SUmmPry
Conditions for tracheal intubation at 90 seconds, time to onset of maximum block and duration of clinical relaxation afterjive different doses of atracurium, which ranged from
Key wordsNeuromuscular relaxants; atracurium.The clinical use of atracurium, a bisquaternary nondepolarising relaxant, was first described by Payne and Hughes.' Subsequent reports confirmed its efficacy and safety in relatively small series of patients*-* and showed it to be a drug with an intermediate duration of action. The use of atracurium in over 200 patients was reported by Rowlandss but that study provided no information about the onset or duration of block. The present study describes the evaluation of atracurium in 200 patients during routine anaesthesia in doses ranging from 0 . 4 1 .O mg/kg, using intravenous or inhalational supplements.
Patients and methodsTwo hundred adult patients, who conformed to ASA grades 1 or 2, aged 1 8 4 5 years were to undergo elective surgery which required the use of a competitive neuromuscular blocking drug. Informed consent was obtained from each patient and the study was approved by the local ethical committee. One hour after premedication with diazepam 10-15 mg orally, anaesthesia was induced with thiopentone 5 mg/kg. Atracurium was given in one of five doses at the loss of eyelash reflex, 0.4, 0.5, 0.6, 0.75, or 1.0 mglkg, chosen at random. Tracheal intubation was attempted 90 seconds after administration of the relaxant. Anaesthesia was maintained with 67% nitrous oxide in oxygen and either fentanyl ( 2 4 pg/kg) or 0.5%4.75% halothane. Forty patients received each dose of atracurium and within each of these groups, half received halothane and half fentanyl, as supplements to anaesthesia.Atracurium wasevaluated at each dosage with respect to the conditions for tracheal intubation. the time to onset of maximum block, the duration of clinical relaxation of initial and repeat doses and the ease of reversal with anticholinesterases. Aclose watch was kept for any side effects including clinical signs of histamine release.Conditions for intubation were graded excellent, satisfactory, fair or poor and were based on jaw relaxation, cord relaxation and overall responses to in- tubation. as described Excellent and satisfactory grades were considered clinically acceptable; a poor grade meant a failed intubation. In such a case intubation was accomplished later when maximum block had developed.Neuromuscular block was monitored using a peripheral nerve stimulator (Myotest, Biometer Ltd). delivering a train-of-four (TOF) stimulus, at 2Hz every 10 seconds, to the ulnar nerve at the wrist via cutaneous electrodes. The technique involved counting the number of contractions felt in a slightly abducted thumb in response to a TOF stimulation as described by VibyMogensene and previously used by the authors.' The time to onset of complete block was taken as the period from the end of injection of atracurium to the loss of all four twitches in response to TOF stimulation. The duration of clinical relaxation w...