Literature DB >> 29703952

The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results.

Yvonne Bombard1,2, Marc Clausen3, Chloe Mighton4,3, Lindsay Carlsson5, Selina Casalino3, Emily Glogowski6, Kasmintan Schrader7, Michael Evans4,3, Adena Scheer3,8,9, Nancy Baxter4,3,8,9,10, Jada G Hamilton11, Jordan Lerner-Ellis12,13, Kenneth Offit11, Mark Robson11, Andreas Laupacis4,3.   

Abstract

Guidelines recommend patients be informed of their incidental results (IR) when undergoing genomic sequencing (GS), yet there are limited tools to support patients' decisions about learning IR. The aim of this study is to develop and test the usability of a decision aid (DA) to guide patients' selection of IR, and to describe patients' preferences for learning IR following use of the DA. We developed and evaluated a DA using an iterative, mixed-methods process consisting of (1) prototype development, (2) feasibility testing, (3) cognitive interviews, (4) design and programming, and (5) usability testing. We created an interactive online DA called the Genomics ADvISER, a genomics decision AiD about Incidental SEquencing Results. The Genomics ADvISER begins with an educational whiteboard video, and then engages users in a values clarification exercise, knowledge quiz and final choice step, based on a 'binning' framework. Participants found the DA acceptable and intuitive to use. They were enthusiastic towards GS and IR; all selected multiple categories of IR. The Genomics ADvISER is a new patient-centered tool to support the clinical delivery of incidental GS results. The Genomics ADvISER fills critical care gaps, given the health care system's limited genomics expertise and capacity to convey the large volume of IR and their myriad of implications.

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Year:  2018        PMID: 29703952      PMCID: PMC6018661          DOI: 10.1038/s41431-018-0144-0

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  41 in total

1.  Translating personalized genomic medicine into clinical practice: evidence, values, and health policy.

Authors:  Yvonne Bombard
Journal:  Genome       Date:  2015-11-18       Impact factor: 2.166

Review 2.  Decision aids for people facing health treatment or screening decisions.

Authors:  Dawn Stacey; France Légaré; Krystina Lewis; Michael J Barry; Carol L Bennett; Karen B Eden; Margaret Holmes-Rovner; Hilary Llewellyn-Thomas; Anne Lyddiatt; Richard Thomson; Lyndal Trevena
Journal:  Cochrane Database Syst Rev       Date:  2017-04-12

Review 3.  Sampling in qualitative research. Purposeful and theoretical sampling; merging or clear boundaries?

Authors:  I T Coyne
Journal:  J Adv Nurs       Date:  1997-09       Impact factor: 3.187

4.  Are you SURE?: Assessing patient decisional conflict with a 4-item screening test.

Authors:  France Légaré; Stephen Kearing; Kate Clay; Susie Gagnon; Denis D'Amours; Michel Rousseau; Annette O'Connor
Journal:  Can Fam Physician       Date:  2010-08       Impact factor: 3.275

5.  Development and testing of a decision aid for breast cancer prevention for women with a BRCA1 or BRCA2 mutation.

Authors:  K A Metcalfe; A Poll; A O'Connor; S Gershman; S Armel; A Finch; R Demsky; B Rosen; S A Narod
Journal:  Clin Genet       Date:  2007-09       Impact factor: 4.438

6.  Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.

Authors:  Sarah S Kalia; Kathy Adelman; Sherri J Bale; Wendy K Chung; Christine Eng; James P Evans; Gail E Herman; Sophia B Hufnagel; Teri E Klein; Bruce R Korf; Kent D McKelvey; Kelly E Ormond; C Sue Richards; Christopher N Vlangos; Michael Watson; Christa L Martin; David T Miller
Journal:  Genet Med       Date:  2016-11-17       Impact factor: 8.822

7.  Incidental findings in clinical genomics: a clarification.

Authors: 
Journal:  Genet Med       Date:  2013-07-04       Impact factor: 8.822

8.  The usefulness of whole-exome sequencing in routine clinical practice.

Authors:  Alejandro Iglesias; Kwame Anyane-Yeboa; Julia Wynn; Ashley Wilson; Megan Truitt Cho; Edwin Guzman; Rebecca Sisson; Claire Egan; Wendy K Chung
Journal:  Genet Med       Date:  2014-06-05       Impact factor: 8.822

Review 9.  Incidental Findings with Genomic Testing: Implications for Genetic Counseling Practice.

Authors:  Myra I Roche; Jonathan S Berg
Journal:  Curr Genet Med Rep       Date:  2015-08-25

10.  Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public.

Authors:  Saskia C Sanderson; Sabrina A Suckiel; Micol Zweig; Erwin P Bottinger; Ethylin Wang Jabs; Lynne D Richardson
Journal:  Genet Med       Date:  2015-09-03       Impact factor: 8.822

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  14 in total

Review 1.  The clinical utility of exome and genome sequencing across clinical indications: a systematic review.

