Comparison of the incidence of complications at induction and emergence in infants receiving oral atropine vs no premedication.

We studied 120 patients less than 1 yr of age, allocated randomly to receive atropine 40 micrograms kg-1 orally 1 h before operation (group A) or no premedication (group B). All patients underwent a standardized anaesthetic, including inhalation induction with halothane followed by atracurium 0.5 mg kg-1, tracheal intubation and positive pressure ventilation. Monitoring during anaesthesia included heart rate, arterial oxygen saturation, temperature and airway conditions at induction and emergence. The incidence of a decrease in arterial oxygen saturation to 94% or less at induction and recovery was similar in both groups (30.5% at induction, 39% at extubation in group A; 31% at induction, 41% at extubation in group B). There were significantly more airway complications in group B both at induction and emergence (25% and 49%, respectively, compared with 9% and 25% in group A; P < 0.015). Mean heart rate at induction and in the peroperative period was significantly higher in the group receiving atropine (P < or = 0.001). There was an increased incidence of bradycardia (decrease in heart rate of > or = 20%) at induction in the non-premedicated group (23% in group B compared with 10% in group A), but this was not statistically significant. We conclude that the incidence of airway complications at induction and emergence was reduced by orally administered atropine premedication.

[1]  D. Hatch,et al.  New inhalation agents in paediatric anaesthesia. , 1999, British journal of anaesthesia.

[2]  M. Jöhr Is it time to question the routine use of anticholinergic agents in paediatric anaesthesia? , 1999, Paediatric anaesthesia.

[3]  W. Dick,et al.  Plasma concentration following oral and intramuscular atropine in children and their clinical effects , 1997, Paediatric anaesthesia.

[4]  S. Parnis,et al.  A National Survey of Atropine Use by Australian Anaesthetists , 1994, Anaesthesia and intensive care.

[5]  L. Brennan,et al.  An audit of induction of anaesthesia in neonates and small infants using pulse oximetry , 1992, Anaesthesia.

[6]  R. Mirakhur Anticholinergic drugs in anaesthesia. , 1991, British journal of hospital medicine.

[7]  P. Crean,et al.  The influence of atropine premedication on the induction of anaesthesia with isoflurane in children , 1991 .

[8]  D. Dull,et al.  Haemodynamic effects of atropine during halothane or isoflurane anaesthesia in infants and small children , 1989, Canadian journal of anaesthesia = Journal canadien d'anesthesie.

[9]  L. Mcnicol,et al.  Hypoxaemia during induction of anaesthesia—an audit of children who underwent general anaesthesia for routine elective surgery , 1988, Anaesthesia.

[10]  K. Pihlajamäki,et al.  Comparison of Pharmacokinetic and Pharmacodynamic Parameters following Oral or Intramuscular Atropine in Children , 1985, Acta anaesthesiologica Scandinavica.

[11]  R. Davies,et al.  Atropine—a safe drug , 1980, Anaesthesia.

[12]  R. Mirakhur,et al.  Anticholinergic drugs in anesthesia. A survey of their present position , 1979 .

[13]  P. Barash,et al.  Ventricular Function in Children during Halothane Anesthesia: An Echocardiographic Evaluation , 1978, Anesthesiology.

[14]  J. Dundee,et al.  Anticholinergic drugs in anaesthesia , 1978, Anaesthesia.

[15]  J. Sagarminaga,et al.  Atropine and the electrical activity of the heart during induction of anaesthesia in children , 1963, Canadian Anaesthetists' Society journal.

[16]  M. Meeroff Anticholinergic drugs , 1963, Revista brasileira de gastroenterologia.

[17]  A. Holt Premedication with atropine should not be routine. , 1962, Lancet.