Abstract:OBJECTIVE:
To identify factors associated with testing for and diagnosis of trichomoniasis in pregnancy and to describe patterns of treatment and tests of reinfection or persistence.
METHODS:
We conducted a retrospective cohort study of women who delivered from July 2016 to June 2018 at one institution. Testing for Trichomonas vaginalis infection was done by wet mount microscopy or by nucleic acid amplification testing for routine prenatal testing or sy… Show more
“…Compared to NAAT, the sensitivity of wet mount has been reported between 26%-68%. 23,24 At our institution wet mount missed one of 3 cases of trichomoniasis. NAAT is clearly more sensitive and thus preferable in settings able to offer it.…”
Background The Centers for Disease Control and Prevention recommends universal retesting within 3 months after treatment of Trichomonas vaginalis infection given high rates of persistent infection or reinfection, or if this is not possible, within 12 months following treatment. Data is lacking on how often this is actually done. Methods We analyzed the demographic and clinical characteristics, rate of return for the recommended retesting, concordance between wet prep and nucleic acid amplification testing, and percent positivity for T. vaginalis on repeat vaginal specimens at a local public health department in Durham, North Carolina, United States. Results Of 193 females treated for trichomoniasis between March 1, 2021 – May 31, 2022, 83% were Black or African American and 44% between the ages of 20 and 29 years. Of these individuals, 32% had retesting performed within 3 months and 50% within 365 days after treatment. Females between the ages of 20 and 29 years were more likely to return for retesting than those between the ages of 30 and 39 years. Of those who returned for retesting, 10% were positive on repeat testing. Conclusion In this study, 50% of females diagnosed with trichomoniasis completed retesting within 365 days. Improved scheduling of clients at the time of trichomoniasis treatment and improved identification in our electronic health record of individuals diagnosed with trichomoniasis within the prior year would likely improve retesting rates. Given the high prevalence of trichomoniasis, expanded screening of asymptomatic females in settings where this is feasible may be warranted.
“…Compared to NAAT, the sensitivity of wet mount has been reported between 26%-68%. 23,24 At our institution wet mount missed one of 3 cases of trichomoniasis. NAAT is clearly more sensitive and thus preferable in settings able to offer it.…”
Background The Centers for Disease Control and Prevention recommends universal retesting within 3 months after treatment of Trichomonas vaginalis infection given high rates of persistent infection or reinfection, or if this is not possible, within 12 months following treatment. Data is lacking on how often this is actually done. Methods We analyzed the demographic and clinical characteristics, rate of return for the recommended retesting, concordance between wet prep and nucleic acid amplification testing, and percent positivity for T. vaginalis on repeat vaginal specimens at a local public health department in Durham, North Carolina, United States. Results Of 193 females treated for trichomoniasis between March 1, 2021 – May 31, 2022, 83% were Black or African American and 44% between the ages of 20 and 29 years. Of these individuals, 32% had retesting performed within 3 months and 50% within 365 days after treatment. Females between the ages of 20 and 29 years were more likely to return for retesting than those between the ages of 30 and 39 years. Of those who returned for retesting, 10% were positive on repeat testing. Conclusion In this study, 50% of females diagnosed with trichomoniasis completed retesting within 365 days. Improved scheduling of clients at the time of trichomoniasis treatment and improved identification in our electronic health record of individuals diagnosed with trichomoniasis within the prior year would likely improve retesting rates. Given the high prevalence of trichomoniasis, expanded screening of asymptomatic females in settings where this is feasible may be warranted.
“…Of note, although delayed treatment was not associated with increased odds of preterm birth above that of timely treated cases, it is possible that treatment delays are associated with other adverse pregnancy outcomes not addressed in this analysis. Strategies such as point of care testing and expedited partner therapy should be considered to reduce the frequent treatment delays seen in our cohort 26–28 . Behavioral interventions and specific counseling messages to reduce STI acquisition and increase condom use among pregnant women are urgently needed.…”
Section: Discussionmentioning
confidence: 99%
“…Strategies such as point of care testing and expedited partner therapy should be considered to reduce the frequent treatment delays seen in our cohort. [26][27][28] Behavioral interventions and specific counseling messages to reduce STI acquisition and increase condom use among pregnant women are urgently needed.…”
Background: Treating chlamydia and gonorrhea in pregnancy has been shown to decrease the associated risk of preterm birth in some studies. Delayed treatment of these infections among nonpregnant patients carries known consequences. It is unclear whether delayed treatment in pregnancy similarly increases adverse outcomes.
