Kathleen Kelly, Susanne Marschner, Alisha Chitrakar, Micaela Jones, Jeffrey M Finlon, David Buesing, Kimberly A Thomas
{"title":"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。","authors":"Kathleen Kelly, Susanne Marschner, Alisha Chitrakar, Micaela Jones, Jeffrey M Finlon, David Buesing, Kimberly A Thomas","doi":"10.1111/vox.70099","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objectives: </strong>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.</p><p><strong>Materials and methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>Aggregate formation in CSPs appears to be donor-dependent, and not impacted by shelf style or label placement.</p>","PeriodicalId":23631,"journal":{"name":"Vox Sanguinis","volume":" ","pages":""},"PeriodicalIF":1.6000,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Aggregate formation in cold-stored platelet products is associated with donor source, not with storage shelf style nor label orientation.\",\"authors\":\"Kathleen Kelly, Susanne Marschner, Alisha Chitrakar, Micaela Jones, Jeffrey M Finlon, David Buesing, Kimberly A Thomas\",\"doi\":\"10.1111/vox.70099\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and objectives: </strong>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.</p><p><strong>Materials and methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>Aggregate formation in CSPs appears to be donor-dependent, and not impacted by shelf style or label placement.</p>\",\"PeriodicalId\":23631,\"journal\":{\"name\":\"Vox Sanguinis\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-08-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Vox Sanguinis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/vox.70099\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vox Sanguinis","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/vox.70099","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
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.
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.