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IPS186 Fagbamigbe, A. F.
            3.  Data Analysis
                There  were  a  total  of  7,011  children  aged  6-59  months  across  all  the
            households visited during the survey. Basic descriptive statistics were used to
            describe the under-five children with respect to the characteristics of their
            mothers. The McNemar paired test and the Kappa statistics were used to test
            the hypothesis of non-agreement and to determine the level of agreement
            between the outcomes of the diagnostic tests respectively. Diagnostic test
            parameters  including  sensitivity,  specificity,  positive  predictive  value  (PPV),
            and negative predictive value (NPV) was used to determine the accuracy of
            the malaria RDT results in comparison with the “Gold standard” results from
            microscopy tests. Let X denote the true state of a person (microscopy test
            results) with microscopy positive = D+ and negative = D-. Also, let Y be the
            outcome of the RDT test, with RDT positive = T+ and negative = T-. Then,

                                       +
                                                                     −
                                +
            Sensitivity = ( = T |X = D ); pecificity = ( = T  | = D ). The positive
                                                             −
            likelihood ratio (LR+) and the negative likelihood ratio (LR-) are calculated as
                                1−
                     LR+=      =                and LR-=       =
                            1−    

            as  proposed  by  Simel  et  al.  [23].  The  unique  statistics  produced  by  the
            likelihood  ratios  have  made  it  the  optimal  choice  for  reporting  diagnostic
            accuracy for clinically meaningful thresholds[18].
                However,  there  is  a  need  to  determine  the  predictive  values  since
            sensitivities  and  specificities  are  not  measures  of  prediction[18].  Predictive
            values depend on disease prevalence, and their conclusions are transposable
            to  other  settings.  The  predictive  values  help  to  determine  how  likely  the
            disease is, given the test result. The PPV is the probability that the disease is
            present, given that the diagnostic test is positive. It is computed as TP/ (TP+FP)
            while the NPV is the probability that the disease is not present given that the
            test is negative, computed as TN/ (TN+FN). A diagnostic test could be said to
            be perfect if it can predict perfectly, i.e., if PPV = NPV=1. The PPV decreases
            with decreasing prevalence.
                                            +
                                               +
                                                             −
                                 PPV = ( D |T ); NPV = ( D |T ) .
                                                               −
               The  accuracy  of  a  test  =  (TP+TN)/(TP+TN+FP+FN)  and  its  confidence
            intervals are the standard logits as given by Mercaldo et al[24]. The pretest
            probability is the same as the prevalence as determined by the gold standard,
            the pretest odds is prevalence/(1-prevalence), posttest odds= pretest odds
            *likelihood  ratio  and  the  posttest  probability=posttest  odds/(1+positive
            odds).
               The ROC analysis is used in diagnostic screening evaluation to quantify the
            accuracy of diagnostic
            95 tests [25].


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