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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Main Authors: Dimel K Bhuva, Jitendra H Vachhani
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2017-01-01
Series:Asian Journal of Transfusion Science
Subjects:
Online Access:http://www.ajts.org/article.asp?issn=0973-6247;year=2017;volume=11;issue=2;spage=115;epage=120;aulast=Bhuva
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author Dimel K Bhuva
Jitendra H Vachhani
author_facet Dimel K Bhuva
Jitendra H Vachhani
author_sort Dimel K Bhuva
collection DOAJ
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 doaj.art-4f884f9c54e341a0bf2ef76a0a4be23f2022-12-21T23:22:41ZengWolters Kluwer Medknow PublicationsAsian Journal of Transfusion Science0973-62471998-35652017-01-0111211512010.4103/0973-6247.214347Red cell alloimmunization in repeatedly transfused patientsDimel K BhuvaJitendra H VachhaniIntroduction: 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.http://www.ajts.org/article.asp?issn=0973-6247;year=2017;volume=11;issue=2;spage=115;epage=120;aulast=BhuvaAlloantibodiesantibody identificationantibody screening
spellingShingle Dimel K Bhuva
Jitendra H Vachhani
Red cell alloimmunization in repeatedly transfused patients
Asian Journal of Transfusion Science
Alloantibodies
antibody identification
antibody screening
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 Alloantibodies
antibody identification
antibody screening
url http://www.ajts.org/article.asp?issn=0973-6247;year=2017;volume=11;issue=2;spage=115;epage=120;aulast=Bhuva
work_keys_str_mv AT dimelkbhuva redcellalloimmunizationinrepeatedlytransfusedpatients
AT jitendrahvachhani redcellalloimmunizationinrepeatedlytransfusedpatients