Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

< Back to Article

Fig 1.

Flowchart of entire work.

N: normal people; P: CHF patients, in which 1 is of NYHA I-II, 2 is of NYHA III, 3 is of NYHA III-IV; S1: basic measures of 24-h RR interval data, which reflect long-term data variation); S2: basic measures of the second 5-min segment, which representing a stable measurement condition of short-term data; S3: mid-value of basic measures of 5-min segments, which showing an intermediate state of short-term data; D1: mean value of basic measures of 5-min segments, for robustness improvement; D2: standard deviation of each basic measure of 5-min segments; D3: root mean square of each basic measure of 5-min segments; D4: coefficient variation of each basic measure of 5-min segments; D5: percentage of abnormal value (value intervening M±S) of each basic measure of 5-min segments; D6: sample entropy of each basic measure of 5-min segments; D7: fuzzy entropy of each basic measure of 5-min segments.; DT-SVM: decision tree based support vector machine.

More »

Fig 1 Expand

Fig 2.

Multistage classification algorithm based on DT-SVM for risk assessment.

Upper diagram: tree-structured classifier. Lower diagram: wrappers for feature selection. N: normal samples; P: CHF patients, in which 1 is of NYHA I-II, 2 is of NYHA III, 3 is of NYHA III-IV; DSF: disease screening function; RAF: risk assessment function, in which I is for discriminating the higher risk from the lower risk, II is for distinction of moderate risk and mild risk; BE: backward elimination; SD: significance difference.

More »

Fig 2 Expand

Table 1.

Classification performance of classical SVM in 4-level risk assessment.

More »

Table 1 Expand

Table 2.

Performance of different feature combinations for disease detection and quantification.

More »

Table 2 Expand

Table 3.

Result of node selection for level 1 among all samples.

More »

Table 3 Expand

Table 4.

Result of node selection for level 2 among CHF patients.

More »

Table 4 Expand

Fig 3.

Multistage risk assessment model of CHF.

DSF: disease screening function to detect normal from patients; RAF: risk assessment function, in which I is for discriminating the higher risk from the lower risk, II is for distinction of moderate risk and mild risk; N: normal samples; P: CHF patients, in which 1 is of NYHA I-II, 2 is of NYHA III, 3 is of NYHA III-IV.

More »

Fig 3 Expand

Table 5.

Selected optimal feature subsets for each level with backward elimination.

More »

Table 5 Expand

Fig 4.

Confusion matrices.

N: normal samples; P: CHF patients, in which 1 is of NYHA I-II, 2 is of NYHA III, 3 is of NYHA III-IV.

More »

Fig 4 Expand

Table 6.

Classification performance.

More »

Table 6 Expand

Table 7.

Highlight.

More »

Table 7 Expand