Methods:We conducted a retrospective cohort study of women who delivered at a safety-net hospital from July 2016 to June 2018. Women with at least one visit who were tested for chlamydia and gonorrhea were included. Women diagnosed after 36 weeks (preterm analysis) or 31 weeks (early preterm analysis) were excluded. We used multivariable logistic regression to examine the association between no infection, timely treatment (<1 week), and delayed treatment (>1 week, not treated) with preterm (<37 weeks) and early preterm (<32 weeks) birth.Results: Among 3154 deliveries, 389 (12%) were preterm. Among 3107 deliveries, 74 (2%) were early preterm. In adjusted models, women with timely (adjusted odds ratio [aOR]; 1.7, 95% confidence interval [CI], 1.0-2.7) and delayed (aOR, 1.7; 95% CI, 1.1-2.5) treatments had increased odds of preterm birth. Similarly, women with timely (aOR, 2.5; 95% CI, 1.0-6.2) and delayed (aOR, 2.4; 95% CI, 1.2-4.9) treatments had increased odds of early preterm birth. Among women who tested positive, multiple infections were not associated with an increase in preterm birth (preterm: 17% vs. 20%, P = 0.53; early preterm: 5% vs. 6%, P = 0.74).Conclusions: Chlamydia and gonorrhea are associated with preterm and early preterm births, regardless of time to treatment. Creative solutions are needed to improve the prevention of these infections in pregnancy.P reterm birth is the major driver of neonatal morbidity and mortality in the United States. 1 Maternal chlamydial infection and From the
“…Because routine testing for TV in pregnancy in the absence of symptoms is not standard of care 10 and not all delivering women were tested during pregnancy, to assess the potential for selection bias, we used logistic regression to model factors associated with having been tested for TV with NAAT and then generated predicted probabilities of testing and estimated inverse probability of testing weights 20 . Variables used to generate the inverse probability of testing weight model were informed by our prior work on TV testing at our institution 13 and included the following: age, race, use of an interpreter for consenting, date of delivery (6-month period), parity, Kotelchuck prenatal care utilization index, number of triage visits, chronic hypertension, past or current intimate partner violence, history of TV infection in a prior pregnancy, diagnosis of CT during the current pregnancy, and BV diagnosis during the current pregnancy. We then used these probabilities in a weighted logistic regression model of sPTB.…”
Section: Methodsmentioning
confidence: 99%
“…Although routine screening for TV is not recommended by the Centers for Disease Control and Prevention in HIV-negative individuals, 10 our prior work has shown a high proportion of testing among asymptomatic women in this population, likely because of provider preference in the setting of a high population prevalence of TV. 13 To eliminate potential bias from nonindependence of observations, if a woman had more than 1 delivery during the study period, only her first delivery at our facility was included. Because multifetal gestation is an independent risk factor for PTB, only singleton pregnancies were included in the analysis.…”
Background: Trichomonas vaginalis (TV) is the most prevalent nonviral sexually transmitted infection globally, but routine screening is not recommended in HIV-negative individuals. There is a significant racial/ethnic health disparity in TV infection rates. Evidence regarding the association between TV and adverse perinatal outcomes is conflicting, but a recent large meta-analysis found a modest increased risk of preterm birth with TV infection (odds ratio, 1.27; 95% confidence interval, 1.08-1.50). The current study was undertaken to evaluate whether TV infection increases the risk of spontaneous preterm birth (sPTB) in a high-risk obstetric cohort in Atlanta, GA.
Methods:We conducted a retrospective cohort study of women delivering at a safety-net hospital in Atlanta between July 2016 and June 2018. Women delivering a singleton live fetus at >20 weeks' gestation were included. The diagnosis of TV was by nucleic acid amplification testing. The outcome of interest was sPTB before 37 weeks' gestation. Multivariable Cox proportional hazards modeling was used to estimate the effect of TVon sPTB, controlling for confounding variables, including clinical and demographic characteristics. Several sensitivity analyses were undertaken.Results: There were 3723 deliveries during the study period, and approximately half (46%) were screened for TV with nucleic acid amplification testing. After exclusions, the analytic cohort included 1629 women. Median age was 26 years (interquartile range, 22-31 years), and 70% of participants were listed as non-Hispanic Black in the electronic medical record. The prevalence of TV was 16% (n = 257). The sPTB rate was 7% (n = 112). In multivariable Cox proportional hazards modeling, TV infection was not associated with a statistically significantly increased risk of sPTB (hazard ratio, 1.34; 95% confidence interval, 0.84-2.13; P = 0.22). Factors associated with sPTB included history of PTB, adequate plus or transfer of prenatal care (vs. adequate/intermediate prenatal care utilization using the Kotelchuck index), recreational substance use, and Chlamydia trachomatis diagnosed during the current pregnancy. Results were not substantively different in sensitivity analyses.
Conclusions:The prevalence of TV was high in this cohort. Its infection was not associated with a statistically significantly increased risk of sPTB. Nevertheless, the magnitude of effect is consistent with prior meta-analyses.
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