Comparison of neostigmine-induced recovery with spontaneous recovery from mivacurium-induced neuromuscular block

Br J Anaesth. 1994 Dec;73(6):791-4. doi: 10.1093/bja/73.6.791.

Abstract

In 24 ASA I-II adults anaesthetized with thiopentone, fentanyl and nitrous oxide in oxygen, we studied neuromuscular transmission with isometric adductor pollicis monitoring. Patients received mivacurium 0.2 mg kg-1 followed by an infusion lasting at least 60 min and adjusted to maintain twitch height at 1-5%. After termination of the mivacurium infusion, when twitch height spontaneously regained 25% of its control value, the patients were allocated to two groups of 12 patients each. In group NEO patients received neostigmine 40 micrograms kg-1 and atropine 15 micrograms kg-1 and in group SPO neuromuscular transmission was allowed to recover spontaneously. Twitch height was measured every 10 s and train-of-four (TOF) (2 Hz) every 3 min. After 15 min, residual force after tetanic stimulation (50 and 100 Hz, 5-s duration (RF50HZ, RF100HZ), 1 min apart) were recorded sequentially. At 15 min, mean TOF ratio was greater in group NEO (0.94 (SEM 0.01)) than in group SPO (0.87 (0.02)) (P < 0.01). All patients in group NEO recovered to a TOF ratio greater than 0.7 after 6 min compared with 15 min in group SPO (P < 0.005). A TOF ratio greater than 0.9 was observed in all patients in group NEO compared with only six in group SPO (P < 0.025). Nevertheless, RF50HZ and RF100HZ did not differ significantly (0.92 (0.01) (group NEO), 0.91 (0.01) (group SPO) and 0.83 (0.02) (group NEO), 0.78 (0.03) (group SPO), respectively).(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Analysis of Variance
  • Anesthesia Recovery Period
  • Elective Surgical Procedures
  • Fentanyl
  • Humans
  • Isometric Contraction
  • Isoquinolines*
  • Leg / surgery
  • Mivacurium
  • Motor Endplate
  • Neostigmine / administration & dosage*
  • Neostigmine / pharmacology
  • Nerve Block*
  • Neuromuscular Junction / drug effects*
  • Neuromuscular Nondepolarizing Agents*
  • Nitrous Oxide
  • Synaptic Transmission
  • Thiopental

Substances

  • Isoquinolines
  • Neuromuscular Nondepolarizing Agents
  • Neostigmine
  • Mivacurium
  • Thiopental
  • Nitrous Oxide
  • Fentanyl