Evidence map›Paper›PMID 32987879›Full record

ArticleJournal of personalized medicine2020

"They're Not Going to Do Nothing for Me": Research Participants' Attitudes towards Elective Genetic Counseling.

Erica J Sutton, Annika T Beck, Kylie O Gamm, Jennifer B McCormick, Iftikhar J Kullo, Richard R Sharp

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.4field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
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 4 institutions in 1 country.

Erica J SuttonBiomedical Ethics Research Program, Mayo Clinic, Rochester, MN 55905, USA.
Annika T BeckBiomedical Ethics Research Program, Mayo Clinic, Rochester, MN 55905, USA.
Kylie O GammDepartment of Psychiatry and Psychology, Mayo Clinic, Rochester, MN 55905, USA.
Jennifer B McCormickCollege of Medicine, Department of Humanities, Pennsylvania State University, Hershey, PA 17033, USA.
Iftikhar J KulloDivision of Cardiovascular Diseases, Mayo Clinic, Rochester, MN 55905, USA.
Richard R SharpBiomedical Ethics Research Program, Mayo Clinic, Rochester, MN 55905, USA.ORCID 0000-0001-5441-2084
Mayo Clinic in Florida · USMayo Clinic · USMayo Clinic in Arizona · USPennsylvania State University · US

Funding

Genomic Basis of Susceptibility to COVID-19 Infection and its ComplicationsU01HG006379 · NHGRI · MAYO CLINIC ROCHESTER · PI Richard R. Sharp · 2011 to 2026
$16.5M
NHGRI NIH HHS U01 HG006379
6 · The paper itself

Abstract

As applications of genomic sequencing have expanded, offering genetic counseling support to all patients is arguably no longer practical. Additionally, whether individuals desire and value genetic counseling services for genomic screening is unclear. We offered elective genetic counseling to 5110 individuals prior to undergoing sequencing and 2310 participants who received neutral results to assess demand. A total of 0.2% of the study participants accessed genetic counseling services prior to sequencing, and 0.3% reached out after receiving neutral results. We later conducted 50 interviews with participants to understand why they did not access these services. Many interviewees did not recall the availability of genetic counseling and were unfamiliar with the profession. Interviewees described not needing counseling before sequencing because they understood the study and felt that they could cope with any result. Counseling was considered equally unnecessary after learning neutral results. Although the participants had questions about their results, they did not feel that speaking with a genetic counselor would be helpful. Genomic screening efforts that employ opt-in models of genetic counseling may need to clarify the potential value of genetic counseling support from the outset and feature genetic counseling services more prominently in program materials.

Indexed as

and social implicationsethicalgenetic counselinggenomic sequencinginformed consentlegalpatient communicationpatient educationreturn of results

Identifiers

PMID32987879
PMCPMC7711758
OpenAlexW3088903318

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.