Abstract

BackgroundSepsis is one of the most significant causes of mortality in intensive care units. It indicates crosstalk between inflammation and coagulation. In this study, we aimed to identify prognostic markers among sepsis biomarkers and coagulation/fibrinolysis markers.MethodsPatients with sepsis according to the Sepsis-3 criteria were enrolled from January 2013 to September 2015. Univariate and multivariate logistic regression analyses were performed to identify an independent predictive marker of 28-day mortality among sepsis biomarkers and coagulation/fibrinolysis markers on ICU admission. Receiver operating characteristic analysis was performed; the optimal cutoff value of 28-day mortality was calculated using the predictive marker. Patients were classified into two groups according to the cutoff level of the predictive marker. Patient characteristics were compared between the groups.ResultsA total of 186 patients were enrolled in this study; the 28-day mortality was 19.4% (36/186). PAI-1 was identified as the only independent predictive marker of 28-day mortality by univariate and multivariate logistic regression. The area under the curve was 0.72; the optimal cutoff level was 83 ng/ml (sensitivity, 75%; specificity, 61%). Patients were classified into a higher group (PAI-1 level ≥83 ng/ml; n = 85) and a lower group (PAI-1 level <83 ng/ml; n = 101). All disseminated intravascular coagulation (DIC) scores and Sequential Organ Failure Assessment score were significantly higher in the higher group than in the lower group.ConclusionsPAI-1 can predict prognosis in sepsis patients. PAI-1 reflects DIC with suppressed fibrinolysis and organ failure, with microthrombi leading to microcirculatory dysfunction.

Highlights

  • Sepsis is one of the most significant causes of mortality in intensive care units

  • The usefulness of sepsis biomarkers, such as procalcitonin (PCT) and presepsin (PSEP), has been reported; PCT and PSEP have been reported to be superior to C-reactive protein (CRP) and interleukin-6 for sepsis diagnosis and assessment of sepsis severity [4,5,6]

  • With respect to the comparison of sepsis biomarkers and coagulation/fibrinolysis markers, PCT, PT-INR, APTT, thrombin-antithrombin complex (TAT), soluble fibrin (SF), and plasminogen activator inhibitor-1 (PAI-1) levels were significantly higher in the non-survivor group than in the survivor group

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Summary

Introduction

Sepsis is one of the most significant causes of mortality in intensive care units. It indicates crosstalk between inflammation and coagulation. We aimed to identify prognostic markers among sepsis biomarkers and coagulation/fibrinolysis markers. Sepsis is one of the most significant causes of mortality in intensive care units [1], and mortality among septic shock patients has been reported to be 30–50% [2, 3]. If left uncontrolled, immunothrombosis can eventually lead to disseminated intravascular coagulation (DIC) [8, 9]. It is important to measure coagulation/fibrinolysis markers as well as sepsis biomarkers in sepsis to assess the presence of crosstalk between inflammation and coagulation

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