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从采血管采血后 24 小时内冷冻的血浆中制备的冷沉淀含有可接受水平的纤维蛋白原和 VIII 因子。

Cryoprecipitate prepared from plasma frozen within 24 hours after phlebotomy contains acceptable levels of fibrinogen and VIIIC.

机构信息

Institute for Transfusion Medicine, Pittsburgh, Pennsylvania, USA.

出版信息

Transfusion. 2010 May;50(5):1014-8. doi: 10.1111/j.1537-2995.2009.02535.x. Epub 2009 Dec 9.

Abstract

BACKGROUND

As blood centers prepare fewer plasma products from female donors to avoid HLA antibodies, the standard starting material for cryoprecipitate (cryo), fresh-frozen plasma (FFP), might become increasingly scarce. A unit of cryo must contain at a minimum 80 IU of VIIIC and 150 mg of fibrinogen. Plasma frozen within 24 hours after phlebotomy (FP24) contains nearly equivalent levels of clotting factors as FFP at the time of thawing and, although not AABB/FDA approved for this purpose, might be a suitable starting material for cryo (cryo24) manufacture.

STUDY DESIGN AND METHODS

FP24 was collected from 20 male donors and cryo24 was subsequently prepared according to standard blood center protocols. The cryo24 was then thawed and VIIIC, von Willebrand factor (VWF) antigen, and fibrinogen levels were measured in these cryo24 units and compared to the corresponding levels in 20 randomly selected units of standard cryo (prepared from FFP).

RESULTS

The mean (+/-SD) levels in cryo and cryo24 at the time of thawing were as follows: fibrinogen (mg/unit) 455.8 (+/-172.6) and 575.8 (+/-185.9; p = 0.04), VIIIC (IU/unit) 216.1 (+/-52.3) and 252.4 (+/-70.1; p = 0.07), and VWF (IU/unit) 448.1 (+/-118.9) and 505.9 (+/-135.1; p = 0.16), respectively. All units of standard cryo and cryo24 met the current minimum content standards.

CONCLUSION

All units of cryo24 in this pilot study met the current minimum content standards for cryo. While clinical studies of its efficacy are warranted, cryo24's in vitro characteristics are at least equivalent to that of standard cryo.

摘要

背景

由于血液中心准备从女性供体中制备更少的血浆产品以避免 HLA 抗体,因此作为制备冷沉淀(cryo)的标准起始材料,新鲜冷冻血浆(FFP)可能会变得越来越稀缺。一个单位的 cryo 必须至少含有 80IU 的 VIII 因子和 150mg 的纤维蛋白原。在采血后 24 小时内冷冻的血浆(FP24)在解冻时几乎具有与 FFP 相同的凝血因子水平,尽管它没有获得 AABB/FDA 的批准用于此目的,但可能是制备 cryo(cryo24)的合适起始材料。

研究设计和方法

从 20 名男性供体中采集 FP24,并根据标准的血液中心方案制备 cryo24。然后解冻 cryo24,并测量这些 cryo24 单位中的 VIII 因子、血管性血友病因子(VWF)抗原和纤维蛋白原水平,并与 20 个随机选择的标准 cryo 单位(从 FFP 制备)的相应水平进行比较。

结果

解冻时 cryo 和 cryo24 的平均(+/-SD)水平如下:纤维蛋白原(mg/单位)455.8(+/-172.6)和 575.8(+/-185.9;p=0.04),VIII 因子(IU/单位)216.1(+/-52.3)和 252.4(+/-70.1;p=0.07),以及 VWF(IU/单位)448.1(+/-118.9)和 505.9(+/-135.1;p=0.16)。所有标准 cryo 和 cryo24 单位均符合当前的最低含量标准。

结论

在这项试点研究中,所有 cryo24 单位均符合当前 cryo 的最低含量标准。虽然需要进行其疗效的临床研究,但 cryo24 的体外特性至少与标准 cryo 相当。

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