Evidence map›Paper›PMID 42383906›Full record

ArticleSexually transmitted diseases2026

The Potential for Combined Treponemal/Nontreponemal Rapid Point-of-Care Test and Treponema pallidum Polymerase Chain Reaction in the Diagnosis of Gestational and Congenital Syphilis in a Low-Resource, High-Prevalence Setting: Pilot Data From Malawi.

Deirdre J Foley, Vita Nyasulu, Chifundo Kondoni, Annie Kuyere, Fatima Mtonga, George Shaba, James Jafali, Chelsea Morroni, Michael Marks, Patrick Mallon and 6 more

Abstract read
In one paragraph

Article in Sexually transmitted diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

16 authors.

Deirdre J FoleyFrom the School of Medicine, University College Dublin.
Vita NyasuluMalawi Liverpool Wellcome Research Program, Blantyre, Malawi.
Chifundo KondoniMalawi Liverpool Wellcome Research Program, Blantyre, Malawi.
Annie KuyereMalawi Liverpool Wellcome Research Program, Blantyre, Malawi.
Fatima MtongaMalawi Liverpool Wellcome Research Program, Blantyre, Malawi.
George ShabaMalawi Liverpool Wellcome Research Program, Blantyre, Malawi.
James JafaliMalawi Liverpool Wellcome Research Program, Blantyre, Malawi.
Chelsea MorroniCentre for Reproductive Health, University of Edinburgh, Edinburgh, Scotland, United Kingdom.
Michael MarksClinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine.
Patrick MallonCentre for Experimental Host Pathogen Research and Faculty of Paediatrics, University College Dublin, Dublin, Ireland.
David LissauerMalawi Liverpool Wellcome Research Program, Blantyre, Malawi.
Gladys GadamaDepartment of Obstetrics.
Luis GadamaDepartment of Obstetrics.
Kondwani KawazaClinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine.
Charlotte van der VeerMalawi Liverpool Wellcome Research Program, Blantyre, Malawi.
Bridget FreyneFrom the School of Medicine, University College Dublin.

Funding

ESPID Springboard Award
6 · The paper itself

Abstract

backgroundCongenital syphilis (CS) remains a major cause of stillbirth and neonatal morbidity, with an estimated 700,000 cases and 390,000 adverse birth outcomes annually. We evaluated the diagnostic utility of combined treponemal (TT) and nontreponemal (NTT) rapid point-of-care test and Treponema pallidum polymerase chain reaction (PCR) for detecting active maternal syphilis, CS, and treatment response in a high-prevalence, low-resource setting.

methodsSecondary analyses were conducted from a prospective case-control study at Queen Elizabeth Central Hospital, Malawi. Women were recruited ≤48 h postpartum. Maternal and infant sera underwent testing with the DPP® Syphilis Screen and Confirm (Dual rapid diagnostic test [RDT]) and T. pallidum PCR (maternal vaginal swabs and infant nasopharyngeal swabs), with predefined clinical-serological reference standards based on qualitative rapid plasma reagin (RPR).

resultsAmong 504 of 510 women with complete data, Dual RDT identified 110 seropositive cases at delivery, including 86 new maternal syphilis diagnoses. The NTT band showed good performance in mothers versus RPR (sensitivity: 84.8% [95% confidence interval: 77.4%-92.1%]; specificity 92.7% [95% confidence interval: 90.3%-95.1%]) but reduced sensitivity in infants, increasing from 51.9% to 80.0% with RPR titer. Laboratory visual and microreader interpretation showed high concordance (99.5%), while bedside visual accuracy was lower (77.4%). Any Dual RDT positivity identified 19 high-risk infants, of whom 7 of 19 (36.8%) were NTT positive. PCR detected maternal infection in 11 of 504 (2.2%), including 3 serology-negative cases.

conclusionsDual RDT improves detection over TT alone. The NTT band without quantitation is insufficient for treatment monitoring or infant diagnosis. Combining Dual RDT with PCR may enhance detection of active maternal infection and CS in high-burden settings.

Indexed as

Polymerase Chain ReactionPregnancy Complications, InfectiousSyphilisSyphilis, CongenitalTreponema pallidumAdultCase-Control StudiesFemaleHumansInfant, NewbornMalawiPilot ProjectsPoint-of-Care SystemsPoint-of-Care TestingPregnancyPrevalence

Identifiers

PMID42383906
PMCPMC13326932

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LicenceCC BY
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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.