Evidence map›Paper›PMID 36938783›Full record

ArticleJournal of genetic counseling2023

Medical interpreter-mediated genetic counseling for Spanish preferring adults at risk for a hereditary cancer syndrome.

Galen Joseph, Nangel M Lindberg, Claudia Guerra, Cindy Hernandez, Leah S Karliner, Marian J Gilmore, Jamilyn Zepp, Bradley A Rolf, Mikaella Caruncho, Leslie Riddle and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of genetic counseling, 2023. 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
3.9field-weighted citation impact, top 7% 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, 9 citations in OpenAlex.

  1. Trial
  2. Article
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  5. 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

13 authors at 7 institutions in 1 country.

Galen JosephDepartment of Humanities and Social Sciences, University of California, San Francisco, San Francisco, California, USA.ORCID 0000-0001-9179-7075
Nangel M LindbergKaiser Permanente Center for Health Research, Portland, Oregon, USA.
Claudia GuerraDepartment of Humanities and Social Sciences, University of California, San Francisco, San Francisco, California, USA.
Cindy HernandezCancer Genetics and Prevention Program, University of California, San Francisco, San Francisco, California, USA.
Leah S KarlinerDepartment of General Internal Medicine, University of California, San Francisco, San Francisco, California, USA.ORCID 0000-0003-2204-5114
Marian J GilmoreDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Jamilyn ZeppDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Bradley A RolfDivision of Medical Genetics, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA.
Mikaella CarunchoDepartment of Medical Humanities and Ethics, Columbia University, New York, New York, USA.
Leslie RiddleDepartment of Humanities and Social Sciences, University of California, San Francisco, San Francisco, California, USA.
Tia L KauffmanKaiser Permanente Center for Health Research, Portland, Oregon, USA.
Michael C LeoKaiser Permanente Center for Health Research, Portland, Oregon, USA.
Benjamin S WilfondSeattle Children's Research Institute, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-2671-9860
Kaiser Permanente Center for Health Research · USUniversity of California, San Francisco · USColumbia University Irving Medical Center · USSan Francisco General Hospital · USSeattle Children's Hospital · USThe University of Texas MD Anderson Cancer Center · USUniversity of Washington Medical Center · US

Funding

Exome sequencing in Diverse Populations in Colorado & OregonU01HG007292 · NHGRI · KAISER FOUNDATION RESEARCH INSTITUTE · PI LEO, MICHAEL C, WILFOND, BENJAMIN SIMON · 2017 to 2021
$15.7M
Evolving Our Partnership: The CSER2 Centralized Support Coordinating CenterU24HG007307 · NHGRI · UNIVERSITY OF WASHINGTON · PI FULLERTON, STEPHANIE MALIA, JARVIK, GAIL PAIRITZ · 2017 to 2021
$5.8M
NHGRI NIH HHS U01 HG007292NHGRI NIH HHS U24 HG007307
6 · The paper itself

Abstract

The objective of this study was to identify interpretation challenges specific to exome sequencing and errors of potential clinical significance in the context of genetic counseling for adults at risk for a hereditary cancer syndrome. Thirty transcripts of interpreter-mediated telephone results disclosure genetic counseling appointments were coded for errors by bilingual researchers, and the coders applied an overall rating to denote the degree to which the errors interfered with communication overall. Genetic counselors reviewed a subset of errors flagged for potential clinical significance to identify those likely to have clinical impact. Qualitative interviews with 19 interpreters were analyzed to elucidate the challenges they face in interpreting for genetic counseling appointments. Our analysis identified common interpretation errors such as raising the register, omissions, and additions. Further, we found errors specific to genetic counseling concepts and content that appeared to impact the ability of the genetic counselor to accurately assess risk. These errors also may have impacted the patient's ability to understand their results, access appropriate follow-up care, and communicate with family members. Among interpreters' strengths was the use of requests for clarification; in fact, even more use of clarification would have been beneficial in these encounters. Qualitative interviews surfaced challenges stemming from the structure of interpreter work, such as switching from medical and nonmedical interpretations without substantial breaks. Importantly, while errors were frequent, most did not impede communication overall, and most were not likely to impact clinical care. Nevertheless, potentially clinically impactful errors in communication of genetics concepts may contribute to inequitable care for limited English proficient patients and suggest that additional training in genetics and specialization in healthcare may be warranted. In addition, training for genetic counselors and guidance for patients in working effectively with interpreters could enhance interpreters' transmission of complex genetic concepts.

Indexed as

Genetic CounselingNeoplastic Syndromes, HereditaryAdultCommunication BarriersCounselingHumansTranslatingexome sequencinggenetic counselinghealth care interpretersHispaniclanguage accessLatinolimited english proficiencymedical interpreters

Identifiers

PMID36938783
PMCPMC10509308
OpenAlexW4327892659

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.