Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Feb;7(1):58-70.
doi: 10.1525/jer.2012.7.1.58.

Considerations in the construction of an instrument to assess attitudes regarding critical illness gene variation research

Affiliations

Considerations in the construction of an instrument to assess attitudes regarding critical illness gene variation research

Bradley D Freeman et al. J Empir Res Hum Res Ethics. 2012 Feb.

Abstract

Clinical studies conducted in intensive care units are associated with logistical and ethical challenges. Diseases investigated are precipitous and life-threatening, care is highly technological, and patients are often incapacitated and decision-making is provided by surrogates. These investigations increasingly involve collection of genetic data. The manner in which the exigencies of critical illness impact attitudes regarding genetic data collection is unstudied. Given interest in understanding stakeholder preferences as a foundation for the ethical conduct of research, filling this knowledge gap is timely. The conduct of opinion research in the critical care arena is novel. This brief report describes the development of parallel patient/surrogate decision-maker quantitative survey instruments for use in this environment. Future research employing this instrument or a variant of it with diverse populations promises to inform research practices in critical illness gene variation research.

PubMed Disclaimer

Figures

FIG. 1
FIG. 1
Overview of studies examining perceptions and attitudes pertaining to gene variation research (GVR)2
FIG. 2
FIG. 2
Conceptual model guiding the development of survey instrument.3

Similar articles

Cited by

References

    1. Achter P, Parrott R, Silk K. African Americans’ opinions about human-genetics research. Politics and the Life Sciences. 2005;23(1):60–66. - PubMed
    1. Ad Hoc Statement Committee of the American Thoracic Society. The ethical conduct of clinical research involving critically ill patients in the United States and Canada. American Journal of Respiratory and Critical Care Medicine. 2004;170(12):1375–1384. - PubMed
    1. Basson F, Futter MJ, Greenberg J. Qualitative research methodology in the exploration of patients’ perceptions of participating in a genetic research program. Ophthalmic Genetics. 2007;28(3):143–149. - PubMed
    1. Bates BR, Lynch JA, Bevan JL, Condit CM. Warranted concerns, warranted outlooks: A focus group study of public understandings of genetic research. Social Science and Medicine. 2005;60(2):331–344. - PubMed
    1. Bell J. The new genetics in clinical practice. British Medical Journal. 1998;316:618–620. - PMC - PubMed

Publication types

LinkOut - more resources