Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1782284168799977472 |
---|---|
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. |
format | Online Article Text |
id | pubmed-3771126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mastronardicherie processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT schubertpeter processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT levinelena processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT bhaktavarsha processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT yiqilong processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT hansenadele processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT stewarttamiko processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT jenkinscraig processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT lefresnewanda processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT sheffieldwilliam processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod AT ackerjasonp processimprovementbyeliminatingmixingofwholebloodunitsafteranovernightholdpriortocomponentproductionusingthebuffycoatmethod |