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Although previous studies evaluating the relationship between case volume and outcome in critical care have produced conflicting results [ 8- 13, 22], positive volume outcome relationships have been reported in critically ill patients [ 13], including those with sepsis [ 12] and those requiring mechanical ventilation [ 11].
A large range of adverse effects related to RBCs storage have been reported in critically ill patients when RBC stored for 2 to 4 weeks are transfused.
Incidence rates of approximately 10 % have been reported in critically ill patients at the medical ICU [3, 4, 6, 7], and mortality rate in these patients was more than 50%% [1, 4, 5].
Reversible myocardial dysfunction or myocardial stunning is frequently described in patients with episodes of acute coronary syndrome and has recently been reported in critically ill patients without ischaemic heart disease.
Because of the overall increased survival that has been reported in critically ill patients with cancer, we outline an easy-to-use and evidence-based ICU admission triage criteria that may help avoid depriving life support to patients with cancer who can benefit.
To our knowledge, activin B levels have not been reported in critically ill patients.
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Mortality rates of up to 80% are reported in critically ill cirrhotic patients, progressively increasing with the number of organs failing [4 6].
Major discrepancy rates between premortem clinical diagnoses and postmortem autopsy findings continue to be reported in critically ill patients admitted to the intensive care unit (ICU) [ 1- 22].
Se deficiency is reported in critically ill patients due to deficient dietetic intake, unsupplemented parenteral nutrition, catabolic state and increased losses.
Furthermore, improved liver function was reported in critically ill patients when including a fraction of FO in the parenteral nutrition [ 10], and parenteral nutrition-associated liver disease was reversed in a cohort of children receiving long-term parenteral nutrition when exchanging a SO-based lipid emulsion for a FO-based lipid emulsion [ 11].
The fact that comparable white matter lesions have not been reported in nonsepsis critically ill patients [ 8] is consistent with an inflammatory process.
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