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Red Blood Cell Alloimmunization in Multitransfused Pediatric Population in a Tertiary Care Hospital
A P Poornima1, Shiffi Fazal2, P S Shaiji2
1Department of Transfusion Medicine, Government Medical College, Thiruvananthapuram, Kerala, 695011, India. drpoornimaap@gmail.com.
Insights
Red blood cell (RBC) alloimmunization affects 6.35% of pediatric patients receiving multiple transfusions, primarily against Rh antigens. Early first transfusion may reduce alloimmunization risk.
Area of Science:
- Hematology
- Immunology
- Transfusion Medicine
Background:
- Red blood cell (RBC) alloimmunization is a known complication in patients requiring multiple transfusions.
- Understanding the prevalence and specificities of alloantibodies is crucial for managing transfusion reactions.
Purpose of the Study:
- To determine the prevalence and specificity patterns of RBC alloimmunization in pediatric patients undergoing multiple transfusions.
- To identify patient-related factors associated with the development of RBC alloimmunization.
Main Methods:
- A descriptive cross-sectional study was conducted over two years.
- Clinical data from multitransfused pediatric patients were collected.
- RBC antibody screening and identification were performed, followed by analysis of patient factors.
Main Results:
- RBC alloantibodies were detected in 6.35% (4/63) of patients; one patient (1.59%) had an autoantibody.
- Identified alloantibodies were against Rh antigens: anti-E, anti-c, anti-Cw, and anti-D + anti-C.
- A significant association was found between alloimmunization and receiving the first transfusion after two years of age.
Conclusions:
- RBC alloimmunization against Rh antigens is a significant concern in multitransfused children.
- Extended RBC phenotyping for Rh antigens and providing antigen-matched RBCs are recommended for children with ongoing transfusion needs.
Objectives:
To estimate the prevalence and specificity pattern of red blood cell (RBC) alloimmunization among pediatric multitransfused patients, and to identify the factors associated with alloimmunization.
Methods:
This was a descriptive cross-sectional study conducted among mutitransfused pediatric patients over a period of two years. The relevant clinical details of patients were collected, and RBC antibody screening was done. Samples with positive antibody screen were subjected to antibody identification. Patient factors were analysed to find any significant relation to the development of RBC alloimmunization.
Results:
Alloantibodies were obtained in 4 (6.35%) of the total 63 patients, and autoantibody in 1 (1.59%). The specificities of alloantibodies identified were all against Rh antigens-one each of anti E, anti c, anti Cw and anti D + anti C. A significant association was seen between development of alloimmunization and first transfusion at more than 2 y of age.
Conclusions:
RBC alloimmunization against Rhesus (Rh) antigens is a significant problem for multitransfused children in our population. Extended RBC phenotyping at least for antigens of the Rh system and provision of antigen matched RBCs may be an option for such children, where ongoing transfusion requirement is anticipated.
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