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. 2015 Jun 18;53(7):2215–2224. doi: 10.1128/JCM.00137-15

TABLE 3.

Evaluation of different MALDI-TOF MS Hib/non-Hib classification methods

Results by no. of spectra for: Hib (n = 33) Non-Hib (n = 77) Sensitivity (%)a Specificity (%)a AU-ROCb Reproducibility (%)c
ClinProTools
    6 spectra 100 98.7 0.994 97.6
        Hib 33 1
        Uncertain 0 0
        Non-Hib 0 76
    2 spectra 100 97.4 0.987 100
        Hib 33 2
        Non-Hib 0 75
Biotyper MSPs:
    Regular
        6 spectra 100 98.7 0.994 90.5
            Hib 33 0
            Uncertain 0 1
            Non-Hib 0 76
        2 spectra 100 97.4 0.987 95.2
            Hib 33 2
            Non-Hib 0 75
    Subtyping
        6 spectra 97.0 100 0.985 92.9d
            Hib 32 0
            Uncertain 1 0
            Non-Hib 0 77
        2 spectra 100 100 1.000 100d
            Hib 33 0
            Non-Hib 0 77
    Specially designed
        6 spectra 81.8 100 0.909 76.2
            Hib 27 0
            Uncertain 3 0
            Non-Hib 3 77
        2 spectra 97.0 98.7 0.978 85.7
            Hib 32 1
            Non-Hib 1 76
a

Sensitivity and specificity were calculated based on the results from the original laboratory (Malmö).

b

Area under the receiver operator characteristic curve calculated based on correct or false result from the measurements with the microflex instrument compared to those with PCR. All uncertain isolates were considered falsely identified. AU-ROC values were calculated using SPSS Statistics 22.0 (IBM, Armonk, NY).

c

Reproducibility was calculated as the percentage of isolates MALDI-TOF MS measured on both the microflex and ultrafleXtreme instrument, which were identified to the same category (Hib, uncertain, or non-Hib) on both instruments.

d

Reproducibility with adjusted cutoff.