Evidence map›Paper›PMID 40162498›Full record

Trial reportBJOG : an international journal of obstetrics and gynaecology2025

Human Papillomavirus (HPV) Screening With Universal Access to Vaginal Self-Testing: Outcomes of an Implementation Trial.

Peter Sykes, Carrie Innes, Rebecca Bell, Janine Nip, John McMenamin, Lynn McBain, Ben Hudson, Melanie Gibson, Sarah Te Whaiti, Alexandria Tino and 3 more

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in BJOG : an international journal of obstetrics and gynaecology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. 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

13 authors.

Peter SykesDepartment of Obstetrics & Gynaecology, University of Otago, Christchurch, New Zealand.ORCID https://orcid.org/0000-0001-6772-719X
Carrie InnesDepartment of Obstetrics & Gynaecology, University of Otago, Christchurch, New Zealand.
Rebecca BellDepartment of Obstetrics & Gynaecology, University of Otago, Christchurch, New Zealand.
Janine NipDepartment of Obstetrics & Gynaecology, University of Otago, Christchurch, New Zealand.
John McMenaminHealth and Research Collaborative, Whanganui, New Zealand.
Lynn McBainDepartment of Primary Health Care & General Practice, University of Otago, Wellington, New Zealand.
Ben HudsonDepartment of Primary Care and Clinical Simulation, University of Otago, Christchurch, New Zealand.
Melanie GibsonTe Tātai Hauora o Hine-National Centre for Women's Health Research Aotearoa (NCWHRA), Te Herenga Waka-Victoria University of Wellington, Wellington, New Zealand.ORCID https://orcid.org/0000-0002-5043-8786
Sarah Te WhaitiDepartment of Obstetrics & Gynaecology, University of Otago, Christchurch, New Zealand.
Alexandria TinoDepartment of Obstetrics & Gynaecology, University of Otago, Christchurch, New Zealand.
Jonathan WillimanDepartment of Population Health, University of Otago, Christchurch, New Zealand.
Andrew MillerAnatomical Pathology, Canterbury Health Laboratories, Christchurch, New Zealand.
Beverley LawtonTe Tātai Hauora o Hine-National Centre for Women's Health Research Aotearoa (NCWHRA), Te Herenga Waka-Victoria University of Wellington, Wellington, New Zealand.

Funding

Te Whatu Ora Health New Zealand
6 · The paper itself

Abstract

objectiveDetermine the feasibility of high-risk human papillomavirus (HPV)-based cervical screening that included the option of a vaginal swab HPV test (vaginal self-test).

designImplementation trial.

setting17 primary care practices. POPULATION OR SAMPLE: People due for a cervical screening test.

methodsParticipants could choose a clinician-taken cervical test or a vaginal self-test (undertaken in clinic or at home), unless a cervical co-test (HPV and cytology) was clinically indicated.

main outcome measuresProportion of participants who had (a) a vaginal self-test, (b) an HPV-detected result and (c) HPV detected on a vaginal self-test and returned for further investigation.

results3121 people were enrolled. Participation rates were high for people of all recorded ethnicities. A vaginal self-test was undertaken by 95% (2954/3121, 95% confidence interval [CI] [93.8, 95.4]) of people. HPV was detected in 12.9% (404/3121, 95% CI [11.8, 14.2]) of people. 95% (384/404, 95% CI [92.5, 97.0]) of people with HPV detected had follow-up cytology or colposcopy. 2.6% (82/3121, 95% CI [2.1, 3.2]) had HPV 16/18 detected, all of whom attended colposcopy. Cytology triage was completed for 92% (276/301, 95% CI [88.0, 94.3]) of people with non-16/18 HPV types (HPV other) detected on a vaginal self-test. This varied by ethnicity and screening history.

conclusionThis study confirms the feasibility of cervical screening with the universal option of a vaginal self-test and demonstrated a clear preference for the vaginal self-test. Challenges remain in relation to equitable provision of cytology triage. Ongoing programme monitoring is imperative.

trial registrationAustralia and New Zealand Clinical Trial Register. ANZCTR Reference number: ACTRN12622000699763 (https://anzctr.org.au/).

Indexed as

Early Detection of CancerMass ScreeningPapillomavirus InfectionsSelf CareUterine Cervical DysplasiaUterine Cervical NeoplasmsVaginal SmearsAdultAgedFeasibility StudiesFemaleHuman Papillomavirus VirusesHumansMiddle AgedPapillomaviridaeYoung Adultcervical cancer screeningcolposcopyhealth inequityhuman papillomavirusself‐testingvaginal swab

Identifiers

PMID40162498
PMCPMC12232538

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.