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男性性接触者和跨性别女性中 3 个解剖部位联合检测沙眼衣原体和淋病奈瑟菌的性能。

The Performance of Pooled 3 Anatomic Site Testing for Chlamydia trachomatis and Neisseria gonorrhoeae Among Men Who Have Sex With Men and Transgender Women.

机构信息

From the Division of Infectious Disease and Global Public Health, Department of Medicine, University of California San Diego.

出版信息

Sex Transm Dis. 2021 Oct 1;48(10):733-737. doi: 10.1097/OLQ.0000000000001411.

Abstract

BACKGROUND

Although molecular testing for Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) is highly sensitive, the cost can be prohibitive. Those high costs are amplified when the recommended screening approach is used, which requires separate testing of specimens from 3 anatomic sites (rectal, pharyngeal and urogenital). Although individual molecular testing is standard of care, pooled testing may offer a cost-saving alternative.

METHODS

Using the Xpert® CT/NG assay (Cepheid, Sunnyvale, CA) we tested urine, rectal and pharyngeal swabs for CT and NG in a high-risk cohort of participants assigned male at birth who reported sex with other persons who were assigned male at birth. Remnant specimens (0.34 mL from each anatomic site) were combined to perform a single 'pooled' test. We calculated positive and negative percent agreement between the pooled testing results with standard of care Xpert CT/NG test results as the reference.

RESULTS

We conducted 644 pooled tests. Of those, 598 (92.3%) gave CT and NG results. The CT-positive and -negative percent agreement were 90.1% (95% confidence interval [CI], 80.7-95.9%) and 99.2% (98.1-99.8%), respectively. The NG-positive and -negative percent agreement were 96.2% (95% CI, 86.8-99.5%) and 99.8% (95% CI, 99.0-100%), respectively. Pooled testing identified 4 CT and 1 NG infections that were negative at all anatomic sites by individual testing.

CONCLUSIONS

Three-site pooled CT and NG testing performs similarly to single anatomic site testing among tests providing a valid result. Future cost analyses should evaluate the cost effectiveness of pooled 3-site testing to determine if such a strategy improves the feasibility and accessibility of molecular sexually transmitted infection testing.

摘要

背景

虽然针对沙眼衣原体(CT)和淋病奈瑟菌(NG)的分子检测具有高度敏感性,但成本可能过高。当推荐的筛查方法(需要分别检测来自 3 个解剖部位(直肠、咽和泌尿生殖道)的标本)被采用时,这些高成本会被放大。尽管个体分子检测是标准护理,但汇集检测可能提供一种节省成本的替代方法。

方法

我们使用 Xpert® CT/NG 检测试剂盒(Cepheid,加利福尼亚州森尼韦尔),对报告与其他男性发生性行为的高风险出生时为男性的参与者的尿液、直肠和咽拭子进行 CT 和 NG 检测。将剩余的标本(每个解剖部位 0.34 毫升)混合在一起进行单次“汇集”检测。我们计算了汇集检测结果与标准护理 Xpert CT/NG 检测结果之间的阳性和阴性百分一致率,后者作为参考。

结果

我们进行了 644 次汇集检测。其中 598 次(92.3%)提供了 CT 和 NG 结果。CT 阳性和阴性百分一致率分别为 90.1%(95%置信区间[CI],80.7-95.9%)和 99.2%(98.1-99.8%)。NG 阳性和阴性百分一致率分别为 96.2%(95%CI,86.8-99.5%)和 99.8%(95%CI,99.0-100%)。汇集检测在所有解剖部位的个体检测均为阴性的情况下,发现了 4 例 CT 和 1 例 NG 感染。

结论

在提供有效结果的检测中,3 部位汇集 CT 和 NG 检测的性能与单个解剖部位检测相似。未来的成本分析应评估汇集 3 部位检测的成本效益,以确定这种策略是否能提高分子性传播感染检测的可行性和可及性。

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