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Pelvic inflammatory disease associated with Chlamydia trachomatis but not Mycoplasma genitalium in New Zealand
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Background
There is a paucity of studies looking at associations between Mycoplasma genitalium and pelvic inflammatory disease (PID). The objectives of this study were to estimate the prevalence of M. genitalium in women attending a sexual health service in New Zealand and secondly to examine for an association of M. genitalium with PID. Methods: Women consecutively attending the service for a sexual health screen (Chlamydia trachomatis, Neisseria gonorrhoeae and Trichomonas vaginalis) were recruited to establish a baseline prevalence of M. genitalium. An extra cervical swab was taken for the detection of M. genitalium. Recruitment of additional women with a clinical diagnosis of PID continued until a sufficient sample size was obtained to examine the association of PID with M. genitalium. Women in the baseline sample without PID were used as the control group. Results: The control group included 250 women, with M. genitalium diagnosed in 8.7% (95% CI 5.8–12.9%) and C. trachomatis in 9.9% (95% CI 6.8–14.2%). Ninety-one women were recruited with PID; M. genitalium was diagnosed in 9.9% (95% CI 5.3–17.7%) and C. trachomatis in 27.5% (95% CI 19.4–37.4%). Multivariate analysis using clinically relevant variables showed that a diagnosis of C. trachomatis (OR 2.44, 95% CI 1.24–4.81) but not M. genitalium (OR 0.91, 95% CI 0.38–2.20) was significantly associated with a PID diagnosis. Conclusions:M. genitalium was almost as commonly diagnosed as C. trachomatis in this population. C. trachomatis was the only infection that was significantly associated with PID.
Title: Pelvic inflammatory disease associated with Chlamydia trachomatis but not Mycoplasma genitalium in New Zealand
Description:
Background
There is a paucity of studies looking at associations between Mycoplasma genitalium and pelvic inflammatory disease (PID).
The objectives of this study were to estimate the prevalence of M.
genitalium in women attending a sexual health service in New Zealand and secondly to examine for an association of M.
genitalium with PID.
Methods: Women consecutively attending the service for a sexual health screen (Chlamydia trachomatis, Neisseria gonorrhoeae and Trichomonas vaginalis) were recruited to establish a baseline prevalence of M.
genitalium.
An extra cervical swab was taken for the detection of M.
genitalium.
Recruitment of additional women with a clinical diagnosis of PID continued until a sufficient sample size was obtained to examine the association of PID with M.
genitalium.
Women in the baseline sample without PID were used as the control group.
Results: The control group included 250 women, with M.
genitalium diagnosed in 8.
7% (95% CI 5.
8–12.
9%) and C.
trachomatis in 9.
9% (95% CI 6.
8–14.
2%).
Ninety-one women were recruited with PID; M.
genitalium was diagnosed in 9.
9% (95% CI 5.
3–17.
7%) and C.
trachomatis in 27.
5% (95% CI 19.
4–37.
4%).
Multivariate analysis using clinically relevant variables showed that a diagnosis of C.
trachomatis (OR 2.
44, 95% CI 1.
24–4.
81) but not M.
genitalium (OR 0.
91, 95% CI 0.
38–2.
20) was significantly associated with a PID diagnosis.
Conclusions:M.
genitalium was almost as commonly diagnosed as C.
trachomatis in this population.
C.
trachomatis was the only infection that was significantly associated with PID.
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