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Many supposed low-risk intensive care unit (ICU) admissions develop acute organ failure (AOF).
We routinely screen for and treat hyperglycaemia with insulin in our PICU, and have reported that about 20% of all our admissions develop CIH [ 35].
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Two hundred ninety-five admissions developed HH (15%%) during their stay at the ICU.
Of all 1948 admissions studied during the observation period, 55%% (1054 admissions) developed AKI within 48 h after ICU admission.
He added that "active patients" means patient who are on an "open treatment pathway with us," and patients admitted in emergencies in some circumstances — given there may also be a risk of A&E admissions developing AKI.
Over 9 months, 40 8.8%) children of 452 admissions developed ALI.
We had an incidence of positive blood cultures of almost 32% of the total admissions; 19.4% of admissions developed bloodstream infections.
In this 5 month study, 46% (n = 1618) of ICU admissions developed sepsis, equating to 0.77 cases per 1000 population, per annum, in Scotland.
Four (29%) out of 14 patients without ACLF on admission developed ACLF within 48 h after ROSC.
New MODS was diagnosed if a patient with no organ dysfunction or one organ dysfunction at the time of PICU admission developed two or more organ dysfunctions during PICU stay or if he/she died; progressive MODS was diagnosed if a patient who already had MODS at PICU admission developed dysfunction of at least one other organ during PICU stay or if he/she died.
In a combined analysis of 243 patients recruited to two malaria treatment trials in western Cambodia, 20/43 (47%) of those with P. falciparum gametocytes on admission developed P. vivax malaria by Day 28 of follow-up.
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