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. 2013 Sep;51(9):2869–2874. doi: 10.1128/JCM.00488-13

Table 2.

ChromID MRSA agar culture, LightCycler MRSA Advanced Test, and in-house duplex real-time PCR assay performance in detection of MRSA

Assay No. of samples with the indicated resulta
Performance (% [95% CI])h
Positive Negative True positiveb False positive False negative True negativec Sensitivity Specificity Positive predictive value Negative predictive value
Direct ChromID MRSA agar culture 147 1,099 147 0 27 1,072 84.5 (78.3–89.2) 100 (99.7–100.0) 100 (97.8–100.0) 97.5 (96.4–98.3)
LightCycler MRSA Advanced Test 156d 1,090 145e 11f 29 1,061 83.3 (77.0–88.5) 99.0 (98.2–99.5) 92.9 (87.7–96.1) 97.3 (96.2–98.2)
In-house duplex real-time PCR assay 148 1,098g 133 15 41 1,057 76.4 (69.6–82.2) 98.6 (97.7–99.2) 89.9 (83.9–93.9) 96.3 (95.0–97.3)
a

A total of 1,246 samples were used to evaluate the performance of culture and real-time PCR assays for the detection of MRSA nasal colonization.

b

A total of 174 samples were considered true positive for MRSA based on the overall results of cultures and real-time PCR assays (also see Table 1).

c

A total of 1,072 samples were considered true negative for MRSA based on the overall results of cultures and real-time PCR assays (also see Table 1).

d

Among 156 positive samples from the LightCycler test, 92 showed Tm values of 59°C, whereas 64 showed Tm values of 55°C.

e

Among 145 true-positive samples indicated by the LightCycler test, 85 showed Tm values of 59°C, whereas 60 showed Tm values of 55°C.

f

The 11 false-positive samples from the LightCycler test included 7 samples with Tm values of 59°C and 4 samples with Tm values of 55°C.

g

A total of 18 samples with positive amplification for both sau and mecA genes were considered negative in the in-house duplex PCR assay because their ΔCp values were >3 cycles.

h

Results were determined as percentages and 95% confidence intervals (CIs) by an adjusted Wald method.