Evidence map›Paper›PMID 27322592›Full record

Trial reportClinical genetics2017

EMR documentation of physician-patient communication following genomic counseling for actionable complex disease and pharmacogenomic results.

K Sweet, A C Sturm, T Schmidlen, S Hovick, J Peng, K Manickam, A Salikhova, J McElroy, L Scheinfeldt, A E Toland and 2 more

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical genetics, 2017. 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
1.8field-weighted citation impact, top 13% 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
  3. Article
  4. Article
  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

12 authors at 6 institutions in 2 countries.

K SweetDivision of Human Genetics, Ohio State University Wexner Medical Center, Columbus, OH, USA.
A C SturmDivision of Human Genetics, Ohio State University Wexner Medical Center, Columbus, OH, USA.
T SchmidlenCoriell Personalized Medicine Collaborative, Coriell Institute for Medical Research, Camden, NJ, USA.
S HovickSchool of Communication, Ohio State University, Columbus, OH, USA.
J PengDepartment of Biomedical Informatics, Center for Biostatistics, Columbus, OH, USA.
K ManickamDivision of Human Genetics, Ohio State University Wexner Medical Center, Columbus, OH, USA.
A SalikhovaOhio State University Comprehensive Cancer Center, Columbus, OH, USA.
J McElroyDepartment of Biomedical Informatics, Center for Biostatistics, Columbus, OH, USA.
L ScheinfeldtCoriell Personalized Medicine Collaborative, Coriell Institute for Medical Research, Camden, NJ, USA.
A E TolandDivision of Human Genetics, Ohio State University Wexner Medical Center, Columbus, OH, USA.
J S RobertsDepartment of Health Behaviour & Health Education, University of Michigan School of Public Health, Ann Arbor, MI, USA.
M ChristmanCoriell Personalized Medicine Collaborative, Coriell Institute for Medical Research, Camden, NJ, USA.
The Ohio State University Wexner Medical Center · USCoriell Institute For Medical Research · USThe Ohio State University · USColumbus Center · USInstitute for Medical Informatics and Biostatistics · CHMichigan Department of Health and Human Services · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
Pharmacogenomics of Anti-platlet Intervention-2 (PAPI-2) StudyU01HL105198 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI SHULDINER, ALAN R. · 2010 to 2014
$13.6M
Expression Genetics in Drug TherapyU01GM092655 · NIGMS · OHIO STATE UNIVERSITY · PI SADEE, WOLFGANG · 2010 to 2014
$8.6M
Assessing the utility of genomic counseling for common complex diseasesR21HG006575 · NHGRI · OHIO STATE UNIVERSITY · PI CHRISTMAN, MICHAEL F, SWEET, KEVIN M. · 2013 to 2014
$477k
NCATS NIH HHS UL1 TR001070NCI NIH HHS P30 CA016058NHGRI NIH HHS R21 HG006575NHLBI NIH HHS U01 HL105198NIGMS NIH HHS U01 GM092655
6 · The paper itself

Abstract

Genomic risk information for potentially actionable complex diseases and pharmacogenomics communicated through genomic counseling (GC) may motivate physicians and patients to take preventive actions. The Ohio State University-Coriell Personalized Medicine Collaborative is a randomized trial to measure the effects of in-person GC on chronic disease patients provided with multiplex results. Nine personalized genomic risk reports were provided to patients through a web portal, and to physicians via electronic medical record (EMR). Active arm participants (98, 39% female) received GC within 1 month of report viewing; control arm subjects (101, 54% female) could access counseling 3-months post-report viewing. We examined whether GC affected documentation of physician-patient communication by reviewing the first clinical note following the patient's GC visit or report upload to the EMR. Multivariable logistic regression modeling estimated the independent effect of GC on physician-patient communication, as intention to treat (ITT) and per protocol (PP), adjusted for physician educational intervention. Counselees in the active arm had more physician-patient communications than control subjects [ITT, odds ratio (OR): 3.76 (95% confidence interval (CI): 1.38-10.22, p < 0.0094); PP, OR: 5.53 (95% CI: 2.20-13.90, p = 0.0017). In conclusion, GC appreciably affected physician-patient communication following receipt of potentially actionable genomic risk information.

Indexed as

Electronic Health RecordsPharmacogeneticsPhysician-Patient RelationsAdultAgedAged, 80 and overCardiovascular DiseasesCommunicationFemaleGenetic CounselingGenome, HumanHumansMaleMiddle AgedOhioPhysicianscomplex diseasecounselingelectronic medical recordgeneticgenomicpharmacogenomicsphysician-patient communication

Identifiers

PMID27322592
PMCPMC5173448
OpenAlexW2464025955

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.