Literature DB >> 24158054

Informed consent for return of incidental findings in genomic research.

Paul S Appelbaum1, Cameron R Waldman2, Abby Fyer1, Robert Klitzman1, Erik Parens2, Josue Martinez3, W Nicholson Price4, Wendy K Chung5.   

Abstract

PURPOSE: Researchers face the dilemma of how to obtain consent for return of incidental findings from genomic research. We surveyed and interviewed investigators and study participants, with the goal of providing suggestions for how to shape the consent process.
METHODS: We performed an online survey of 254 US genetic researchers identified through the NIH RePORTER database, abstracts from the 2011 American Society of Human Genetics meeting, and qualitative semi-structured interviews with 28 genomic researchers and 20 research participants.
RESULTS: Most researchers and participants endorsed disclosure of a wide range of information about return of incidental findings, including risks, benefits, impact on family members, data security, and procedures, for return of results in the event of death or incapacity and for recontact. However, most researchers were willing to devote 30 min or less to this process and expressed concerns that disclosed information would overwhelm participants, a concern shared by many participants themselves.
CONCLUSION: There is a disjunction between the views of investigators and participants about the amount of information that should be disclosed and the practical realities of the research setting, including the time available for consent discussions. This strongly suggests the need for innovative approaches to the informed consent process.

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Mesh:

Year:  2013        PMID: 24158054      PMCID: PMC3999314          DOI: 10.1038/gim.2013.145

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  30 in total

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3.  The incidentalome: a threat to genomic medicine.

Authors:  Isaac S Kohane; Daniel R Masys; Russ B Altman
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4.  Medicine. Reestablishing the researcher-patient compact.

Authors:  Isaac S Kohane; Kenneth D Mandl; Patrick L Taylor; Ingrid A Holm; Daniel J Nigrin; Louis M Kunkel
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Review 5.  Interventions to improve patient comprehension in informed consent for medical and surgical procedures: a systematic review.

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Journal:  Med Decis Making       Date:  2010-03-31       Impact factor: 2.583

Review 6.  The law of incidental findings in human subjects research: establishing researchers' duties.

Authors:  Susan M Wolf; Jordan Paradise; Charlisse Caga-anan
Journal:  J Law Med Ethics       Date:  2008       Impact factor: 1.718

7.  Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project.

Authors:  Leslie G Biesecker
Journal:  Genet Med       Date:  2012-02-16       Impact factor: 8.822

8.  Processes and factors involved in decisions regarding return of incidental genomic findings in research.

Authors:  Robert Klitzman; Brigitte Buquez; Paul S Appelbaum; Abby Fyer; Wendy K Chung
Journal:  Genet Med       Date:  2013-09-26       Impact factor: 8.822

9.  Subjects matter: a survey of public opinions about a large genetic cohort study.

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10.  ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.

Authors:  Robert C Green; Jonathan S Berg; Wayne W Grody; Sarah S Kalia; Bruce R Korf; Christa L Martin; Amy L McGuire; Robert L Nussbaum; Julianne M O'Daniel; Kelly E Ormond; Heidi L Rehm; Michael S Watson; Marc S Williams; Leslie G Biesecker
Journal:  Genet Med       Date:  2013-06-20       Impact factor: 8.822

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  29 in total

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2.  Much ado about nothing: A qualitative study of the experiences of an average-risk population receiving results of exome sequencing.

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3.  Return of individual results in epilepsy genomic research: A view from the field.

Authors:  Ruth Ottman; Catharine Freyer; Heather C Mefford; Annapurna Poduri; Daniel H Lowenstein
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4.  Attitudes among South African university staff and students towards disclosing secondary genetic findings.

Authors:  Georgina Spies; Jolynne Mokaya; Jacqui Steadman; Nicole Schuitmaker; Martin Kidd; S M J Hemmings; Jonathan A Carr; Helena Kuivaniemi; Soraya Seedat
Journal:  J Community Genet       Date:  2020-11-20

5.  Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual Understanding.

Authors:  Leandra K Tolusso; Kathleen Collins; Xue Zhang; Jennifer R Holle; C Alexander Valencia; Melanie F Myers
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6.  Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot.

Authors:  Julie C Sapp; Jennifer J Johnston; Kate Driscoll; Alexis R Heidlebaugh; Ane Miren Sagardia; D Nadine Dogbe; Kendall L Umstead; Erin Turbitt; Ilias Alevizos; Jeffrey Baron; Carsten Bönnemann; Brian Brooks; Sandra Donkervoort; Youn Hee Jee; W Marston Linehan; Francis J McMahon; Joel Moss; James C Mullikin; Deborah Nielsen; Eileen Pelayo; Alan T Remaley; Richard Siegel; Helen Su; Carlos Zarate; Teri A Manolio; Barbara B Biesecker; Leslie G Biesecker
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7.  Research Participants' Preferences for Hypothetical Secondary Results from Genomic Research.

Authors:  Julia Wynn; Josue Martinez; Jimmy Duong; Codruta Chiuzan; Jo C Phelan; Abby Fyer; Robert L Klitzman; Paul S Appelbaum; Wendy K Chung
Journal:  J Genet Couns       Date:  2016-12-29       Impact factor: 2.537

8.  "Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.

Authors:  Ashley N Tomlinson; Debra Skinner; Denise L Perry; Sarah R Scollon; Myra I Roche; Barbara A Bernhardt
Journal:  J Genet Couns       Date:  2015-04-26       Impact factor: 2.537

Review 9.  Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.

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10.  Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine.

Authors:  Robert C Green; Katrina A B Goddard; Gail P Jarvik; Laura M Amendola; Paul S Appelbaum; Jonathan S Berg; Barbara A Bernhardt; Leslie G Biesecker; Sawona Biswas; Carrie L Blout; Kevin M Bowling; Kyle B Brothers; Wylie Burke; Charlisse F Caga-Anan; Arul M Chinnaiyan; Wendy K Chung; Ellen W Clayton; Gregory M Cooper; Kelly East; James P Evans; Stephanie M Fullerton; Levi A Garraway; Jeremy R Garrett; Stacy W Gray; Gail E Henderson; Lucia A Hindorff; Ingrid A Holm; Michelle Huckaby Lewis; Carolyn M Hutter; Pasi A Janne; Steven Joffe; David Kaufman; Bartha M Knoppers; Barbara A Koenig; Ian D Krantz; Teri A Manolio; Laurence McCullough; Jean McEwen; Amy McGuire; Donna Muzny; Richard M Myers; Deborah A Nickerson; Jeffrey Ou; Donald W Parsons; Gloria M Petersen; Sharon E Plon; Heidi L Rehm; J Scott Roberts; Dan Robinson; Joseph S Salama; Sarah Scollon; Richard R Sharp; Brian Shirts; Nancy B Spinner; Holly K Tabor; Peter Tarczy-Hornoch; David L Veenstra; Nikhil Wagle; Karen Weck; Benjamin S Wilfond; Kirk Wilhelmsen; Susan M Wolf; Julia Wynn; Joon-Ho Yu
Journal:  Am J Hum Genet       Date:  2016-05-12       Impact factor: 11.025

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