Table 1.

Association Between Baseline Characteristics and Incident Trichomonas vaginalis (TV) Infection in 18 Women With 25 Episodes of TV Infection (Cases) and 50 Women Matched to Each Episode Who Remained Uninfected (Controls)

VariableUnique Participants (n = 68)aCases (n = 25)Controls (n = 50)RR (95% CI)Pb
Age, y 36.2 ± 9.236.4 ± 7.136.5 ± 10.11.00 (.97–1.04)1.0
Education duration, y8.4 ± 3.48.1 ± 3.08.6 ± 3.50.97 (.88–1.08).6
Contraceptive method
 None/condoms38 (55.9)17 (68.0)27 (54.0)Reference
 Hormonal20 (29.4)3 (12.0)17 (34.0)0.39 (.12–1.23).1
 Other10 (14.7)5 (20.0)6 (12.0)1.18 (.50–2.80).7
Menstrual status
 Follicular19 (27.9)10 (40.0)11 (22.0)Reference
 Luteal15 (22.1)6 (24.0)12 (24.0)0.70 (.35–1.39).3
 Otherc8 (11.8)4 (16.0)5 (10.0)0.93 (.39–2.21).9
 Amenorrheicd26 (38.2)5 (20.0)22 (44.0)0.39 (.16–.96).04
  Clinical amenorrheae5 (7.4)3 (12.0)3 (6.0)
  Menopause11 (16.2)1 (4.0)10 (20.0)
  Depot medroxyprogesterone9 (13.2)1 (4.0)8 (16.0)
  Pregnancy1 (1.5)01 (2.0)
Sex partners in past wk, no.2.5 ± 3.53.0 ± 3.42.3 ± 3.41.04 (.96–1.12).4
Sex acts in past wk, no.2.9 ± 3.63.4 ± 3.52.7 ± 3.41.04 (.96–1.12).4
Any unprotected sex in past wk11 (16.2)6 (24.0)8 (16.0)1.38 (.68–2.78).4
Genital ulceration2 (2.9)1 (4.0)1 (2.0)1.52 (.36–6.47).6
Nugent criteriaf
 Normal45 (66.2)15 (60.0)33 (66.0)Reference
 Intermediate6 (8.8)4 (16.0)4 (8.0)1.60 (.72–3.55).2
 BV17 (25.0)6 (24.0)13 (26.0)1.01 (.49–2.08)1.0
Any gonorrhea or Chlamydia infection1 (1.5)1 (4.0)03.08 (2.03–4.69)<.001
Presence of vaginal yeast9 (13.2)3 (12.0)7 (12.0)0.89 (.34–2.30).8
VariableUnique Participants (n = 68)aCases (n = 25)Controls (n = 50)RR (95% CI)Pb
Age, y 36.2 ± 9.236.4 ± 7.136.5 ± 10.11.00 (.97–1.04)1.0
Education duration, y8.4 ± 3.48.1 ± 3.08.6 ± 3.50.97 (.88–1.08).6
Contraceptive method
 None/condoms38 (55.9)17 (68.0)27 (54.0)Reference
 Hormonal20 (29.4)3 (12.0)17 (34.0)0.39 (.12–1.23).1
 Other10 (14.7)5 (20.0)6 (12.0)1.18 (.50–2.80).7
Menstrual status
 Follicular19 (27.9)10 (40.0)11 (22.0)Reference
 Luteal15 (22.1)6 (24.0)12 (24.0)0.70 (.35–1.39).3
 Otherc8 (11.8)4 (16.0)5 (10.0)0.93 (.39–2.21).9
 Amenorrheicd26 (38.2)5 (20.0)22 (44.0)0.39 (.16–.96).04
  Clinical amenorrheae5 (7.4)3 (12.0)3 (6.0)
  Menopause11 (16.2)1 (4.0)10 (20.0)
  Depot medroxyprogesterone9 (13.2)1 (4.0)8 (16.0)
  Pregnancy1 (1.5)01 (2.0)
Sex partners in past wk, no.2.5 ± 3.53.0 ± 3.42.3 ± 3.41.04 (.96–1.12).4
Sex acts in past wk, no.2.9 ± 3.63.4 ± 3.52.7 ± 3.41.04 (.96–1.12).4
Any unprotected sex in past wk11 (16.2)6 (24.0)8 (16.0)1.38 (.68–2.78).4
Genital ulceration2 (2.9)1 (4.0)1 (2.0)1.52 (.36–6.47).6
Nugent criteriaf
 Normal45 (66.2)15 (60.0)33 (66.0)Reference
 Intermediate6 (8.8)4 (16.0)4 (8.0)1.60 (.72–3.55).2
 BV17 (25.0)6 (24.0)13 (26.0)1.01 (.49–2.08)1.0
Any gonorrhea or Chlamydia infection1 (1.5)1 (4.0)03.08 (2.03–4.69)<.001
Presence of vaginal yeast9 (13.2)3 (12.0)7 (12.0)0.89 (.34–2.30).8

Data are mean ± SD or no. (%) of participants, unless otherwise indicated.

Abbreviations: BV, bacterial vaginosis; CI, confidence interval; RR, risk ratio.

aData are for 18 unique participants who acquired TV and 50 participants who remained uninfected. Data are from the time of the first case of TV infection for those who contributed >1 case of TV infection.

bValues <.05 are considered statistically significant.

cData are for women whose last menstrual period was 29–84 days ago and for whom the menstrual phase could not be estimated on the basis of a 28-day cycle.

dData are for clinical amenorrhea, menopause, pregnancy, or depot medroxyprogesterone acetate use.

eDefined as >84 days since the last menstrual period.

fA score of 0–3 indicates normal; 4–6, intermediate; and 7–10, BV.

