Field Nigel, Clifton Soazig, Alexander Sarah, Ison Catherine A, Hughes Gwenda, Beddows Simon, Tanton Clare, Soldan Kate, Coelho da Silva Filomeno, Mercer Catherine H, Wellings Kaye, Johnson Anne M, Sonnenberg Pam
Research Department of Infection & Population Health, University College London, Mortimer Market Centre, London, UK.
Research Department of Infection & Population Health, University College London, Mortimer Market Centre, London, UK NatCen Social Research, London, UK.
Sex Transm Infect. 2015 Aug;91(5):338-41. doi: 10.1136/sextrans-2014-051850. Epub 2014 Dec 15.
To investigate the occurrence of unconfirmed positive gonorrhoea results when using molecular testing within a large population-based survey.
DESIGN, SETTING AND PARTICIPANTS: Between 2010 and 2012, we did a probability sample survey of 15,162 men and women aged 16-74 years in Britain. Urine from participants aged 16-44 years reporting ≥1 lifetime sexual partner was tested for Neisseria gonorrhoeae and Chlamydia trachomatis using the Aptima Combo 2 (AC2) assay, with positive or equivocal results confirmed with molecular assays using different nucleic acid targets.
A total of 4550 participants aged 16-44 years had urine test results (1885 men; 2665 women). For gonorrhoea, 18 samples initially tested positive and eight were equivocal. Only five out of 26 confirmed, giving a positive predictive value (PPV) for the initial testing of 19% (95% CI 4% to 34%). Most (86% (18/21)) participants with unconfirmed positive results for gonorrhoea reported zero or one sexual partner without condoms in the past year and none had chlamydia co-infection, whereas all five with confirmed gonorrhoea reported at least two recent sexual partners without condoms, and four had chlamydia co-infection. The weighted prevalence for gonorrhoea positivity fell from 0.4% (0.3% to 0.7%) after initial screening to <0.1% (0.0% to 0.1%) after confirmatory testing. By comparison, 103 samples tested positive or equivocal for chlamydia and 98 were confirmed (PPV=95% (91% to 99%)).
We highlight the low PPV for gonorrhoea of an unconfirmed reactive test when deploying molecular testing in a low-prevalence population. Failure to undertake confirmatory testing in low-prevalence settings may lead to inappropriate diagnoses, unnecessary treatment and overestimation of population prevalence.
在一项基于人群的大型调查中,研究使用分子检测时未确诊的淋病阳性结果的发生情况。
设计、背景和参与者:2010年至2012年期间,我们对英国15162名年龄在16 - 74岁的男性和女性进行了概率抽样调查。对报告有≥1个终身性伴侣的16 - 44岁参与者的尿液进行淋病奈瑟菌和沙眼衣原体检测,采用Aptima Combo 2(AC2)检测法,阳性或疑似阳性结果通过使用不同核酸靶点的分子检测法进行确认。
共有4550名年龄在16 - 44岁的参与者有尿液检测结果(1885名男性;2665名女性)。对于淋病,最初有18个样本检测呈阳性,8个为疑似阳性。在26个经确认的样本中只有5个呈阳性,初始检测的阳性预测值(PPV)为19%(95%置信区间4%至34%)。大多数(86%(18/21))淋病检测结果未确诊为阳性的参与者报告在过去一年中无避孕套性行为的性伴侣为零个或一个,且无人合并衣原体感染,而所有5个确诊为淋病的参与者均报告近期至少有两个无避孕套性行为的性伴侣,其中4人合并衣原体感染。淋病阳性的加权患病率从初始筛查后的0.4%(0.3%至0.7%)降至确认检测后的<0.1%(0.0%至0.1%)。相比之下,103个样本衣原体检测呈阳性或疑似阳性,98个得到确认(PPV = 95%(91%至99%))。
我们强调在低流行人群中采用分子检测时,未确诊的反应性检测对淋病的阳性预测值较低。在低流行环境中不进行确认检测可能导致不适当的诊断、不必要的治疗以及对人群患病率的高估。