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Abstract Presentation Date: 6/9/2024 Presentation Start Time: 2:30:00 PM Background Sickle cell disease (SCD) is an inherited blood disorder which causes acute and chronic complications and can result in early death. About three-fourth of patients with SCD live in sub-Saharan Africa; in Ghana, 1 in 50 newborns are affected with SCD. Foetal hemoglobin (Hb F) level is a strong modifier of SCD severity. High levels of Hb F inhibit sickling and hemolysis and reduce disease morbidity and mortality. Hb F monitoring is also used to assess adherence and response to disease modifying therapy such as hydroxyurea. Standard hemoglobin electrophoretic techniques are unable to quantify Hb F. In resource-limited settings like Ghana, the use of high-performance liquid chromatography (HPLC) for Hb F quantification is often challenging due to cost and logistic constraints such limited availability of adequate technology and appropriately trained personnel. In this study, we assessed the performance of a low-cost, point-of-care (POC), microchip based cellulose acetate electrophoresis “GazelleTM” compared to HPLC for Hb F quantification in children with SCD in Ghana. GazelleTM is a fast ( 8 minutes), easy-to-use test which can be performed by minimally trained end-users using only a finger-prick volume of blood. Methods This cross-sectional study was conducted at the paediatric SCD Clinic in Korle Bu Teaching Hospital, Accra, Ghana. Study participants were children of ages ≥ 1 year to 16 years who were known to have sickle cell disease and were about to commence or were on hydroxyurea therapy and followed at the SCD clinic. Results A total of 532 children were included in the analysis. Gazelle showed a correlation of 0.98 (Pearson correlation) when compared to HPLC. Conclusions Haemoglobin variants are quantified by Gazelle offering the ability to monitor disease modifying therapy in SCD such as hydroxyurea, where quantification of Hb F levels is important in assessing treatment adherence and determining response to therapy. Gazelle has the potential to be utilized as a POC test for quantification of Hb F levels in monitoring hydroxyurea therapy for children with SCD, especially in limited-resource settings.
Segbefia et al. (Sat,) studied this question.