Evidence map›Paper›PMID 26237256›Full record

ArticleJournal of clinical medicine2014

Preferences for Prenatal Tests for Cystic Fibrosis: A Discrete Choice Experiment to Compare the Views of Adult Patients, Carriers of Cystic Fibrosis and Health Professionals.

Melissa Hill, Ranjan Suri, Edward F Nash, Stephen Morris, Lyn S Chitty

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 3 pooled it
1.9field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 3 syntheses or guidelines pooled it, 33 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Preferences for prenatal diagnosis of sickle-cell disorder: A discrete choice experiment comparing potential service users and health-care providers.Health expectations : an international journal of public participation in health care and health policy · 2017
    Article
  12. Article
  13. 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

5 authors at 3 institutions in 1 country.

Melissa HillClinical and Molecular Genetics, Institute of Child Health and Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3BH, UK. melissa.hill@ucl.ac.uk.
Ranjan SuriDepartment of Respiratory Paediatrics, Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3JH, UK. ranjan.suri@gosh.nhs.uk.
Edward F NashWest Midlands Adult Cystic Fibrosis Centre, Heart of England NHS Foundation Trust, Birmingham B9 5SS, UK. edward.nash@heartofengland.nhs.uk.
Stephen MorrisResearch Department of Applied Health Research, University College London, London WC1H 0AJ, UK. steve.morris@ucl.ac.uk.
Lyn S ChittyClinical and Molecular Genetics, Institute of Child Health and Great Ormond Street Hospital for Children NHS Foundation Trust, London WC1N 3BH, UK. l.chitty@ucl.ac.uk.
Great Ormond Street Hospital for Children NHS Foundation Trust · GBHeart of England NHS Foundation Trust · GBUniversity College London · GB

Funding

Department of Health RP-PG-0707-10107
6 · The paper itself

Abstract

As new technologies enable the development of non-invasive prenatal diagnosis (NIPD) for cystic fibrosis (CF), research examining stakeholder views is essential for the preparation of implementation strategies. Here, we compare the views of potential service users with those of health professionals who provide counselling for prenatal tests. A questionnaire incorporating a discrete choice experiment examined preferences for key attributes of NIPD and explored views on NIPD for CF. Adult patients (n = 92) and carriers of CF (n = 50) were recruited from one children's and one adult NHS specialist CF centre. Health professionals (n = 70) were recruited via an e-mail invitation to relevant professional bodies. The key attribute affecting service user testing preferences was no miscarriage risk, while for health professionals, accuracy and early testing were important. The uptake of NIPD by service users was predicted to be high and includes couples that would currently decline invasive testing. Many service users (47%) and health professionals (55.2%) thought the availability of NIPD for CF would increase the pressure to undergo prenatal testing. Most service users (68.5%) thought NIPD for CF should be offered to all pregnant women, whereas more health professionals (68.2%) thought NIPD should be reserved for known carrier couples. The implications for clinical practice are discussed.

Indexed as

cystic fibrosisdiscrete choice experimentnon-invasive prenatal diagnosis (NIPD)

Identifiers

PMID26237256
PMCPMC4449661
OpenAlexW2112446277

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.