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Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results

Authors :
Kyle B. Brothers
Kelly M. East
Whitley V. Kelley
M. Frances Wright
Matthew J. Westbrook
Carla A. Rich
Kevin M. Bowling
Edward J. Lose
E. Martina Bebin
Shirley Simmons
John A. Myers
Greg Barsh
Richard M. Myers
Greg M. Cooper
Jill M. Pulley
Mark A. Rothstein
Ellen Wright Clayton
Source :
Genetics in medicine : official journal of the American College of Medical Genetics
Publication Year :
2017
Publisher :
Elsevier BV, 2017.

Abstract

Purpose Eliciting and understanding patient and research participant preferences regarding return of secondary test results is a key aspect of genomic medicine. A valid instrument should be easily understood without extensive pre-test counseling, while still faithfully eliciting patients’ preferences. Methods We conducted focus groups with 110 adults to understand patient perspectives on secondary genomic findings and the role preferences should play. We then developed and refined a draft instrument, and used it to elicit preferences from parents participating in a genomic sequencing study in children with intellectual disabilities. Results Patients preferred filtering of secondary genomic results to avoid information overload and to avoid learning what the future holds, among other reasons. Patients preferred to make autonomous choices about which categories of results to receive and to have their choices applied automatically before results are returned to them and their clinicians. The Preferences Instrument for Genomic Secondary Results (PIGSR) is designed to be completed by patients or research participants without assistance and to guide bioinformatic analysis of genomic raw data. Most participants wanted to receive all secondary results, but a significant minority indicated other preferences. Conclusions Our novel instrument – PIGSR – should be useful in a wide range of clinical and research settings.

Details

ISSN :
10983600
Volume :
19
Database :
OpenAIRE
Journal :
Genetics in Medicine
Accession number :
edsair.doi.dedup.....0ef62a94007769e11602454c3ce5b731
Full Text :
https://doi.org/10.1038/gim.2016.110