Red Cell Phenotyping in Thalassemia Patient at Songklanagarind Hospital
The purpose of this study was to determine the frequency of Rh, Kidd and Duffy phenotypes in thalassemia major patients with regular transfusion which may develop antibodies to red cell antigens that can be a significant complication of transfusion therapy. Red cell phenotyping for thalassemic patie...
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doaj-08c582ee95aa4a27adac320875a598c42020-11-25T02:38:12ZengPrince of Songkla UniversityJournal of Health Science and Medical Research (JHSMR)2586-99812630-05592016-06-01343131139162Red Cell Phenotyping in Thalassemia Patient at Songklanagarind HospitalPornkanok Saksrisirisakul0Wanwimon Yindee1Nardsuda Thawornsuk2Department of Pathorogy, Faculty of Medicine, Prince of Songkla, University, Hat Yai, Songkhla 90110,Department of Pathorogy, Faculty of Medicine, Prince of Songkla, University, Hat Yai, Songkhla 90110,Department of Pathorogy, Faculty of Medicine, Prince of Songkla, University, Hat Yai, Songkhla 90110,The purpose of this study was to determine the frequency of Rh, Kidd and Duffy phenotypes in thalassemia major patients with regular transfusion which may develop antibodies to red cell antigens that can be a significant complication of transfusion therapy. Red cell phenotyping for thalassemic patients at Songklanagarind Hospital will be helpful in antibody identification of single or multiple alloantibodies such as anti-C, anti-c, anti-e, anti-Jka, anti-Jkb, anti-Fya, and anti-Fyb. In addition, to understand phenotypes, antigens, and other blood group information may help in choosing the right blood for the patients. A total of 100 thalassemic patients between 2002-2014 who had not been previously typed, were the subjects of this study. Antigens of Rh, Kidd and Duffy systems were determined by the standard conventional tube method of red cell typing, column agglutination technique (CAT) and gel technique. The results of probable genotype in Rh system were DCe/DCe (R1R1) = 41%, DCe/DcE (R1R2) = 41%, DCe/Dce (R1R0) = 11%, DcE/DcE (R2R2) = 3%, DCE/DcE (RZR2) = 3% and DcE/Dce (R2R0) = 1%. In Kidd system, the phenotypes were Jk (a+b+) = 61%, Jk (a-b+) = 27%, Jk (a+b-) = 12%, and Jk (a-b-) = 0% and in Duffy system, the phenotypes were Fy (a+b+) = 55% Fy (a+b-) = 42%, Fy (a-b+) = 2% and Fy (a-b-) = 1%. This study showed that 41% of the patients had all antigens in Rh system (C, c, D, E, e), 61% of the patients were Jk (a+b+) phenotype and 55% of the patients were Fy (a+b+) phenotype. In conclusion, studying the frequency of Rh, Kidd and Duffy antigens in thalassemic major patients can be helpful in selecting antigen negative blood in order to prevent red all alloimmunization espectially in emergency situation.https://www.jhsmr.org/index.php/jhsmr/article/view/148antigenred cellthalassemia |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Pornkanok Saksrisirisakul Wanwimon Yindee Nardsuda Thawornsuk |
spellingShingle |
Pornkanok Saksrisirisakul Wanwimon Yindee Nardsuda Thawornsuk Red Cell Phenotyping in Thalassemia Patient at Songklanagarind Hospital Journal of Health Science and Medical Research (JHSMR) antigen red cell thalassemia |
author_facet |
Pornkanok Saksrisirisakul Wanwimon Yindee Nardsuda Thawornsuk |
author_sort |
Pornkanok Saksrisirisakul |
title |
Red Cell Phenotyping in Thalassemia Patient at Songklanagarind Hospital |
title_short |
Red Cell Phenotyping in Thalassemia Patient at Songklanagarind Hospital |
title_full |
Red Cell Phenotyping in Thalassemia Patient at Songklanagarind Hospital |
title_fullStr |
Red Cell Phenotyping in Thalassemia Patient at Songklanagarind Hospital |
title_full_unstemmed |
Red Cell Phenotyping in Thalassemia Patient at Songklanagarind Hospital |
title_sort |
red cell phenotyping in thalassemia patient at songklanagarind hospital |
publisher |
Prince of Songkla University |
series |
Journal of Health Science and Medical Research (JHSMR) |
issn |
2586-9981 2630-0559 |
publishDate |
2016-06-01 |
description |
The purpose of this study was to determine the frequency of Rh, Kidd and Duffy phenotypes in thalassemia major patients with regular transfusion which may develop antibodies to red cell antigens that can be a significant complication of transfusion therapy. Red cell phenotyping for thalassemic patients at Songklanagarind Hospital will be helpful in antibody identification of single or multiple alloantibodies such as anti-C, anti-c, anti-e, anti-Jka, anti-Jkb, anti-Fya, and anti-Fyb. In addition, to understand phenotypes, antigens, and other blood group information may help in choosing the right blood for the patients.
A total of 100 thalassemic patients between 2002-2014 who had not been previously typed, were the subjects of this study. Antigens of Rh, Kidd and Duffy systems were determined by the standard conventional tube method of red cell typing, column agglutination technique (CAT) and gel technique.
The results of probable genotype in Rh system were DCe/DCe (R1R1) = 41%, DCe/DcE (R1R2) = 41%, DCe/Dce (R1R0) = 11%, DcE/DcE (R2R2) = 3%, DCE/DcE (RZR2) = 3% and DcE/Dce (R2R0) = 1%. In Kidd system, the phenotypes were Jk (a+b+) = 61%, Jk (a-b+) = 27%, Jk (a+b-) = 12%, and Jk (a-b-) = 0% and in Duffy system, the phenotypes were Fy (a+b+) = 55% Fy (a+b-) = 42%, Fy (a-b+) = 2% and Fy (a-b-) = 1%. This study showed that 41% of the patients had all antigens in Rh system (C, c, D, E, e), 61% of the patients were Jk (a+b+) phenotype and 55% of the patients were Fy (a+b+) phenotype.
In conclusion, studying the frequency of Rh, Kidd and Duffy antigens in thalassemic major patients can be helpful in selecting antigen negative blood in order to prevent red all alloimmunization espectially in emergency situation. |
topic |
antigen red cell thalassemia |
url |
https://www.jhsmr.org/index.php/jhsmr/article/view/148 |
work_keys_str_mv |
AT pornkanoksaksrisirisakul redcellphenotypinginthalassemiapatientatsongklanagarindhospital AT wanwimonyindee redcellphenotypinginthalassemiapatientatsongklanagarindhospital AT nardsudathawornsuk redcellphenotypinginthalassemiapatientatsongklanagarindhospital |
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