Vanderbilt University Medical Center
Nashville, Tennessee, 37212, United States
NCT Number: NCT03098472
Delirium is a syndrome of acute brain dysfunction involving attention and cognition that affects up to half of older hospitalized patients and 50%-75% of critically ill ICU patients, such that millions of patients worldwide experience this acute threat to their health and well being every year. One-third to half of critical illness survivors struggle with a dementia-like disorder similar in severity to moderate-to-severe traumatic brain injury or Alzheimer's Disease, and the only proven risk factor that is potentially modifiable is delirium in the ICU. Despite the frequency and impact of delirium in the ICU, little is known regarding the biological mechanisms that lead to this form of organ dysfunction during critical illness. A widely held hypothesis proposes that inflammation is regulated by the cholinergic system, and that this interaction plays a pivotal role whether delirium developments in the setting of acute illness. Acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE) are enzymes that hydrolyze the neurotransmitter acetylcholine. Changes in the activity of these enzymes, which can be measured in whole blood, reflect altered regulation of circulating acetylcholine. AChE and BuChE activities have promise as both predictors of delirium (when found to be low at admission) and biomarkers of delirium (when low during serial measurement). Neither of these biomarkers, however, have been studied in the ICU setting where delirium risk is the highest. The current investigation, therefore will be the first to determine the validity of circulating AChE and BuChE activities as biomarkers of delirium during critical illness and subsequent cognitive impairment after discharge. This study will measure whole blood AChE and butyrylcholinesterase BuChE activities within the framework of the ICU Delirium and Cognitive Impairment Study Group's ongoing clinical trials in critically ill patients.
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Notify Me18 year and older
All sexes
Observational
Nashville, Tennessee, 37212, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: During hospital stay until death or hospital discharge, whichever comes first, up to 30 days
Confusion Assessment Method for the ICU
Time frame: At 3, 6, and/or 12 months after hospital discharge up to 18 months after discharge
Neuropsychological battery
Time frame: At 3, 6, and/or 12 months after hospital discharge up to 18 months after discharge
Katz Index of Independence in Activities of Daily Living
Time frame: At 3, 6, and/or 12 months after hospital discharge up to 18 months after discharge
Functional activities questionnaire
Time frame: At 3, 6, and/or 12 months after hospital discharge up to 18 months after discharge
EQ-5D
Time frame: During hospital stay until death or hospital discharge, whichever comes first, up to 30 days
Richmond Agitation Sedation Scale
Vanderbilt University Medical Center
Other
Acronym: CADUCeuS
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