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. 2013 Nov 20;8(11):e81236. doi: 10.1371/journal.pone.0081236

Table 2. Case-level analyses on the associations between potential covariates and Chlamydia trachomatis-positive samples (positivity) and load from days 23–51 after treatment.

Positivity, Days 23–51 Load, Days 23–51
OR 95% CI a Difference log load
(IFU/ml) 95% CI a
Time post treatment (per day) 1.004 (1.00;1.01) # 0.01 (0.001;0.02) *
Anorectal case 1.16 (0.92;1.45) 0.19 (−0.22;0.61)
Age <23 years 1.06 (0.90;1.24) −0.05 (−0.41;0.32)
History of Ct diagnosis 0.96 (0.81;1.14) 0.14 (−0.39;0.69)
Pre-treatment load >75% percentile b 1.01 (0.83;1.23) Anorectal: 0.99 (0.04;2.02)c *
Cervicovaginal: −0.16 (−0.75;0.42)c
Current symptoms d , e 1.02 (0.89;1.16) −0.20 (−0.47;0.07)
Pre-treatment symptoms d , f 0.94 (0.80;1.11) −0.31 (−0.71; −0.09)
Current menstruation f 0.96 (0.86;1.07) 0.03 (−0.33;0.40)
Sexual re-exposure risk: unsafe sex 0.99 (0.69;1.09) −0.07 (−0.45;0.32)
with a new partner/unknown behavior

Abbreviations: OR: Odds Ratio; CI: Confidence Interval; IFU/ml: Inclusion-forming units per milliliter.

#: P = 0.06,

*P<0.05; tested using generalized estimating equations (positivity) or mixed models (load).

a

estimates adjusted for potential confounding by sexual re-exposure risk, anatomic site, and repeated measurements; in models with bacterial load as outcome, anatomic site was included as an effect-modifier as the interaction-term was statistically significant.

b

>159 IFU/ml for anorectal cases and >1299 IFU/ml for cervicovaginal cases.

c

presented separately for anatomic sites due to significant interactions between pre-treatment load and site (P = 0.008).

d

dysuria; irregular menstruation; lower abdominal pain; pain during intercourse; vaginal discharge.

e

anal discharge; anal blood loss during/after intercourse; anal pain during/after intercourse.

f

only evaluated for cervicovaginal cases.