Evidence map›Paper›PMID 36731925›Full record

ArticleBMJ open2023

Estimating the prevalence of non-cervical human papillomavirus infection in mainland China (PROGRESS-Plus): protocol of a national cross-sectional study.

Wei Wang, Smita Kothari-Talwar, Craig Roberts, Qingbin Lu, Nuria Lara, Ravi Panchal, Edith Morais, Ya-Ting Chen, Youlin Qiao, Fuqiang Cui

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 5 institutions in 4 countries.

Wei WangMerck & Co Inc, Rahway, New Jersey, USA wei.wang40@merck.com.ORCID 0000-0002-0855-0002
Smita Kothari-TalwarMerck & Co Inc, Rahway, New Jersey, USA.
Craig RobertsMerck & Co Inc, Rahway, New Jersey, USA.
Qingbin LuSchool of Public Health, Peking University, Beijing, China.
Nuria LaraIMS Health Barcelona, Barcelona, Spain.
Ravi PanchalIQVIA, Bangalore, India.
Edith MoraisMSD France, Courbevoie, France.
Ya-Ting ChenMerck & Co Inc, Rahway, New Jersey, USA.
Youlin QiaoCancer Epidemiology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Fuqiang CuiPeking University Health Science Centre, Beijing, China.ORCID 0000-0002-9592-4286
Merck & Co., Inc., Rahway, NJ, USA (United States) · USPeking University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNIQVIA (India) · INMSD (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionHuman papillomavirus (HPV) infection is the most common sexually transmissible infection worldwide. Although the prevalence of cervical HPV infection has been extensively reported in women worldwide, few epidemiological studies have examined the prevalence of non-cervical HPV infection among both women and men, especially in China. METHODS AND ANALYSIS: PROGRESS-Plus is a national, multisite, cross-sectional study that aims to estimate the prevalence of non-cervical HPV infection in women and men aged 18-60 years residing in mainland China. More specifically, PROGRESS-Plus will estimate the prevalence rate of HPV DNA in oral samples from both women and men, and that of anogenital samples from men. The secondary study objectives are to (1) report the aforementioned prevalence rates by HPV genotype, age and geographical region, (2) examine the concordance (ie, prevalence of the same HPV genotype) between the oral and anogenital samples among men, (3) explore risk factors associated with oral (in both women and men) and anogenital (in men only) HPV infection and (4) describe study participants' health-related quality of life, health behaviour, sexual behaviour and health status. ETHICS AND DISSEMINATION: The study protocol and all required documents have been submitted for review and approval to the Independent Ethics Committees of all the participating sites. All participants will provide their written informed consent on study entry, and all the recorded data will be treated as confidential.

Indexed as

Papillomavirus InfectionsChinaCross-Sectional StudiesFemaleGenotypeHuman Papillomavirus VirusesHumansMalePapillomaviridaePrevalenceQuality of LifeEpidemiologyINFECTIOUS DISEASESPREVENTIVE MEDICINEPublic health

Identifiers

PMID36731925
PMCPMC9896211
OpenAlexW4318986991

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.