Iron deficiency anemia (IDA) is of concern for regular blood donors. Studies have found red blood cell (RBC) indices particularly useful in the early detection and prevention of IDA (1). The mean corpuscular volume (MCV) and the RBC distribution width (RDW) are especially useful, as these parameters often become abnormal before anemia becomes noticeable in other routine testing (2, 3).
Donor-induced iron deficiency (DIID)
A blood transfusion can in many cases be the only therapy available to treat an acute or chronic health condition. Voluntary blood donors are paramount to blood transfusion services. However, regular donations can cause significant depletion of the body’s iron stores, which might adversely affect the donor’s health as well as the quality of the donated blood (1).
Iron-deficient erythropoiesis results in unevenly small (microcytic) RBCs, and anisocytosis (increased RDW) can be the first laboratory finding that indicates anemia well before hemoglobin levels degrease below reference internals. A prompt detection of subclinical iron deficiency in regular donors is therefore necessary (1).
Singh and colleagues at the Rajarshi Dashrath Autonomous State Medical College, Ayodhya, Uttar Pradesh, India used the Medonic M-series M20M hematology system to evaluate the usefulness of MCV, MCH, and RDW in detection of iron deficiency at an early stage (1). They found significantly lower MCV and MCH values and significantly increased RDW in recurring donors and concluded that proper use of these parameters will be helpful to prevent the development of clinically evident IDA.
Wigina and collegues at the Technical University of Mombasa, School of Applied and Health Sciences, Mombasa, Kenya also used the Medonic M-series M20M hematology system to identify RBC abnormalities in blood donors (4). They found 31.05% of the donor cells exhibiting one or more of assayed abnormalities, with 9.91 % of the donor red cells having MCV values below the reference interval.
Distinguishing IDA from thalassemia
Thalassemia is another cause of microcytic anemia (5). However, while IDA is a nutrient disorder that can be treated with iron supplementation, thalassemia is an inherited disorder that lacks management protocol and for which blood transfusion is a mainstay of treatment (6, 7). The ability to differentiate IDA from thalassemia is important, as blood hemoglobin will not be improved by iron supplementation in thalassemia patients (8).
Together with determination of, for example, serum iron levels, RBC indices can be of good help (5, 8). Many formulas that include the RBC indices have been suggested to discriminate thalassemia from IDA (Table 1).