Evidence map›Paper›PMID 15043057›Full record

ArticleJournal of genetic counseling2003

An investigation of genetic counselors' discussion of genetic discrimination with cancer risk patients.

Nicole L Pfeffer, Patricia McCarthy Veach, Bonnie S LeRoy

Abstract read
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In one paragraph

Article in Journal of genetic counseling, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

3 authors.

Nicole L PfefferDepartment of Educational Psychology, 139 Burton Hall, University of Minnesota, Minneapolis, Minnesota 55455, USA. veach001@umn.edu
Patricia McCarthy Veach
Bonnie S LeRoy

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Twenty-five genetic counselors who see familial cancer risk patients were interviewed about their definitions of genetic discrimination, perceptions of patient risk for discrimination, frequency and type of discrimination experienced by their patients, sources of information about discrimination, and what they tell patients about genetic discrimination. There was variability in participant definitions and content of discussions of genetic discrimination. Although 82% regarded risk to be low to theoretical, 40% reported possible instances of genetic discrimination, including insurance companies requiring results to cover procedures, denial of life/health insurance, social discrimination, and employment discrimination. Ninety-six percent of the sample reported always or almost always discussing genetic discrimination, and one or more of the following: insurance discrimination risks, protective legislation, no known cases positively documenting discrimination, strategies to avoid discrimination, and uncertainty of protective measures. The majority use current literature and research as information sources. Practice, policy, and research implications are discussed.

Indexed as

Attitude of Health PersonnelEmploymentInsuranceInsurance Selection BiasPrejudiceAdultCommunicationData CollectionDisclosureEthics, ProfessionalGenetic CounselingGenetic Predisposition to DiseaseGenetic TestingHumansInformed ConsentLegislation, MedicalEmpirical ApproachGenetics and Reproduction

Identifiers

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.