Evidence map›Paper›PMID 14707527›Full record

ArticleFamilial cancer2003

What motivates interest in attending a familial cancer genetics clinic?

L Fraser, S Bramald, C Chapman, C Chu, V Cornelius, F Douglas, A Lucassen, A Nehammer, S Sutton, M Trivella and 1 more

Abstract readComparative StudyMulticenter Study
PubMed Publisher
In one paragraph

Article in Familial cancer, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Trial
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  4. Review
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  8. Genomics in general practice: Generation Genome.The British journal of general practice : the journal of the Royal College of General Practitioners · 2017
    Article
  9. Article
  10. Communicating with biobank participants: preferences for receiving and providing updates to researchers.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2015
    Article
  11. Article
  12. Characteristics associated with genetic counseling referral and BRCA1/2 testing among women in a large integrated health system.Genetics in medicine : official journal of the American College of Medical Genetics · 2015
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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

11 authors at 8 institutions in 1 country.

L FraserDepartment of Medical & Molecular Genetics, Guy's Hospital, London, UK. l.fraser@qmul.ac.uk
S Bramald
C Chapman
C Chu
V Cornelius
F Douglas
A Lucassen
A Nehammer
S Sutton
M Trivella
S Hodgson
Cancer Research UK · GBChurchill Hospital · GBGuy's Hospital · GBPrincess Anne Hospital · GBQueen Mary University of London · GBRoyal Victoria Infirmary · GBSt James's University Hospital · GBUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The motivation of people who seek advice about a family history of cancer was explored in a cross sectional study of new cancer referrals to five regional cancer genetics centres in England: the PACT (patient and clinical team) psychosocial study. One hundred sixty-two people took part. Measures were source of referral, estimated and perceived cancer risk, level of cancer worry, and personal and family-centred reasons for wanting to be seen in clinic. General practitioners referred more people than hospital doctors, and referred a larger proportion of people at low genetic risk of developing cancer. More than half of the participants had been the first to raise the issue of their family history of cancer. Personal motivation for referral is clearly different for those who have had a diagnosis of cancer and for those with children, compared to unaffected and childless people, and is characterised by altruistic concern for other family members rather than a perception of increased personal risk. Men and people from ethnic minorities are very significantly under-represented. Understanding people's motivation may be useful in targeting genetic counselling for people with a family history of cancer.

Indexed as

Attitude to HealthAdultAge DistributionAmbulatory Care FacilitiesAnalysis of VarianceChi-Square DistributionCross-Sectional StudiesFemaleGenetic CounselingGenetic Diseases, InbornGenetic TestingHumansMaleMiddle AgedMotivationNeoplasms

Identifiers

PMID14707527
OpenAlexW2066706469

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.