#ExistRefRangeSet>
Reference Interval:
#ExistRefRangeTable> | Test Number
| Components
| Reference Interval
| | 0065059 | Chlamydia trachomatis DNA Probe
| Positive: Presence of C. trachomatis by nucleic acid probe. Negative: Absence of C. trachomatis by nucleic acid probe.
| | 0060223 | Neisseria gonorrhoeae DNA Probe
| Positive: Presence of N. gonorrhoeae by nucleic acid probe. Negative: Absence of N. gonorrhoeae by nucleic acid probe.
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*ExistRefRangeTable>
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*ExistRefRangeSet>
#ExistNote>
| Note: |
Amplification tests are recommended for detection of Chlamydia trachomatis & Neisseria gonorrhoeae from genitourinary sources. Refer to Chlamydia trachomatis & Neisseria gonorrhoeae by Amplified Detection (APTIMA®) (0060241). Direct DNA probe testing is appropriate only for endocervical, and urethral specimens. Specimens must be collected and transported in test-specific kits provided by the manufacturer. Culture is recommended for Chlamydia trachomatis and Neisseria gonorrhoeae detection in cases of suspected sexual abuse or suspected failure of therapy.
Specimens must be collected and transported in the manufacturer's test specific kits.
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*ExistNote>
#ExistCPT>
| CPT Code(s): |
87800
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*ExistCPT>
#ExistCrossReferences>
Cross References: |
Neisseria gonorrhoeae and Chlamydia trachomatis, DNA Probe |
*ExistCrossReferences>