新型 HemoClear 重力驱动微滤细胞挽救系统与传统离心 XTRA™ 自动输血设备的体外试验研究比较。

IF 1.6 Q2 ANESTHESIOLOGY Anesthesiology Research and Practice Pub Date : 2020-09-08 eCollection Date: 2020-01-01 DOI:10.1155/2020/9584186
Anneloes Hoetink, Sabine F Scherphof, Frederik J Mooi, Paul Westers, Jack van Dijk, Sjef J van de Leur, Arno P Nierich
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引用次数: 0

摘要

背景:2013 年,世界卫生组织报告称,红细胞单位短缺达 1700 万个,且这一数字仍在不断增长。缓解这一短缺的措施主要集中在异体采血上。然而,自体输血可以部分缓解目前对血库系统的压力和依赖。要实现这一目标,目前的黄金标准自体输血设备应辅以广泛使用、成本效益高、时间效率高的设备。新型的 HemoClear 细胞挽救装置(HemoClear BV,荷兰兹沃勒)是一种重力驱动的微型过滤器,具有广泛应用的潜力。与离心式 XTRA™ 自动输血装置相比,我们对其在心脏术后的性能进行了评估:方法:在一项分单元研究(n = 18)中,心胸手术后 18 小时收集的脱落血液被分成两个等量的体积。一半用 XTRA™ 设备处理,另一半用 HemoClear 血液分离系统处理。在这种配对设置中,两种方法使用的洗涤量相等。通过测量两种浓缩液和滤液中的全血细胞计数、游离血红蛋白、补体 C3、补体 C4 和 D-二聚体,确定了洗涤效果和细胞回收率。此外,还对处理时间和处理量进行了评估:结果:HemoClear 和 XTRA™ 设备在浓缩红细胞和白细胞方面效果相当。两种方法都能将补体 C3、补体 C4 和 D-二聚体减少≥90%。离心装置能更显著地减少溶质,降幅高达 99%。XTRA™ 和 HemoClear 的游离血红蛋白负荷分别降低了 12.9% 和 15.5%:结论:与传统的离心 XTRA™ 自体输血设备相比,HemoClear 设备能有效地产生洗涤浓缩红细胞。虽然离心 XTRA™ 设备减少的杂质明显更多,但 HemoClear 设备的血液质量可以接受,在金标准细胞保存器负担不起或不实用的情况下,HemoClear 设备似乎很有前途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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An In Vitro Pilot Study Comparing the Novel HemoClear Gravity-Driven Microfiltration Cell Salvage System with the Conventional Centrifugal XTRA™ Autotransfusion Device.

Background: In 2013, the World Health Organization reported a shortage of 17 million red blood cell units, a number that remains growing. Acts to relieve this shortage have primarily focused on allogeneic blood collection. Nevertheless, autologous transfusion can partially alleviate the current pressure and dependence on blood banking systems. To achieve this, current gold standard autotransfusion devices should be complemented with widely available, cost-efficient, and time-efficient devices. The novel HemoClear cell salvage device (HemoClear BV, Zwolle, Netherlands), a gravity-driven microfilter, potentially is widely employable. We evaluated its performance in the cardiac postoperative setting compared to the centrifugal XTRA™ autotransfusion device.

Methods: In a split-unit study (n = 18), shed blood collected 18 hours after cardiothoracic surgery was divided into two equal volumes. One-half was processed by the XTRA™ device and the other with the HemoClear blood separation system. In this paired set-up, equal washing volumes were used for both methods. Washing effectivity and cellular recovery were determined by measuring of complete blood count, free hemoglobin, complement C3, complement C4, and D-dimer in both concentrate as filtrate. Also, processing times and volumes were evaluated.

Results: The HemoClear and XTRA™ devices showed equal effectiveness in concentrating erythrocytes and leucocytes. Both methods reduced complement C3, complement C4, and D-dimer by ≥90%. The centrifugal device reduced solutes more significantly by up to 99%. Free hemoglobin load was reduced to 12.9% and 15.5% by the XTRA™ and HemoClear, respectively.

Conclusion: The HemoClear device effectively produced washed concentrated red blood cells comparably to the conventional centrifugal XTRA™ autotransfusion device. Although the centrifugal XTRA™ device achieved a significantly higher reduction in contaminants, the HemoClear device achieved acceptable blood quality and seems promising in settings where gold standard cell savers are unaffordable or unpractical.

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CiteScore
3.10
自引率
0.00%
发文量
29
审稿时长
18 weeks
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