Literature DB >> 22521718

Usability of a novel clinician interface for genetic results.

Pamela M Neri1, Stephanie E Pollard, Lynn A Volk, Lisa P Newmark, Matthew Varugheese, Samantha Baxter, Samuel J Aronson, Heidi L Rehm, David W Bates.   

Abstract

The complexity and rapid growth of genetic data demand investment in information technology to support effective use of this information. Creating infrastructure to communicate genetic information to healthcare providers and enable them to manage that data can positively affect a patient's care in many ways. However, genetic data are complex and present many challenges. We report on the usability of a novel application designed to assist providers in receiving and managing a patient's genetic profile, including ongoing updated interpretations of the genetic variants in those patients. Because these interpretations are constantly evolving, managing them represents a challenge. We conducted usability tests with potential users of this application and reported findings to the application development team, many of which were addressed in subsequent versions. Clinicians were excited about the value this tool provides in pushing out variant updates to providers and overall gave the application high usability ratings, but had some difficulty interpreting elements of the interface. Many issues identified required relatively little development effort to fix suggesting that consistently incorporating this type of analysis in the development process can be highly beneficial. For genetic decision support applications, our findings suggest the importance of designing a system that can deliver the most current knowledge and highlight the significance of new genetic information for clinical care. Our results demonstrate that using a development and design process that is user focused helped optimize the value of this application for personalized medicine.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22521718      PMCID: PMC3426649          DOI: 10.1016/j.jbi.2012.03.007

Source DB:  PubMed          Journal:  J Biomed Inform        ISSN: 1532-0464            Impact factor:   6.317


  16 in total

1.  Ten commandments for effective clinical decision support: making the practice of evidence-based medicine a reality.

Authors:  David W Bates; Gilad J Kuperman; Samuel Wang; Tejal Gandhi; Anne Kittler; Lynn Volk; Cynthia Spurr; Ramin Khorasani; Milenko Tanasijevic; Blackford Middleton
Journal:  J Am Med Inform Assoc       Date:  2003-08-04       Impact factor: 4.497

2.  The path to personalized medicine.

Authors:  Margaret A Hamburg; Francis S Collins
Journal:  N Engl J Med       Date:  2010-06-15       Impact factor: 91.245

Review 3.  Use and interpretation of genetic tests in cardiovascular genetics.

Authors:  Colleen Caleshu; Sharlene Day; Heidi L Rehm; Samantha Baxter
Journal:  Heart       Date:  2010-10       Impact factor: 5.994

4.  The extent and importance of unintended consequences related to computerized provider order entry.

Authors:  Joan S Ash; Dean F Sittig; Eric G Poon; Kenneth Guappone; Emily Campbell; Richard H Dykstra
Journal:  J Am Med Inform Assoc       Date:  2007-04-25       Impact factor: 4.497

5.  The think aloud method: a guide to user interface design.

Authors:  Monique W M Jaspers; Thiemo Steen; Cor van den Bos; Maud Geenen
Journal:  Int J Med Inform       Date:  2004-11       Impact factor: 4.046

6.  The GeneInsight Suite: a platform to support laboratory and provider use of DNA-based genetic testing.

Authors:  Samuel J Aronson; Eugene H Clark; Lawrence J Babb; Samantha Baxter; Lisa M Farwell; Birgit H Funke; Amy Lovelette Hernandez; Victoria A Joshi; Elaine Lyon; Andrew R Parthum; Franklin J Russell; Matthew Varugheese; Thomas C Venman; Heidi L Rehm
Journal:  Hum Mutat       Date:  2011-03-22       Impact factor: 4.878

7.  Conclusion: You need human factors engineering expertise to see design hazards that are hiding in "plain sight!".

Authors:  John W Gosbee
Journal:  Jt Comm J Qual Saf       Date:  2004-12

8.  ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.

Authors:  C Sue Richards; Sherri Bale; Daniel B Bellissimo; Soma Das; Wayne W Grody; Madhuri R Hegde; Elaine Lyon; Brian E Ward
Journal:  Genet Med       Date:  2008-04       Impact factor: 8.822

9.  Are electronic health records ready for genomic medicine?

Authors:  Maren T Scheuner; Han de Vries; Benjamin Kim; Robin C Meili; Sarah H Olmstead; Stephanie Teleki
Journal:  Genet Med       Date:  2009-07       Impact factor: 8.822

10.  Deficiency of knowledge of genetics and genetic tests among general practitioners, gynecologists, and pediatricians: a global problem.

