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Total Intravenous Anesthesia Versus Inhalation Anesthesia on Postoperative Liver Function

Not Applicable
Completed
Conditions
Laparoscopic Sleeve Gastrectomy
Interventions
Drug: Total intravenous anesthesia group
Registration Number
NCT06423846
Lead Sponsor
Benha University
Brief Summary

The pandemic of obesity has become a serious issue of public health worldwide as the size of the obese population has almost tripled over the last four decades and continues to riseزThe epidemic of obesity has led to a significant increase in the prevalence of non-alcoholic fatty liver disease (NAFLD). NAFLD is currently the most common chronic liver disease, with an estimated global prevalence at 25-30%, rising up to 90% in morbidly obese patients

Detailed Description

Anesthesia and surgery may deteriorate liver function in patients with elevated liver enzyme levels; therefore, in these patients, choosing anaesthetics with less hepatotoxicity may be important. Halothane, which is a typical inhalational anesthetic, is known for its liver and kidney toxicity. The latest anesthetic agents, including sevoflurane and desflurane, are associated with less hepatotoxicity, although rare cases of acute liver injury have been reported with these agentsزPropofol (2,6-diisopropylphenol) is an intravenous anesthetic. Its pharmacokinetic profile makes it very suitable for total intravenous anesthesia (TIVA) and this is a widely used technique in many centers. Its use results in a rapid onset and offset with fewer side effects including postoperative nausea and vomiting, making it particularly favorable in the ambulatory setting

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
Inclusion Criteria
  • Obese patients
  • had ASA I-III
  • diagnosed with non-alcoholic steatohepatitis (NASH) liver disease
  • undergoing laparoscopic sleeve gastrectomy
Exclusion Criteria
  • cases wherein surgeries were performed using anesthetic methods that were not clearly identified as TIVA or INHA
  • heart surgery or cesarean section, and cases of neuromuscular diseases

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
sevoflurane groupsevoflurane groupgeneral anesthesia was induced with propofol 2 mg/kg, fentanyl 1 ug/kg and then maintained with sevoflurane in air and oxygen, dexmedetomidine 1 ug/kg/hour.
total intravenous anesthesia groupTotal intravenous anesthesia groupPatients in the TIVA group had anesthesia induced with propofol 2 mg/kg , fentanyl 1 ug/kg and maintained with propofol.
Primary Outcome Measures
NameTimeMethod
visual analogue scalevisual analogue scale was measured at day one and day two postoperatively

Pain was assessed by using the visual analogue scale (VAS) score for pain (0-no pain, 10-worst imaginable pain)

Secondary Outcome Measures
NameTimeMethod
Patient satisfaction24 hours postoperatively

5-point Likert scale, (1=extremely dissatisfied; 5=extremely satisfied)

Trial Locations

Locations (1)

Benha University

🇪🇬

Banha, Egypt

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