Literature DB >> 2404085

A simulation of neuromuscular function and heart rate during induction, maintenance, and reversal of neuromuscular blockade.

R R Jaklitsch1, D R Westenskow.   

Abstract

We developed a two-compartment model to simulate neuromuscular function and heart rate following the administration of four nondepolarizing neuromuscular blocking agents (atracurium, vecuronium, pancuronium, and d-tubocurarine), three neuromuscular block reversal agents (edrophonium, neostigmine, and pyridostigmine), and two anticholinergic agents (atropine and glycopyrrolate). Twitch depression, train-of-four ratio, and heart rate were modeled during fentanyl, halothane, enflurane, or isoflurane anesthesia, optionally supplemented with nitrous oxide. Simulation results, compared with published values for each drug, fell within the clinical accuracy range (onset time 6.1 +/- 3.9% [mean +/- SEM]; duration, 1.7 +/- 3.5%, 50% effective dose, 0.5 +/- 5.7%; and 95% effective dose, 2.1 +/- 1.1%). The simulation graphically demonstrates the pharmacokinetics, pharmacodynamics, and interactions between neuromuscular blocking agents, reversal agents, and anticholinergic agents. During a simulation, the need for frequent monitoring and repeated delivery of a neuromuscular blocking agent to keep neuromuscular blockade stable becomes apparent, especially with the intermediate-acting neuromuscular blocking agents. When inhalational agents are given concomitantly, the task becomes even more difficult, since potentiation changes with anesthetic uptake. Recurarization, tachycardia, or bradycardia may be seen with the simulation if an improper drug regimen is followed. Concurrent simulation of two identical patients allows comparison of different modes of administration, choice of anesthetic agents, and drug doses.

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Year:  1990        PMID: 2404085     DOI: 10.1007/bf02832179

Source DB:  PubMed          Journal:  J Clin Monit        ISSN: 0748-1977


  70 in total

1.  The dependence of pancuronium- and d-tubocurarine-induced neuromuscular blockades on alveolar concentrations of halothane and forane.

Authors:  R D Miller; W L Way; W M Dolan; W C Stevens; E I Eger
Journal:  Anesthesiology       Date:  1972-12       Impact factor: 7.892

2.  Comparative study of atracurium, vecuronium (Org NC 45) and pancuronium.

Authors:  L Gramstad; P Lilleaasen; B Minsaas
Journal:  Br J Anaesth       Date:  1983       Impact factor: 9.166

3.  Neostigmine antagonism of vecuronium paralysis during fentanyl, halothane, isoflurane, and enflurane anesthesia.

Authors:  B Dernovoi; S Agoston; L Barvais; M Baurain; R Lefebvre; A d'Hollander
Journal:  Anesthesiology       Date:  1987-05       Impact factor: 7.892

4.  Recovery characteristics following antagonism of atracurium with neostigmine or edrophonium.

Authors:  R M Jones; A C Pearce; J P Williams
Journal:  Br J Anaesth       Date:  1984-05       Impact factor: 9.166

5.  Reversal of atracurium with edrophonium.

Authors:  W L Baird; W J Kerr
Journal:  Br J Anaesth       Date:  1983       Impact factor: 9.166

6.  Modification of atracurium blockade by halothane and by suxamethonium. A review of clinical experience.

Authors:  J A Stirt; R L Katz; A L Murray; D L Schehl; C Lee
Journal:  Br J Anaesth       Date:  1983       Impact factor: 9.166

7.  Pharmacokinetics, pharmacodynamics and dose-response relationships of atracurium administered i.v.

Authors:  B C Weatherley; S G Williams; E A Neill
Journal:  Br J Anaesth       Date:  1983       Impact factor: 9.166

8.  Comparison of the effects of atracurium and tubocurarine on heart rate and arterial pressure in anaesthetized man.

Authors:  P K Barnes; V J Thomas; I Boyd; T Hollway
Journal:  Br J Anaesth       Date:  1983       Impact factor: 9.166

9.  Comparison of atropine and glycopyrrolate in a mixture with pyridostigmine for the antagonism of neuromuscular block.

Authors:  R K Mirakhur; L P Briggs; R S Clarke; J W Dundee; H M Johnston
Journal:  Br J Anaesth       Date:  1981-12       Impact factor: 9.166

10.  Atracurium and vecuronium: effect of dose on the time of onset.

Authors:  T E Healy; N D Pugh; B Kay; T Sivalingam; H V Petts
Journal:  Br J Anaesth       Date:  1986-06       Impact factor: 9.166

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