The findings and conclusions in these presentations have not been formally disseminated by the Centers for Disease Control and Prevention and should not be construed to represent any agency determination or policy.

Tuesday, March 11, 2008
P83

Time to Clearance of Ribosomal RNA Using Transcription-mediated Amplification in Women Treated for Chlamydial Infection

Cybele A. Renault1, Vivian Levy2, Dennis M. Israelski2, Bruce K. Fujikawa2, Timothy A. Kellogg3, and Jeffrey D. Klausner4. (1) Division of Infectious Diseases and Geographic Medicine, Stanford University School of Medicine, Stanford University Medical Center, 300 Pasteur Drive, Grant Building, S-169, Stanford, CA, USA, (2) San Mateo Medical Center and Health Department, San Mateo, CA, USA, (3) San Francisco Department of Public Health, San Francisco, CA, USA, (4) STD Prevention and Control Services, San Francisco Department of Public Health, San Francisco, CA, USA


Background:
Recommendations from the Centers for Disease Control and Prevention (CDC) suggest that women treated for Chlamydia trachomatis (CT) wait at least 3 weeks before being tested for cure. This recommendation is based on expert opinion, as the duration of CT detection following treatment is uncertain. Prior studies have demonstrated that DNA-based tests may remain positive for up to 2 weeks following treatment. Transcription-mediated amplification (TMA) amplifies CT ribosomal RNA (rRNA) and has improved sensitivity compared to the DNA-based assays. The time to clearance of rRNA following treatment for chlamydial infection is unknown.

Objective:
To evaluate the time to clearance of rRNA following treatment for cervical chlamydial infection using TMA on self-collected vaginal swabs, in order to evaluate TMA as a possible test-of-cure.

Method:
Twenty women with cervical chlamydia diagnosed with a positive TMA urine test self-obtained a vaginal swab on the day of treatment (day 0) and on days 3, 7, 10 and 14 following treatment with 1 gram of azithromycin. Sixteen subjects reported abstinence during the fourteen-day period and were included in the analysis.

Result:
Twelve of 16 subjects (75%) had a negative swab at day 14. The median time to a negative vaginal TMA in these subjects was 10 days. Subjects with a negative TMA at each timepoint were as follows: 0/16 (0%) on day 0, 2/16 (12.5%) on day 3, 6/16 (37.5%) on day 7, 12/16 (75%) on day 10, and 12/16 (75%) on day 14.

Conclusion:
After treatment, chlamydia rRNA by TMA declined with time. As rRNA was undetectable in only 75% of the subjects fourteen days after treatment, TMA should not be used as a test-of-cure in the fourteen-day period following treatment.

Implications:
Given the sensitivity of TMA for persistent chlamydia rRNA, at least 2 weeks must elapse before repeat testing for test-of-cure is warranted.