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Red cell alloimmunization in repeatedly transfused patients

INTRODUCTION: Repeated blood transfusions can result in the production of alloantibodies against one or more red cell antigens, which complicates subsequent transfusions. Aims: The study was done to find incidence of various red cell alloantibodies; to determine the type of alloantibody; to identify...

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Autores principales: Bhuva, Dimel K., Vachhani, Jitendra H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613416/
https://www.ncbi.nlm.nih.gov/pubmed/28970677
http://dx.doi.org/10.4103/0973-6247.214347
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author Bhuva, Dimel K.
Vachhani, Jitendra H.
author_facet Bhuva, Dimel K.
Vachhani, Jitendra H.
author_sort Bhuva, Dimel K.
collection PubMed
description INTRODUCTION: Repeated blood transfusions can result in the production of alloantibodies against one or more red cell antigens, which complicates subsequent transfusions. Aims: The study was done to find incidence of various red cell alloantibodies; to determine the type of alloantibody; to identify the factors such as frequency of transfusion, splenectomy status, donor ethnicity and gender and their association with the development of antibody in repeatedly transfused patients. MATERIALS AND METHODS: This study was carried out in Dept. of IHBT, Shree M. P. Shah Medical College, Jamnagar, Gujarat. Blood was taken from the patients of thalassemia major, sickle cell disease, chronic renal failure, post partum haemorrhage, aplastic anemia, Myelodysplastic syndrome with more than 10 red cell transfusions. The plasma/serum was used for antibody screening and antibody identification test. Three cell antibody screening was performed using antihuman globulin gel cards (ID-Card LISS/Coombs) and three cell panel (ID-DiaCell I, II, III-Asia). Those with positive antibody screening were analyzed further for antibody identification test using eleven cell panel (Set ID-Dia Panel). RESULTS: Antibody screening and identification was done in 2 consecutive set of samples (n = 300) which showed, nine (9) patients (3%) were alloimmunized. All repeatedly transfused patients had developed alloantibody before the starting of study period, no patient developed new alloantibody during study period. CONCLUSIONS: Alloantibodies should be identified in repeatedly transfused patients and should be given corresponding antigen negative blood unit which will minimize the antibody mediated destruction of transfused red cells.
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spelling pubmed-56134162017-10-02 Red cell alloimmunization in repeatedly transfused patients Bhuva, Dimel K. Vachhani, Jitendra H. Asian J Transfus Sci Original Article INTRODUCTION: Repeated blood transfusions can result in the production of alloantibodies against one or more red cell antigens, which complicates subsequent transfusions. Aims: The study was done to find incidence of various red cell alloantibodies; to determine the type of alloantibody; to identify the factors such as frequency of transfusion, splenectomy status, donor ethnicity and gender and their association with the development of antibody in repeatedly transfused patients. MATERIALS AND METHODS: This study was carried out in Dept. of IHBT, Shree M. P. Shah Medical College, Jamnagar, Gujarat. Blood was taken from the patients of thalassemia major, sickle cell disease, chronic renal failure, post partum haemorrhage, aplastic anemia, Myelodysplastic syndrome with more than 10 red cell transfusions. The plasma/serum was used for antibody screening and antibody identification test. Three cell antibody screening was performed using antihuman globulin gel cards (ID-Card LISS/Coombs) and three cell panel (ID-DiaCell I, II, III-Asia). Those with positive antibody screening were analyzed further for antibody identification test using eleven cell panel (Set ID-Dia Panel). RESULTS: Antibody screening and identification was done in 2 consecutive set of samples (n = 300) which showed, nine (9) patients (3%) were alloimmunized. All repeatedly transfused patients had developed alloantibody before the starting of study period, no patient developed new alloantibody during study period. CONCLUSIONS: Alloantibodies should be identified in repeatedly transfused patients and should be given corresponding antigen negative blood unit which will minimize the antibody mediated destruction of transfused red cells. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5613416/ /pubmed/28970677 http://dx.doi.org/10.4103/0973-6247.214347 Text en Copyright: © 2017 Asian Journal of Transfusion Science http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Bhuva, Dimel K.
Vachhani, Jitendra H.
Red cell alloimmunization in repeatedly transfused patients
title Red cell alloimmunization in repeatedly transfused patients
title_full Red cell alloimmunization in repeatedly transfused patients
title_fullStr Red cell alloimmunization in repeatedly transfused patients
title_full_unstemmed Red cell alloimmunization in repeatedly transfused patients
title_short Red cell alloimmunization in repeatedly transfused patients
title_sort red cell alloimmunization in repeatedly transfused patients
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5613416/
https://www.ncbi.nlm.nih.gov/pubmed/28970677
http://dx.doi.org/10.4103/0973-6247.214347
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