Study population: A total of 90 consecutive patients of decompensated cirrhosis of any etiology, presenting to the Institute of Liver and Biliary Sciences with SBP with septic shock will be included. Study design: Randomized controlled trial Study period: August 2019 to December 2021. Sample size: Assuming that the response rate is 90% with GM-CSF and 60% without GM-CSF after day 5. With alpha 5 and power 80,we need to enroll 76 cases (38 cases with each). Further assuming 20 % drop-out due to various reasons, it was decided to enroll 90 cases randomly allocated into two groups (i.e., 45 in each) by block randomization method by taking block size as 6. So for the present study, it was decided to enroll 90 cases in all. Group A will be given Imipenem and Tigecycline. Patients with recent hospitalisation will be given Colistin in addition. Group B will be given: To another group we will give Imipenem and Tigecycline and GMCSF.Patients with recent hospitalisation will be given Colistin in addition. The dose of antibiotic will be given at dosage Inj Imipenem 1gm i.v. TDS Inj Tigecycline 100mg stat f/b 50mg i.v. OD Inj GM-CSF 500mcg s.c. OD Inj Colistin 9 MIU i.v. stat f/b 4.5 MIU i.v. BD Monitoring and assessment At the baseline, all patients will undergo investigational evaluation as described Daily monitoring of following parameters: * Haemoglobin, * Total peripheral leucocyte counts, * Platelet counts, * Renal function tests * Liver function tests and * Chest X rays will be undertaken * Ascitic fluid analysis will be done on day 0, day 2 and day 5 Stopping rule:If the patient develops a TLC of more than 50,000, the dose of the GM CSF will be reduced to half and the treatment continued. If, even after the reduction, the TLC rises to more than 50,000, then the treatment will be stopped and the patient excluded. Expected outcome of the project: Addition of GM-CSF to standard antibiotic regimen helps resolve SBP and improves outcome in decompensated liver cirrhotic patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
90
Inj Imipenem 1gm i.v. TDS
Inj Tigecycline 100mg stat f/b 50mg i.v. OD
Inj GM-CSF 500mcg s.c. OD
Inj Colistin 9 MIU i.v. stat f/b 4.5 MIU i.v. BD
Institute of Liver and Biliary Sciences
New Delhi, National Capital Territory of Delhi, India
RECRUITINGResolution of Spontaneous Bacterial peritonitis in both groups
Response is defined by resolution of SBP in terms of total counts \< 500,Neutrophil\<250
Time frame: Day 5
Reversal of shock in both groups
Blood pressure more than 90/60 mmHg with no inotropes requirement
Time frame: Day 2
Survival in both groups
Time frame: Day 7
Survival in both groups
Time frame: Day 28
Change in ascitic fluid metabolites Nitric Oxide in both groups
change is defined as percentage reduction in nitric oxide
Time frame: Day 28
Change in ascitic fluid macrophage population in both groups
change is defined as percentage reduction in macrophage population
Time frame: Day 28
Development of Hepatic Encephalopathy in both groups.
Hepatic Encephalopathy will be measured as per West Haven criteria
Time frame: Day 28
Development of Acute Kidney Injury in both groups
AKIN criteria will be used for Acute kidney injury
Time frame: Day 28
Development of Pneumonia in both groups.
Pneumonia will be confirmed based on imaging and clinically
Time frame: Day 28
Development of organ failures in both groups.
Organ failure will be as per APACHE score
Time frame: Day 28
Development of coagulopathy in both groups.
Coagulopathy is defined as INR \> 1.5
Time frame: Day 28
Resolution of Spontaneous Bacterial peritonitis in both groups
Response is defined by resolution of SBP in terms of total counts \< 500,Neutrophil\<250
Time frame: Day 2
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