血液学MCS 3p血细胞分离器在血小板提取中不同方案产品质量参数的比较。

R Moog, N Müller
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引用次数: 5

摘要

背景:在血小板分离术中,间歇流式细胞分离器产生的血小板浓缩物(PC)比连续流式血细胞分离器产生的白细胞污染更高。新的不连续流式细胞分离器Haemonetics MCS 3p为PC提供了低白细胞解决方案。本文对MCS 3p制得的PC的质量进行了研究。设计:前瞻性研究。地点:一所大学诊所的采血单位。患者:采血单位的健康献血者。材料和方法:研究了三种不同方案下血小板(PLT)产率、分离效率和白细胞(WBC)污染。两种方案使用血液计算器,根据供体的物理特性和所需的PLT产量计算靶体积。协议I使用3,000 ml作为目标工艺体积,协议II使用3.3 x 10(11)作为期望的PLT产率。方案III不使用血液计算器。通过葡萄糖、乳酸、乳酸脱氢酶(LDH)、形态学评分和pH值的测定来考察PC的质量。结果:三种方法的血小板得率和分离效率无统计学差异。在没有血液计算器的方案中,白细胞污染最低(中位数:3.15 × 10(6),范围0.4-20.8 × 10(6))。葡萄糖、乳酸、乳酸脱氢酶和pH值在三种治疗方案中无统计学差异。方案III的形态学评分最高。结论:使用MCS 3p血细胞分离器收集血小板可获得足够的血小板产量。使用血液计算器我们不能达到期望的血小板产量。由于这个原因,并且由于方案II中白细胞污染较高,我们更倾向于不使用血球计算器的PLT采集。血小板浓缩物的葡萄糖、乳酸、乳酸脱氢酶、形态学评分和pH等指标均较好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparison of different protocols in plateletpheresis with the haemonetics MCS 3p blood cell separator with respect to parameters of product quality.

Background: In thrombocytapheresis, intermittent flow cell separators produce platelet concentrates (PC) with a higher leucocyte contamination than continuous flow blood cell separators. The new discontinuous flow cell separator Haemonetics MCS 3p offers a low-leucocyte solution for PC. The quality of PC obtained by the MCS 3p was investigated in this study.

Design: Prospective study.

Setting: Haemapheresis Unit of a University Clinic.

Patients: Healthy blood donors from the haemapheresis unit.

Materials and methods: Platelet (PLT) yield, separation efficiency and white blood cell (WBC) contamination were studied in three different protocols. Two protocols used a haemocalculator, which calculated the target volume based on the donor's physical characteristics and the desired PLT yield for the procedure. Protocol I used 3,000 ml as target process volume and protocol II 3.3 x 10(11) as desired PLT yield. Protocol III was used without haemocalculator. Glucose, lactate, lactate dehydrogenase (LDH), morphology score and pH value were analysed to investigate the quality of the PC.

Results: Platelet yield and separation efficiency were not statistically different in the three protocols. Leucocyte contamination was lowest in the protocol without haemocalculator (median: 3.15 x 10(6), range 0.4-20.8 x 10(6)). Glucose, lactate, LDH and pH were not statistically different in the three protocols. Morphology score was best in protocol III.

Conclusions: PLT collection with the MCS 3p blood cell separator results in sufficient thrombocyte yields. Using the haemocalculator we were not able to achieve the desired platelet yield. For this reason, and because of the higher WBC contamination in protocol II we prefer PLT collection without the haemocalculator. The quality of the platelet concentrates was good with respect to the parameters glucose, lactate, LDH, morphology score and pH.

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