Table 2.
Performance characteristics of three commercially-available Chlamydia trachomatis molecular screening platforms per manufacturer-provided data. Ranges reflect differences in performance characteristics between specimens collected from symptomatic and asymptomatic individuals (when specified).
| Commercial assay | Gender | Specimen | Performance indices | |
|---|---|---|---|---|
| Sensitivity range (%) | Specificity range (%) | |||
| AMPLICOR | Female | Endocervical | 87.4–94.0 | 98.6 |
| Urine | 84.3–89.5 | 98.0–98.8 | ||
| Male | Urethral | 96.3–98.7 | 95.2–97.7 | |
| Urine | 87.6–92.0 | 91.9–95.7 | ||
|
| ||||
| BD ProbeTec ET | Female | Endocervical | 88.7–96.8 | 97.9–98.5 |
| Urine | 77.0–83.9 | 98.2–98.3 | ||
| Male | Urethral | 89.5–95.5 | 92.9–97.0 | |
| Urine | 89.5–95.4 | 89.4–95.8 | ||
|
| ||||
| APTIMA Combo 2† | Female | Endocervical | 92.4–98.4 | 96.7–98.8 |
| Urine | 93.8–96.8 | 98.8–99.0 | ||
| Male | Urethral | 94.6–96.4 | 96.9–98.4 | |
| Urine | 96.3–98.5 | 98.4–98.8 | ||
†APTIMA Combo 2 clinician-collected vaginal swab sensitivity range 96.5–96.7%, specificity range 96.4–97.2%; APTIMA Combo 2 patient-collected vaginal swab sensitivity 98.4%, specificity 96.8%.