Meeting unique requirements: Community consultation and public disclosure for research in emergency setting using exception from informed consent
- PMID: 33872426
- PMCID: PMC8523587
- DOI: 10.1111/acem.14264
Meeting unique requirements: Community consultation and public disclosure for research in emergency setting using exception from informed consent
Abstract
Background: Exception from informed consent (EFIC) regulations for research in emergency settings contain unique requirements for community consultation and public disclosure. These requirements address ethical challenges intrinsic to this research context. Multiple approaches have evolved to accomplish these activities that may reflect and advance different aims. This scoping review was designed to identify areas of consensus and lingering uncertainty in the literature.
Methods: Scoping review methodology was used. Conceptual and empirical literature related to community consultation and public disclosure for EFIC research was included and identified through a structured search using Embase, HEIN Online, PubMed, and Web of Science. Data were extracted using a standardized tool with domains for major literature categories.
Results: Among 84 manuscripts, major domains included conceptual or policy issues, reports of community consultation processes and results, and reports of public disclosure processes and results. Areas of consensus related to community consultation included the need for a two-way exchange of information and use of multiple methods. Public acceptance of personal EFIC enrollment is commonly 64% to 85%. There is less consensus regarding how to assess attitudes, what "communities" to prioritize, and how to determine adequacy for individual projects. Core goals of public disclosure are less well developed; no metrics exist for assessing adequacy.
Conclusions: Multiple methods are used to meet community consultation and public disclosure requirements. There remain no settled norms for assessing adequacy of public disclosure, and there is lingering debate about needed breadth and depth of community consultation.
Keywords: clinical trials as topic; community-institutional relations; critical care; disclosure; emergencies; informed consent.
© 2021 by the Society for Academic Emergency Medicine.
Conflict of interest statement
CONFLICT OF INTEREST
The authors’ institutions receive funding from NIH. ND reports research funding from AHRQ and the Greenwall Foundation. The other authors have no potential conflicts to disclose.
References
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- U.S. Food and Drug Administration. Title 21 (Code of Federal Regulations), Part 50.24 Protection of Human Subjects. 2004.
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- Guidance for Institutional Review Boards, Clinical Investigators, and Sponsors. Exception from Informed Consent Requirements for Emergency Research. U.S. Food and Drug Administration website. 2013. Accessed August 18, 2013. www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM249673.pdf
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- Tricco AC, Lillie E, Zarin W, et al. PRISMA extension for scoping reviews (PRISMA-ScR): checklist and explanation. Ann Intern Med. 2018;169:467–473. - PubMed
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- Biros MH. The people speak: community consultation in emergency research. Ann Emerg Med. 2011;57:355–356. - PubMed
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