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一种快速沙眼衣原体和淋病重组酶聚合酶扩增检测试剂盒的诊断准确性:一项多中心横断面临床前评估。

Diagnostic accuracy of a prototype rapid chlamydia and gonorrhoea recombinase polymerase amplification assay: a multicentre cross-sectional preclinical evaluation.

机构信息

Applied Diagnostic Research & Evaluation Unit (ADREU), Institute for Infection & Immunity, St George's University of London, London, UK; HIV/STI Department, National Infection Service, Public Health England, London, UK.

Applied Diagnostic Research & Evaluation Unit (ADREU), Institute for Infection & Immunity, St George's University of London, London, UK.

出版信息

Clin Microbiol Infect. 2019 Mar;25(3):380.e1-380.e7. doi: 10.1016/j.cmi.2018.06.003. Epub 2018 Jun 12.

Abstract

OBJECTIVES

Rapid and accurate sexually transmitted infection diagnosis can reduce onward transmission and improve treatment efficacy. We evaluated the accuracy of a 15-minute run-time recombinase polymerase amplification-based prototype point-of-care test (TwistDx) for Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG).

METHODS

Prospective, multicentre study of symptomatic and asymptomatic patients attending three English sexual health clinics. Research samples provided were additional self-collected vulvovaginal swab (SCVS) (female participants) and first-catch urine (FCU) aliquot (female and male participants). Samples were processed blind to the comparator (routine clinic CT/NG nucleic acid amplification test (NAAT)) results. Discrepancies were resolved using Cepheid CT/NG GeneXpert.

RESULTS

Both recombinase polymerase amplification and routine clinic NAAT results were available for 392 male and 395 female participants. CT positivity was 8.9% (35/392) (male FCU), 7.3% (29/395) (female FCU) and 7.1% (28/395) (SCVS). Corresponding NG positivity was 3.1% (12/392), 0.8% (3/395) and 0.8% (3/395). Specificity and positive predictive values were 100% for all sample types and both organisms, except male CT FCU (99.7% specificity (95% confidence interval (CI) 98.4-100.0; 356/357), 97.1% positive predictive value (95% CI 84.7-99.9; 33/34)). For CT, sensitivity was ≥94.3% for FCU and SCVS. CT sensitivity for female FCU was higher (100%; 95% CI, 88.1-100; 29/29) than for SCVS (96.4%; 95% CI, 81.7-99.9; 27/28). NG sensitivity and negative predictive values were 100% in FCU (male and female).

CONCLUSIONS

This prototype test has excellent performance characteristics, comparable to currently used NAATs, and fulfils several World Health Organization ASSURED criteria. Its rapidity without loss of performance suggests that once further developed and commercialized, this test could positively affect clinical practice and public health.

摘要

目的

快速准确地诊断性传播感染可以减少传播,并提高治疗效果。我们评估了一种 15 分钟运行时间的基于重组酶聚合酶扩增的原型即时护理检测(TwistDx)对沙眼衣原体(CT)和淋病奈瑟菌(NG)的准确性。

方法

对三个英国性健康诊所就诊的有症状和无症状患者进行前瞻性、多中心研究。研究样本是额外的自我采集的阴道外阴拭子(SCVS)(女性参与者)和首次采集的尿液(FCU)等分试样(女性和男性参与者)。样本的处理对比较器(常规诊所 CT/NG 核酸扩增检测(NAAT))的结果是盲目的。差异使用 Cepheid CT/NG GeneXpert 解决。

结果

男性和女性参与者各有 392 名和 395 名,均有重组酶聚合酶扩增和常规诊所 NAAT 结果。CT 阳性率为 8.9%(35/392)(男性 FCU)、7.3%(29/395)(女性 FCU)和 7.1%(28/395)(SCVS)。相应的 NG 阳性率为 3.1%(12/392)、0.8%(3/395)和 0.8%(3/395)。所有样本类型和两种病原体的特异性和阳性预测值均为 100%,除了男性 CT FCU(99.7%特异性(95%置信区间(CI)98.4-100.0;356/357)、97.1%阳性预测值(95%CI 84.7-99.9;33/34))。对于 CT,FCU 和 SCVS 的敏感性均≥94.3%。女性 FCU 的 CT 敏感性(100%;95%CI,88.1-100;29/29)高于 SCVS(96.4%;95%CI,81.7-99.9;27/28)。FCU(男性和女性)的 NG 敏感性和阴性预测值均为 100%。

结论

该原型测试具有出色的性能特征,与目前使用的 NAAT 相当,并满足世界卫生组织 ASSURED 标准的几个要求。其快速性而不影响性能表明,一旦进一步开发和商业化,该测试可能会对临床实践和公共卫生产生积极影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84ee/6420679/1ef69d124870/gr1.jpg

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