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Process Improvement by Eliminating Mixing of Whole Blood Units after an Overnight Hold Prior to Component Production Using the Buffy Coat Method

The elimination of a thorough manual mixing of whole blood (WB) which takes place following the overnight hold, but before the first centrifugation step, during buffy coat component production at Canadian Blood Services (CBS) was investigated. WB was pooled after donation and split. Pairs of platele...

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Autores principales: Mastronardi, Cherie, Schubert, Peter, Levin, Elena, Bhakta, Varsha, Yi, Qi-Long, Hansen, Adele, Stewart, Tamiko, Jenkins, Craig, Lefresne, Wanda, Sheffield, William, Acker, Jason P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771126/
https://www.ncbi.nlm.nih.gov/pubmed/24066260
http://dx.doi.org/10.1155/2013/154838
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author Mastronardi, Cherie
Schubert, Peter
Levin, Elena
Bhakta, Varsha
Yi, Qi-Long
Hansen, Adele
Stewart, Tamiko
Jenkins, Craig
Lefresne, Wanda
Sheffield, William
Acker, Jason P.
author_facet Mastronardi, Cherie
Schubert, Peter
Levin, Elena
Bhakta, Varsha
Yi, Qi-Long
Hansen, Adele
Stewart, Tamiko
Jenkins, Craig
Lefresne, Wanda
Sheffield, William
Acker, Jason P.
author_sort Mastronardi, Cherie
collection PubMed
description The elimination of a thorough manual mixing of whole blood (WB) which takes place following the overnight hold, but before the first centrifugation step, during buffy coat component production at Canadian Blood Services (CBS) was investigated. WB was pooled after donation and split. Pairs of platelet, red blood cell (RBC), and plasma components were produced, with half using the standard method and half using a method in which the mixing step was eliminated. Quality assessments included yield, pH, CD62P expression and morphology for platelets, hemoglobin, hematocrit, hemolysis, and supernatant K(+) for RBCs, and volume and factor VIII activity levels for plasma. All components, produced using either method, met CBS quality control criteria. There were no significant differences in platelet yield between components produced with and without mixing. A significant difference was seen for RBC hemolysis at expiry (P = 0.03), but for both groups, levels met quality control requirements. Noninferiority of components produced without mixing was confirmed for all parameters. Manual mixing is laborious and has a risk of repetitive strain for production staff and its significance is unclear. Elimination of this step will improve process efficiencies without compromising quality.
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spelling pubmed-37711262013-09-24 Process Improvement by Eliminating Mixing of Whole Blood Units after an Overnight Hold Prior to Component Production Using the Buffy Coat Method Mastronardi, Cherie Schubert, Peter Levin, Elena Bhakta, Varsha Yi, Qi-Long Hansen, Adele Stewart, Tamiko Jenkins, Craig Lefresne, Wanda Sheffield, William Acker, Jason P. J Blood Transfus Research Article The elimination of a thorough manual mixing of whole blood (WB) which takes place following the overnight hold, but before the first centrifugation step, during buffy coat component production at Canadian Blood Services (CBS) was investigated. WB was pooled after donation and split. Pairs of platelet, red blood cell (RBC), and plasma components were produced, with half using the standard method and half using a method in which the mixing step was eliminated. Quality assessments included yield, pH, CD62P expression and morphology for platelets, hemoglobin, hematocrit, hemolysis, and supernatant K(+) for RBCs, and volume and factor VIII activity levels for plasma. All components, produced using either method, met CBS quality control criteria. There were no significant differences in platelet yield between components produced with and without mixing. A significant difference was seen for RBC hemolysis at expiry (P = 0.03), but for both groups, levels met quality control requirements. Noninferiority of components produced without mixing was confirmed for all parameters. Manual mixing is laborious and has a risk of repetitive strain for production staff and its significance is unclear. Elimination of this step will improve process efficiencies without compromising quality. Hindawi Publishing Corporation 2013 2013-06-05 /pmc/articles/PMC3771126/ /pubmed/24066260 http://dx.doi.org/10.1155/2013/154838 Text en Copyright © 2013 Cherie Mastronardi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Mastronardi, Cherie
Schubert, Peter
Levin, Elena
Bhakta, Varsha
Yi, Qi-Long
Hansen, Adele
Stewart, Tamiko
Jenkins, Craig
Lefresne, Wanda
Sheffield, William
Acker, Jason P.
Process Improvement by Eliminating Mixing of Whole Blood Units after an Overnight Hold Prior to Component Production Using the Buffy Coat Method
title Process Improvement by Eliminating Mixing of Whole Blood Units after an Overnight Hold Prior to Component Production Using the Buffy Coat Method
title_full Process Improvement by Eliminating Mixing of Whole Blood Units after an Overnight Hold Prior to Component Production Using the Buffy Coat Method
title_fullStr Process Improvement by Eliminating Mixing of Whole Blood Units after an Overnight Hold Prior to Component Production Using the Buffy Coat Method
title_full_unstemmed Process Improvement by Eliminating Mixing of Whole Blood Units after an Overnight Hold Prior to Component Production Using the Buffy Coat Method
title_short Process Improvement by Eliminating Mixing of Whole Blood Units after an Overnight Hold Prior to Component Production Using the Buffy Coat Method
title_sort process improvement by eliminating mixing of whole blood units after an overnight hold prior to component production using the buffy coat method
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771126/
https://www.ncbi.nlm.nih.gov/pubmed/24066260
http://dx.doi.org/10.1155/2013/154838
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