Evidence map›Paper›PMID 8019277›Full record

Trial reportBMJ (Clinical research ed.)1994

Antenatal screening for cystic fibrosis: a trial of the couple model.

J Livingstone, R A Axton, A Gilfillan, M Mennie, M Compton, W A Liston, A A Calder, A J Gordon, D J Brock

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in BMJ (Clinical research ed.), 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
14.0field-weighted citation impact, top 1% 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

18 citing papers in PubMed, 84 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Costs, effects, and savings of screening for cystic fibrosis gene carriers.Journal of epidemiology and community health · 1998
    Article
  5. Article
  6. Article
  7. Article
  8. The views of general practitioners on community carrier screening for cystic fibrosis.The British journal of general practice : the journal of the Royal College of General Practitioners · 1996
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Carrier screening in the community.Journal of inherited metabolic disease · 1995
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Screening for carriers of cystic fibrosis.BMJ (Clinical research ed.) · 1994
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

J LivingstoneHuman Genetics Unit, University of Edinburgh, Western General Hospital.
R A Axton
A Gilfillan
M Mennie
M Compton
W A Liston
A A Calder
A J Gordon
D J Brock
Western General Hospital · GBUniversity of Edinburgh · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo assess the delivery and acceptability of antenatal couple screening for cystic fibrosis. Carrier status was notified only when both members of a partnership had cystic fibrosis alleles and therefore a one in four risk of having an affected child.

designMouthwash samples were tested when both partners participated. Results were returned only to positive couples.

settingTwo large maternity hospitals in Edinburgh. SUBJECTS: Screening was offered to all couples who booked at one of the two hospitals.

main outcome measures(a) The take up of screening, carriers and carrier couples identified, take up of prenatal diagnosis, and numbers of affected fetuses detected; (b) questionnaire measures of patient satisfaction and stress.

resultsScreening was offered to 8536 couples. 714 (8.4%) were regarded as ineligible, usually because of late booking or absence of a partner. 1900 (24.3%) of the remainder declined screening. Among the 5922 screened couples, four tested positive--that is, both partners were cystic fibrosis heterozygotes. All four elected to have prenatal diagnosis. There were three terminations of pregnancy because of an affected fetus, one couple having two successive pregnancies with affected fetuses. The participation rate was 76% for eligible couples (5922/7822) and 69% for all couples (5922/8536). Only 89 screened couples (1.5%) requested information on individual carrier status. No anxiety was detected among a cohort of the screened population, and 99% of questioned participants expressed satisfaction with the concept of couple screening.

conclusionsAntenatal couple screening is a satisfactory and acceptable way of screening for cystic fibrosis and has been adopted as routine in the two trial hospitals.

Indexed as

Pregnant PeopleAnxietyCystic FibrosisFemaleFetal DiseasesGenetic Carrier ScreeningGenetic CounselingGenetic TestingHeterozygoteHumansMalePatient SatisfactionPregnancyPrenatal DiagnosisTime FactorsEdinburghEmpirical ApproachGenetics and Reproduction

Identifiers

PMID8019277
PMCPMC2540322
OpenAlexW2044057469

What OpenQuestion holds

Textmetadata
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.