Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
Transfusion & Transplantation Medicine Program, Alberta Precision Laboratories, Edmonton, Alberta, Canada.
Transfusion. 2024 Jul;64(7):1279-1286. doi: 10.1111/trf.17873. Epub 2024 May 25.
Platelet inventory constraints necessitate ABO-incompatible platelet transfusion. Many minimize the hemolytic impact by confirming low titre (LT) donor isohemagglutinins. This process is costly. Pathogen-reduced platelets (PRP) in platelet additive solutions (PAS) will dilute plasma and decrease high-titre isohemagglutinins (HT). We determined the proportion of HT platelets and incompatible transfusions for units suspended in plasma to reassess the need for titres following introduction of PRP/PAS.
Our titre method is manual tube (1:50) dilution of platelet supernatant from apheresis or whole blood derived buffy coat pools suspended in plasma, tested with A1/B red cells. Testing included 49,058 pooled and 11,738 apheresis platelets over 4 years. The HT proportion, rate of out-of-group transfusions, and hemolytic reactions were determined. The impact of PAS dilution was estimated.
Totally 60,796 platelet units were tested. Group O pooled and group B apheresis platelets had HT in 6.6% and 5.7%, respectively. Group A pooled and apheresis platelets included 2% with HT. Approximately 25% of platelets transfused were ABO-incompatible and no hemolytic reactions were reported. Based on the proportions of PAS-E and plasma for PRP platelets, plasma from each donor comprises 11 mL (6% of total volume) vs 20-257 mL in untreated pools. PAS-E will replace and dilute residual plasma by at least 50%.
Rare platelet pools may demonstrate HT. PRP platelets with PAS will reduce titres and may abrogate the need for titration. A strategy of group specific transfusion or transfusion of group A PRP platelet transfusions may be a safe alternative.
血小板库存限制需要进行 ABO 不相容的血小板输注。许多人通过确认低滴度(LT)供体同种凝集素来最大限度地减少溶血的影响。这个过程成本很高。血小板添加剂溶液(PAS)中的减毒血小板(PRP)会稀释血浆并减少高滴度同种凝集素(HT)。我们确定了在血浆中悬浮的单位中的 HT 血小板和不相容输血的比例,以重新评估在引入 PRP/PAS 后对滴度的需求。
我们的滴度方法是手动管(1:50)稀释从血浆悬浮的单采或全血衍生的浓缩血小板上清液,用 A1/B 红细胞进行测试。测试包括在 4 年中对 49058 个 pooled 和 11738 个单采血小板进行了测试。确定了 HT 比例、外组输血率和溶血反应。还估计了 PAS 稀释的影响。
共检测了 60796 个血小板单位。O 型 pooled 和 B 型单采血小板的 HT 比例分别为 6.6%和 5.7%。A 型 pooled 和单采血小板中 HT 比例为 2%。约 25%的血小板输血是 ABO 不相容的,没有报告溶血反应。根据 PRP 血小板 PAS-E 和血浆的比例,每个供体的血浆占 11mL(总体积的 6%),而未处理的 pooled 血浆占 20-257mL。PAS-E 将至少替代和稀释 50%的残留血浆。
罕见的血小板 pool 可能表现出 HT。用 PAS 的 PRP 血小板将降低滴度,并可能取消对滴定的需求。特异性输血或输注 A 组 PRP 血小板输血的策略可能是一种安全的替代方案。