Authors:  Marieke J H Baars; Lidewij Henneman; Leo P Ten Kate
Journal:  Genet Med       Date:  2005 Nov-Dec       Impact factor: 8.822

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  16 in total

1.  Evaluation: A Qualitative Pilot Study of Novel Information Technology Infrastructure to Communicate Genetic Variant Updates.

Authors:  Stephanie Klinkenberg-Ramirez; Pamela M Neri; Lynn A Volk; Sara J Samaha; Lisa P Newmark; Stephanie Pollard; Matthew Varugheese; Samantha Baxter; Samuel J Aronson; Heidi L Rehm; David W Bates
Journal:  Appl Clin Inform       Date:  2016-06-01       Impact factor: 2.342

2.  A novel clinician interface to improve clinician access to up-to-date genetic results.

Authors:  Allison R Wilcox; Pamela M Neri; Lynn A Volk; Lisa P Newmark; Eugene H Clark; Lawrence J Babb; Matthew Varugheese; Samuel J Aronson; Heidi L Rehm; David W Bates
Journal:  J Am Med Inform Assoc       Date:  2013-09-07       Impact factor: 4.497

3.  Genomic medicine in primary care: barriers and assets.

Authors:  Jason L Vassy; Robert C Green; Lisa Soleymani Lehmann
Journal:  Postgrad Med J       Date:  2013-11       Impact factor: 2.401

4.  CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.

Authors:  Brian H Shirts; Joseph S Salama; Samuel J Aronson; Wendy K Chung; Stacy W Gray; Lucia A Hindorff; Gail P Jarvik; Sharon E Plon; Elena M Stoffel; Peter Z Tarczy-Hornoch; Eliezer M Van Allen; Karen E Weck; Christopher G Chute; Robert R Freimuth; Robert W Grundmeier; Andrea L Hartzler; Rongling Li; Peggy L Peissig; Josh F Peterson; Luke V Rasmussen; Justin B Starren; Marc S Williams; Casey L Overby
Journal:  J Am Med Inform Assoc       Date:  2015-07-03       Impact factor: 4.497

5.  Healthcare provider education to support integration of pharmacogenomics in practice: the eMERGE Network experience.

Authors:  Carolyn R Rohrer Vitek; Noura S Abul-Husn; John J Connolly; Andrea L Hartzler; Terrie Kitchner; Josh F Peterson; Luke V Rasmussen; Maureen E Smith; Sarah Stallings; Marc S Williams; Wendy A Wolf; Cynthia A Prows
Journal:  Pharmacogenomics       Date:  2017-06-22       Impact factor: 2.533

6.  Bringing clinical pharmacogenomics information to pharmacists: A qualitative study of information needs and resource requirements.

Authors:  Katrina M Romagnoli; Richard D Boyce; Philip E Empey; Solomon Adams; Harry Hochheiser
Journal:  Int J Med Inform       Date:  2015-11-30       Impact factor: 4.046

7.  The use of think-aloud and instant data analysis in evaluation research: Exemplar and lessons learned.

Authors:  Jonathan Joe; Shomir Chaudhuri; Thai Le; Hilaire Thompson; George Demiris
Journal:  J Biomed Inform       Date:  2015-06-10       Impact factor: 6.317

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

Authors:  Yvonne Bombard; Marc Clausen; Chloe Mighton; Lindsay Carlsson; Selina Casalino; Emily Glogowski; Kasmintan Schrader; Michael Evans; Adena Scheer; Nancy Baxter; Jada G Hamilton; Jordan Lerner-Ellis; Kenneth Offit; Mark Robson; Andreas Laupacis
Journal:  Eur J Hum Genet       Date:  2018-04-27       Impact factor: 4.246

9.  Usability evaluation of pharmacogenomics clinical decision support aids and clinical knowledge resources in a computerized provider order entry system: a mixed methods approach.

Authors:  Emily Beth Devine; Chia-Ju Lee; Casey L Overby; Neil Abernethy; Jeannine McCune; Joe W Smith; Peter Tarczy-Hornoch
Journal:  Int J Med Inform       Date:  2014-05-09       Impact factor: 4.046

10.  User-centered design of multi-gene sequencing panel reports for clinicians.

Authors:  Elizabeth Cutting; Meghan Banchero; Amber L Beitelshees; James J Cimino; Guilherme Del Fiol; Ayse P Gurses; Mark A Hoffman; Linda Jo Bone Jeng; Kensaku Kawamoto; Mark Kelemen; Harold Alan Pincus; Alan R Shuldiner; Marc S Williams; Toni I Pollin; Casey Lynnette Overby
Journal:  J Biomed Inform       Date:  2016-07-14       Impact factor: 6.317

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