Evidence map›Paper›PMID 32245369›Full record

ArticleBMC infectious diseases2020

Evaluation of the effectiveness of high-risk human papilloma self-sampling test for cervical cancer screening in Bolivia.

Gustavo Allende, Pedro Surriabre, Neli Ovando, Pamela Calle, Andrea Torrico, Jaime Villarroel, Michel Bossens, Véronique Fontaine, Patricia Rodriguez

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in BMC infectious diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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

9 authors at 2 institutions in 2 countries.

Gustavo AllendeLaboratory of Virology, Faculty of Medicine, Universidad Mayor de San Simón, Cochabamba, Bolivia.
Pedro SurriabreLaboratory of Virology, Faculty of Medicine, Universidad Mayor de San Simón, Cochabamba, Bolivia.
Neli OvandoLaboratory of Virology, Faculty of Medicine, Universidad Mayor de San Simón, Cochabamba, Bolivia.
Pamela CalleLaboratory of Virology, Faculty of Medicine, Universidad Mayor de San Simón, Cochabamba, Bolivia.
Andrea TorricoLaboratory of Virology, Faculty of Medicine, Universidad Mayor de San Simón, Cochabamba, Bolivia.
Jaime VillarroelAnatomopathology Laboratory of the Bolivian-Japanese hospital, Cochabamba, Bolivia.
Michel BossensResearch Laboratory in Human Reproduction, Campus Erasme, Faculty of Medicine, Universite libre de Bruxelles, Brussels, ULB, Belgium.
Véronique FontaineUnité de Microbiologie Pharmaceutique et Hygiène, Faculté de Pharmacie, Université Libre de Bruxelles (ULB), CP205/2, Campus Plaine, Boulevard du Triomphe, 1050, Brussels, Belgium.
Patricia RodriguezLaboratory of Virology, Faculty of Medicine, Universidad Mayor de San Simón, Cochabamba, Bolivia. p.rodriguez@umss.edu.bo.
University of San Simón · BOUniversité Libre de Bruxelles · BE

Funding

ARES-CCD PRD 2013
6 · The paper itself

Abstract

backgroundIn Bolivia the incidence and mortality rates of uterine cervix cancer are the highest in America. The main factor contributing to this situation is the difficulty of establishing and maintaining quality prevention programs based on cytology. We aimed to evaluate the effectiveness of HR-HPV testing on self-collected samples to detect cervical intra-epithelial neoplasia and identify the best combination of screening tests.

methodsA total of 469 women, divided in two groups, were included in this study. The first group included 362 women that underwent three consecutively primary screening tests: self-collected sampling for HR-HPV detection, conventional cervical cytology and visual inspection under acetic acid (VIA). The second group included 107 women referred with a positive HR-HPV test that underwent conventional cervical cytology and VIA. The presence of high grade intraepithelial lesion (CIN 2+) or invasive cancer was verified by colposcopy and biopsy.

resultIn the screening group the sensitivity to detect high grade intraepithelial lesion (CIN 2+) or invasive cancer were 100, 76, 44% for the VIA, HR-HPV test and cytology, respectively. In the referred group, the sensitivity to detect high grade intraepithelial lesion (CIN 2+) or invasive cancer by VIA and cytology were 100 and 81%, respectively.

conclusionsVIA and HR-HPV self-sampling were the best combination to detect CIN2+ lesions. Cytology analysis gave the poorest performance.

Indexed as

AdultBoliviaColposcopyCross-Sectional StudiesEarly Detection of CancerFemaleHumansIncidenceMass ScreeningMiddle AgedPapanicolaou TestPapillomaviridaePapillomavirus InfectionsPolymerase Chain ReactionPrognosisSensitivity and SpecificityCervical intra-epithelial neoplasiaCytologyHuman papillomavirus testing, visual inspection with acetic acid

Identifiers

PMID32245369
PMCPMC7119273
OpenAlexW3014817092

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.