Evidence map›Paper›PMID 31683813›Full record

ArticleJournal of personalized medicine2019

Physician Experience with Direct-To-Consumer Genetic Testing in Kaiser Permanente.

M Cabell Jonas, Pim Suwannarat, Andrea Burnett-Hartman, Nikki Carroll, Michelle Turner, Kristen Janes, Christine Truong, Erica Blum-Barnett, Nazneen Aziz, Elizabeth A McGlynn

Abstract read
In one paragraph

Article in Journal of personalized medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 2 pooled it
–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

10 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Direct-to-Consumer Genetic Testing: A Comprehensive Review.Therapeutic innovation & regulatory science · 2023
    Review
  7. Article
  8. Identifying rare, medically relevant variation via population-based genomic screening in Alabama: opportunities and pitfalls.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
  9. Article
  10. Article
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

10 authors.

M Cabell JonasMid-Atlantic Permanente Research Institute, Mid-Atlantic Permanente Medical Group, Kaiser Permanente Mid-Atlantic States, Rockville, MD 20852, USA. Cabell.Jonas@kp.org.
Pim SuwannaratMid-Atlantic Permanente Medical Group, Kaiser Permanente Mid-Atlantic States, Rockville, MD 20852, USA. Pim.Suwannarat@kp.org.
Andrea Burnett-HartmanInstitute for Health Research, Kaiser Permanente Colorado, Aurora, CO 80014, USA. Andrea.N.Burnett-Hartman@kp.org.
Nikki CarrollInstitute for Health Research, Kaiser Permanente Colorado, Aurora, CO 80014, USA. Nikki.M.Carroll@kp.org.
Michelle TurnerUniversity of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA. Michelle.Turner@cuanschutz.edu.
Kristen JanesKaiser Permanente National Quality, Oakland, CA 94611, USA. Kristen.X.Janes@kp.org.
Christine TruongMid-Atlantic Permanente Medical Group, Kaiser Permanente Mid-Atlantic States, Rockville, MD 20852, USA. ChristinexTruong@gmail.com.
Erica Blum-BarnettInstitute for Health Research, Kaiser Permanente Colorado, Aurora, CO 80014, USA. Erica.Blum-Barnett@kp.org.
Nazneen AzizVariant Genomics, Inc., Oakland, CA 94611, USA. Nazneen.Aziz@variant-genomics.com.
Elizabeth A McGlynnKaiser Permanente Research, Pasadena, CA 91101, USA. Elizabeth.A.McGlynn@kp.org.

Funding

Garfield Memorial Fund n/a
6 · The paper itself

Abstract

Health systems and physicians nationwide aspire to consistently and reliably apply genetic and genomic information to guide disease prevention, management, and treatment. However, clinical information, including genetics/genomics data from within and outside of the care delivery system, is expanding rapidly. Between November 2017 and April 2018, we surveyed 1502 Permanente Medical Group primary care and specialist physicians to assess the degree to which direct-to-consumer genetic test results were being presented to physicians and identify genetics educational needs among physicians (response rate 15%). Adjusted logistic regression (according to respondent characteristics) was used to calculate adjusted odds ratios (ORs) and 95% confidence intervals (CIs) comparing responses within groups. Results showed 35% and 12% of respondents reported receiving at least one direct-to-consumer health risk genetic result (DTC-health risk) or direct-to-consumer pharmacogenomic test result (DTC-PGx), respectively, from a patient in the past year. Of those receiving at least one test result, 40% (DTC-health risk) and 39% (DTC-PGx) of physicians reported 1+ referral(s); 78% (DTC-health risk) and 42% (DTC-PGx) of referrals were to clinical genetics. In total, 85% of physicians would spend ≥2 h/year on genetics/genomics education.

Indexed as

direct-to-consumer genetic testinggeneticsgenomicspharmacogenomic testingphysician educationphysician survey

Identifiers

PMID31683813
PMCPMC6963876

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.