Wonju Severance Christian Hospital
Wŏnju, Gangwon-do, 26426, South Korea
NCT Number: NCT05441787
1) Research Hypothesis
1. Trauma -> Inflammation -> Severe inflammation -> Poor prognosis 2. If the degree of inflammation in the serum is precisely measurable, the prognosis of patients with trauma can be predicted. In addition, if inflammatory processes linked to serum mitochondrial DNA copy number (smtDNAcn) and delta neutrophil index (DNI) are demonstrated, early intervention to improve outcomes in patients with trauma and a poor prognosis may be possible.
2) Basis of Research Hypothesis
1. The Sequential Organ Failure Assessment (SOFA) score is currently used as a measurement tool to evaluate the severity and prognosis of critically ill patients. Recently, some studies reported that the DNI, an inflammatory index, is useful as a prognostic index. Although DNI is a simple prognostic index, further studies are necessary to investigate its usefulness as a reliable prognostic index for severely injured patients. 2. Therefore, this study aimed to:
i. prospectively analyze the effectiveness of DNI by measuring the degree of inflammation in severely injured patients;
ii. Measure serum mitochondrial DNA, which is suggested as a mechanism preceding DNI elevation, and identify the sequence of inflammatory steps leading to circulating mitochondrial DNA as a damage-associated molecular pattern (DAMP), DNI, neutrophils, and inflammatory cytokines; and
iii. Establish the effectiveness of each indicator as a prognostic factor, construct a prediction model for poor prognosis, and prove the effectiveness of the final risk model.
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Notify Me19 year and older
All sexes
Observational
Wŏnju, Gangwon-do, 26426, South Korea
i. 1st and 2nd year (until construction of prognostic scoring system): 200 patients (MODS:50, mortality: 50)
ii. 3rd year (for validation): 100 patients (MODS: 30, mortality: 30)
i. Blood sampling: At the initial presentation and again on trauma days #1 and #2.
ii. smtDNAcn, cytokines (IL-1β/2/6/12, IFN-ℽ, TNF-α, IL-4/10) by PCR, multiplex, and DNI using an automatic cell analyzer.
i. Statistical analysis of inflammatory markers such as smtDNAcn, cytokines (IL-1β/2/6/12, IFN-ℽ, TNF-α, IL-4/10) measured at the initial presentation, on trauma day #1, and #2 between severely injured patients with no poor outcomes and those with poor outcomes such as MODS and mortality risk.
i. Recruitment of 100 severely injured patients for validation on 3rd year during study period
ii. The recruited patients were divided into low-risk and high-risk groups according to the new risk model, cut-off value of each inflammatory marker, and SOFA score.
iii. Comparison of sensitivity and specificity of the new risk model, inflammatory markers, and SOFA score.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Within 30 days after trauma
The number of deaths
Time frame: Within 30 days after trauma
The number of patients with SOFA ≥ 6
Time frame: From date of the admission until the date of first discharge from the hospital, assessed up to 60 days
Measured in days from admission to discharge
Time frame: From date of ICU admission (in cases of ICU admission at the initial presentation) until the date of first discharge from ICU, assessed up to 60 days
Measured in days from ICU admission to ICU out
Wonju Severance Christian Hospital
Other
Comparison of Inflammatory Markers (Serum Mitochondrial DNA, Delta Neutrophil Index, Inflammatory Cytokines) According to the Injury Severity, and Development of Risk Prediction Model Using Inflammatory Markers for Trauma Patients
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