Key result
A clinical decision tree utilizing baseline SOFA score, antithrombin activity, infection site, age, and sex accurately classified 28-day mortality risk in 86.1% of patients with sepsis-associated DIC.
Why the study?
DIC frequently complicates sepsis and increases mortality, and anticoagulant therapy may benefit select patients with high disease severity and antithrombin deficiency.
Can baseline SOFA score, antithrombin activity, and demographic data predict 28-day mortality in patients with sepsis-associated DIC treated with antithrombin concentrate?
Cohort (n=1,562)
Yes
Can baseline SOFA score, antithrombin activity, and demographic data predict 28-day mortality in patients with sepsis-associated DIC treated with antithrombin concentrate?
Baseline SOFA score, antithrombin activity, and demographic factors can be used in a decision tree to effectively stratify 28-day mortality risk in patients with sepsis-associated DIC.
May aid mortality stratification in sepsis-associated DIC; hypothesis-generating pending prospective validation.
Disseminated intravascular coagulation (DIC) is a frequent complication in patients with sepsis and is associated with increased mortality. Anticoagulant therapy may be appropriate for certain patients with DIC, particularly those with increased disease severity and deficiency in the physiologic anticoagulant antithrombin. We retrospectively analyzed post-marketing survey data from 1562 patients with sepsis-associated DIC and antithrombin activity of 70% or less. All the patients were treated with antithrombin concentrates. Baseline sequential organ failure assessment (SOFA) score, DIC score, and antithrombin activity were assessed. Cox multivariate regression analysis, Kaplan-Meier curve analysis, and receiver operating characteristic (ROC) curve analysis were performed to evaluate the performance of variables used to assess mortality. Furthermore, a decision tree was constructed to classify the risk of 28-day mortality. COX multivariate regression analysis demonstrated a significant association of age, sex, baseline SOFA score, baseline antithrombin activity, and the presence of pneumonia or skin/soft tissue infection with increased mortality. The area under the curve of SOFA score or antithrombin activity for mortality was 0.700 and 0.614, respectively. Kaplan-Meier analysis demonstrated that mortality was significantly higher in patients with SOFA score ≥ 12 and antithrombin activity < 47%. The decision tree analysis accurately classified the risk of death into high (> 40%), medium (40%-20%), and low (< 20%) categories in 86.1% of the cohort. Twenty eight-day mortality can be strongly predicted using baseline SOFA score, antithrombin activity, infection site, age, and sex as variables in the clinical decision tree for patients with sepsis-associated disseminated intravascular coagulation (DIC).
No takes yet. Share an insight, caveat, or question.
Iba et al. (2023) conducted a cohort in Sepsis-associated disseminated intravascular coagulation (DIC) (n=1,562). Baseline SOFA score, antithrombin activity, and demographic data was evaluated on 28-day mortality. A clinical decision tree utilizing baseline SOFA score, antithrombin activity, infection site, age, and sex accurately classified 28-day mortality risk in 86.1% of patients with sepsis-associated DIC.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: