About this trial
This prospective observational cohort study evaluates if fluid balance in the first 48 hours of ICU admission is linked to acute kidney injury (AKI) in critically ill adults. Patients without AKI at entry will have fluids tracked hourly via charts, weights, and labs to assess AKI risk by KDIGO criteria within 7 days. Findings may guide better fluid management to lower AKI rates.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adults aged 18 years or older admitted to the ICU.
Patients with no AKI at ICU admission.
AKI secondary to (prerenal cause-renal and post renal with manifestation of hypovolemia)-postoperative settings-On top of CKD up to Stage 111b-Compansated heart failure with indication of fluid therapy
Disqualifiers
Patients with pre-existing end-stage renal disease requiring dialysis.
Patients with known chronic kidney disease stage 4 or higher.
ICU readmissions during the same hospitalization.
Patients who received renal replacement therapy before ICU admission
Trial population
Adult patients aged 18 years or older admitted to the intensive care unit (ICU) at Assiut University Hospital without acute kidney injury (AKI) at admission. Eligible cases include prerenal, renal, postrenal AKI with hypovolemia; postoperative; CKD up to stage IIIb; compensated heart failure needing fluids.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Incidence of Acute Kidney Injury (AKI)
Development of AKI defined by KDIGO criteria (increase in serum creatinine by ≥0.3 mg/dL within 48 hours or ≥1.5 times baseline within 7 days, or urine output \<0.5 mL/kg/h for 6 hours).
Secondary outcomes
AKI Stage by KDIGO Criteria
Worst stage of AKI (Stage 1: SCr 1.5-2.9x baseline or UO \<0.5 mL/kg/h ≥6h; Stage 2: SCr 3-5.9x or UO \<0.5 mL/kg/h ≥12h; Stage 3: SCr ≥6x or ≥4.0 mg/dL or RIFLE F/ESRD, UO \<0.3 mL/kg/h ≥24h or anuria ≥12h).
Locations
Sponsors and contacts
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