Sepsis is a life-threatening organ dysfunction caused by a dysregulated host response to infection. For clinical operationalization, organ dysfunction can be represented by an increase in the Sequential Organ Failure Assessment (SOFA) score of 2 points or more, which is associated with an in-hospital mortality greater than 10%. pancreatic stone protein has been studied as biomarker of sepsis and results suggests that it has higher diagnostic performance. The main objective of this study is to identify ability of pancreatic stone protein (PSP) as a new biomarker for diagnosis of urosepsis in Intensive Care Units comparison to other biomarkers and its role as a prognostic marker for mortality
Study Type
OBSERVATIONAL
Enrollment
80
Blood samples will be collected for biomarker (PCT, CRP, and PSP) measurements in admission and 24 hours, 72 hours from admission and patients will be followed until death or discharge from the ICU or for 30 days, whichever occurred.
PSP ability to detect urinary sepsis
time course of PSP serum levels above normal range 20-50ng/ml in absence or presence of infection.
Time frame: measurements from admission and patients will be followed until death or discharge from or for 30 days whichever occurred the ICU
PSP ability to predict prognosis of sepsis in ICU.
value of serial serum PSP levels from admission in ICU to predict infection severity and complications.
Time frame: measurements from admission and patients will be followed until death or discharge from or for 30 days whichever occurred the ICU
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