Relationship Among Clinically Obtained Biomarkers of Inflammation, Hypercoagulability, and Macrophage Activation, and Delirium in Critically Ill Patients With COVID-19.
作者信息
Khan Sikandar H, Perkins Anthony J, Chi Rosalyn, Seyffert Sarah, Conrad Peter, Lindroth Heidi, Wang Sophia, Mulkey Malissa, Gao Sujuan, Khan Babar
机构信息
Division of Pulmonary, Critical Care, Sleep and Occupational Medicine, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN.
Indiana University Center for Aging Research, Regenstrief Institute, Indianapolis, IN.
出版信息
Crit Care Explor. 2023 Jan 18;5(1):e0851. doi: 10.1097/CCE.0000000000000851. eCollection 2023 Jan.
UNLABELLED
Critically ill patients with COVID-19 experience high rates of delirium and coma. Whether delirium occurs through novel mechanisms in COVID-19 is not known. We analyzed the relationship among biomarkers of inflammation (C-reactive protein [CRP]), hypercoagulability (d-dimer), and lung macrophage activation (ferritin), and the primary composite outcome of delirium/coma next day. We also measured associations between biomarkers and next day delirium and coma independently, and delirium severity.
DESIGN
Retrospective, observational cohort study.
SETTING
ICUs at two large, urban, academic referral hospitals.
PATIENTS
All consecutive adult patients admitted to the ICU from March 1, 2020, to June 7, 2020, with COVID-19 with clinical biomarkers and delirium assessments performed.
INTERVENTIONS
None.
MEASUREMENTS AND MAIN RESULTS
Daily concentrations of CRP, d-dimer, and ferritin were obtained. Coma (assessed by Richmond Agitation-Sedation Scale) and delirium (assessed by Confusion Assessment Method for the ICU/Confusion Assessment Method for the ICU-7) were measured bid. A cohort of 197 ICU patients with COVID-19 were included. Higher d-dimer (odds ratio [OR], 1.57; 95% CI, 1.17-2.12; < 0.01) and ferritin quartiles (OR, 1.36; 95% CI, 1.02-1.81; < 0.01) were associated with greater odds of the composite outcome of delirium/coma next day. d-dimer was associated with greater odds of next day delirium (OR, 1.49; 95% CI, 1.14-1.94; < 0.01) and coma independently (OR, 1.52; 95% CI, 1.08-2.14; = 0.017). Higher ferritin quartiles were associated with greater odds of next day delirium (OR, 1.33; 95% CI, 1.04-1.70; = 0.026) and coma independently (OR, 1.59; 95% CI, 1.14-2.23; < 0.01). Higher CRP quartiles were associated with coma (OR, 1.36; 95% CI, 1.03-1.79; = 0.030) and delirium severity the next day (β = 0.30; se, 0.07; ≤ 0.01).
CONCLUSIONS
Our hypothesis-generating study found d-dimer and ferritin were associated with delirium/coma the following day, as well as delirium and coma independently. CRP was associated with next day coma and delirium severity. Larger studies to validate these results are needed.
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