Evidence map›Paper›PMID 29699549›Full record

ArticleBMC women's health2018

Evaluation of human-papillomavirus testing and visual inspection for cervical cancer screening in Rwanda.

M Chantal Umulisa, Silvia Franceschi, Iacopo Baussano, Vanessa Tenet, Mathilde Uwimbabazi, Belson Rugwizangoga, Daniëlle A M Heideman, Anne M Uyterlinde, Teresa M Darragh, Peter J F Snijders and 2 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC women's health, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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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

12 authors at 6 institutions in 5 countries.

M Chantal UmulisaMinistry of Health of Rwanda, Kigali, Rwanda.
Silvia FranceschiCancer Epidemiology Unit, Aviano National Cancer Institute IRCCS, Aviano, Italy.
Iacopo BaussanoInternational Agency for Research on Cancer, 150 cours Albert Thomas, 69372 Lyon Cedex 08, France.
Vanessa TenetInternational Agency for Research on Cancer, 150 cours Albert Thomas, 69372 Lyon Cedex 08, France.
Mathilde UwimbabaziMuhima District Hospital, Kigali, Rwanda.
Belson RugwizangogaDepartment of Pathology, University Teaching Hospital of Kigali, Kigali, Rwanda.
Daniëlle A M HeidemanDepartment of Pathology, VU University Medical Center, Amsterdam, the Netherlands.
Anne M UyterlindeDepartment of Pathology, VU University Medical Center, Amsterdam, the Netherlands.
Teresa M DarraghUniversity of California, San Francisco, CA, USA.
Peter J F SnijdersDepartment of Pathology, VU University Medical Center, Amsterdam, the Netherlands.
Felix SayinzogaMinistry of Health of Rwanda, Kigali, Rwanda.
Gary M CliffordInternational Agency for Research on Cancer, 150 cours Albert Thomas, 69372 Lyon Cedex 08, France. cliffordg@iarc.fr.ORCID 0000-0001-7534-333X
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLCentre international de recherche sur le cancer · FRMinistry of Health · RWCentro di Riferimento Oncologico · ITUniversity of California, San Francisco · USUniversity of Rwanda · RW

Funding

World Health Organization 001
6 · The paper itself

Abstract

backgroundA pilot screening campaign in Rwanda, based on careHPV-testing followed by visual inspection with acetic acid triage (careHPV+VIA triage), was evaluated against other WHO-recommended screening options, namely HPV screen-and-treat and VIA screen-and-treat.

methods764 women aged 30-69 underwent at visit 1: i) VIA, and cervical cell collection for ii) careHPV in Rwanda, and iii) liquid-based cytology and GP5+/6+ HR-HPV PCR in The Netherlands. All 177 women positive by VIA, careHPV and/or PCR were recalled, of whom 84% attended. At visit 2, VIA was again used to triage screen-positive women for treatment and to obtain biopsies from all women either from visible lesions or at 12 o'clock of the squamocolumnar junction. Cross-sectional screening indices were estimated primarily against histological high-grade squamous intraepithelial lesions or worse (hHSIL+), after imputation of missing histology data, based on 1-visit or 2-visit approaches.

resultsIn a 1-visit screen-and-treat approach, VIA had sensitivity and specificity of 41% and 96%, respectively, versus 71% and 88% for careHPV, and 88% and 86% for PCR. In a 2-visit approach (in which hHSIL+ imputed among women without visit 2 were considered untreated) careHPV sensitivity dropped to 59% due to loss of 13% of hHSIL+. For careHPV+VIA triage, sensitivity dropped further to 35%, as another 24% of hHSIL+ were triaged to no treatment.

conclusionsCareHPV was not as sensitive as gold-standard PCR, but detected considerably more hHSIL+ than VIA. However, due to careHPV-positive hHSIL+ women being lost to follow-up and/or triaged to no treatment, 2-visit careHPV+VIA triage did not perform better than VIA screen-and-treat.

Indexed as

Acetic AcidAdultAgedDNA, ViralEarly Detection of CancerFemaleHumansMiddle AgedPapillomaviridaePapillomavirus InfectionsRwandaSensitivity and SpecificitySquamous Intraepithelial Lesions of the CervixUterine Cervical NeoplasmsAcetic AcidDNA, ViralCervical cancerHuman papillomavirusRwandaScreeningVisual inspection

Identifiers

PMID29699549
PMCPMC5921370
OpenAlexW2806515478

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.