Acute Kidney Injury, Sepsis
Conditions
Brief summary
The aim of this study is to investigate the prognostic value of Blood Urea Nitrogen to serum Albumin ratio in septic Acute Kidney Injury patients Follow-up will be conducted for all enrolled patients for 30 days from admission to record mortality and the cause of death.
Detailed description
A complete medical history will be obtained from all patients including age, sex, comorbidities, cause of sepsis, and SOFA and APACHE II scores at admission. Blood samples will be collected within 24 hours of AKI diagnosis for analysis of Blood Urea Nitrogen (BUN) and serum Albumin levels. Blood Urea Nitrogen to serum Albumin ratio (B/A) will be calculated by dividing the BUN of a patient by their serum Albumin levels. Laboratory parameters also will include pH, lactate (Lac), base excess (BE), hemoglobin (Hb), platelet (PLT) count, white blood cell (WBC) count, bilirubin, hematocrit (HCT), creatinine (Cr), serum sodium (Na), serum potassium (K), serum calcium (Ca), serum magnesium (Mg), triglyceride (TG), aspartate aminotransferase (ALT), alanine aminotransferase (AST), prothrombin time (PT), and activated partial thromboplastin time (APTT) values. Follow-up will be conducted for all enrolled patients for 30 days from admission to record mortality and the cause of death. Study population will be divided into survival and non-survival groups based on their 30-day survival status
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
1. 18 - 60 years of age 2. Fulfilled the diagnostic criteria of Sepsis 3.0 (defined as a suspected or confirmed infection with a sequential organ failure assessment (SOFA) score of 2 or higher) 3. Developed AKI during hospitalization according to Kidney Disease: Improving Global Outcomes (KDIGO) guideline
Exclusion criteria
1. ICU length of stay\<24 h 2. AKI occurred before current hospital admission. 3. AKI is supposed to be secondary to causes other than sepsis. 4. Receiving renal replacement therapy at the time of admission. 5. Diagnosis with chronic kidney disease. 6. Diagnosis with liver failure. 7. Pregnant or lactating. 8. There was insufficient data for analysis. 9. Patients who had received Human serum Albumin infusion 3 days before ICU admission.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| mortality | 30 days | number of cases of mortality |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| mechanical ventilation | 30 days | number of participants who needed mechanical ventilation |
| stage-3 AKI | 30 days | number of participants who developed stage-3 AKI |
| renal replacement therapy | 30 days | number of participants who needed renal replacement therapy |
| septic shock | 30 days | number of participants who developed septic shock |
| length of ICU stay | 30 days | length of ICU stay in days |
Countries
Egypt