Skip Navigation


BJA Advance Access originally published online on August 5, 2007
British Journal of Anaesthesia 2007 99(5):679-685; doi:10.1093/bja/aem212
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
99/5/679    most recent
aem212v1
Right arrow E-Letters: Submit a response to the article
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Cortínez, L. I.
Right arrow Articles by Muñoz, H. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Cortínez, L. I.
Right arrow Articles by Muñoz, H. R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?


© The Board of Management and Trustees of the British Journal of Anaesthesia 2007. All rights reserved. For Permissions, please e-mail: journals.permissions@oxfordjournals.org

Estimation of the plasma–effect-site equilibration rate constant (ke0) of rocuronium by the time of maximum effect: a comparison with non-parametric and parametric approaches

L. I. Cortínez*, C. Nazar and H. R. Muñoz

Departamento de Anestesiología, Facultad de Medicina, Hospital Clínico U.C., Pontificia Universidad Católica de Chile, PO Box 114-D, Marcoleta 367, Santiago, Chile

* Corresponding author. E-mail: licorti{at}med.puc.cl

Background: The first order plasma–effect-site equilibration rate constant (ke0) links the pharmacokinetics (PK) and pharmacodynamics (PD) of a given drug. For the calculation of the ke0, one method uses a single point of the response curve corresponding to the time to peak effect of a drug (tpeak); however, it has not been validated. This study compares the ke0 calculated with the method of tpeak and the ke0 calculated with traditional non-parametric and parametric methods.

Methods: Fifteen adult patients receiving total intravenous anaesthesia (TIVA) were studied. All patients were monitored with an NMT Monitor 221 (GE Healthcare, Helsinki, Finland) to obtain the evoked compound EMG of the adductor pollicis to a train-of-four stimuli at 10 s intervals. During TIVA, rocuronium 0.15 mg kg–1 was given i.v. as a bolus, and the neuromuscular response was recorded until recovery from block. Using the tpeak and the complete response curve, ke0 of rocuronium was calculated with the three methods using the predicted plasma concentrations of rocuronium from a PK model. Values of ke0 are median (range).

Results: The ke0s obtained were 0.19 min–1 (0.09–0.72) with the ‘tpeak’ method, 0.20 min–1 (0.14–0.44) with the non-parametric method, and 0.19 min–1 (0.11–0.38) [typical value (range)] with the parametric method (NS).

Conclusions: If the tpeak can be adequately estimated from the data, the tpeak method’ is a valid alternative to traditional methods to calculate the ke0.

Keywords: neuromuscular block, rocuronium; pharmacokinetics; pharmacology, rocuronium


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.