Evidence map›Paper›PMID 41918401›Full record

ArticleBJOG : an international journal of obstetrics and gynaecology2026

Comparison of Cervical Screening at 6- and 12-Weeks Postnatal: A Paired-Sample Feasibility Study.

Victoria A Cullimore, Tessa Dean, Kim Chu, Adam Brentnall, Karin Denton, Katherine Hunt, Alexandra Sargent, Laura Johns, Katharine Edey, Sarah L Coleridge and 6 more

Abstract readComparative Study
In one paragraph

Article in BJOG : an international journal of obstetrics and gynaecology, 2026. 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
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.

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

16 authors.

Victoria A CullimoreDepartment of Gynaecological Oncology, GRACE Centre, Musgrove Park Hospital, Somerset NHS Foundation Trust, Taunton, Somerset, UK.ORCID https://orcid.org/0000-0003-0966-0964
Tessa DeanDepartment of Gynaecological Oncology, GRACE Centre, Musgrove Park Hospital, Somerset NHS Foundation Trust, Taunton, Somerset, UK.ORCID https://orcid.org/0000-0001-6318-1337
Kim ChuWolfson Institute of Population Health, Queen Mary University of London, Charterhouse Square, London, UK.ORCID https://orcid.org/0009-0006-0692-1451
Adam BrentnallWolfson Institute of Population Health, Queen Mary University of London, Charterhouse Square, London, UK.ORCID https://orcid.org/0000-0001-6327-4357
Karin DentonDepartment of Cytopathology, North Bristol Trust, Bristol, UK.ORCID https://orcid.org/0000-0001-6957-895X
Katherine HuntDepartment of Cytopathology, North Bristol Trust, Bristol, UK.
Alexandra SargentGynae Cytology Department, Manchester University NHS FT, Manchester, UK.ORCID https://orcid.org/0000-0002-9354-7720
Laura JohnsDepartment of Obstetrics and Gynaecology, Royal Devon and Exeter, Exeter, UK.
Katharine EdeyDepartment of Obstetrics and Gynaecology, Royal Devon and Exeter, Exeter, UK.
Sarah L ColeridgeDepartment of Obstetrics and Gynaecology, Royal Devon and Exeter, Exeter, UK.
Jane BorleyDepartment of Gynaecological Oncology, Royal Cornwall Hospital, Truro, UK.
Rebecca NewhouseDepartment of Gynaecological Oncology, GRACE Centre, Musgrove Park Hospital, Somerset NHS Foundation Trust, Taunton, Somerset, UK.ORCID https://orcid.org/0000-0003-3162-2438
Holly Baker-RandDepartment of Gynaecological Oncology, GRACE Centre, Musgrove Park Hospital, Somerset NHS Foundation Trust, Taunton, Somerset, UK.ORCID https://orcid.org/0009-0005-9301-6929
Lorna McWilliamsManchester Centre for Health Psychology, Division of Psychology & Mental Health, School of Health Sciences, The University of Manchester, Manchester, UK.
Emma J DavidsonCancer Prevention & Early Detection Research, NIHR Manchester Biomedical Research Centre, Faculty of Biology, Medicine & Health, The University of Manchester, St Mary's Hospital, Manchester, UK.ORCID https://orcid.org/0000-0003-0284-8630
Jo MorrisonDepartment of Gynaecological Oncology, GRACE Centre, Musgrove Park Hospital, Somerset NHS Foundation Trust, Taunton, Somerset, UK.ORCID https://orcid.org/0000-0003-0000-520X

Funding

Cancer Research UKManchester Biomedical Research CentreMedical Research CouncilNational Institute for Health and Care ResearchNational Institute for Health and Care Research (NIHR) Associate Scheme
6 · The paper itself

Abstract

objectiveFeasibility of a paired-sample study comparing cervical screening and urine self-sampling at 6- and 12-weeks postnatal.

designPaired-sample feasibility study.

settingAcute hospital. POPULATION OR SAMPLE: Females within 6 weeks of childbirth.

methodsPaired-sample study comparing cervical screening and high-risk human papillomavirus (HPV) testing from clinician-taken samples and urine self-samples at 6- and 12-weeks postnatal.

main outcome measuresUptake rates, patient-reported outcomes, adverse events, HPV detection, relative HPV sensitivity and specificity.

resultsOf 245 potential participants, 115 (47%) consented, 102 (89%) and 96 (83%) attended their 6- and 12-week screening visits, respectively. Median pain scores for cervical screening did not differ (6-weeks = 1; 12-weeks = 1; p = 0.76). Most would be happy for future screening at 6-weeks postnatal, 97/102 (95%) and 85/95 (89%) when asked at 6- and 12-week study visits, respectively. Agreement rate of clinician-taken HPV tests between 6- and 12-weeks was 94.8% (91/96, 95% confidence interval [CI], 88.4%-97.8%), with no inadequate combination HPV/cytology tests (6 vs. 12-week: sensitivity 80% [95% CI, 44.4-97.5]; specificity 96.5% [95% CI 90.1-99.3]). Relative to 12-week clinician-taken samples, urine self-sampling may have lower sensitivity for HPV (e.g., 6-week: sensitivity 60.0% [95% CI 26.2-87.8]; specificity 96.5% [95% CI 90.1-99.3]; NPV 95.4% [95% CI 88.6-98.7]).

conclusionsA paired-sample study of cervical screening at 6- and 12-weeks is feasible. Inadequacy rates of cervical screening were low, with high agreement. Urine self-sampling may be less sensitive in this population.

Indexed as

Early Detection of CancerPapillomavirus InfectionsUterine Cervical NeoplasmsVaginal SmearsAdultFeasibility StudiesFemaleHuman Papillomavirus VirusesHumansMass ScreeningPregnancySensitivity and SpecificityYoung Adultcervical screeningpostnatalself‐sampling

Identifiers

PMID41918401
PMCPMC13485450

What OpenQuestion holds

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Registered trials

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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.