- Open Access
Red blood cell distribution width and iron deficiency anemia among pregnant Sudanese women
© Abdelrahman et al.; licensee BioMed Central Ltd. 2012
- Received: 16 October 2012
- Accepted: 28 November 2012
- Published: 3 December 2012
Iron deficiency anemia (IDA) is a major health problem during pregnancy and it has adverse effects on the mother and the newborn. Red cell distribution width (RDW), which is a quantitative measure for red cell size variation (anisocytosis), is a predictor of IDA. Little is known regarding RDW and IDA during pregnancy.
A cross sectional study was conducted at the antenatal clinic of Khartoum Hospital, Sudan, to determine the performance of RDW in the diagnosis of IDA using serum ferritin as a gold standard.
Among 194 pregnant women with a gestational period of 21.4 ± 6.5 weeks, 57 (29.4%) had IDA according to serum ferritin levels (<15 μg/l) and 61 (31.4%) had IDA according to RDW (>14.5). The sensitivity, specificity, positive predictive value, and negative predictive value of RDW where serum ferritin was the gold standard were 43.8% (95% CI: 31.4–57.0%), 73.7% (95% CI: 65.8–80.5%), 41.0% (95% CI: 29.2–53.6%), and 76.0% (95% CI: 68.1–82.6%), respectively.
In this study, we found that RDW has a poor performance in diagnosing IDA among pregnant women compared with serum ferritin as the gold standard.
The virtual slides for this article can be found here: http://www.diagnosticpathology.diagnomx.eu/vs/1721072967826303
- Red cell distribution width
It has been estimated that the highest proportions of individuals affected by anemia are in Africa, e.g. in neighboring Ethiopia, anemia is a major problem for both pregnant (62.7%) and non-pregnant (52.3%) women of child-bearing age . However, the prevalence of anemia varies significantly both within and between countries, which indicates a need for local data to help improve preventive programs. Anemia during pregnancy is associated with increased maternal morbidity and mortality, and contributes to 20% of the maternal mortality in Africa [2–5]. Anemia is one of the most common nutritional deficiency disorders in the world . The World Health Organization (WHO) defines iron deficiency anemia (IDA) as anemia accompanied by depleted iron stores and signs of a compromised supply of iron to the tissues [7, 8].
Anemia during pregnancy is a large health problem in Sudan, where pregnant women in different regions of Sudan are more susceptible to anemia, irrespective of their age or parity [9, 10]. Furthermore, anemia is associated with poor maternal and perinatal outcomes, such as maternal and perinatal mortality [10–12].
A cross-sectional descriptive study was carried out at the antenatal clinic of Khartoum Hospital, Sudan during the period of January to March, 2012 to investigate the performance of RDW in diagnosing IDA where serum ferritin was the gold standard. A sample size of 190 subjects was calculated based on a 2-sided hypothesis tests using Epiinfo with 80% power and a confidence interval (CI) of 95%. After signing an informed consent, pregnant women attending the antenatal clinic for the first time with singletons were approached to participate in the study.
Those subjects having any of the following: diabetes mellitus, hypertension, taking iron supplements or a history of blood transfusion within the last 3 months were excluded. The obstetric and medical history was determined using pretested questionnaires. A total of 5 ml of blood was collected through an aseptic venipuncture from the antecubital vein. Two milliliters of blood was taken in an ethylene diamine tetra acetic acid and immediately analyzed for a complete hemogram, including hemoglobin, white blood count (WBC), and RDW, using an automated hematology analyzer . Details of the hemoanalyzer are provided in our previous study . In summary, the Sysmex KX21N  is an automated blood cell counter intended for in vitro diagnostic use in clinical laboratories. It is a compact, fully automated hematology analyzer with simultaneous analysis of 18 parameters in whole blood mode and capillary blood mode. This analyzer counts blood cells as routine in a few minutes. The test was performed as stated in the manufacturer’s manual .
The remaining 3 mls of blood were delivered into a dry clean plain container, centrifuged after clotting and kept at –20 °C until analysis for the serum iron profile. Ferritin levels were measured by immunofluorescent assay using Immulite kits (Siemens, Los Angeles, CA, USA).
IDA was defined as hemoglobin less than 11 g/dl and serum ferritin level (<15 μg/l). Those women with severe anemia (hemoglobin <7 g/dl) and with leukocytosis (WBC >17.1 × 109/L were excluded.  RDW >14.5% is considered as abnormal and diagnostic for IDA . The serum ferritin level (<15 μg/l) was the gold standard for the diagnosis of IDA in this study.
