Literature DB >> 28872658

Evidence of hysteresis in propofol pharmacodynamics.

P O Sepúlveda1, E Carrasco1, L F Tapia1, M Ramos1, F Cruz1, P Conget2, Q F B Olivares3, I Cortínez4.   

Abstract

It is commonly assumed that loss of responsiveness and recovery of responsiveness occur at similar concentrations of propofol. However, the 'conscious' and 'anaesthetised' conditions produced by general anaesthetics may behave as two bistable states. We hypothesised that loss of responsiveness and recovery of responsiveness occur at different propofol concentrations. Propofol was administered to 19 healthy volunteers by effect-site target-controlled infusion using increasing and decreasing stable concentration steps of 7 min. Propofol serum concentrations were measured from venous blood samples at the end of each 7-min step. A long step of 14 min was performed at loss of responsiveness. At this step, propofol concentrations were measured at 7 and 14 min. Propofol concentrations measured at loss of responsiveness and recovery of responsiveness were 2.6 (1.2-4.7) μg.ml-1 and 1.6 (0.6-3.3) μg.ml-1 , respectively (p < 0.001). Propofol plasma concentration and the corresponding bispectral index values measured at minute 7 and minute 14 of the long step performed at loss of responsiveness were 2.6 (1.2-4.7) vs. 2.6 (1.3-4.3) at recovery of responsiveness, (p = 0.96) and 61.2 (49.0-77.0) vs. 58.4 (45.0-74.0), (p = 0.058), respectively. Loss of responsiveness and recovery of responsiveness appear to occur at different propofol concentrations. However, it is possible that, if equilibration was not achieved between plasma and effect-sites at the end of each 7-min step, the higher concentrations found at loss of responsiveness compared with those observed during recovery of responsiveness could be explained by a possible bias in estimations of the effect-site concentrations of propofol by the Schnider model, rather than neural inertia.
© 2017 The Association of Anaesthetists of Great Britain and Ireland.

Entities:  

Keywords:  administration guidelines; pharmacodynamic; pharmacokinetic; propofol

Mesh:

Substances:

Year:  2017        PMID: 28872658     DOI: 10.1111/anae.14009

Source DB:  PubMed          Journal:  Anaesthesia        ISSN: 0003-2409            Impact factor:   6.955


  6 in total

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2.  Dynamics of recovery from anaesthesia-induced unconsciousness across primate neocortex.

Authors:  Shaun R Patel; Jesus J Ballesteros; Omar J Ahmed; Pamela Huang; Jessica Briscoe; Emad N Eskandar; Yumiko Ishizawa
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3.  Performance of blink reflex in patients during anesthesia induction with propofol and remifentanil: prediction probabilities and multinomial logistic analysis.

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Review 4.  Molecular Diversity of Anesthetic Actions Is Evident in Electroencephalogram Effects in Humans and Animals.

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Review 5.  Why do We Use the Concepts of Adult Anesthesia Pharmacology in Developing Brains? Will It Have an Impact on Outcomes? Challenges in Neuromonitoring and Pharmacology in Pediatric Anesthesia.

Authors:  Pablo O Sepúlveda; Valeria Epulef; Gustavo Campos
Journal:  J Clin Med       Date:  2021-05-18       Impact factor: 4.241

6.  Effect of Hemodynamic Changes in Plasma Propofol Concentrations Associated with Knee-Chest Position in Spinal Surgery: A Prospective Study.

Authors:  Daniela Chalo; Sara Pedrosa; Pedro Amorim; Aura Silva; Paula Guedes de Pinho; Rui Correia; Sonia Gouveia; Consuelo Sancho
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  6 in total

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