Background and Objectives
Mismatched red blood cell phenotypes between donors and recipients in multiple blood
transfusions can result in the development of alloimmunization in recipients. We studied in this
research the effect of alloantibodies on the increase of need of blood transfusion in major
thalassemiacs.
Materials and Methods
This is a descriptive study in which 2 groups of major thalassemiacs with more and less than
20 days of blood transfusion intervals (27 patients vs. 25) were evaluated for the presence and
frequency of alloantibodies and related factors. We used t-test and t-student tables for
evaluating the results.
Results
55% of patients in the first group had developed alloantibodies and their annual transfused
blood volume was more than those who were not immunized (p<0.005). Male gender and
initial blood transfusion in children under 3 years old were related to the absence of
alloantibodies. 100% of patients in the second group were immunized, and those who received
higher amounts of blood units annually (493 ml/kg and 508 ml/kg) were patients with more
than two types of alloantibodies. Alloimmunization involved K (27.5%), N (12.5%),
CW, s, Fyb (5%), C, S, E, e and M (2.5%) antigens. 100% of antibodies were of warm
immunoglobulin type, and 16% both warm and cold. 17.3% of thalassemiacs were
splenectomized and their need for transfused blood was less than unsplenectomized patients
(p<0.005). In most cases, annual blood transfusion in both groups was estimated to be much
more than what was expected.
Conclusions
We conclude that red blood cell matching, at least for Kell and Rh systems, is necessary to
prevent alloimmunization in thalassemiacs. Hypersplenism and low quality of blood, that can
increase the need for transfused blood, should be taken into consideration.