Surrogate consent for genomics research in intensive care

Am J Crit Care. 2009 Sep;18(5):418-26; quiz 427. doi: 10.4037/ajcc2009473.

Abstract

Surrogate decision makers may be poorly prepared to give informed consent for genomics research for their loved ones in intensive care. A review of the challenges and strategies associated with obtaining surrogates' consent for genomics research in intensive care patients revealed that few well-controlled studies have been done on this topic. Yet, a major theme in the literature is the role of health care professionals in guiding surrogates through the informed consent process rather than simply witnessing a signature. Informed consent requires explicit strategies to approach potential surrogates effectively, educate them, and ensure that informed consent has been attained.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Biomedical Research / ethics*
  • Critical Care
  • Critical Illness
  • Decision Making*
  • Genetic Testing / ethics*
  • Humans
  • Intensive Care Units
  • Third-Party Consent / ethics*