Literature DB >> 27917391

Adrift in the Gray Zone: IRB Perspectives on Research in the Learning Health System.

Sandra Soo-Jin Lee, Maureen Kelley, Mildred K Cho, Stephanie Alessi Kraft, Cyan James, Melissa Constantine, Adrienne N Meyer, Douglas Diekema, Alexander M Capron, Benjamin S Wilfond, David Magnus.   

Abstract

BACKGROUND: Human subjects protection in healthcare contexts rests on the premise that a principled boundary distinguishes clinical research and clinical practice. However, growing use of evidence-based clinical practices by health systems makes it increasingly difficult to disentangle research from a wide range of clinical activities that are sometimes called "research on medical practice" (ROMP), including quality improvement activities and comparative effectiveness research. The recent growth of ROMP activities has created an ethical and regulatory gray zone with significant implications for the oversight of human subjects research.
METHODS: We conducted six semi-structured, open-ended focus group discussions with IRB members to understand their experiences and perspectives on ethical oversight of ROMP, including randomization of patients to standard treatments.
RESULTS: Our study revealed that IRB members are unclear or divided on the central questions at stake in the current policy debate over ethical oversight of ROMP: IRB members struggle to make a clear distinction between clinical research and medical practice improvement, lack consensus on when ROMP requires IRB review and oversight, and are uncertain about what constitutes incremental risk when patients are randomized to different treatments, any of which may be offered in usual care. They characterized the central challenge as a balancing act, between, on the one hand, making information fully transparent to patients and providing adequate oversight, and on the other hand, avoiding a chilling effect on the research process or harming the physician-patient relationship.
CONCLUSIONS: Evidence-based guidance that supports IRB members in providing adequate and effective oversight of ROMP without impeding the research process or harming the physician-patient relationship is necessary to realize the full benefits of the learning health system.

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Year:  2016        PMID: 27917391      PMCID: PMC5130156          DOI: 10.1080/23294515.2016.1155674

Source DB:  PubMed          Journal:  AJOB Empir Bioeth        ISSN: 2329-4515


  12 in total

1.  Addressing low-risk comparative effectiveness research in proposed changes to US federal regulations governing research.

Authors:  Nancy Kass; Ruth Faden; Sean Tunis
Journal:  JAMA       Date:  2012-04-18       Impact factor: 56.272

2.  The research-clinical practice distinction, learning health systems, and relationships.

Authors:  Howard Brody; Franklin G Miller
Journal:  Hastings Cent Rep       Date:  2013 Sep-Oct       Impact factor: 2.683

3.  Managing conflicts of interest in the conduct of clinical trials.

Authors:  Karine Morin; Herbert Rakatansky; Frank A Riddick; Leonard J Morse; John M O'Bannon; Michael S Goldrich; Priscilla Ray; Matthew Weiss; Robert M Sade; Monique A Spillman
Journal:  JAMA       Date:  2002-01-02       Impact factor: 56.272

4.  Research on medical practices and the ethics of disclosure.

Authors:  David Magnus; Benjamin S Wilfond
Journal:  Pediatrics       Date:  2015-01-12       Impact factor: 7.124

5.  An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.

Authors:  Ruth R Faden; Nancy E Kass; Steven N Goodman; Peter Pronovost; Sean Tunis; Tom L Beauchamp
Journal:  Hastings Cent Rep       Date:  2013 Jan-Feb       Impact factor: 2.683

6.  Determining when quality improvement initiatives should be considered research: proposed criteria and potential implications.

Authors:  D Casarett; J H Karlawish; J Sugarman
Journal:  JAMA       Date:  2000-05-03       Impact factor: 56.272

7.  The ethics of using quality improvement methods in health care.

Authors:  Joanne Lynn; Mary Ann Baily; Melissa Bottrell; Bruce Jennings; Robert J Levine; Frank Davidoff; David Casarett; Janet Corrigan; Ellen Fox; Matthew K Wynia; George J Agich; Margaret O'Kane; Theodore Speroff; Paul Schyve; Paul Batalden; Sean Tunis; Nancy Berlinger; Linda Cronenwett; J Michael Fitzmaurice; Nancy Neveloff Dubler; Brent James
Journal:  Ann Intern Med       Date:  2007-04-16       Impact factor: 25.391

8.  Can research and care be ethically integrated?

Authors:  Emily A Largent; Steven Joffe; Franklin G Miller
Journal:  Hastings Cent Rep       Date:  2011 Jul-Aug       Impact factor: 2.683

