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机采血小板中因子 V 活性:对 FV 缺乏症管理的影响。

Factor V activity in apheresis platelets: Implications for management of FV deficiency.

机构信息

Department of Laboratory Medicine, Yale School of Medicine, New Haven, Connecticut, USA.

Department of Pediatrics, Yale School of Medicine, New Haven, Connecticut, USA.

出版信息

Transfusion. 2021 Feb;61(2):405-409. doi: 10.1111/trf.16179. Epub 2020 Nov 9.

Abstract

BACKGROUND

Allogeneic platelet (PLT) infusion is a strategy to raise Factor V (FV) levels in patients with congenital FV deficiency. However, since FV is labile in vitro, we hypothesized that FV activity could be low in PLT units.

STUDY DESIGN AND METHODS

FV activity was tested using a prothrombin time-based platform in the supernatant and platelet lysate (PL) of apheresis PLT units (16 units stored in PLT additive solution with acetate and phosphate [PAS-C] and 10 units stored in plasma only), on post-collection days 3-6. Statistical analysis was performed using Student's t test (P < .05).

RESULTS

FV activity was severely diminished in PAS-C PLTs (N = 16) supernatant (3.70% ± 1.02%) and PL (3.26% ± 1.02%). FV activity in plasma-only PLTs (N = 10) was lower in both supernatant (44.55% ± 6.46%) and lysate (39.67% ± 6.33%) relative to normal plasma levels, but both were significantly higher (P < .0001) compared to PAS-C PLTs. In a separate set of experiments, FV activity in PAS-C PLTs examined serially over storage time (N = 3 for these experiments) showed that FV levels were reduced by day 3 and not significantly different by day 5 of storage (Day 3 supernatant 5.03% ± 1.41%; Day 5 supernatant: 3.10% ± 0.57%; P = .2; Day 3 lysate: 3.89% ± 1.03%; Day 5 lysate: 2.61% ± 0.41%; P = .4).

CONCLUSION

Plasma should be considered over PLTs as first-line therapy for non-complex FV deficiency-associated hemorrhage. If PLTs are considered for transfusion, plasma-only PLT units should be preferentially utilized, as PAS-C PLT have near-absent FV activity.

摘要

背景

异体血小板(PLT)输注是提高先天性 FV 缺乏症患者 FV 水平的一种策略。然而,由于 FV 在体外不稳定,我们假设 PLT 单位中的 FV 活性可能较低。

研究设计和方法

使用基于凝血酶原时间的平台检测在收集后第 3-6 天的 16 个单位的在含醋酸盐和磷酸盐的 PLT 添加剂溶液(PAS-C)中保存的异体 PLT 单位(APheresis PLT 单位)的上清液和血小板溶解物(PL)中的 FV 活性(N = 16)和仅在血浆中保存的 10 个单位的 PLT 单位的上清液(N = 10)和 PL(N = 10)。使用学生 t 检验进行统计分析(P <.05)。

结果

PAS-C PLT 的上清液(3.70% ± 1.02%)和 PL(3.26% ± 1.02%)中 FV 活性严重降低。仅在血浆中保存的 PLT(N = 10)的上清液(44.55% ± 6.46%)和 PL(39.67% ± 6.33%)中的 FV 活性均低于正常血浆水平,但与 PAS-C PLT 相比,两者均显著升高(P <.0001)。在另一组实验中,在存储时间内对 PAS-C PLT 中 FV 活性进行了连续检测(这些实验中 N = 3),结果表明 FV 水平在第 3 天降低,在第 5 天存储时无显著差异(第 3 天的上清液 5.03% ± 1.41%;第 5 天的上清液:3.10% ± 0.57%;P =.2;第 3 天的 PL:3.89% ± 1.03%;第 5 天的 PL:2.61% ± 0.41%;P =.4)。

结论

如果考虑输注 PLT,则应将血浆视为治疗非复杂性 FV 缺乏相关出血的一线疗法。如果考虑输注 PLT,则应优先使用仅含血浆的 PLT 单位,因为 PAS-C PLT 几乎没有 FV 活性。

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