Literature DB >> 19490581

Set-up and routine use of a database of 10,555 genotyped blood donors to facilitate the screening of compatible blood components for alloimmunized patients.

J Perreault1, J Lavoie, P Painchaud, M Côté, J Constanzo-Yanez, R Côté, G Delage, F Gendron, S Dubuc, B Caron, R Lemieux, M St-Louis.   

Abstract

BACKGROUND AND OBJECTIVES: Large-scale genotyping of blood donors for red blood cell and platelet antigens has been predicted to replace phenotyping assays in the screening of compatible blood components for alloimmunized patients. Although several genotyping platforms have been described, novel procedures and processes are needed to perform genotyping efficiently and to maximize its benefits for blood banks.
MATERIALS AND METHODS: Here we describe the processes and procedures developed to introduce large-scale genotyping in our routine operations.
RESULTS: Preliminary cost-benefit analysis indicated that genotyping must target frequent blood donors (> 3 donations/year) to be efficiently used. A custom-designed computer application was developed to manage the whole project. It selects frequent donors among recent donations, prints coded labels to identify blood samples sent to the external genotyping laboratory, and stores genotyping results. It can search for donors compatible for any combination of the 22 genotyped antigens as well as consult the current inventory for the presence of the corresponding blood components. The phenotype of recovered components is confirmed by standard serology techniques prior to shipment to hospitals.
CONCLUSION: Since October 2007, 10 555 blood donors have been genotyped. The database is used on a regular basis to find compatible blood components with a genotype-phenotype concordance of 99.6%.

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Year:  2009        PMID: 19490581     DOI: 10.1111/j.1423-0410.2009.01177.x

Source DB:  PubMed          Journal:  Vox Sang        ISSN: 0042-9007            Impact factor:   2.144


  8 in total

1.  Evaluation of red blood cell and platelet antigen genotyping platforms (ID CORE XT/ID HPA XT) in routine clinical practice.

Authors:  Kirstin Finning; Radhika Bhandari; Fiona Sellers; Nicoletta Revelli; Maria Antonietta Villa; Eduardo Muñiz-Díaz; Núria Nogués
Journal:  Blood Transfus       Date:  2015-10-29       Impact factor: 3.443

2.  Applying molecular immunohaematology to regularly transfused thalassaemic patients in Thailand.

Authors:  Pairaya Rujirojindakul; Willy A Flegel
Journal:  Blood Transfus       Date:  2013-10-03       Impact factor: 3.443

3.  ABO genotyping: the quest for clinical applications.

Authors:  Willy A Flegel
Journal:  Blood Transfus       Date:  2012-11-27       Impact factor: 3.443

4.  Molecular typing for blood group antigens within 40 min by direct polymerase chain reaction from plasma or serum.

Authors:  Franz F Wagner; Willy A Flegel; Rita Bittner; Andrea Döscher
Journal:  Br J Haematol       Date:  2016-12-19       Impact factor: 6.998

Review 5.  The molecular genetics of blood group polymorphism.

Authors:  Geoff Daniels
Journal:  Hum Genet       Date:  2009-08-29       Impact factor: 4.132

Review 6.  Evolution of technology for molecular genotyping in blood group systems.

Authors:  Ajit Gorakshakar; Harita Gogri; Kanjaksha Ghosh
Journal:  Indian J Med Res       Date:  2017-09       Impact factor: 2.375

7.  Alternative blood products and clinical needs in transfusion medicine.

Authors:  Carolyn Whitsett; Stefania Vaglio; Giuliano Grazzini
Journal:  Stem Cells Int       Date:  2012-04-08       Impact factor: 5.443

8.  Extended Donor Typing by Pooled Capillary Electrophoresis: Impact in a Routine Setting.

Authors:  Franz F Wagner; Andrea Doescher; Rita Bittner; Thomas H Müller
Journal:  Transfus Med Hemother       Date:  2018-07-12       Impact factor: 3.747

  8 in total

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