Consecutive patients with ACLF (Acute on Chronic Liver Failure) and septic shock with AKI (Acute Kidney Injury) who give written informed consent will be included in this prospective trial at ILBS. At baseline s, endotoxin levels, NT-Pro BNP, , urine N-GAL will be done for all patients. A 10 ml serum sample will be stored for doing a cytokine profile. Septic shock will be defined by the presence of two or more diagnostic criteria for the systemic inflammatory response syndrome, proven or suspected infection with hypotension non-responsive to adequate fluid resuscitation assessed by no evidence of stroke volume variation on flow track and need of a vasopressor to achieve a target mean arterial pressure (MAP) of ≥ 65 mm Hg. A record of CVP, IVC diameter and B-lines on ultrasound lung would also be done. Patients with age less than 18 years, severe known cardiopulmonary disease (structural or valvular heart disease, coronary artery disease, COPD) pregnancy, chronic kidney disease, patients already meeting emergency criteria for immediate hemodialysis at the time of randomization as specified in the late group, patients transferred from other hospitals who have already been on hemodialysis before their arrival in the intensive care unit, extremely moribund patients with an expected life expectancy of less than 24 hours, failure to give informed consent from family members.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
150
Continous Renal Replacement Therapy
Continous Renal Replacement Therapy
Standard Medical Therapy
Institute of Liver and Biliary Sciences
New Delhi, National Capital Territory of Delhi, India
RECRUITINGTransplant Free Survival
Time frame: 28 days
Incidence of intradialytic hypotension i.e. defined as a decrease in systolic blood pressure by ≥20 mm Hg or a decrease in MAP by 10 mm Hg associated with symptoms
Time frame: 1 year
Hemodynamic stability i.e. maintenance of MAP on dialysis without increase in the vasopressors
Time frame: 1 year
Dialysis efficiency as measured by Urea Reduction ratio at 48 hours
Time frame: 2 days
Achievement of target ultrafiltration goals
Time frame: 1 year
Recovery in renal functions defined as an increase in urine output to more than 400 ml/day
Time frame: 1 year
Duration of mechanical ventilation and ICU (Intensive Care Unit) stay
Time frame: 1 year
Improvement in SOFA (Sequential Organ Failure Assessment ) ( by 2 points) scores
Time frame: 1 year
Improvement in APACHE (Acute Physiology and Chronic Health Evaluation) ( by 2 points) scores
Time frame: 1 year
Improvement in MELD (Model for End Stage Liver Disease) ( by 2 points) scores
Time frame: 1 year
Improvement in lactic acidosis and lactate clearance at 6 hours after initiation of CRRT
Time frame: within 6 hours
Improvement in lactic acidosis and lactate clearance at 12 hours after initiation of CRRT
Time frame: within 12 hours
Improvement in lactic acidosis and lactate clearance at 24 hours after initiation of CRRT
Time frame: within 24 hours
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.