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Total Intravenous Anesthesia in Percutaneous Transhepatic Cholangiography

Conditions
Percutaneous Transhepatic Cholangiography
Interventions
Procedure: Percutaneous transhepatic cholangiography
Registration Number
NCT03103672
Lead Sponsor
Inonu University
Brief Summary

Percutaneous transhepatic cholangiography is a disturbing procedure for patients.

TIVA with short-acting anesthetics such as propofol and remifentanil is characterized by hemodynamic stability and better compilation profile The purpose of this study; To compare total intravenous anesthesia with inhalation anesthesia in patients undergoing percutaneous transhepatic cholangiography under general anesthesia.

Detailed Description

Percutaneous transhepatic cholangiography is a disturbing procedure for patients. Especially pain at the time of dilation can be a serious problem. These situations may be required local anesthetics, intravenous narcotics and sedatives or general anesthesia (1).

TIVA with short-acting anesthetics such as propofol and remifentanil is characterized by hemodynamic stability and better compilation profile (2).

The purpose of this study; To compare total intravenous anesthesia with inhalation anesthesia in patients undergoing percutaneous transhepatic cholangiography under general anesthesia and Determine their advantages and disadvantages.

1. Michael J. Lee, Peter R. Mueller, Sanjay Saini, Peter F. Hahn, Stewen L. Dawson. Percutaneous Dilatation of Benign Biliary Strictures: Single-Season Therapy with General Anesthesia. AJR: 157, December 1991: 1263-1266

2. Xiaoqian Deng, Tao Zhu. Clinical comparison of propofol-remifentanil TCI with sevoflurane induction / maintenance anesthesia in laparoscopic cholecystectomy. Pak J Med Sci 2014 Vol. 30 No. 5: 1017-1021

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Adult patients undergoing percutaneous transhepatic cholangiography with general anesthesia
Exclusion Criteria
  • Essential data were missing
  • Patient participating in other research projects
  • Drug allergy
  • Anesthetic complication story

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Groupe IPercutaneous transhepatic cholangiographyPatients who will receive inhalation anesthesia
Groupe 2Percutaneous transhepatic cholangiographyPatients who will receive total intravenous anesthesia
Primary Outcome Measures
NameTimeMethod
Recovery time from anesthesiaup to postoperative 1 hours

Time for Modified Aldrete Score 9 and over

Secondary Outcome Measures
NameTimeMethod
Heart rateup to postoperative 1 hours

Every 5 minutes during the process

Mean blood pressureup to postoperative 1 hours

Every 5 minutes during the process

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