Albumin is commonly used plasma expander in patients of decompensated cirrhosis and has been found to have many beneficial effects, with few studies showing that maintenance of serum albumin levels above 3 g/dl has improved outcomes and mortality leading to widespread utilization in patients with cirrhosis of the liver. While 20% human albumin solution has been subject to in-depth analysis along several fronts, it's effects on coagulation parameters is unknown. With cirrhosis being a state of dysregulated clotting and bleeding, it is imperative to know the effects of such a widely used plasma expander on coagulation. The aim of this study is to evaluate the effects of albumin on coagulation parameters in patients of decompensated cirrhosis.
Aim and Objective: To study the effects of 20% human albumin infusions on coagulation parameters in patients with decompensated cirrhosis of the liver. Methodology: \- Study population: All patients aged ≥ 18 years and ≤ 70 years admitted in Institute of Liver and Biliary Sciences, New Delhi with decompensated cirrhosis of any cause and S. Albumin ≤ 2.5 g/dl upon presentation and are giving written consent for participation in the study. * Study design - Single center, Open label, Randomized controlled trial * Study period - 1 year * Monitoring and assessment - * ABG prior to enrollment * Investigations - tests performed on Day 0, 1, 3, 5 and 7 or till discharge (whichever is earlier) * Routine: CBC, RFT, LFT, apTT, PT/INR, CXR * Coagulation parameter: ROTEM (EXTEM, FIBTEM), Fibrinogen * Inflammatory markers: ESR, CRP, IL-6, TNF-⍺ * Endothelial dysfunction: vWF, ADAMTS-13 * Cardiac function: NT-proBNP, PRA * 2 D Echo,PFT with DLCO will be done at 0,1 and 7 days. * Statistical Analysis: The data will be represented as mean±SD. The categorical data will be analysed using Chi-square test. The continuous data will be analysed by student T test, or Mann-Whitney test, whichever is applicable. Besides this, Cox regression will be applied to analyse the variables. For all tests, p≤ 0.05 will be considered statistically significant. * Adverse effects * Allergic reactions to albumin. * Features of symptomatic volume overload. * Stopping rule * Day 7, or discharge (whichever is earlier) * Allergic reaction to albumin * Features of symptomatic volume overload * Variceal bleeding * Requirement of coagulation correct Expected outcome of the project: Derangement of ROTEM in the group of patients receiving human albumin solution
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
120
20% human albumin solution infusion, to raise and maintain serum albumin levels above 3.0 g/dl. Human albumin solution will be given to those enrolled in the study having serum albumin levels ≤ 3 g/dl to maintain the serum albumin levels above 3 g/dl.
Standard treatment that the patient would receive had they not been included in the trial.
Institute of Liver & Biliary Sciences
New Delhi, National Capital Territory of Delhi, India
Change in ROTEM based coagulation parameters with albumin infusion in decompensated cirrhotic patients.
ROTEM based parameters includes CT,CFT,A10,A20,MCF (EXTEM). CT,CFT,A10,A20 (FIBTEM)
Time frame: 3 days
Changes in inflammatory parameters like ESR.
Time frame: 3 days
Changes in inflammatory parameters like CRP.
Time frame: 3 days
Changes in inflammatory parameters like IL-6
Time frame: 3 days
Changes in inflammatory parameters like TNF-alpha.
Time frame: 3 days
Changes in endothelial dysfunction like VWF.
Time frame: 3 days
Changes in endothelial dysfunction like ADAMTS-13.
Time frame: 3 days
Effect on pulmonary function by Pulmonary function test
Time frame: 3 days
Effect on renal function by s.creatinine.
Time frame: 3 days
Adverse effects of Human Albumin Solution
Time frame: 3 days
Change in the albuminome in both the groups
Albumin bound metabolites and lipids will be studied and the effect of albumin infusion on this albuminome.
Time frame: 3 days
Duration of hospital stay
Time frame: 28 days
Mortality at 28 days
Time frame: 28 days
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