4.1 Article

Confirmatory assays are essential when using molecular testing for Neisseria gonorrhoeae in low-prevalence settings: insights from the third National Survey of Sexual Attitudes and Lifestyles (Natsal-3)

Journal

SEXUALLY TRANSMITTED INFECTIONS
Volume 91, Issue 5, Pages 338-341

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/sextrans-2014-051850

Keywords

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Funding

  1. Medical Research Council [G0701757]
  2. Wellcome Trust [084840]
  3. Economic and Social Research Council
  4. Department of Health
  5. MRC [G0701757] Funding Source: UKRI
  6. National Institute for Health Research [CL-2010-18-010, NF-SI-0508-10244] Funding Source: researchfish

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Objectives 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. Results 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%)). Conclusions 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.

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