Evidence map›Paper›PMID 23795206›Full record

ArticlePersonalized medicine2012

Incorporating direct-to-consumer genomic information into patient care: attitudes and experiences of primary care physicians.

Barbara A Bernhardt, Cara Zayac, Erynn S Gordon, Lisa Wawak, Reed E Pyeritz, Sarah E Gollust

Open access · greenAbstract read
In one paragraph

Article in Personalized medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 6 pooled it
3.1field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 6 syntheses or guidelines pooled it, 51 citations in OpenAlex.

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  5. Delivering genomic medicine in the United Kingdom National Health Service: a systematic review and narrative synthesis.Genetics in medicine : official journal of the American College of Medical Genetics · 2019
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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

6 authors at 3 institutions in 1 country.

Barbara A BernhardtDivision of Translational Medicine & Human Genetics, Perelman School of Medicine, University of Pennsylvania, 3400 Spruce Street, Penn Tower Room 1115, Philadelphia, PA 19104, USA ; Penn Center for the Integration of Genetic Healthcare Technologies, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cara Zayac
Erynn S Gordon
Lisa Wawak
Reed E Pyeritz
Sarah E Gollust
University of Pennsylvania · USCoriell Institute For Medical Research · USMinnesota Department of Health · US

Funding

Penn Center for ELSI Research in Emerging Genetic Technologies in Health CareP50HG004487 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI PYERITZ, REED E · 2007 to 2012
$6.2M
Assessing Attitudes and Experiences of Early Adopters of Personalized GenomicsRC1HG005369 · NHGRI · UNIVERSITY OF PENNSYLVANIA · PI BERNHARDT, BARBARA A. · 2009 to 2010
$647k
NHGRI NIH HHS P50 HG004487NHGRI NIH HHS RC1 HG005369
6 · The paper itself

Abstract

aimDespite predictions of increased clinical applications, little is known about primary care providers' (PCPs') readiness to apply genomics to patient care. The aim was to assess PCPs' current experience with genetic testing, their assessment of the understandability and clinical utility of information in sample direct-to-consumer reports for genomic assessment of disease risk and warfarin dosing and attitudes toward genomic medicine. MATERIALS &

methodsA web-based survey of PCPs who are members of Knowledge Networks' Physician Consulting Network was conducted.

resultsOf the 502 respondents (23.3% response rate), most ordered genetic tests infrequently. When presented with the direct-to-consumer genomic testing reports, most believed the reports were understandable, and would be willing to review results with a patient, and many believed the results would be helpful in patient management.

conclusionDespite limited experience with genetic tests, PCPs are open to helping patients understand genomic information. However, additional physician education is needed.

Indexed as

geneticsgenetic testinggenomicspharmacogenomicsphysician experiencephysician readiness

Identifiers

PMID23795206
PMCPMC3684987
OpenAlexW2161781518

What OpenQuestion holds

Textmetadata
LicenceTDM
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.