Evidence map›Paper›PMID 42497228›Full record

ArticlePLOS global public health2026

Leveraging current capacity to address the high prevalence of Chlamydia trachomatis, Neisseria gonorrhoeae, and Trichomonas vaginalis in South Africa: Modelling potential costs and benefits of near point-of-care GeneXpert testing for STIs.

Nkgomeleng A Lekodeba, Katherine Snyman, Brooke E Nichols, Lise Jamieson

Abstract read
In one paragraph

Article in PLOS global public health, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Nkgomeleng A LekodebaHealth Economics and Epidemiology Research Office, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.ORCID https://orcid.org/0000-0001-7951-7333
Katherine SnymanHealth Economics and Epidemiology Research Office, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.ORCID https://orcid.org/0000-0002-0074-2720
Brooke E NicholsHealth Economics and Epidemiology Research Office, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.ORCID https://orcid.org/0000-0003-4682-4999
Lise JamiesonHealth Economics and Epidemiology Research Office, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

South Africa has high sexually transmitted infections (STIs) prevalence and currently implements syndromic management, which has limitations including untreated asymptomatic infections and excess antibiotic use. Diagnostic tools like GeneXpert may offer potential improvements. We evaluated potential costs and benefits of GeneXpert for STIs testing. We developed a static analytical model using existing data over a one-year time horizon (January-December 2024) from a provider perspective. We estimated costs (2024 USD), outcomes, cost-effectiveness, and budget impact of syndromic management and multiple near point-of-care (i.e., off-site laboratory) GeneXpert testing scenarios for Neisseria gonorrhoeae, Chlamydia trachomatis, and Trichomonas vaginalis. Target groups included symptomatic individuals, antenatal care (ANC) attendees, and HIV testers. Deterministic sensitivity analysis was conducted on key parameters. Cost per person, and per person correctly diagnosed and treated ranged from $21-$29 under syndromic management and $88-$755 in GeneXpert scenarios. Syndromic management cost the healthcare system an estimated $24.1 million per year; symptomatic GeneXpert testing would cost substantially more: $102.1-$207.8 million, and $300.9 million-$2.1 billion for GeneXpert scenarios involving symptomatic individuals, ANC attendees, and HIV testers. GeneXpert testing reduces excess antibiotic use by up to 88% compared to syndromic management. Of scenarios modelled, three were on the cost-effectiveness frontier: syndromic management, S4: symptomatic adults and adolescent girls and young women HIV testers, and S8: symptomatic adults, ANC attendees and HIV testers. While syndromic management was least costly, incremental cost per additional person correctly diagnosed and treated was $863 (S4) and $1,064 (S8). These scenarios would cost $3.5 and $12.0 billion over 5-years, respectively, compared to $146.0 million in syndromic management. Staff and diagnostic cost were the most influential parameter in sensitivity analysis. Prioritizing GeneXpert testing for symptomatic individuals and high-risk groups (e.g., HIV testers) can improve STI management but requires additional investment. These findings support the need for targeted strategies to optimise STI control.

Identifiers

PMID42497228
PMCPMC13399335

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.