Which factors influence the resort to surrogate consent in stroke trials, and what are the patient outcomes in this context?. Mendyk AM, Labreuche J, Henon H, Girot M, Cordonnier C, Duhamel A, Leys D, & Bordet R BMC Med. Ethics, 2015.
Which factors influence the resort to surrogate consent in stroke trials, and what are the patient outcomes in this context? [link]Paper  doi  bibtex   
@article{mendyk_am_which_2015,
title = {Which factors influence the resort to surrogate consent in stroke trials, and what are the patient outcomes in this context?},
volume = {16},
issn = {1472-6939},
url = {http://www.ncbi.nlm.nih.gov/pubmed/25903471},
DOI = {10.1186/s12910-015-0018-8},
Language = {English},
Journal = {BMC Med. Ethics},
author = {{Mendyk AM} and {Labreuche J} and {Henon H} and {Girot M} and {Cordonnier C} and {Duhamel A} and {Leys D} and {Bordet R}},
year = {2015},
keywords = {Age Factors, Aged, Aged, 80 and over, Aphasia, Biomedical Research*/ethics, Cognition, Cognition Disorders, Decision Making, Female, Humans, Informed Consent*, Male, Middle Aged, Patient Selection*/ethics, Proxy*, Research Design, Research Subjects*, Severity of Illness Index*, Stroke*, United States},
}

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