Evidence map›Paper›PMID 33947741›Full record

ArticleBMJ open2021

Cervical ripening at home or in-hospital-prospective cohort study and process evaluation (CHOICE) study: a protocol.

Sarah Jane Stock, Amarnath Bhide, Heather Richardson, Mairead Black, Cassandra Yuill, Mairi Harkness, Maggie Reid, Fiona Wee, Helen Cheyne, Christine McCourt and 10 more

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Article
  7. 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

20 authors at 13 institutions in 5 countries.

Sarah Jane StockCentre for Medical Informatics, Usher Institute, University of Edinburgh, Edinburgh, UK sarah.stock@ed.ac.uk.ORCID 0000-0003-4308-856X
Amarnath BhideObstetrics and Gynaecology, St George's University Hospitals Trust, London, UK.
Heather RichardsonWomen and Children's Health, NHS Lothian University Hospitals Division, Edinburgh, UK.
Mairead BlackInstitute of Applied Health Sciences, University of Aberdeen, Aberdeen, UK.
Cassandra YuillCentre for Maternal & Child Health Research, School of Health Sciences, City University of London, London, UK.
Mairi HarknessNursing, Midwifery and Allied Health Professions Research Unit (NMAHP), University of Stirling, Stirling, UK.
Maggie ReidCentre for Medical Informatics, Usher Institute, University of Edinburgh, Edinburgh, UK.
Fiona WeeEdinburgh Clinical Trials Unit (ECTU) Usher Institute, University of Edinburgh, Edinburgh, UK.ORCID 0000-0001-9161-1955
Helen CheyneNursing, Midwifery and Allied Health Professions Research Unit (NMAHP), University of Stirling, Stirling, UK.ORCID 0000-0001-5738-8390
Christine McCourtCentre for Maternal & Child Health Research, School of Health Sciences, City University of London, London, UK.
Dikshyanta RanaInstitute of Health and Well Being, University of Glasgow, Glasgow, UK.ORCID 0000-0001-9133-3094
Kathleen Anne BoydInstitute of Health and Well Being, University of Glasgow, Glasgow, UK.
Julia SandersSchool of Healthcare Sciences, Cardiff University, Cardiff, UK.
Neelam HeeraPatient and Public Involvement Representative, Edinburgh, UK.
Jane HuddlestonPatient and Public Involvement Representative, Edinburgh, UK.
Fiona DenisonMRC Centre for Reproductive Health, The University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-0371-2014
Dharmintra PasupathyFaculty of Medicine and Health, The University of Sydney, Sydney, New South Wales, Australia.
Neena ModiDepartment of Medicine, Imperial College London, London, UK.
Gordon SmithDepartment of Obstetrics and Gynaecology, University of Cambridge, Cambridge, UK.
John NorrieEdinburgh Clinical Trials Unit (ECTU) Usher Institute, University of Edinburgh, Edinburgh, UK.
City, University of London · GBHealth & Life (Taiwan) · TWInstitute for Medical Research · MYUniversity of Edinburgh · GBUniversity of Stirling · GBCardiff University · GBImperial College London · GBMRC Centre for Reproductive Health · GBNHS Lothian · GBSt George’s University Hospitals NHS Foundation Trust · GBThe University of Sydney · AUUniversity of Aberdeen · GBUniversity of Cambridge · GB

Funding

Wellcome TrustWellcome Trust 209560/Z/17/Z
6 · The paper itself

Abstract

introductionThe aim of the cervical ripening at home or in-hospital-prospective cohort study and process evaluation (CHOICE) study is to compare home versus in-hospital cervical ripening to determine whether home cervical ripening is safe (for the primary outcome of neonatal unit (NNU) admission), acceptable to women and cost-effective from the perspective of both women and the National Health Service (NHS). METHODS AND ANALYSIS: We will perform a prospective multicentre observational cohort study with an internal pilot phase. We will obtain data from electronic health records from at least 14 maternity units offering only in-hospital cervical ripening and 12 offering dinoprostone home cervical ripening. We will also conduct a cost-effectiveness analysis and a mixed methods study to evaluate processes and women/partner experiences. Our primary sample size is 8533 women with singleton pregnancies undergoing induction of labour (IOL) at 39+0 weeks' gestation or more. To achieve this and contextualise our findings, we will collect data relating to a cohort of approximately 41 000 women undergoing IOL after 37 weeks. We will use mixed effects logistic regression for the non-inferiority comparison of NNU admission and propensity score matched adjustment to control for treatment indication bias. The economic analysis will be undertaken from the perspective of the NHS and Personal Social Services (PSS) and the pregnant woman. It will include a within-study cost-effectiveness analysis and a lifetime cost-utility analysis to account for any long-term impacts of the cervical ripening strategies. Outcomes will be reported as incremental cost per NNU admission avoided and incremental cost per quality adjusted life year gained. RESEARCH ETHICS APPROVAL AND DISSEMINATION: CHOICE has been funded and approved by the National Institute of Healthcare Research Health Technology and Assessment, and the results will be disseminated via publication in peer-reviewed journals. TRIAL REGISTRATION NUMBER: ISRCTN32652461.

Indexed as

Cervical RipeningState MedicineCohort StudiesFemaleHospitalsHumansInfant, NewbornObservational Studies as TopicPregnancyProspective Studiesfetal medicinematernal medicineobstetrics

Identifiers

PMID33947741
PMCPMC8098973
OpenAlexW3159452916

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.