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Major and minor subgroup profile of blood in patients receiving multiple transfusions and donors

OBJECTIVE: It was aimed to profile the blood subgroups of our region and to reveal the prevalence of auto/alloimmune sensitization in patients who had to undergo multiple erythrocyte transfusions and to establish the sensitization profile by screening major and minor subgroups. MATERIALS AND METHODS...

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Autores principales: Orhan, Mehmet Fatih, Adigül, Merve Pilavci, Altindiş, Mustafa, Köroğlu, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9855220/
https://www.ncbi.nlm.nih.gov/pubmed/36687545
http://dx.doi.org/10.4103/ajts.ajts_17_21
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author Orhan, Mehmet Fatih
Adigül, Merve Pilavci
Altindiş, Mustafa
Köroğlu, Mehmet
author_facet Orhan, Mehmet Fatih
Adigül, Merve Pilavci
Altindiş, Mustafa
Köroğlu, Mehmet
author_sort Orhan, Mehmet Fatih
collection PubMed
description OBJECTIVE: It was aimed to profile the blood subgroups of our region and to reveal the prevalence of auto/alloimmune sensitization in patients who had to undergo multiple erythrocyte transfusions and to establish the sensitization profile by screening major and minor subgroups. MATERIALS AND METHODS: In this study, the distribution of ABO and Rh system major subgroups was studied in 100 donor blood. As the patient group, 50 patients who received three or more red blood cell transfusions were included. In addition to this group, Kell, Lewis, Duffy blood group systems were studied. RESULTS: According to the ABO system, 35% of the donors were in O, 33% in A, 17% in AB, and 15% in B. According to the Rh system, 75% is Dvi positive. Rh system is 99% e positive and 33% E positive in major subgroups and Kell1 positivity is 8%. In the patient group, 22% D(-) was determined compared to Rh blood group. Among the major subgroups of Rh, C was 68%, E was 14%, c was 76%, and e positivity was found to be 100%. The Kell1 negativity rate is 96%. The highest negativity was found in 86% Lea antigen in Lewis system, in 36% S antigen in MNS system, 34% Fyb antigen in Duffy system, and 24% Jka antigen in Kidd system. When inappropriate blood is given for any antigen, a double population is formed. The double negativities we detected in our study occurred as follows according to blood group systems: E 18%, C 12%, c 8%, Cw 2%, Kell 1 2%, M 8%, N 4%, S 18%, s 6%, Fya 8%, Jka 6%, Jkb 22%. Indirect Agglutination Test (IAT) was negative in all patients. CONCLUSION: IAT negativity in all patient groups suggests that we do not develop alloimmunization, but the high rates of double population suggest a high risk of alloimmunization.
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spelling pubmed-98552202023-01-21 Major and minor subgroup profile of blood in patients receiving multiple transfusions and donors Orhan, Mehmet Fatih Adigül, Merve Pilavci Altindiş, Mustafa Köroğlu, Mehmet Asian J Transfus Sci Original Article OBJECTIVE: It was aimed to profile the blood subgroups of our region and to reveal the prevalence of auto/alloimmune sensitization in patients who had to undergo multiple erythrocyte transfusions and to establish the sensitization profile by screening major and minor subgroups. MATERIALS AND METHODS: In this study, the distribution of ABO and Rh system major subgroups was studied in 100 donor blood. As the patient group, 50 patients who received three or more red blood cell transfusions were included. In addition to this group, Kell, Lewis, Duffy blood group systems were studied. RESULTS: According to the ABO system, 35% of the donors were in O, 33% in A, 17% in AB, and 15% in B. According to the Rh system, 75% is Dvi positive. Rh system is 99% e positive and 33% E positive in major subgroups and Kell1 positivity is 8%. In the patient group, 22% D(-) was determined compared to Rh blood group. Among the major subgroups of Rh, C was 68%, E was 14%, c was 76%, and e positivity was found to be 100%. The Kell1 negativity rate is 96%. The highest negativity was found in 86% Lea antigen in Lewis system, in 36% S antigen in MNS system, 34% Fyb antigen in Duffy system, and 24% Jka antigen in Kidd system. When inappropriate blood is given for any antigen, a double population is formed. The double negativities we detected in our study occurred as follows according to blood group systems: E 18%, C 12%, c 8%, Cw 2%, Kell 1 2%, M 8%, N 4%, S 18%, s 6%, Fya 8%, Jka 6%, Jkb 22%. Indirect Agglutination Test (IAT) was negative in all patients. CONCLUSION: IAT negativity in all patient groups suggests that we do not develop alloimmunization, but the high rates of double population suggest a high risk of alloimmunization. Wolters Kluwer - Medknow 2022 2022-11-12 /pmc/articles/PMC9855220/ /pubmed/36687545 http://dx.doi.org/10.4103/ajts.ajts_17_21 Text en Copyright: © 2022 Asian Journal of Transfusion Science https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Orhan, Mehmet Fatih
Adigül, Merve Pilavci
Altindiş, Mustafa
Köroğlu, Mehmet
Major and minor subgroup profile of blood in patients receiving multiple transfusions and donors
title Major and minor subgroup profile of blood in patients receiving multiple transfusions and donors
title_full Major and minor subgroup profile of blood in patients receiving multiple transfusions and donors
title_fullStr Major and minor subgroup profile of blood in patients receiving multiple transfusions and donors
title_full_unstemmed Major and minor subgroup profile of blood in patients receiving multiple transfusions and donors
title_short Major and minor subgroup profile of blood in patients receiving multiple transfusions and donors
title_sort major and minor subgroup profile of blood in patients receiving multiple transfusions and donors
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9855220/
https://www.ncbi.nlm.nih.gov/pubmed/36687545
http://dx.doi.org/10.4103/ajts.ajts_17_21
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