About this trial
AKI causes high mortality and morbidity, especially in critically ill patients, and prolongs the patient's stay in the intensive care unit. Due to the high morbidity and mortality associated with AKI, many researchers are studying several new biomarkers for earlier detection of AKI, determination of etiologies, and prediction of outcomes. However, the use of these new biomarkers may be limited due to reimbursement issues. In addition to the therapeutic role of furosemide in fluid balance, blood pressure control, and hypercalcemia management, Chawla et al. recommend the furosemide stress test (FST) as a tool to predict AKI progression. Designing a test that predicts the probability of AKI progression will help us make better decisions regarding the optimal timing of RRT initiation. In this study, we aimed to evaluate the feasibility of using the FST test in determining the progression of AKI in patients hospitalized in the intensive care unit and the need for RRT using the noninvasive procedure furosemide stress test.
Eligibility criteria
Qualifiers
Those who meet KDIGO AKI stage 1 and stage 2 criteria in the first 24 hours
Those with sufficient fluid volume (CVP≥6 cmH20)
Female and male patients over the age of 18 will be included in the study
Disqualifiers
Pregnant patients
Hospitalization due to intoxication
Liver or kidney transplant
Glomerular filtration rate below 30 ml/min/1.73m2
Trial design
Treatments tested in this trial
- Furosemide