Sanna Susila, Teemu Silver, Tuukka Helin, Timo Jama, Jouni Lauronen, Lotta Joutsi-Korhonen, Minna Ilmakunnas
{"title":"白细胞诱导和长时间保存对冷藏全血凝血作用的体外研究。","authors":"Sanna Susila, Teemu Silver, Tuukka Helin, Timo Jama, Jouni Lauronen, Lotta Joutsi-Korhonen, Minna Ilmakunnas","doi":"10.1111/vox.70075","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objectives: </strong>Cold-stored whole blood (CSWB) for haemodynamically unstable bleeding patients is especially convenient when platelets are otherwise unavailable and simple logistics are favoured, as in prehospital situations. Storage times exceeding the currently common 21 days would be beneficial in situations where normal blood processing and distribution is disturbed. To better understand extended-storage CSWB haemostatic properties, we studied leukoreduced CSWB (LR-CSWB) and non-leukoreduced CSWB (non-LR-CSWB) for 5 weeks of cold storage.</p><p><strong>Materials and methods: </strong>Non-LR-CSWB was donated by seven donors and refrigerated for 5 weeks. Eight units of 20-day-old LR-CSWB returned from clinical rotation unused were stored for an additional 2 weeks. Previously published results were used for early-storage LR-CSWB data. Blood counts, coagulation assays, multiple electrode aggregometry, thrombin generation, rotational thromboelastometry and sonorheometry were analysed.</p><p><strong>Results: </strong>Regardless of leukoreduction, markedly reduced platelet aggregation and increasing FXIII levels as a sign of platelet activation were seen during storage. Coagulation factors generally decreased and clotting times increased during storage, but endogenous thrombin potential remained normal at 5 weeks in both groups. Viscoelastic assays displayed conflicting results later during storage, with extremely low clot stiffness in sonorheometry concomitantly with apparently adequate clotting in thromboelastometry.</p><p><strong>Conclusion: </strong>Most haemostatic changes in LR-CSWB and non-LR-CSWB occur within the first 2 weeks of storage. Little difference remains between LR-CSWB and non-LR-CSWB aged 5 weeks. Differences in viscoelastic properties suggest that clot strength may be weaker than thought already in 14-day-old CSWB regardless of leukoreduction.</p>","PeriodicalId":23631,"journal":{"name":"Vox Sanguinis","volume":" ","pages":"881-891"},"PeriodicalIF":1.6000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12422834/pdf/","citationCount":"0","resultStr":"{\"title\":\"The effect of leukoreduction and prolonged storage on coagulation in cold-stored whole blood: An in vitro study.\",\"authors\":\"Sanna Susila, Teemu Silver, Tuukka Helin, Timo Jama, Jouni Lauronen, Lotta Joutsi-Korhonen, Minna Ilmakunnas\",\"doi\":\"10.1111/vox.70075\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background and objectives: </strong>Cold-stored whole blood (CSWB) for haemodynamically unstable bleeding patients is especially convenient when platelets are otherwise unavailable and simple logistics are favoured, as in prehospital situations. Storage times exceeding the currently common 21 days would be beneficial in situations where normal blood processing and distribution is disturbed. To better understand extended-storage CSWB haemostatic properties, we studied leukoreduced CSWB (LR-CSWB) and non-leukoreduced CSWB (non-LR-CSWB) for 5 weeks of cold storage.</p><p><strong>Materials and methods: </strong>Non-LR-CSWB was donated by seven donors and refrigerated for 5 weeks. Eight units of 20-day-old LR-CSWB returned from clinical rotation unused were stored for an additional 2 weeks. Previously published results were used for early-storage LR-CSWB data. Blood counts, coagulation assays, multiple electrode aggregometry, thrombin generation, rotational thromboelastometry and sonorheometry were analysed.</p><p><strong>Results: </strong>Regardless of leukoreduction, markedly reduced platelet aggregation and increasing FXIII levels as a sign of platelet activation were seen during storage. Coagulation factors generally decreased and clotting times increased during storage, but endogenous thrombin potential remained normal at 5 weeks in both groups. Viscoelastic assays displayed conflicting results later during storage, with extremely low clot stiffness in sonorheometry concomitantly with apparently adequate clotting in thromboelastometry.</p><p><strong>Conclusion: </strong>Most haemostatic changes in LR-CSWB and non-LR-CSWB occur within the first 2 weeks of storage. Little difference remains between LR-CSWB and non-LR-CSWB aged 5 weeks. Differences in viscoelastic properties suggest that clot strength may be weaker than thought already in 14-day-old CSWB regardless of leukoreduction.</p>\",\"PeriodicalId\":23631,\"journal\":{\"name\":\"Vox Sanguinis\",\"volume\":\" \",\"pages\":\"881-891\"},\"PeriodicalIF\":1.6000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12422834/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Vox Sanguinis\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1111/vox.70075\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/5 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"HEMATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Vox Sanguinis","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/vox.70075","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/5 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
The effect of leukoreduction and prolonged storage on coagulation in cold-stored whole blood: An in vitro study.
Background and objectives: Cold-stored whole blood (CSWB) for haemodynamically unstable bleeding patients is especially convenient when platelets are otherwise unavailable and simple logistics are favoured, as in prehospital situations. Storage times exceeding the currently common 21 days would be beneficial in situations where normal blood processing and distribution is disturbed. To better understand extended-storage CSWB haemostatic properties, we studied leukoreduced CSWB (LR-CSWB) and non-leukoreduced CSWB (non-LR-CSWB) for 5 weeks of cold storage.
Materials and methods: Non-LR-CSWB was donated by seven donors and refrigerated for 5 weeks. Eight units of 20-day-old LR-CSWB returned from clinical rotation unused were stored for an additional 2 weeks. Previously published results were used for early-storage LR-CSWB data. Blood counts, coagulation assays, multiple electrode aggregometry, thrombin generation, rotational thromboelastometry and sonorheometry were analysed.
Results: Regardless of leukoreduction, markedly reduced platelet aggregation and increasing FXIII levels as a sign of platelet activation were seen during storage. Coagulation factors generally decreased and clotting times increased during storage, but endogenous thrombin potential remained normal at 5 weeks in both groups. Viscoelastic assays displayed conflicting results later during storage, with extremely low clot stiffness in sonorheometry concomitantly with apparently adequate clotting in thromboelastometry.
Conclusion: Most haemostatic changes in LR-CSWB and non-LR-CSWB occur within the first 2 weeks of storage. Little difference remains between LR-CSWB and non-LR-CSWB aged 5 weeks. Differences in viscoelastic properties suggest that clot strength may be weaker than thought already in 14-day-old CSWB regardless of leukoreduction.
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.