne K.,
Wardrop Katherine Jane
Publication year - 2020
Publication title -
journal of veterinary emergency and critical care
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.886
H-Index - 47
eISSN - 1476-4431
pISSN - 1479-3261
DOI - 10.1111/vec.13031
Subject(s) - platelet , lactate dehydrogenase , medicine , whole blood , in vivo , platelet rich plasma , ex vivo , andrology , zoology , in vitro , chemistry , biochemistry , biology , enzyme , microbiology and biotechnology
Objective To determine if platelet additive solutions (PAS) decrease the occurrence and degree of platelet storage lesions, maintain platelet function, and extend storage time in vitro beyond 5 days at 22°C when compared to platelets stored in plasma only. Design Prospective, ex vivo experimental controlled study. Setting Research laboratory in a school of veterinary medicine. Animals Twelve units of canine platelet concentrate prepared from fresh whole blood donations. Interventions Platelet concentrates were aliquoted into 4 units and stored at room temperature (22°C) under constant agitation in either 100% plasma (control) or 35% plasma and 65% of 1 of 3 different PAS (Plasma‐Lyte A, Isoplate, and InterSol) for 7 days. At days 0, 3, 5, and 7, samples were analyzed for presence of swirling, degree of aggregate formation, platelet count, platelet indices, glucose, lactate, lactate dehydrogenase, Pv o 2 , and Pv co 2 concentrations, aggregation via light aggregometry, and activation percentage based on flow cytometric measurement of surface P‐selectin. Bacterial cultures were performed on days 0, 5, and 7. Measurements and main results Isoplate had a higher incidence of aggregate formation on day 0 (n = 2), and Plasma‐Lyte A had a higher incidence of loss of swirl on day 7 (n = 5). Plasma‐stored samples had significantly higher platelet counts ( P  < 0.001), pH ( P  < 0.05), Pv co 2 ( P  < 0.001), and lactate ( P  < 0.001), and significantly lower lactate dehydrogenase ( P  < 0.05) as compared to all PAS. The mean pH remained above 7.2 in PAS and plasma. There was no difference in platelet activation between plasma and PAS. Changes in platelet indices, glucose consumption, and maximum aggregation varied by storage solution. There was no bacterial growth seen in any samples. Conclusions The 3 PAS performed similarly and could all be considered as potential replacements for plasma during the room temperature storage of canine platelet concentrate for up to 7 days.

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