Oral atropine premedication in infants attenuates cardiovascular depression during halothane anesthesia

Anesth Analg. 1988 Feb;67(2):180-5.

Abstract

The efficacy of oral atropine premedication in attenuation of the cardiovascular depression associated with halothane anesthesia has not been previously evaluated. A solution containing either oral atropine 0.04 mg/kg (HI), 0.02 mg/kg (LO), or a placebo (NO) was randomly administered to 36 infants 1-6 months old and 36 infants 7-15 months old 30-90 minutes before induction of anesthesia. The onset of action of atropine was approximately 25 minutes after administration as determined by a 15% increase in heart rate (HR) above baseline levels. Heart rate, systolic blood pressure (SBP), and mean arterial blood pressure (MAP) were then measured at 1-minute intervals starting just before induction of anesthesia and continuing until onset of surgical stimulation during anesthesia with halothane (up to 3%), nitrous oxide (60%), and oxygen (40%). In infants 1-6 months old, either dosage of oral atropine preserved HR and SBP as compared with placebo. In infants 7-15 months old, either dosage preserved HR but not SBP. The severity of hypotension was greatest in infants 1-6 months of age given placebos. No significant differences existed between oral atropine 0.04 mg/kg or 0.02 mg/kg in either age range. It is concluded that premedication with oral atropine 0.02 mg/kg is effective in attenuating the cardiovascular depression associated with halothane anesthesia in infants.

Publication types

  • Clinical Trial
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Analysis of Variance
  • Atropine / administration & dosage*
  • Atropine / adverse effects
  • Atropine / therapeutic use
  • Blood Pressure / drug effects*
  • Clinical Trials as Topic
  • Double-Blind Method
  • Halothane / adverse effects
  • Halothane / antagonists & inhibitors*
  • Heart Rate / drug effects*
  • Humans
  • Infant
  • Premedication*
  • Prospective Studies
  • Random Allocation
  • Systole / drug effects
  • Time Factors

Substances

  • Atropine
  • Halothane