Cargando…

Pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil

PURPOSE: Regulations have broadened to allow moderate sedation administration for gastrointestinal endoscopy by non-anesthesia personnel. The line between moderate and deep sedation is ambiguous. Deep sedation offers patient comfort as well as greater safety concerns. Unintended deep sedation can oc...

Descripción completa

Detalles Bibliográficos
Autores principales: Liou, Jing-Yang, Kuo, I-Ting, Chang, Weng-Kuei, Ting, Chien-Kun, Tsou, Mei-Yung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843845/
https://www.ncbi.nlm.nih.gov/pubmed/36647160
http://dx.doi.org/10.1186/s40360-023-00642-5
_version_ 1784870485183430656
author Liou, Jing-Yang
Kuo, I-Ting
Chang, Weng-Kuei
Ting, Chien-Kun
Tsou, Mei-Yung
author_facet Liou, Jing-Yang
Kuo, I-Ting
Chang, Weng-Kuei
Ting, Chien-Kun
Tsou, Mei-Yung
author_sort Liou, Jing-Yang
collection PubMed
description PURPOSE: Regulations have broadened to allow moderate sedation administration for gastrointestinal endoscopy by non-anesthesia personnel. The line between moderate and deep sedation is ambiguous. Deep sedation offers patient comfort as well as greater safety concerns. Unintended deep sedation can occur if drug interactions are overlooked. We present a pharmacodynamic model for moderate sedation using midazolam, alfentanil and propofol. The model is suitable for training and devising rationales for appropriate dosing. METHODS: The study consists of two parts: modeling and validation. In modeling, patients scheduled for esophagogastroduodenoscopy (EGD) or colonoscopy sedation are enrolled. The modified observer’s assessment of alertness/sedation (MOAA/S) score < 4 is defined as loss of response to represent moderate sedation. Two patient groups receiving bronchoscopy or endoscopic retrograde cholangiopancreatography (ERCP) are used for validation. Model performance is assessed by receiver operating characteristic (ROC) curves and area under the curve (AUC). Simulations are performed to demonstrate how the model is used to rationally determine drug regimen for moderate sedation. RESULTS: Interaction between propofol and alfentanil is stronger than the other pairwise combinations. Additional synergy is observed with three drugs. ROC AUC is 0.83 for the modeling group, and 0.96 and 0.93 for ERCP and bronchoscopy groups respectively. Model simulation suggests that 1 mg midazolam, 250 µg alfentanil and propofol maximally benefits from drug interactions and suitable for moderate sedation. CONCLUSION: We demonstrate the accurate prediction of a three-drug response surface model for moderate sedation and simulation suggests a rational dosing strategy for moderate sedation with midazolam, alfentanil and propofol. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40360-023-00642-5.
format Online
Article
Text
id pubmed-9843845
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-98438452023-01-18 Pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil Liou, Jing-Yang Kuo, I-Ting Chang, Weng-Kuei Ting, Chien-Kun Tsou, Mei-Yung BMC Pharmacol Toxicol Research PURPOSE: Regulations have broadened to allow moderate sedation administration for gastrointestinal endoscopy by non-anesthesia personnel. The line between moderate and deep sedation is ambiguous. Deep sedation offers patient comfort as well as greater safety concerns. Unintended deep sedation can occur if drug interactions are overlooked. We present a pharmacodynamic model for moderate sedation using midazolam, alfentanil and propofol. The model is suitable for training and devising rationales for appropriate dosing. METHODS: The study consists of two parts: modeling and validation. In modeling, patients scheduled for esophagogastroduodenoscopy (EGD) or colonoscopy sedation are enrolled. The modified observer’s assessment of alertness/sedation (MOAA/S) score < 4 is defined as loss of response to represent moderate sedation. Two patient groups receiving bronchoscopy or endoscopic retrograde cholangiopancreatography (ERCP) are used for validation. Model performance is assessed by receiver operating characteristic (ROC) curves and area under the curve (AUC). Simulations are performed to demonstrate how the model is used to rationally determine drug regimen for moderate sedation. RESULTS: Interaction between propofol and alfentanil is stronger than the other pairwise combinations. Additional synergy is observed with three drugs. ROC AUC is 0.83 for the modeling group, and 0.96 and 0.93 for ERCP and bronchoscopy groups respectively. Model simulation suggests that 1 mg midazolam, 250 µg alfentanil and propofol maximally benefits from drug interactions and suitable for moderate sedation. CONCLUSION: We demonstrate the accurate prediction of a three-drug response surface model for moderate sedation and simulation suggests a rational dosing strategy for moderate sedation with midazolam, alfentanil and propofol. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40360-023-00642-5. BioMed Central 2023-01-16 /pmc/articles/PMC9843845/ /pubmed/36647160 http://dx.doi.org/10.1186/s40360-023-00642-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liou, Jing-Yang
Kuo, I-Ting
Chang, Weng-Kuei
Ting, Chien-Kun
Tsou, Mei-Yung
Pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil
title Pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil
title_full Pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil
title_fullStr Pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil
title_full_unstemmed Pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil
title_short Pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil
title_sort pharmacodynamic modeling of moderate sedation and rationale for dosing using midazolam, propofol and alfentanil
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9843845/
https://www.ncbi.nlm.nih.gov/pubmed/36647160
http://dx.doi.org/10.1186/s40360-023-00642-5
work_keys_str_mv AT lioujingyang pharmacodynamicmodelingofmoderatesedationandrationalefordosingusingmidazolampropofolandalfentanil
AT kuoiting pharmacodynamicmodelingofmoderatesedationandrationalefordosingusingmidazolampropofolandalfentanil
AT changwengkuei pharmacodynamicmodelingofmoderatesedationandrationalefordosingusingmidazolampropofolandalfentanil
AT tingchienkun pharmacodynamicmodelingofmoderatesedationandrationalefordosingusingmidazolampropofolandalfentanil
AT tsoumeiyung pharmacodynamicmodelingofmoderatesedationandrationalefordosingusingmidazolampropofolandalfentanil