Table 4

Distribution of CT-DNA and viable CT at the vaginal and the rectal site at the follow-up visit (just prior to treatment) a median of 9 days later, in 560 women who were previously CT diagnosed (FemCure)

Group AGroup BGroup CGroup D
vCT and rCTvCT (rCT untested)vCT (rCT negative)rCT (vCT negative)
n=155, n (%)n=351, n (%)n=25, n (%)n=29, n (%)
CT-DNA (PCR positive) at follow-up
 No CT-DNA at vaginal and rectal site1 (0.6)19 (5.4)8 (32.0)8 (27.6)
 CT-DNA detected at the vaginal site only20 (12.9)60 (17.1)8 (32.0)0 (0)
 CT-DNA detected at the rectal site only2 (1.3)2 (0.6)*0 (0)21 (72.4)
 CT-DNA detected at the vaginal and rectal site132 (85.2)270 (76.9)*9 (36.0)†0 (0)
Viable CT (PCR and V-PCR positive) at follow-up
 No CT-DNA or only non-viable CT at vaginal and rectal site6 (3.9)33 (9.4)13 (52.0)12 (41.4)
 CT-DNA and viable CT at the vaginal site only48 (31.0)148 (42.2)10 (40.0)0 (0)
 CT-DNA and viable CT at the rectal site only4 (2.6)6 (1.7)*0 (0)17 (58.6)
 CT-DNA and viable CT at the vaginal and rectal site97 (62.6)164 (46.7)*2 (8.0)†0 (0)
  • CT-DNA is assessed with a quantitative PCR; viable CT is assessed with a viability PCR.

  • *The rectal site was initially not tested, thus could be positive or negative. The fact that at follow-up (just prior to treatment), some women rectally had CT-DNA or viable CT-DNA suggests that in those women the rectal site was initially positive (350/351 patients reported no anal sex in 2 weeks prior to treatment).

  • †The rectal site was initially tested CT-DNA negative. The fact that at follow-up (just prior to treatment), women rectally had CT-DNA or viable CT-DNA suggests that new infections may have occurred at the rectal site between diagnosis and treatment (6/9 patients reported no anal sex in the 2 weeks prior to treatment).

  • rCT, rectal Chlamydia trachomatis; vCT, vaginal Chlamydia trachomatis.