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A comparison of three column agglutination tests for red blood cell alloantibody identification

OBJECTIVE: Commercial kits of column tests for pre-transfusion testing have progressively replaced conventional tube tests in most laboratories. Aim of this study was to compare three commercial test cell panels for the identification of irregular red blood cell (RBC) alloantibodies. Overall, 44 sam...

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Autores principales: Blomme, Siska, De Maertelaere, Emilie, Verhoye, Eline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057655/
https://www.ncbi.nlm.nih.gov/pubmed/32131887
http://dx.doi.org/10.1186/s13104-020-04974-x
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author Blomme, Siska
De Maertelaere, Emilie
Verhoye, Eline
author_facet Blomme, Siska
De Maertelaere, Emilie
Verhoye, Eline
author_sort Blomme, Siska
collection PubMed
description OBJECTIVE: Commercial kits of column tests for pre-transfusion testing have progressively replaced conventional tube tests in most laboratories. Aim of this study was to compare three commercial test cell panels for the identification of irregular red blood cell (RBC) alloantibodies. Overall, 44 samples with a positive indirect antiglobulin test (IAT) by routine testing were used for comparison of following panels: Ortho RESOLVE(®) panelC (Ortho Clinical Diagnostics (OCD), Milan, Italy), ID-DiaPanel(-P) (Bio-Rad Laboratories, CA, USA) and Identisera Diana(P) (Grifols, Barcelona, Spain). Column agglutination techniques were used, with microtubes containing either microgel (Bio-Rad/Grifols) or glass bead microparticles (Ortho). RESULTS: Alloantibody identification was possible in 38 samples, of which identical identification was shown in 33 samples by all methods. The remaining samples showed differences between certain methods, with the gel card system being superior to the glass card system for analyzing stored samples Considering that not all samples were evaluated in all three methods, the concordance rate reached 100% between Bio-Rad and Grifols, 90.5% between Bio-Rad and OCD, 86.5% between OCD and Grifols and 90.5% between all methods. Although differences in sensitivities were seen for specific antibodies, the three methods showed comparable performance for the identification of RBC alloantibodies.
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spelling pubmed-70576552020-03-10 A comparison of three column agglutination tests for red blood cell alloantibody identification Blomme, Siska De Maertelaere, Emilie Verhoye, Eline BMC Res Notes Research Note OBJECTIVE: Commercial kits of column tests for pre-transfusion testing have progressively replaced conventional tube tests in most laboratories. Aim of this study was to compare three commercial test cell panels for the identification of irregular red blood cell (RBC) alloantibodies. Overall, 44 samples with a positive indirect antiglobulin test (IAT) by routine testing were used for comparison of following panels: Ortho RESOLVE(®) panelC (Ortho Clinical Diagnostics (OCD), Milan, Italy), ID-DiaPanel(-P) (Bio-Rad Laboratories, CA, USA) and Identisera Diana(P) (Grifols, Barcelona, Spain). Column agglutination techniques were used, with microtubes containing either microgel (Bio-Rad/Grifols) or glass bead microparticles (Ortho). RESULTS: Alloantibody identification was possible in 38 samples, of which identical identification was shown in 33 samples by all methods. The remaining samples showed differences between certain methods, with the gel card system being superior to the glass card system for analyzing stored samples Considering that not all samples were evaluated in all three methods, the concordance rate reached 100% between Bio-Rad and Grifols, 90.5% between Bio-Rad and OCD, 86.5% between OCD and Grifols and 90.5% between all methods. Although differences in sensitivities were seen for specific antibodies, the three methods showed comparable performance for the identification of RBC alloantibodies. BioMed Central 2020-03-04 /pmc/articles/PMC7057655/ /pubmed/32131887 http://dx.doi.org/10.1186/s13104-020-04974-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Note
Blomme, Siska
De Maertelaere, Emilie
Verhoye, Eline
A comparison of three column agglutination tests for red blood cell alloantibody identification
title A comparison of three column agglutination tests for red blood cell alloantibody identification
title_full A comparison of three column agglutination tests for red blood cell alloantibody identification
title_fullStr A comparison of three column agglutination tests for red blood cell alloantibody identification
title_full_unstemmed A comparison of three column agglutination tests for red blood cell alloantibody identification
title_short A comparison of three column agglutination tests for red blood cell alloantibody identification
title_sort comparison of three column agglutination tests for red blood cell alloantibody identification
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057655/
https://www.ncbi.nlm.nih.gov/pubmed/32131887
http://dx.doi.org/10.1186/s13104-020-04974-x
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