The aim of the current study is to assess the predictive value of renal cell arrest biomarkers (urinary TIMP2 and IGFBP7), renal damage biomarkers (urinary KIM-1) and microscopic examination of urinary sediment in progression and outcome of sepsis associated AKI.
Acute kidney injury occurred in about 45-53% of patients with sepsis, and most septic AKI was mild or moderate AKI (KDIGO stage 1 or stage 2). However, previous study showed that up to 40% of these mild or moderate AKI would progress to more severe AKI (KDIGO stage 3), of which 30% required dialysis and the risk of death increased by 3-fold, as high as 70%. Therefore, early identifying patients at high risk for progressive AKI might help clinicians to enhance individualized monitoring and personalized management in patient with septic AKI, which might prevent or halt the ongoing renal injury and improve the outcome of patients with sepsis.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
80
measurement of TIMP2 and IGFBP7, KIM-1
Faculty of Medicine, Aexandria University
Alexandria, Egypt
Urinary TIMP2 and IGFBP7 estimation
both will be measured by the ELISA technique
Time frame: 90 days
Urinary KIM-1 estimation
will be measured by the ELISA technique
Time frame: 90 days
Examination of urine sediment
by calculating Perazella score
Time frame: 7 days
progression of AKI
by assessing change in eGFR
Time frame: 90 days
Examination of urine sediment
by calculating Chawla score
Time frame: 7 days
need for renal replacement therapy
need of any dialysis modality
Time frame: 90 days
mortality
death
Time frame: 90 days
length of ICU and hospital stay
duration of stay
Time frame: 90 days
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