Evidence map›Paper›PMID 8401130›Full record

ArticleBMJ (Clinical research ed.)1993

Screening for carriers of cystic fibrosis--a general practitioner's perspective.

M Modell

Abstract read
In one paragraph

Article in BMJ (Clinical research ed.), 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  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. 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
  6. Article
  7. Article
  8. Clinical genetics meets primary care.BMJ (Clinical research ed.) · 1993
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

M ModellDepartment of Primary Health Care, University College London Medical School, Whittington Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of the gene for cystic fibrosis has led to the possibility of population based screening for carriers of cystic fibrosis to identify couples at risk of having an affected child. Pilot studies have shown that screening is feasible and does not cause untoward anxiety, though the uptake of testing varies considerably with the setting and method of invitation. Screening offered at times when individuals (and health professionals) perceive it as directly relevant will probably gradually become established in the United Kingdom. This review examines the role of general practice in genetic carrier screening as exemplified by cystic fibrosis. General practice has a pivotal role from the beginning in providing individuals and couples with information, facilitating testing of patients' relatives and of carriers identified by screening elsewhere (such as antenatal clinics), and offering testing in the context of reproduction. Screening for the cystic fibrosis gene will probably be followed by other genetic screening programmes.

Indexed as

Genetic TestingHeterozygoteCystic FibrosisDecision MakingFamily HealthFamily PracticeFemaleGenetic Carrier ScreeningGenetic Diseases, InbornHealth PromotionHumansMalePatient Acceptance of Health CarePilot ProjectsRisk AssessmentRisk FactorsGenetics and ReproductionHealth Care and Public Health

Identifiers

PMID8401130
PMCPMC1678878

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.