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Predicting Cardiovascular Risks using Pattern Recognition and Data ...

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equivalent rates for “High risk” are very poor (0.93; 0.84 vs 0.09; 0.19 on average). The two radialbasis function classifiers, CM1-RBF <strong>and</strong> CM2-RBF, predicted all expected “High risk” patients as“Low risk”. This again shows the technique‟s disadvantages for use with the thesis data.Confusion MatrixClassifiersRiskHigh riskLow riskACC Sen Spec PPV NPVCM1-MLPCM1-RBFCM1-SVMCM2-MLPCM2-RBFCM2-SVMHigh risk 9 117Low risk 34 679High risk 0 126Low risk 0 713High risk 30 96Low risk 112 601High risk 6 133Low risk 27 673High risk 0 139Low risk 0 700High risk 24 115Low risk 125 5750.82 0.07 0.95 0.21 0.850.85 0.00 1.00 N/A 0.850.75 0.24 0.84 0.21 0.860.81 0.04 0.96 0.18 0.830.83 0.00 1.00 N/A 0.830.71 0.17 0.82 0.16 0.83Table 7.1: Experimental results of CM1 <strong>and</strong> CM2 models.From Table 7.1, the correct predicted “High risk” rates (sensitivity as well as the positive predictivevalue) are very poor (0.09 <strong>and</strong> 0.19 on average except CM1-RBF <strong>and</strong> CM2-RBF). The nature of theproblem <strong>and</strong> the difficulty of measuring influential parameters might be the cause for these poorperformances.7.2.2. Clinical Models CM3a <strong>and</strong> CM4aTable 7.2 shows the results for supervised neural networks on the clinical risk prediction models CM3a<strong>and</strong> CM4a. These models share the same expected outputs but their input sets are different (as indicated108

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