Abstract:
The national screening programme for thalassaemia in Sri Lanka is currently using full blood count with red cell indices as the technique to identify haemoglobinopathies. This approach is likely to miss sickle haemoglobin (Hb-S) as it is well known that sickle haemoglobin is not associated with hypochromic microcytosis. Sickling test is a low cost microscopic screening test which detects sickle cell by its characteristic appearance. Therefore, the present study was undertaken to assess the performance of sickling test in identifying Hb-S among relatively high risk population in Hambantota district. A total of 581 school children (grade 11) were selected randomly from five (5) schools in Hambantota district. A blood sample (2ml) was collected from each participant after obtaining informed assent and consent. Screening panel comprises with sickling test by sodium metabisulphite method, one tube osmotic fragility test, dichlorophenol indophenol test, full blood count and Zinc protoporphyrin test. Haemoglobin phenotyping of each sample was confirmed by capillary electrophoresis technique. Four students out of 581 had sickle trait. Three other types of haemoglobinopathies were detected including β-thalassaemia trait (n=17), haemoglobin D trait (n=2) and haemoglobin E trait (n=1). Iron deficiency was observed in 8% (n=44) of students. All 4 cases with sickle trait were positive for sickling test and all other cases were negative. None of the Hb-S case demonstrated hypochromic microcytosis in full blood count. The average time taken for red cells with sickle haemoglobin to assume the characteristic sickle shape was 28 minutes and 45 seconds. Sickling test demonstrated 100 % sensitivity and 100 % specificity in identifying sickle trait. Inclusion of sickling test in screening individuals for haemoglobinopathies would have an additional advantage as highly specific, sensitive and low cost test for detecting sickle haemoglobin.
