Empirical Analysis of Current Approaches to Incidental Findings

Author:

Lawrenz Frances,Sobotka Suzanne

Abstract

Researchers in the health sciences regularly discover information of potential health importance unrelated to their object of study in the course of their research. However, there appears to be little guidance available on what researchers should do with this information, known in the scientific literature as incidental findings (IFs). The study described here was designed to determine the extent of guidance available to researchers from public sources. This empirical study was part of a larger two-year project funded by the National Human Genome Research Institute (NHGRI) to generate guidance on how incidental findings should be managed in human subjects research, especially genetics, genomics, and imaging research. We generated empirical analysis of publicly available guidance and consent forms to help guide a multidisciplinary Working Group of experts in their formulation of normative recommendations reported in this symposium.

Publisher

Cambridge University Press (CUP)

Subject

Health Policy,General Medicine,Issues, ethics and legal aspects

Reference9 articles.

1. 2. Wolf, S. M. , Sobotka, S. P. , and Lawrenz, F. , “Managing Incidental Findings in Human Subjects Research: Empirical Findings,” manuscript in progress.

2. 4. Department of Veterans Affairs, IRB Guidebook 2005, available at (last visited February 11, 2008).

3. 5. National Institutes of Health Office of Extramural Research, Frequently Asked Questions from Applicants (May 11, 2006), available at (last visited February 11, 2008).

4. 9. Stanford University, Consent Form for Adult Brain Function Imaging with MR, (1.5T and 3.0T) 2002, available at (last visited February 11, 2008).

5. 8. Oregon Health Sciences University, IRB Policy/Procedure Manual, 2002, available at (last visited October 25, 2005; copy on file with author).

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