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Incompatible blood transfusion: Challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia
BACKGROUND AND AIM: Autoimmune hemolytic anemia (AIHA) is characterized by the production of autoantibodies directed against red cell antigens. Most patients of AIHA arrive in the emergency or out-patient department (OPD) with severe anemia requiring urgent blood transfusion. Here we share our exper...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140051/ https://www.ncbi.nlm.nih.gov/pubmed/25161349 http://dx.doi.org/10.4103/0973-6247.137445 |
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author | Das, Sudipta Sekhar Zaman, Rafiq Uz Safi, Mohammad |
author_facet | Das, Sudipta Sekhar Zaman, Rafiq Uz Safi, Mohammad |
author_sort | Das, Sudipta Sekhar |
collection | PubMed |
description | BACKGROUND AND AIM: Autoimmune hemolytic anemia (AIHA) is characterized by the production of autoantibodies directed against red cell antigens. Most patients of AIHA arrive in the emergency or out-patient department (OPD) with severe anemia requiring urgent blood transfusion. Here we share our experience of managing these patients with incompatible blood transfusions and suggest the minimal test required to assure patient safety. MATERIALS AND METHODS: A total of 14 patients admitted with severe anemia, diagnosed with AIHA and requiring blood transfusion urgently were included in the study. A series of immunohematological investigations were performed to confirm the diagnosis and issue best match packed red blood cells (PRBC) to these patients. RESULTS: A total of 167 PRBC units were crossmatched for 14 patients of which 46 units (28%) were found to be best match ones and 26 (56.5%) of these units were transfused. A mean turn around time of 222 min was observed in issuing the “best match” blood. Severe hemolysis was observed in all patients with a median hemoglobin increment of 0.88 g/dl after each unit PRBC transfusion. CONCLUSION: Decision to transfuse in AIHA should be based on the clinical condition of the patient. No critical patient should be denied blood transfusion due to serological incompatibility. Minimum investigations such as direct antiglobulin test (DAT), antibody screening and autocontrol should be performed to ensure transfusion safety in patients. All transfusion services should be capable of issuing “best match” PRBCs in AIHA. |
format | Online Article Text |
id | pubmed-4140051 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41400512014-08-26 Incompatible blood transfusion: Challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia Das, Sudipta Sekhar Zaman, Rafiq Uz Safi, Mohammad Asian J Transfus Sci Original Article BACKGROUND AND AIM: Autoimmune hemolytic anemia (AIHA) is characterized by the production of autoantibodies directed against red cell antigens. Most patients of AIHA arrive in the emergency or out-patient department (OPD) with severe anemia requiring urgent blood transfusion. Here we share our experience of managing these patients with incompatible blood transfusions and suggest the minimal test required to assure patient safety. MATERIALS AND METHODS: A total of 14 patients admitted with severe anemia, diagnosed with AIHA and requiring blood transfusion urgently were included in the study. A series of immunohematological investigations were performed to confirm the diagnosis and issue best match packed red blood cells (PRBC) to these patients. RESULTS: A total of 167 PRBC units were crossmatched for 14 patients of which 46 units (28%) were found to be best match ones and 26 (56.5%) of these units were transfused. A mean turn around time of 222 min was observed in issuing the “best match” blood. Severe hemolysis was observed in all patients with a median hemoglobin increment of 0.88 g/dl after each unit PRBC transfusion. CONCLUSION: Decision to transfuse in AIHA should be based on the clinical condition of the patient. No critical patient should be denied blood transfusion due to serological incompatibility. Minimum investigations such as direct antiglobulin test (DAT), antibody screening and autocontrol should be performed to ensure transfusion safety in patients. All transfusion services should be capable of issuing “best match” PRBCs in AIHA. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4140051/ /pubmed/25161349 http://dx.doi.org/10.4103/0973-6247.137445 Text en Copyright: © 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Das, Sudipta Sekhar Zaman, Rafiq Uz Safi, Mohammad Incompatible blood transfusion: Challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia |
title | Incompatible blood transfusion: Challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia |
title_full | Incompatible blood transfusion: Challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia |
title_fullStr | Incompatible blood transfusion: Challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia |
title_full_unstemmed | Incompatible blood transfusion: Challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia |
title_short | Incompatible blood transfusion: Challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia |
title_sort | incompatible blood transfusion: challenging yet lifesaving in the management of acute severe autoimmune hemolytic anemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4140051/ https://www.ncbi.nlm.nih.gov/pubmed/25161349 http://dx.doi.org/10.4103/0973-6247.137445 |
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