冷库血小板产品的聚集形成与供体来源有关,而与储存货架风格或标签方向无关。

IF 1.6 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-08-26 DOI:10.1111/vox.70099
Kathleen Kelly, Susanne Marschner, Alisha Chitrakar, Micaela Jones, Jeffrey M Finlon, David Buesing, Kimberly A Thomas
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引用次数: 0

摘要

背景和目的:在美国,冷冻血小板(CSPs)储存14天被批准用于无法获得常规室温储存血小板的活动性出血患者。冷藏促进聚集体的形成,但具体的储存条件如何影响聚集体的形成仍然不清楚。由于CSP储存在透气袋中,我们研究了货架样式(穿孔,固体)或标签方向(向上,向下)如何影响CSP聚集体的形成。材料与方法:将17个单供者单采血小板(Trima 100%血浆)平均分成小容量血小板储存袋,每供者4个迷你单位。在以下条件下保存14天(1-6°C):(i)穿孔货架,标签放下;(ii)穿孔货架,贴上标签;(三)牢固置物,标签放下;(四)坚固的架子,贴好标签。对单位的聚集进行视觉评分,并检测血小板计数、平均血小板体积、未成熟血小板分数和代谢参数。在一个单位子集(N = 11个供体)中,我们评估了生理相关血流下的表面受体表达、凝血酶生成、聚集和闭塞。结果:在所有四种储存条件下,总发生率相似,并且相对于供体(变异系数[CV] = 116%)比储存条件(CV = 14%)变化更大。在固体货架上储存的单位与在穿孔货架上储存的单位相比,代谢参数有统计学上的显著差异,而货架类型之间的表型和功能差异不显著。在所有四种情况下,单位的内在止血功能没有差异。结论:csp的聚合形成似乎是供体依赖的,不受货架风格或标签放置的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aggregate formation in cold-stored platelet products is associated with donor source, not with storage shelf style nor label orientation.

Background and objectives: Cold-stored platelets (CSPs) stored out to 14 days are approved in the United States for use in actively bleeding patients when conventional room temperature-stored platelets are unavailable. Cold storage promotes aggregate formation, yet how specific storage conditions impact aggregate formation remains poorly defined. As CSPs are stored in gas-permeable bags, we investigated how the shelving style (perforated, solid) or label orientation (up, down) affects CSP aggregate formation.

Materials and methods: Single-donor apheresis platelets (N = 17, Trima 100% plasma) were split equally into small-volume platelet storage bags to create four mini-units/donor. These were stored for 14 days (1-6°C) under the following conditions: (i) perforated shelving, label down; (ii) perforated shelving, label up; (iii) solid shelving, label down; and (iv) solid shelving, label up. Units were visually scored for aggregates and assayed for platelet count, mean platelet volume, immature platelet fraction and metabolic parameters. In a subset of units (N = 11 donors), we evaluated surface receptor expression, thrombin generation, aggregation and occlusion under physiologically relevant flow.

Results: Aggregate occurrence was similar across all four storage conditions, and varied more with respect to donor (coefficient of variation [CV] = 116%) than storage condition (CV = 14%). While units stored on solid shelves had statistically significant different metabolic parameters compared to units stored on perforated shelves, phenotypical and functional differences between shelving styles were unremarkable. There were no differences in intrinsic haemostatic function of units under all four conditions.

Conclusion: Aggregate formation in CSPs appears to be donor-dependent, and not impacted by shelf style or label placement.

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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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