Authors:  Salma Shickh; Chloe Mighton; Elizabeth Uleryk; Petros Pechlivanoglou; Yvonne Bombard
Journal:  Hum Genet       Date:  2021-08-08       Impact factor: 4.132

Review 2.  Digital health-enabled genomics: Opportunities and challenges.

Authors:  Yvonne Bombard; Geoffrey S Ginsburg; Amy C Sturm; Alicia Y Zhou; Amy A Lemke
Journal:  Am J Hum Genet       Date:  2022-07-07       Impact factor: 11.043

3.  ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.

Authors:  Elizabeth G Liles; Michael C Leo; Amanda S Freed; Kathryn M Porter; Jamilyn M Zepp; Tia L Kauffman; Erin Keast; Carmit K McMullen; Inga Gruß; Barbara B Biesecker; Kristin R Muessig; Donna J Eubanks; Laura M Amendola; Michael O Dorschner; Bradley A Rolf; Gail P Jarvik; Katrina A B Goddard; Benjamin S Wilfond
Journal:  Genet Med       Date:  2022-05-06       Impact factor: 8.864

4.  Engaging Patients in Precision Oncology: Development and Usability of a Web-Based Patient-Facing Genomic Sequencing Report.

Authors:  Ilana B Solomon; Sarah McGraw; Jenny Shen; Adem Albayrak; Gil Alterovitz; Melanie Davies; Catherine Del Vecchio Fitz; Rachel A Freedman; Lisa N Lopez; Lynette M Sholl; Eliezer Van Allen; Joanne Mortimer; Marwan Fakih; Sumanta Pal; Karen L Reckamp; Yuan Yuan; Stacy W Gray
Journal:  JCO Precis Oncol       Date:  2020-04-14

Review 5.  Genetic Counseling and Genome Sequencing in Pediatric Rare Disease.

Authors:  Alison M Elliott
Journal:  Cold Spring Harb Perspect Med       Date:  2020-03-02       Impact factor: 6.915

Review 6.  Informed Consent in the Genomics Era.

Authors:  Shannon Rego; Megan E Grove; Mildred K Cho; Kelly E Ormond
Journal:  Cold Spring Harb Perspect Med       Date:  2020-08-03       Impact factor: 5.159

7.  The role of digital tools in the delivery of genomic medicine: enhancing patient-centered care.

Authors:  Salma Shickh; Sara A Rafferty; Marc Clausen; Rita Kodida; Chloe Mighton; Seema Panchal; Justin Lorentz; Thomas Ward; Nicholas Watkins; Christine Elser; Andrea Eisen; June C Carroll; Emily Glogowski; Kasmintan A Schrader; Jordan Lerner-Ellis; Raymond H Kim; David Chitayat; Cheryl Shuman; Yvonne Bombard
Journal:  Genet Med       Date:  2021-03-02       Impact factor: 8.864

8.  Participant choices for return of genomic results in the eMERGE Network.

Authors:  Christin Hoell; Julia Wynn; Luke V Rasmussen; Keith Marsolo; Sharon A Aufox; Wendy K Chung; John J Connolly; Robert R Freimuth; David Kochan; Hakon Hakonarson; Margaret Harr; Ingrid A Holm; Iftikhar J Kullo; Philip E Lammers; Kathleen A Leppig; Nancy D Leslie; Melanie F Myers; Richard R Sharp; Maureen E Smith; Cynthia A Prows
Journal:  Genet Med       Date:  2020-07-16       Impact factor: 8.864

9.  Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.

Authors:  Salma Shickh; Marc Clausen; Chloe Mighton; Mariana Gutierrez Salazar; Kathleen-Rose Zakoor; Rita Kodida; Emma Reble; Christine Elser; Andrea Eisen; Seema Panchal; Melyssa Aronson; Tracy Graham; Susan Randall Armel; Chantal F Morel; Ramzi Fattouh; Emily Glogowski; Kasmintan A Schrader; Jada G Hamilton; Kenneth Offit; Mark Robson; June C Carroll; Wanrudee Isaranuwatchai; Raymond H Kim; Jordan Lerner-Ellis; Kevin E Thorpe; Andreas Laupacis; Yvonne Bombard
Journal:  BMJ Open       Date:  2019-10-07       Impact factor: 2.692

10.  Next-generation sequencing in precision oncology: Patient understanding and expectations.

Authors:  J Scott Roberts; Michele C Gornick; Lan Q Le; Natalie J Bartnik; Brian J Zikmund-Fisher; Arul M Chinnaiyan
Journal:  Cancer Med       Date:  2019-01-01       Impact factor: 4.452

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