The sensitivity, specificity, positive predictive value, and negative predictive value were calculated. The sensitivity of the RDW was calculated as true positives/(true positive + false negatives), the specificity was calculated as true negatives/(true negatives + false positives), the positive predictive value was calculated as true positives/(true positives + false positives), and the negative predictive value was calculated as true negatives/(true negatives + false negatives) .
The current study received ethical approval from the Department of Obstetrics in Khartoum Hospital, Sudan.
Basic characteristics of the pregnant women included in the study at Khartoum Teaching Hospital, Sudan
Gestational age, weeks
Among the 57 women that had IDA using serum ferritin level as a diagnostic tool, 25 (43.8%) of them had IDA as indicated by RDW. Therefore, the sensitivity of RDW was 43.8% (95% CI: 31.4–57.0%). Among the 137 women who had no IDA using serum ferritin levels as a diagnostic tool, 36 had IDA by using RDW. The specificity of RDW was 73.7% (95% CI: 65.8–80.5%).
Results of RDW compared with serum ferritin levels for diagnosis of IDA among pregnant women at Khartoum Hospital, Sudan
IDA according to the serum ferritin result
IDA according to RDW results
Performance of RDW in the diagnosis of IDA among pregnant women at Khartoum Hospital
Validity test Percentage
Positive predictive value
Negative predictive value
The main findings of the current study were the low sensitivity (43.8%) and moderate specificity (73.7%) of the RDW in the diagnosis of IDA among pregnant women in Sudan. Previously, hemoglobin was the most commonly used hematological parameter and screening test for IDA . However, hemoglobin has its limitation in detecting IDA because sufficient time must elapse for iron to have an effect , and hemoglobin may take up to 2 months to show low levels . A recent study showed that other hematological parameters, which can be estimated via a hemoanalyzer, such as MCV, MCH and MCHC, have poor performance in detecting IDA during pregnancy . It is possible that these red cell indices (MCV, MCH and MCHC) are mean values, which cannot express the small variation of red cell size that occurs in early iron deficiency . Changes in the peripheral blood film (e.g., erythrocyte hypochromia and microcytosis) are less prominent during pregnancy than during the non-pregnant condition, even in moderate iron deficiency . Therefore, there is a need for a screening test that is cheap and has a high reliability and accuracy for identifying iron deficiency.
A recent observation among non-pregnant women of child-bearing age showed that RDW (≥16.1%) had a sensitivity of 59.3% and specificity of 71% . Another study among pregnant women in the first half of pregnancy (<20 weeks gestation) showed that an RDW ≥15 had a sensitivity and specificity of 46.8% and 95.7%, respectively . A high sensitivity (82.3%) and specificity (97.4%) for RDW was reported recently among pregnant women . Different rates of RDW have been reported. For example, Aulakh et al.  found that the sensitivity of RDW was 81.0% and the specificity was 53.4%, and vanZeben et al.  found that the sensitivity of RDW was 94% and the specificity was 59%.
Some points need to be taken into consideration when comparing different studies. First, some reports used a ferritin level of 10 μg/l as a cut-off point for diagnosis of iron deficiency [31–33]. Second, there was a difference in the gestational age between our study and previous studies [16, 28].
It should be noted that because of the high prevalence of IDA in pregnancy, it is customary in many settings to consider/treat empirically pregnant anemic patients with iron supplements. Therefore, most of the studies, including the current study, were focused and designed to have maximum specificity for diagnosing IDA rather than achieving the most sensitivity.
This study has some limitations. Hemoglobin electrophoresis, serum vitamin B12, and folate tests were not performed. Such tests are important for excluding hemoglobinopathies, early macrocytosis due to folic acid, or vitamin B12 deficiency where RDW may increase. Anemia of chronic disorders also could not be excluded by an appropriate investigation in cases where serum ferritin levels might have been misinterpreted. The other parameters of iron status or profile such as serum iron level, total iron binding capacity and transferrin saturation were not investigated. Screening for submicroscopic malaria (as it is one of the commonest causes of anaemia) was not performed.
In this study; RDW has a poorer performance than serum ferritin in diagnosing IDW among pregnant women.
We gratefully acknowledge the pregnant mothers who, despite their suffering, participated in this study. LME and IA were funded by the University of Khartoum, Sudan.
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