Evers Ymke J, van Liere Geneviève A F S, Dukers-Muijrers Nicole H T M, van Bergen Jan, Kuizenga-Wessel Sophie, Hoebe Christian J P A
Department of Sexual Health, Infectious Diseases and Environmental Health, South Limburg Public Health Service, Heerlen, Netherlands; Department of Social Medicine and Medical Microbiology, School of Public Health and Primary Care, Maastricht University Medical Centre, Maastricht, Netherlands.
Department of Sexual Health, Infectious Diseases and Environmental Health, South Limburg Public Health Service, Heerlen, Netherlands; Department of Social Medicine and Medical Microbiology, School of Public Health and Primary Care, Maastricht University Medical Centre, Maastricht, Netherlands.
Lancet Infect Dis. 2022 Apr;22(4):552-561. doi: 10.1016/S1473-3099(21)00465-5. Epub 2021 Dec 15.
Pharyngeal Chlamydia trachomatis in women might contribute to autoinoculation and transmission to sexual partners. Data for effectiveness of different testing practices for pharyngeal C trachomatis are scarce. We therefore aimed to assess the prevalence of pharyngeal C trachomatis, determinants, and effectiveness of different testing practices in women.
We did a retrospective cohort study, in which surveillance data for all women visiting sexually transmitted infection clinics in all regions in the Netherlands between Jan 1, 2008, and Dec 31, 2017, were used. We collected consultation-level data and individual-level data from 2016 onwards for sociodemographic characteristics, sexual behaviour in the past 6 months, self-reported symptoms, and STI diagnoses. The primary outcome was the positivity rate of pharyngeal C trachomatis infection compared between routine universal testing (>85% tested pharyngeally per clinic year), selective testing (5-85% tested pharyngeally per clinic year), and incidental testing (<5% pharyngeally tested per clinic year). We calculated the number of missed infections by extrapolating the positivity rate assessed by routine universal testing to all selectively tested women. We used multivariable generalised estimating equations logistic regression analyses to assess independent risk factors for pharyngeal C trachomatis and used the assessed risk factors as testing indicators for comparing alternative testing scenarios.
Between Jan 1, 2008, and Dec 31, 2017, a total of 550 615 consultations with at least one C trachomatis test was recorded, of which 541 945 (98·4%) consultations (including repeat visits) were included in this analysis. Pharyngeal C trachomatis positivity was lower in the routine universal testing group than in the selective testing group (1081 [2·4%; 95% CI 2·2-2·5] of 45 774 vs 3473 [2·9%; 2·8-3·0] of 121 262; p<0·0001). The positivity rate was also higher among consultations done in the incidental testing group (44 [4·1%; 95% CI 3·1-5·5] of 1073; p<0·0001) than in the routine universal testing group. Based on extrapolation, selective testing would have hypothetically missed 64·4% (95% CI 63·5-65·3; 6363 of 9879) of the estimated total of C trachomatis infections. The proportion of pharyngeal-only C trachomatis was comparable between routinely universally tested women (22·9%) and selectively tested women (20·4%), resulting in a difference of 2·5% (95% CI -0·3 to 5·3; p=0·07). When using risk factors for pharyngeal C trachomatis as testing indicators, 15 484 (79·6%) of 19 459 women would be tested to detect 398 (80·6%) of 494 infections.
No optimal testing scenario was available for pharyngeal C trachomatis, in which only a selection of high-risk women needs to be tested to find most pharyngeal C trachomatis infections. The relative low prevalence of pharyngeal-only C trachomatis (0·5%) and probably limited clinical and public health effect do not provide support for routine universal testing.
Public Health Service South Limburg.
女性咽部沙眼衣原体感染可能导致自身接种感染,并传播给性伴侣。关于不同检测方法对咽部沙眼衣原体检测效果的数据较少。因此,我们旨在评估女性咽部沙眼衣原体的感染率、影响因素以及不同检测方法的效果。
我们进行了一项回顾性队列研究,使用了2008年1月1日至2017年12月31日期间荷兰所有地区性传播感染诊所就诊的所有女性的监测数据。我们收集了2016年起的咨询层面数据和个体层面数据,包括社会人口学特征、过去6个月的性行为、自我报告症状和性传播感染诊断情况。主要结局是比较常规普遍检测(每年每个诊所咽部检测率>85%)、选择性检测(每年每个诊所咽部检测率5%-85%)和偶然检测(每年每个诊所咽部检测率<5%)之间咽部沙眼衣原体感染的阳性率。我们通过将常规普遍检测评估的阳性率外推到所有选择性检测的女性来计算漏检感染数。我们使用多变量广义估计方程逻辑回归分析来评估咽部沙眼衣原体的独立危险因素,并将评估出的危险因素用作比较不同检测方案的检测指标。
2008年1月1日至2017年12月31日期间,共记录了550615次至少进行过一次沙眼衣原体检测的咨询,其中541945次(98.4%)咨询(包括复诊)纳入本分析。常规普遍检测组的咽部沙眼衣原体阳性率低于选择性检测组(45774例中的1081例[2.4%;95%CI 2.2-2.5] vs 121262例中的3473例[2.9%;2.8-3.0];p<0.0001)。偶然检测组咨询的阳性率也高于常规普遍检测组(1073例中的44例[4.1%;95%CI 3.1-5.5];p<0.0001)。根据外推法,选择性检测可能会漏检估计沙眼衣原体感染总数的64.4%(95%CI 63.5-65.3;9879例中的6363例)。仅咽部沙眼衣原体感染的比例在常规普遍检测女性(22.9%)和选择性检测女性(20.4%)之间相当,差异为2.5%(95%CI -0.3至5.3;p=0.07)。当将咽部沙眼衣原体的危险因素用作检测指标时,19459名女性中的15484名(79.6%)将接受检测,以检测494例感染中的398例(80.6%)。
对于咽部沙眼衣原体,没有一种最佳检测方案,即仅对一部分高危女性进行检测就能发现大多数咽部沙眼衣原体感染。仅咽部沙眼衣原体的相对低感染率(0.5%)以及可能有限的临床和公共卫生影响不支持常规普遍检测。
南林堡公共卫生服务局。