9.  Pragmatic Randomized Trials Without Standard Informed Consent?: A National Survey.

Authors:  Rahul K Nayak; David Wendler; Franklin G Miller; Scott Y H Kim
Journal:  Ann Intern Med       Date:  2015-09-01       Impact factor: 25.391

10.  Patient Perspectives on the Learning Health System: The Importance of Trust and Shared Decision Making.

Authors:  Maureen Kelley; Cyan James; Stephanie Alessi Kraft; Diane Korngiebel; Isabelle Wijangco; Emily Rosenthal; Steven Joffe; Mildred K Cho; Benjamin Wilfond; Sandra Soo-Jin Lee
Journal:  Am J Bioeth       Date:  2015       Impact factor: 11.229

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  12 in total

1.  Patient Preferences Regarding Informed Consent Models for Participation in a Learning Health Care System for Oncology.

Authors:  Rochelle D Jones; Chris Krenz; Michele Gornick; Kent A Griffith; Rebecca Spence; Angela R Bradbury; Raymond De Vries; Sarah T Hawley; Rodney A Hayward; Robin Zon; Sage Bolte; Navid Sadeghi; Richard L Schilsky; Reshma Jagsi
Journal:  JCO Oncol Pract       Date:  2020-04-30

2.  Integrating Rules for Genomic Research, Clinical Care, Public Health Screening and DTC Testing: Creating Translational Law for Translational Genomics.

Authors:  Susan M Wolf; Pilar N Ossorio; Susan A Berry; Henry T Greely; Amy L McGuire; Michelle A Penny; Sharon F Terry
Journal:  J Law Med Ethics       Date:  2020-03       Impact factor: 1.718

3.  Patient Experiences, Trust, and Preferences for Health Data Sharing.

Authors:  Rochelle D Jones; Chris Krenz; Kent A Griffith; Rebecca Spence; Angela R Bradbury; Raymond De Vries; Sarah T Hawley; Robin Zon; Sage Bolte; Navid Sadeghi; Richard L Schilsky; Reshma Jagsi
Journal:  JCO Oncol Pract       Date:  2021-12-02

4.  Enhancing diversity to reduce health information disparities and build an evidence base for genomic medicine.

Authors:  Lucia A Hindorff; Vence L Bonham; Lucila Ohno-Machado
Journal:  Per Med       Date:  2018-09-13       Impact factor: 2.512

5.  Public Attitudes toward Consent When Research Is Integrated into Care-Any "Ought" from All the "Is"?

Authors:  Stephanie R Morain; Emily A Largent
Journal:  Hastings Cent Rep       Date:  2021-03       Impact factor: 2.683

6.  Stakeholder perspectives regarding alternate approaches to informed consent for comparative effectiveness research.

Authors:  Stephanie R Morain; Ellen Tambor; Rachael Moloney; Nancy E Kass; Sean Tunis; Kristina Hallez; Ruth R Faden
Journal:  Learn Health Syst       Date:  2017-12-05

7.  Informed consent within a learning health system: A scoping review.

Authors:  Annabelle Cumyn; Adrien Barton; Roxanne Dault; Anne-Marie Cloutier; Rosalie Jalbert; Jean-François Ethier
Journal:  Learn Health Syst       Date:  2019-12-04

8.  Governance of a Learning Health Care System for Oncology: Patient Recommendations.

Authors:  Rochelle D Jones; Chris Krenz; Kent A Griffith; Rebecca Spence; Angela R Bradbury; Raymond De Vries; Sarah T Hawley; Robin Zon; Sage Bolte; Navid Sadeghi; Richard L Schilsky; Reshma Jagsi
Journal:  JCO Oncol Pract       Date:  2020-10-23

9.  Navigating the research-clinical interface in genomic medicine: analysis from the CSER Consortium.

Authors:  Susan M Wolf; Laura M Amendola; Jonathan S Berg; Wendy K Chung; Ellen Wright Clayton; Robert C Green; Julie Harris-Wai; Gail E Henderson; Gail P Jarvik; Barbara A Koenig; Lisa Soleymani Lehmann; Amy L McGuire; Pearl O'Rourke; Carol Somkin; Benjamin S Wilfond; Wylie Burke
Journal:  Genet Med       Date:  2017-08-31       Impact factor: 8.822

10.  Ensuring respect for persons in COMPASS: a cluster randomised pragmatic clinical trial.

Authors:  Joseph E Andrews; J Brian Moore; Richard B Weinberg; Mysha Sissine; Sabina Gesell; Jacquie Halladay; Wayne Rosamond; Cheryl Bushnell; Sara Jones; Paula Means; Nancy M P King; Diana Omoyeni; Pamela W Duncan
Journal:  J Med Ethics       Date:  2018-05-02       Impact factor: 2.903

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