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Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light

BACKGROUND: A triple storage (TS) set allows for pathogen inactivation (PI) treatment of triple‐dose apheresis platelet products with amotosalen + UVA. We evaluated the quality and metabolic parameters of platelet concentrates (PCs) pathogen inactivated and stored for 7 days. MATERIALS AND METHODS:...

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Autores principales: Infanti, Laura, Pehlic, Vildana, Mitrovic, Sandra, Holbro, Andreas, Andresen, Silke, Payrat, Jean‐Marc, Lin, Jin‐Sying, Buser, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087429/
https://www.ncbi.nlm.nih.gov/pubmed/36124649
http://dx.doi.org/10.1111/tme.12913
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author Infanti, Laura
Pehlic, Vildana
Mitrovic, Sandra
Holbro, Andreas
Andresen, Silke
Payrat, Jean‐Marc
Lin, Jin‐Sying
Buser, Andreas
author_facet Infanti, Laura
Pehlic, Vildana
Mitrovic, Sandra
Holbro, Andreas
Andresen, Silke
Payrat, Jean‐Marc
Lin, Jin‐Sying
Buser, Andreas
author_sort Infanti, Laura
collection PubMed
description BACKGROUND: A triple storage (TS) set allows for pathogen inactivation (PI) treatment of triple‐dose apheresis platelet products with amotosalen + UVA. We evaluated the quality and metabolic parameters of platelet concentrates (PCs) pathogen inactivated and stored for 7 days. MATERIALS AND METHODS: Twelve triple‐dose products collected with two different apheresis platforms were treated with amotosalen+UVA. Products were split into three single‐dose units. Testing was made pretreatment, after splitting, at days 5 and 7 of storage. RESULTS: Single‐dose PI PCs had a mean platelet content of 2.89 ± 0.35 x 10(11). From baseline to day 7, pH remained stable (7.1 ± 0.1 vs. 7.0 ± 0.1), pO(2) increased (11.3 ± 2.4 vs. 18.3 ± 3.5 kPa) as did LDH (201 ± 119 vs. 324 ± 203 U/L) and lactate (3.6 ± 1.7 vs. 12.1 ± 1.5 mmol/L) (all p < 0.01); pCO(2) decreased (4.1 ± 0.8 vs. 1.5 ± 0.7 mmHg; p < 0.01) and so did bicarbonate (6.6 ± 1.1 vs. 2.5 ± 1.4 mmol/L), glucose (5.6 ± 1.2 vs. 0.4 ± 0.4 mmol/L) and ATP (3.4 ± 0.9 vs. 2.5 ± 1.4 nmol/10(8) platelets) (all p < 0.05). CONCLUSION: Triple‐dose PCs processed with the TS sets fulfilled the quality requirements and displayed metabolic changes of expected extent during 7‐day storage.
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spelling pubmed-100874292023-04-12 Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light Infanti, Laura Pehlic, Vildana Mitrovic, Sandra Holbro, Andreas Andresen, Silke Payrat, Jean‐Marc Lin, Jin‐Sying Buser, Andreas Transfus Med Short Communications BACKGROUND: A triple storage (TS) set allows for pathogen inactivation (PI) treatment of triple‐dose apheresis platelet products with amotosalen + UVA. We evaluated the quality and metabolic parameters of platelet concentrates (PCs) pathogen inactivated and stored for 7 days. MATERIALS AND METHODS: Twelve triple‐dose products collected with two different apheresis platforms were treated with amotosalen+UVA. Products were split into three single‐dose units. Testing was made pretreatment, after splitting, at days 5 and 7 of storage. RESULTS: Single‐dose PI PCs had a mean platelet content of 2.89 ± 0.35 x 10(11). From baseline to day 7, pH remained stable (7.1 ± 0.1 vs. 7.0 ± 0.1), pO(2) increased (11.3 ± 2.4 vs. 18.3 ± 3.5 kPa) as did LDH (201 ± 119 vs. 324 ± 203 U/L) and lactate (3.6 ± 1.7 vs. 12.1 ± 1.5 mmol/L) (all p < 0.01); pCO(2) decreased (4.1 ± 0.8 vs. 1.5 ± 0.7 mmHg; p < 0.01) and so did bicarbonate (6.6 ± 1.1 vs. 2.5 ± 1.4 mmol/L), glucose (5.6 ± 1.2 vs. 0.4 ± 0.4 mmol/L) and ATP (3.4 ± 0.9 vs. 2.5 ± 1.4 nmol/10(8) platelets) (all p < 0.05). CONCLUSION: Triple‐dose PCs processed with the TS sets fulfilled the quality requirements and displayed metabolic changes of expected extent during 7‐day storage. Blackwell Publishing Ltd 2022-09-20 2022-12 /pmc/articles/PMC10087429/ /pubmed/36124649 http://dx.doi.org/10.1111/tme.12913 Text en © 2022 The Authors. Transfusion Medicine published by John Wiley & Sons Ltd on behalf of British Blood Transfusion Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Short Communications
Infanti, Laura
Pehlic, Vildana
Mitrovic, Sandra
Holbro, Andreas
Andresen, Silke
Payrat, Jean‐Marc
Lin, Jin‐Sying
Buser, Andreas
Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light
title Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light
title_full Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light
title_fullStr Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light
title_full_unstemmed Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light
title_short Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light
title_sort pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light
topic Short Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087429/
https://www.ncbi.nlm.nih.gov/pubmed/36124649
http://dx.doi.org/10.1111/tme.12913
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