Literature DB >> 26509823

A model for integrating molecular-based testing in transfusion services.

S Gerald Sandler1, Trina Horn2, Jessica Keller2, Al Langeberg1, Margaret A Keller2.   

Abstract

BACKGROUND: Molecular-based laboratory tests can predict blood group antigens and supplement serological methods, adding a unique technology to assist in resolving discrepant or incomplete blood group typing or antibody identification. Hospital transfusion services have options for integrating molecular-based methods in their routine operations. We describe here the model of a hospital-reference laboratory partnership.
MATERIALS AND METHODS: Blood samples for compatibility testing were obtained from patients in a 609-bed hospital serving an urban multiethnic and multiracial population. When results of blood group phenotyping by serological methods were inconclusive, samples were referred for molecular-based testing. The reference laboratory used several methods for genotyping, including polymerase chain reaction followed by restriction enzyme-linked polymorphism analysis, sequence-specific primer polymerase chain reaction and array-based approaches. Human erythrocyte antigen, RHCE and RHD single nucleotide polymorphism arrays were integrated into the laboratory as they became commercially available.
RESULTS: The hospital-reference laboratory model made it possible to integrate blood group genotyping promptly by current technology without the expense of new laboratory equipment or adding personnel with technical expertise. We describe ten cases that illustrate the categories of serological problems that were resolved by molecular methods. DISCUSSION: In-hospital molecular testing for transfusion services has logistical advantages, but is financially impractical for most hospitals. Our model demonstrates the advantages of a hospital-reference laboratory partnership. In conclusion, hospital transfusion services can integrate molecular-based testing in their routine services without delay by establishing a partnership with a molecular blood group reference laboratory. The hospital reference-laboratory model promotes genomic medicine without the expense of new equipment and skilled personnel, while supporting the economy of centralised large-scale laboratory operations.

Entities:  

Year:  2015        PMID: 26509823      PMCID: PMC5111386          DOI: 10.2450/2015.0070-15

Source DB:  PubMed          Journal:  Blood Transfus        ISSN: 1723-2007            Impact factor:   3.443


  24 in total

1.  Weak D alleles express distinct phenotypes.

Authors:  F F Wagner; A Frohmajer; B Ladewig; N I Eicher; C B Lonicer; T H Müller; M H Siegel; W A Flegel
Journal:  Blood       Date:  2000-04-15       Impact factor: 22.113

2.  How do we use molecular red blood cell antigen typing to supplement pretransfusion testing?

Authors:  Suneeti Sapatnekar; Priscilla I Figueroa
Journal:  Transfusion       Date:  2014-03-24       Impact factor: 3.157

3.  Do we need to be more concerned about weak D antigens?

Authors:  George Garratty
Journal:  Transfusion       Date:  2005-10       Impact factor: 3.157

4.  Partners for life: the transfusion program for patients with sickle cell disease offered at the American Red Cross Blood Services, Southern Region, Atlanta, Georgia.

Authors:  K L Hillyer; V W Hare; C D Josephson; S B Harris; C D Hillyer
Journal:  Immunohematology       Date:  2006

5.  Applying molecular immunohematology discoveries to standards of practice in blood banks: now is the time.

Authors:  Gregory A Denomme; Willy A Flegel
Journal:  Transfusion       Date:  2008-11       Impact factor: 3.157

6.  How I manage donors and patients with a weak D phenotype.

Authors:  Willy A Flegel
Journal:  Curr Opin Hematol       Date:  2006-11       Impact factor: 3.284

7.  It's time to phase in RHD genotyping for patients with a serologic weak D phenotype. College of American Pathologists Transfusion Medicine Resource Committee Work Group.

Authors:  S Gerald Sandler; Willy A Flegel; Connie M Westhoff; Gregory A Denomme; Meghan Delaney; Margaret A Keller; Susan T Johnson; Louis Katz; John T Queenan; Ralph R Vassallo; Clayton D Simon
Journal:  Transfusion       Date:  2014-12-01       Impact factor: 3.157

8.  The potential of blood group genotyping for transfusion medicine practice.

Authors:  C M Westhoff
Journal:  Immunohematology       Date:  2008

9.  Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals.

Authors:  C Tournamille; Y Colin; J P Cartron; C Le Van Kim
Journal:  Nat Genet       Date:  1995-06       Impact factor: 38.330

10.  Comments on: molecular matching of red blood cells is superior to serological matching in sickle cell disease patients.

Authors:  Sandra Taddie Nance; Margaret A Keller
Journal:  Rev Bras Hematol Hemoter       Date:  2013
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  5 in total

1.  A proposal for a rational transfusion strategy in patients of European and North African descent with weak D type 4.0 and 4.1 phenotypes.

Authors:  Willy A Flegel; Thierry Peyrard; Jacques Chiaroni; Christophe Tournamille; Déborah Jamet; France Pirenne
Journal:  Blood Transfus       Date:  2018-05-03       Impact factor: 3.443

Review 2.  Serological weak D phenotypes: a review and guidance for interpreting the RhD blood type using the RHD genotype.

Authors:  S Gerald Sandler; Leonard N Chen; Willy A Flegel
Journal:  Br J Haematol       Date:  2017-05-16       Impact factor: 6.998

3.  Molecular immunohaematology round table discussions at the AABB Annual Meeting, Orlando 2016.

Authors:  Willy A Flegel; Qing Chen; Lilian Castilho; Margaret A Keller; Ellen B Klapper; William J Lane; France Pirenne; Gary Stack; Maryse St-Louis; Christopher A Tormey; Dan A Waxman; Christof Weinstock; Silvano Wendel; Gregory A Denomme
Journal:  Blood Transfus       Date:  2018-02-14       Impact factor: 3.443

Review 4.  Red Cell Transfusions in the Genomics Era.

Authors:  Jamal H Carter; Willy A Flegel
Journal:  Semin Hematol       Date:  2019-11-08       Impact factor: 3.851

5.  Transfusion Support in Patients with Hematologic Disease: New and Novel Transfusion Modalities.

Authors:  Sandhya R Panch; Bipin N Savani; David F Stroncek
Journal:  Semin Hematol       Date:  2019-10       Impact factor: 3.851

  5 in total

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