학술논문

Sepsis with liver dysfunction and coagulopathy predicts an inflammatory pattern of macrophage activation
Document Type
article
Source
Intensive Care Medicine Experimental. 10(1)
Subject
Biomedical and Clinical Sciences
Clinical Sciences
Clinical Research
Sepsis
Infectious Diseases
Hematology
4.1 Discovery and preclinical testing of markers and technologies
Detection
screening and diagnosis
2.1 Biological and endogenous factors
Aetiology
Infection
Inflammatory and immune system
Good Health and Well Being
ProCESS Investigators
Ferritin
IL-18
Organ dysfunction
Phenotype
Clinical sciences
Language
Abstract
BackgroundInterleukin-1 receptor antagonists can reduce mortality in septic shock patients with hepatobiliary dysfunction and disseminated intravascular coagulation (HBD + DIC), an organ failure pattern with inflammatory features consistent with macrophage activation. Identification of clinical phenotypes in sepsis may allow for improved care. We aim to describe the occurrence of HBD + DIC in a contemporary cohort of patients with sepsis and determine the association of this phenotype with known macrophage activation syndrome (MAS) biomarkers and mortality. We performed a retrospective nested case-control study in adult septic shock patients with concurrent HBD + DIC and an equal number of age-matched controls, with comparative analyses of all-cause mortality and circulating biomarkers between the groups. Multiple logistic regression explored the effect of HBD + DIC on mortality and the discriminatory power of the measured biomarkers for HBD + DIC and mortality.ResultsSix percent of septic shock patients (n = 82/1341) had HBD + DIC, which was an independent risk factor for 90-day mortality (OR = 3.1, 95% CI 1.4-7.5, p = 0.008). Relative to sepsis controls, the HBD + DIC cohort had increased levels of 21 of the 26 biomarkers related to macrophage activation (p