Propofol for Sedation of Postoperative Electively Ventilated Liver Transplant Recipients.

Institute of Liver and Biliary Sciences, India

Status: Unknown

Conditions: Liver Cirrhoses

Study type: Observational

Funder types: Other

Identifiers

NCT03837145

ILBS-TRANSPLANT ANESTHESIA-01

Details and patient eligibility

About

All consenting, adult patients aged 18 years and above who will require elective ventilation after liver transplant recipient surgery will be enrolled for the study. Patients in acute liver failure, hepatic encephalopathy or patients with history of allergic reactions to propofol will be excluded from the study. This is an observational study. As per institute treatment protocol, propofol will be given post-operatively at a dose of 1 mg/kg/hr and than titrated to maintain a Bi-Spectral Index (BIS) score of 60-80 till the patient is on ventilator. There will be no deviation from our routine institutional protocol and no other sedative drugs like opioids or benzodiazepines will be used and no interventions will be done. Hemodynamics will be maintained targeting a mean arterial pressure (MAP) of at least 65 mm Hg. during the study period using appropriate measures.

Enrollment: 30 estimated patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Living donor liver transplant (LDLT) recipient adult patients ≥ 18 years of age requiring postoperative elective ventilation.

Exclusion criteria

• Propofol allergy
• Acute liver failure (ALF).
• Hepatic encephalopathy (HE)

Trial design

30 participants in 1 patient group

Liver transplant recipients

Description:

Adult patients requiring elective post-operative ventilation after a living donor liver transplant receiving intravenous propofol infusion for sedation titrated to Bi-Spectral Index (BIS) score of 60-80,as per our institutional protocol.