Lactate Kinetics as a Predictor of Survival in ACLF With Septic Shock

NCT ID: NCT06116305

Last Updated: 2023-11-03

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 100 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-11-05
• Study Completion Date: 2024-08-30

Brief Summary

Shock is a clinical state of tissue hypoxia. This hypoxia may be brought about by either decreased perfusion or the inability of the cell to extract oxygen in the presence of adequate perfusion. This causes cellular dysfunction. The most encountered form of shock seen in cirrhotics is septic shock. Septic shock has underlying cellular and metabolic abnormalities in addition to circulatory dysfunction. The circulatory dysfunction in sepsis is in the form of severe vasodilatation with high cardiac index. Cirrhosis is a state of hyperdynamic circulation. The mortality of septic shock in these group of patients is still higher. Sepsis-3 definition of septic shock describes it as a dysregulated immune response to an infection, leading to systemic inflammation, vasodilation, and organ impairment (3). Practically, to define septic shock it requires the lactate to be more than 2 mmol/L and there should be requirement of vasopressors after adequate fluid resuscitation.

Increased lactate levels can indicate tissue hypoxia, excessively rapid aerobic glycolysis, or reduced clearance. As lactate is a normal product of glucose and pyruvate metabolism, any increase in glucose metabolism and / or decrease in pyruvate metabolism will increase lactate generation. This was observed even in the presence of adequate tissue oxygenation. In sepsis, the inflammatory response appears to be associated with an increase in glycolysis and impaired pyruvate dehydrogenase activity. Thus, cytoplasmic pyruvate increases with greater lactate formation. The glycolytic enzyme complex lactate dehydrogenase (LDH) regenerates nicotinamide adenine dinucleotide (NAD) when pyruvate is reduced to lactate via a redox-coupled process in anaerobic glycolysis (Embden-Meyerhof pathway). Since lactate is overproduced and underutilised in tissue hypoxia due to poor mitochondrial oxidation, lactate has traditionally been used as a diagnostic marker for tissue hypoxia. However, up to 70% of the body's lactate elimination occurs in the liver

Detailed Description

• We hypothesise that delta lactate at 6 hours would be a better predictor of survival in patients of ACLF with septic shock when compared to admission lactate

Aim and Objective -

• Aim: To study the impact of measurement of dynamic change of lactate on outcomes in ACLF patients with septic shock
• Primary objective: Delta arterial lactate at 6 hours (delta lactate) as a predictor of survival at 7 days in patients of ACLF with septic shock

Secondary objectives:

• To study the lactate kinetics and lactate clearance at different time points (0, 6, 12,24,48 and 72 hours)
• Impact of delta arterial lactate and lactate clearance at 6h on the length of hospital stay, days of ventilation, time taken for reversal of shock and 28-day mortality
• Impact of oxygenation, respiratory acidosis, metabolic acidosis, anion gap
• Effect of etiology of ACLF on lactate kinetics
• Study the impact of type of infection (MDRO) on lactate kinetics
• Study the impact of therapeutic interventions ( CRRT - impact of CRRT in a subgroup / Fluids/ Vasopressors) on lactate kinetics in ACLF patients with septic shock at day 7
• To develop a dynamic predictive model incorporating lactate kinetics to improve risk stratification and prediction of 28-day mortality.

Methodology:

Study population: Patients of ACLF with septic shock who get admitted to our ICU with a diagnosis of septic shock in the age group 18 - 70 years.

Study design: Prospective observational study Study period: 3 months

Study Location: Department of Hepatology, ILBS, New Delhi

Definitions Sepsis will be defined as a SOFA score more than 2 (or increase in SOFA score >2) in a patient with a suspected infection

Septic shock will be defined as Subset of patients with sepsis with hypotension (MAP <65) unresponsive to fluid boluses AND with lactate >2mmol/L despite adequate fluid resuscitation

Reversal of Shock will be defined as maintenance of MAP > 65mmHg after discontinuation of all vasopressors for 6 hours.

Lactic Acidosis

Hyperlactatemia

• Sample size with justification: No study has been done on lactate clearance in ACLF (APASL) with septic shock
• We have taken a sample size of 100 arbitrarily

• Intervention: Not applicable (Observational study)
• Monitoring and assessment:
• Statistical Analysis: Continuous data- Student's t test
• Nonparametric analysis- Mann Whitney test
• Survival outcome By Kaplan-Meier method curve.
• For all tests, p≤ 0.05 will be considered statistically significant.
• Analysis will be performed using SPSS .
• The analysis will be done with intention to treat and per protocol analysis if
• Adverse effects: N/A
• Stopping rule of study: N/A

Conditions

Acute on Chronic Liver Failure

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Interventions

No intervention

No intervention

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Patients of Acute on chronic liver failure with septic shock (APASL, Sepsis -3 definitions)

2. Age 18-70yrs

3. Informed Consent

Exclusion Criteria

1. Acute coronary syndrome, hemodynamically unstable arrhythmias

2. CKD stage 5

3. COPD with acute exacerbation

4. Acute CVA or Seizures

5. Extremely moribund patients

6. Hepato-cellular carcinoma (HCC), intrahepatic or extrahepatic malignancy

7. Pregnancy

8. Diabetic ketoacidosis

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Institute of Liver and Biliary Sciences, India

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Institute of Liver & Biliary Sciences (ILBS)

New Delhi, National Capital Territory of Delhi, India

Countries

India

Central Contacts

Dr Vishnu Girish, MD

Role: CONTACT

vishnugirish@gmail.com

01146300000

Facility Contacts

Dr Vishnu Girish, MD

Role: primary

vishnugirish@gmail.com

01146300000

Other Identifiers

ILBS-ACLF-13

Identifier Type: -

Identifier Source: org_study_id