Incidental Findings
Incidental findings
During the course of research involving humans, findings relating to a subject's health may be discovered that is unrelated to the purpose or objectives of the study. These findings are termed "Incidental Findings" (IFs), which may be of clinical significance that could have potential serious implications for the subject's well-being. In general, a research subject should be allowed to consent if he/she wishes to be re-identified in the case of an IF, if the proposed biomedical research expressly provides for such re-identification, especially if the IFs are both clinically significant and actionable. Ethical management of IFs is thus necessary and researchers have and obligation to anticipate these findings and make a plan in advance of starting the research, that addresses what, when and how findings will be communicated to the research subjects.
In line with NTU's policy on IFs, PIs are to determine from the outset on the potential for IFs occurring, and if these will be released to the subjects. The threshold for reporting IFs, which are the potential medical beneficence of the findings versus the need for respect for persons, should be determined. Based on this, a management plan should be developed by the PI, and these are to be submitted to NTU IRB for review and approval.
[A detailed guideline on this can be found here]
Examples of Incidental Findings
Research Domain | IFs – Key Examples |
---|---|
Genetic Studies | Misattributed paternity |
MRI of Brain | Unexpected mass |
CT Scans | Findings anywhere in torso (e.g. aortic aneurysm, renal neoplasm) not part of original study site |
Recommended classification of Incidental Findings (adopted from NIH)
IF Disclosure Category | Relevant IFs | Recommended Action |
---|---|---|
Strong Net Benefit (IFs whose disclosure is likely to offer markedly more benefit than burden to the research participant) | Information revealing a condition (or significant risk) likely to be life-threatening Examples: | Disclose to research participant as an incident finding, unless he/ she elected not to know. |
Possible Net Benefit (IFs that may offer more benefit than burden to the research participant) | Information revealing a nonfatal condition likely to be grave or serious but that cannot be avoided or ameliorated, when a research participant is likely to deem that information important Examples: | May disclose to research participant as an incidental finding, unless he/ she elected not to know. |
Unlikely Net Benefit (IFs that probably offer more burden than benefit) | Information revealing a condition that is not likely to be of serious health or reproductive importance, or importance cannot be ascertained. Examples: | Do not disclose to research participant as an incidental finding. |
References:
Schaefer GO, Savulescu J. The Right to Know: A Revised Standard for Reporting Incidental Findings. Hastings Cent Rep. 2018 Mar;48(2):22-32.
Susan M. Wolf, et. al.., Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations. J Law Med Ethics. 2008; 36(2): 219–211.