Table 1.

Association Between Baseline Characteristics and Incident Trichomonas vaginalis (TV) Infection in 18 Women With 25 Episodes of TV Infection (Cases) and 50 Women Matched to Each Episode Who Remained Uninfected (Controls)

VariableUnique Participants (n = 68)aCases (n = 25)Controls (n = 50)RR (95% CI)Pb
Age, y 36.2 ± 9.236.4 ± 7.136.5 ± 10.11.00 (.97–1.04)1.0
Education duration, y8.4 ± 3.48.1 ± 3.08.6 ± 3.50.97 (.88–1.08).6
Contraceptive method
 None/condoms38 (55.9)17 (68.0)27 (54.0)Reference
 Hormonal20 (29.4)3 (12.0)17 (34.0)0.39 (.12–1.23).1
 Other10 (14.7)5 (20.0)6 (12.0)1.18 (.50–2.80).7
Menstrual status
 Follicular19 (27.9)10 (40.0)11 (22.0)Reference
 Luteal15 (22.1)6 (24.0)12 (24.0)0.70 (.35–1.39).3
 Otherc8 (11.8)4 (16.0)5 (10.0)0.93 (.39–2.21).9
 Amenorrheicd26 (38.2)5 (20.0)22 (44.0)0.39 (.16–.96).04
  Clinical amenorrheae5 (7.4)3 (12.0)3 (6.0)
  Menopause11 (16.2)1 (4.0)10 (20.0)
  Depot medroxyprogesterone9 (13.2)1 (4.0)8 (16.0)
  Pregnancy1 (1.5)01 (2.0)
Sex partners in past wk, no.2.5 ± 3.53.0 ± 3.42.3 ± 3.41.04 (.96–1.12).4
Sex acts in past wk, no.2.9 ± 3.63.4 ± 3.52.7 ± 3.41.04 (.96–1.12).4
Any unprotected sex in past wk11 (16.2)6 (24.0)8 (16.0)1.38 (.68–2.78).4
Genital ulceration2 (2.9)1 (4.0)1 (2.0)1.52 (.36–6.47).6
Nugent criteriaf
 Normal45 (66.2)15 (60.0)33 (66.0)Reference
 Intermediate6 (8.8)4 (16.0)4 (8.0)1.60 (.72–3.55).2
 BV17 (25.0)6 (24.0)13 (26.0)1.01 (.49–2.08)1.0
Any gonorrhea or Chlamydia infection1 (1.5)1 (4.0)03.08 (2.03–4.69)<.001
Presence of vaginal yeast9 (13.2)3 (12.0)7 (12.0)0.89 (.34–2.30).8
VariableUnique Participants (n = 68)aCases (n = 25)Controls (n = 50)RR (95% CI)Pb
Age, y 36.2 ± 9.236.4 ± 7.136.5 ± 10.11.00 (.97–1.04)1.0
Education duration, y8.4 ± 3.48.1 ± 3.08.6 ± 3.50.97 (.88–1.08).6
Contraceptive method
 None/condoms38 (55.9)17 (68.0)27 (54.0)Reference
 Hormonal20 (29.4)3 (12.0)17 (34.0)0.39 (.12–1.23).1
 Other10 (14.7)5 (20.0)6 (12.0)1.18 (.50–2.80).7
Menstrual status
 Follicular19 (27.9)10 (40.0)11 (22.0)Reference
 Luteal15 (22.1)6 (24.0)12 (24.0)0.70 (.35–1.39).3
 Otherc8 (11.8)4 (16.0)5 (10.0)0.93 (.39–2.21).9
 Amenorrheicd26 (38.2)5 (20.0)22 (44.0)0.39 (.16–.96).04
  Clinical amenorrheae5 (7.4)3 (12.0)3 (6.0)
  Menopause11 (16.2)1 (4.0)10 (20.0)
  Depot medroxyprogesterone9 (13.2)1 (4.0)8 (16.0)
  Pregnancy1 (1.5)01 (2.0)
Sex partners in past wk, no.2.5 ± 3.53.0 ± 3.42.3 ± 3.41.04 (.96–1.12).4
Sex acts in past wk, no.2.9 ± 3.63.4 ± 3.52.7 ± 3.41.04 (.96–1.12).4
Any unprotected sex in past wk11 (16.2)6 (24.0)8 (16.0)1.38 (.68–2.78).4
Genital ulceration2 (2.9)1 (4.0)1 (2.0)1.52 (.36–6.47).6
Nugent criteriaf
 Normal45 (66.2)15 (60.0)33 (66.0)Reference
 Intermediate6 (8.8)4 (16.0)4 (8.0)1.60 (.72–3.55).2
 BV17 (25.0)6 (24.0)13 (26.0)1.01 (.49–2.08)1.0
Any gonorrhea or Chlamydia infection1 (1.5)1 (4.0)03.08 (2.03–4.69)<.001
Presence of vaginal yeast9 (13.2)3 (12.0)7 (12.0)0.89 (.34–2.30).8

Data are mean ± SD or no. (%) of participants, unless otherwise indicated.

Abbreviations: BV, bacterial vaginosis; CI, confidence interval; RR, risk ratio.

aData are for 18 unique participants who acquired TV and 50 participants who remained uninfected. Data are from the time of the first case of TV infection for those who contributed >1 case of TV infection.

bValues <.05 are considered statistically significant.

cData are for women whose last menstrual period was 29–84 days ago and for whom the menstrual phase could not be estimated on the basis of a 28-day cycle.

dData are for clinical amenorrhea, menopause, pregnancy, or depot medroxyprogesterone acetate use.

eDefined as >84 days since the last menstrual period.

fA score of 0–3 indicates normal; 4–6, intermediate; and 7–10, BV.

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