Intravenous remifentanil and propofol for gastroscopy

J Clin Anesth. 2008 Aug;20(5):352-355. doi: 10.1016/j.jclinane.2008.03.006.

Abstract

Study objectives: To evaluate the efficiency and safety of intravenous (i.v.) remifentanil and propofol for gastroscopy in healthy adults.

Design: Randomized, double-blinded study.

Setting: Endoscopy Center, West China Hospital, Sichuan University (Chengdu, People's Republic of China).

Patients: 199 adult ASA physical status I and II patients.

Interventions: Patients were randomly allocated to either the fentanyl group (n = 99) or the remifentanil group (n = 100). Patients received either fentanyl 0.5 microg/kg or remifentanil 0.5 microg/kg, followed by a bolus injection of one mg/kg of propofol. The subsequent doses of propofol were 0.5 mg/kg when the patient was conscious or body movement appeared.

Measurements: Noninvasive blood pressure, heart rate, arterial pulse oxygen saturation, and respiratory rate were recorded before gastroscopy and at two-minute intervals until the end of the gastroscopy procedure. Patients were asked to evaluate their level of cognition using the Digit-Symbol Substitution Test score before gastroscopy and at 10 minutes after discontinuation of the drug injection.

Main results: Recovery time was significantly shorter in the remifentanil group than in the fentanyl group (P < 0.05). Postoperative Digit-Symbol Substitution Test scores were significantly higher in the remifentanil group than in the fentanyl group (P < 0.01). Total dosage of propofol given in the remifentanil group was significantly less than it was in the fentanyl group (P < 0.01). Frequency of apnea was significantly higher in the remifentanil group (P < 0.05). There were no significant differences in frequency of hypoxemia, bag ventilation, or body movement between the two groups (P > 0.05).

Conclusions: Intravenous remifentanil and propofol were more efficient for gastroscopy than i.v. fentanyl and propofol.

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Anesthesia Recovery Period
  • Anesthetics, Combined / adverse effects
  • Anesthetics, Combined / therapeutic use
  • Anesthetics, Intravenous / administration & dosage
  • Anesthetics, Intravenous / adverse effects
  • Anesthetics, Intravenous / therapeutic use*
  • Apnea / chemically induced
  • Cognition / drug effects
  • Dose-Response Relationship, Drug
  • Double-Blind Method
  • Fentanyl / adverse effects
  • Fentanyl / therapeutic use*
  • Gastroscopy / methods
  • Humans
  • Hypoxia / chemically induced
  • Piperidines / adverse effects
  • Piperidines / therapeutic use*
  • Propofol / administration & dosage
  • Propofol / adverse effects
  • Propofol / therapeutic use*
  • Remifentanil
  • Respiration, Artificial

Substances

  • Anesthetics, Combined
  • Anesthetics, Intravenous
  • Piperidines
  • Remifentanil
  • Fentanyl
  • Propofol