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Q In critically ill patients, does implementation of an evidence based algorithm for nutritional support improve the provision of nutritional support and patient outcomes?
METHODS
Design:
cluster randomised controlled trial.
Allocation:
{concealed}*.
Blinding:
{unblinded}*.
Follow up period:
until hospital discharge.
Setting:
intensive care units (ICUs) of 11 community and 3 teaching hospitals in Ontario, Canada.
Patients:
499 patients aged ⩾16 years (mean age 66 y, 61% men) with an expected ICU stay of ⩾48 hours. Exclusion criteria: expected to be receiving sufficient oral nutrition within 24 hours after ICU admission, admitted for palliative care, …
Footnotes
↵* Information provided by author.
For correspondence: Dr C M Martin, Department of Medicine, Faculty of Medicine, University of Western Ontario, London, Ontario, Canada. claudio_m_martinhotmail.com
Source of funding: Nestlé Nutrition, Inc, Toronto, Ontario.