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An experimental comparison and user evaluation of three different dried plasma products
Clinical Immunology and Transfusion Medicine, Karolinska University Hospital, Stockholm, Sweden, (SWE); Department of Center for Hematology and Regenerative Medicine (HERM), Karolinska Institutet, Stockholm, Sweden, (SWE).ORCID iD: 0009-0003-4182-5826
Department of Anaesthesiology and Intensive Care, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden, (SWE); Department of Anaesthesiology, Södra Älvsborgs Sjukhus, Borås, Sweden, (SWE); Helicopter Emergency Medical Service, Västra Götalandsregionen, Gothenburg, Sweden, (SWE).
Institute of Clinical Sciences, Department of Pediatric Anesthesia and Intensive Care, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden, (SWE).
Swedish Defence University, Department of War Studies. Department of Anaesthesiology and Intensive Care, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.ORCID iD: 0000-0001-7352-4356
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2025 (English)In: Vox Sanguinis, ISSN 0042-9007, E-ISSN 1423-0410, Vol. 120, no 11, p. 1051-1189Article in journal (Refereed) Published
Abstract [en]

Background and Objectives: Access to blood components in pre-hospital bleeding resuscitation is challenging. Dried plasma is a logistically superior alternative, and new products are emerging. Therefore, we aimed to evaluate laboratory and practical differences in three differently produced dried plasma products.

Materials and Methods: Single-donor lyophilized LyoPlas®, pooled-donor, lyophilizedand pathogen-reduced OctaplasLG Powder®, and single-donor sprayed-dried FrontlineODP™ along with fresh plasma (in-house, pre-FrontlineODP and Octa-plasLG) as controls were analysed (n = 8). Laboratory tests included measurements of various coagulation factors and thromboelastography. The practical evaluation ofthe dried plasma products included preparation time, time to dissolve the dried plasma and total time, together with subjective opinions from eight clinical users.

Results: The coagulation factor content was within human reference ranges for all dried plasma, with approximately 10%–20% loss compared with fresh plasma. More variations were observed in the single-donor products compared with the pooled products. Clot formation analysed by thromboelastography showed normal graphs. Reconstitution time was similar, ranging from on average 7–9 min. In the user evaluation, the reconstitution time and the possibility of using a plastic bag for the transfusion were emphasized as important, the latter fulfilled by two of the products.

Conclusion: The study supports that dried plasma may be produced with lyophilization or spray-drying technique, as well as with the addition of pathogen reduction, with preserved coagulation capability. The products were reconstituted in acceptable time and deemed feasible for pre-hospital use by eighth test users.

Place, publisher, year, edition, pages
2025. Vol. 120, no 11, p. 1051-1189
Keywords [en]
dried plasma, haemorrhage, major trauma, plasma transfusion, pre-hospital
National Category
Anesthesiology and Intensive Care
Research subject
War Studies
Identifiers
URN: urn:nbn:se:fhs:diva-14222DOI: 10.1111/vox.13798OAI: oai:DiVA.org:fhs-14222DiVA, id: diva2:2015927
Available from: 2025-11-24 Created: 2025-11-24 Last updated: 2025-11-27Bibliographically approved

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