Lokhande Trupti, Thomas Sherin, Kumar Guresh, Bajpai Meenu
Department of Transfusion Medicine, Institute of Liver and Biliary Sciences, New Delhi, 110 070 India.
Department of Biochemistry, Institute of Liver and Biliary Sciences, New Delhi, 110 070 India.
Indian J Hematol Blood Transfus. 2021 Apr;37(2):295-301. doi: 10.1007/s12288-020-01339-z. Epub 2020 Sep 1.
Citrate is the anticoagulant of choice for plateletpheresis. Citrate toxicity is common during plateletpheresis as citrate chelates calcium and causes hypocalcemia in donors. We have conducted this study to analyze the effects of routine citrate infusion during plateletpheresis on laboratory and clinical parameters. We also compared the dose of citrate delivered to donors during plateletpheresis using two different cell separators as Haemonetics MCS + and Trima Accel. The study was conducted on 50 plateletpheresis donors who were eligible for donation. Donor demographics and baseline parameters were recorded. Pre, mid and post-procedure blood samples were collected for hematological and biochemical analysis. We found a significant decrease in baseline iCa (1.23 ± 0.07 mmol/L) from start to mid-procedure (1.19 ± 0.006 mmol/L) which recovered at 30 min post procedure (1.2 ± 0.01 mmol/L). The incidence of citrate toxicity was 10%. In donors with citrate toxicity, the post-procedure recovery of iCa was not seen and there was a further decrease in iCa levels. We also found a significant fall in Hb and platelet count post plateletpheresis. We observed that lower PLT counts (< 200 × 10/µL) necessitated higher blood volume processing and therefore a higher anticoagulant (citrate) dose. The Trima Accel cell separator reached platelet target yield faster but with a higher citrate dose as compared to Hemonetics MCS + . Ionized calcium decreases significantly during plateletpheresis but recovers soon after the completion of the procedure. Serious adverse events were not observed during plateletpheresis. The mild citrate toxicity which occurred was easily managed by slowing the procedure and administering oral calcium to donors. Trima Accel and Hemonetics MCS + both collected platelets efficiently, with minimal donor discomfort.
枸橼酸盐是血小板单采术的首选抗凝剂。在血小板单采过程中,枸橼酸盐毒性很常见,因为枸橼酸盐会螯合钙并导致献血者低钙血症。我们开展这项研究以分析血小板单采过程中常规输注枸橼酸盐对实验室和临床参数的影响。我们还比较了使用两种不同的血细胞分离机(Haemonetics MCS + 和Trima Accel)在血小板单采过程中输送给献血者的枸橼酸盐剂量。该研究对50名符合献血条件的血小板单采献血者进行。记录了献血者的人口统计学数据和基线参数。在术前、术中及术后采集血样进行血液学和生化分析。我们发现,从开始到术中,基线离子钙(iCa)水平显著下降(从1.23±0.07 mmol/L降至1.19±0.006 mmol/L),术后30分钟恢复(1.2±0.01 mmol/L)。枸橼酸盐毒性的发生率为10%。在发生枸橼酸盐毒性的献血者中,未见术后iCa恢复,且iCa水平进一步下降。我们还发现血小板单采术后血红蛋白和血小板计数显著下降。我们观察到,较低的血小板计数(<200×10⁹/µL)需要更高的血容量处理,因此需要更高的抗凝剂(枸橼酸盐)剂量。与Haemonetics MCS + 相比,Trima Accel血细胞分离机更快达到血小板目标采集量,但枸橼酸盐剂量更高。在血小板单采过程中离子钙显著降低,但在操作完成后很快恢复。在血小板单采过程中未观察到严重不良事件。发生的轻度枸橼酸盐毒性通过减慢操作并给献血者口服钙剂很容易得到处理。Trima Accel和Haemonetics MCS + 都能高效采集血小板,献血者不适最小。