Evidence map›Paper›PMID 23326441›Full record

ArticlePloS one2013

Validation of cervical cancer screening methods in HIV positive women from Johannesburg South Africa.

Cynthia Firnhaber, Nomtha Mayisela, Lu Mao, Sophie Williams, Avril Swarts, Mark Faesen, Simon Levin, Pam Michelow, Tanvier Omar, Michael G Hudgens and 4 more

Open access · goldAbstract readValidation Study
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed, 3 pooled it
9.6field-weighted citation impact, top 1% of its field
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

73 citing papers in PubMed, 3 syntheses or guidelines pooled it, 120 citations in OpenAlex.

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  19. The IARC Perspective on Cervical Cancer Screening.The New England journal of medicine · 2021
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  20. Review

13 more citing papers are in PubMed but not listed here.

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

14 authors at 5 institutions in 2 countries.

Cynthia FirnhaberFaculty of Health Science Centre, Department of Medicine, University of Witwatersrand, Johannesburg, South Africa. cindy.firnhaber@righttocare.org
Nomtha Mayisela
Lu Mao
Sophie Williams
Avril Swarts
Mark Faesen
Simon Levin
Pam Michelow
Tanvier Omar
Michael G Hudgens
Anna-Lise Williamson
Bruce Allan
David A Lewis
Jennifer S Smith
National Health Laboratory Service · ZARight to Care · ZAUniversity of North Carolina at Chapel Hill · USUniversity of the Witwatersrand · ZAUniversity of Cape Town · ZA

Funding

Virology, Immunology, and Microbiology CoreP30AI050410 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DAVID M. MARGOLIS · 2001 to 2026
$76.9M
NIAID NIH HHS P30 AI050410NIAID NIH HHS P30-AI50410PEPFAR 674-A-00-08-00007-00
6 · The paper itself

Abstract

backgroundHIV-infected women are at increased risk for developing cervical cancer. Women living in resource-limited countries are especially at risk due to poor access to cervical cancer screening and treatment. We evaluated three cervical cancer screening methods to detect cervical intraepithelial neoplasia grade 2 and above (CIN 2+) in HIV-infected women in South Africa; Pap smear, visual inspection with 5% acetic acid (VIA) and human papillomavirus detection (HPV).

methodsHIV-infected women aged 18-65 were recruited in Johannesburg. A cross-sectional study evaluating three screening methods for the detection of the histologically-defined gold standard CIN-2 + was performed. Women were screened for cervical abnormalities with the Digene HC2 assay (HPV), Pap smear and VIA. VIA was performed by clinic nurses, digital photographs taken and then later reviewed by specialist physicians. The sensitivity, specificity and predictive valves for CIN-2 + were calculated using maximum likelihood estimators.

results1,202 HIV-infected women participated, with a median age of 38 years and CD4 counts of 394 cells/mm(3). One third of women had a high grade lesion on cytology. VIA and HPV were positive in 45% and 61% of women respectively. Estimated sensitivity/specificity for HPV, Pap smear and VIA for CIN 2+ was 92%/51.4%, 75.8%/83.4% and 65.4/68.5% (nurse reading), respectively. Sensitivities were similar, and specificities appeared significantly lower for the HPV test, cytology and VIA among women with CD4 counts ≤200 cells/mm(3) as compared to CD4 counts >350 cells/mm(3).

conclusionsAlthough HPV was the most sensitive screening method for detecting CIN 2+, it was less specific than conventional cytology and VIA with digital imaging review. Screening programs may need to be individualized in context of the resources and capacity in each area.

Indexed as

AdolescentAdultAgedColposcopyDemographyEarly Detection of CancerFemaleHIV SeropositivityHumansMiddle AgedQuality Assurance, Health CareReproducibility of ResultsSensitivity and SpecificitySouth AfricaUterine Cervical NeoplasmsYoung Adult

Identifiers

PMID23326441
PMCPMC3543403
OpenAlexW2066973637

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.