by Khan, Babar A.; Perkins, Anthony J.; Prasad, Nagendra K.;
Shekhar, Anantha; Campbell, Noll L.; Gao, Sujuan; Wang, Sophia; Khan, Sikandar
H.; Marcantonio, Edward R.; Twigg, Homer L. III; Boustani, Malaz A.
Critical Care
Medicine: March 2020 -
Volume 48 - Issue 3 - p 353-361
Objectives: Both
delirium duration and delirium severity are associated with adverse patient
outcomes. Serum biomarkers associated with delirium duration and delirium
severity in ICU patients have not been reliably identified. We conducted our
study to identify peripheral biomarkers representing systemic inflammation,
impaired neuroprotection, and astrocyte activation associated with delirium
duration, delirium severity, and in-hospital mortality.
Design:
Observational study.
Setting: Three
Indianapolis hospitals.
Patients:
Three-hundred twenty-one critically ill delirious patients.
Interventions:
None.
Measurements and Main
Results: We analyzed the associations between biomarkers collected at
delirium onset and delirium-/coma-free days assessed through Richmond
Agitation-Sedation Scale/Confusion Assessment Method for the ICU, delirium
severity assessed through Confusion Assessment Method for the ICU-7, and
in-hospital mortality. After adjusting for age, gender, Acute Physiology and
Chronic Health Evaluation II score, Charlson comorbidity score, sepsis
diagnosis and study intervention group, interleukin-6, -8, and -10, tumor
necrosis factor-α, C-reactive protein, and S-100β levels in quartile 4 were
negatively associated with delirium-/coma-free days by 1 week and 30 days post
enrollment. Insulin-like growth factor-1 levels in quartile 4 were not
associated with delirium-/coma-free days at both time points. Interleukin-6,
-8, and -10, tumor necrosis factor-α, C-reactive protein, and S-100β levels in
quartile 4 were also associated with delirium severity by 1 week. At hospital
discharge, interleukin-6, -8, and -10 retained the association but tumor
necrosis factor-α, C-reactive protein, and S-100β lost their associations with
delirium severity. Insulin-like growth factor-1 levels in quartile 4 were not
associated with delirium severity at both time points. Interleukin-8 and S-100β
levels in quartile 4 were also associated with higher in-hospital mortality.
Interleukin-6 and -10, tumor necrosis factor-α, and insulin-like growth
factor-1 were not found to be associated with in-hospital mortality.
Conclusions:
Biomarkers of systemic inflammation and those for astrocyte and glial
activation were associated with longer delirium duration, higher delirium
severity, and in-hospital mortality. Utility of these biomarkers early in
delirium onset to identify patients at a higher risk of severe and prolonged
delirium, and delirium related complications during hospitalization needs to be
explored in future studies.
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