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. 2015 Oct 28;29(1):1–27. doi: 10.1128/CMR.00108-14

TABLE 9.

PCR-based testing for CPOs in clinical specimens

Target(s) Methodology Specimen type(s)b Sensitivity (%) Specificity (%) Limit(s) of detection (CFU/ml) No. of specimens Reference
KPC PCR ES 92.2 99.6 Not calculated 755 153
KPC qPCR ES 97 96.6 4 × 100–4 × 102 95 155
KPC qPCR S, MC 100 98 5 × 100 CFU/ml 216 190
VIM, IMP, KPC, OXA-48, NDM-1 PCR (Hyplex SuperBug ID) MC 98.0 98.6 Not calculated 236 172
OXA-48 qPCR PC, SS 100 100 101–102 35 182
KPC, NDM-1 qPCR S, SS 100 100 KPC, 104–105; NDM, 103 46/80a 141
KPC qPCR (EasyQ KPC) S 93.3 99 Not calculated 806 193
VIM, OXA-48, NDM, KPC qPCR (Check-MDR Carba) SS 100 100 103–105 25 191
KPC, NDM, VIM qPCR (Xpert MDRO) S, SS 100 99 <3 × 102 328 183
KPC qPCR S 97.9–100 95–96.4 5 × 100 187 152
NDM-1 qPCR SS 100 Not calculated 101–3 × 101 32 189
a

Specificity panel of 80 known negative specimens.

b

ES, stool or perirectal swab with prior enrichment; S: stool, stool swabs, or perirectal swabs; MC, mixed clinical specimens; SS, spiked stool or stool swabs; PC, pure cultures.