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Diagnostic accuracy in field conditions of the sickle SCAN® rapid test for sickle cell disease among children and adults in two West African settings: the DREPATEST study

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Figure

Fig. 1 Flow Chart of participants in Lomé (Togo), Mai-June 2016, (n = 295) (On the left side) and in Bamako (Mali), October 2016, (n = 240)(On the right side)
Table 1 Baseline characteristics between sickle cell anaemia and trait cases and controls in Lomé (Togo) and Bamako (Mali)
Table 2 Aggregate confusion matrix between results achieved by two different reference methods and the Sickle SCAN® device, to2016, (determine the haemoglobin phenotype in Lomé (Togo), May–June 2016, (n = 295) (On the left side) and in Bamako (Mali), Octobern = 240) (On the right side)
Table 3 Sensitivity and specificity for each haemoglobin phenotype identified using the reference standard method (CapillaryElectrophoresis) in Lomé (Togo), May–June 2016

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