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      Effect of Laryngeal Mask Airway Insertion on Parameters Derived From Catacrotic Phase of Photoplethysmography Under Different Concentrations of Remifentanil

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          Abstract

          Background: Some parameters have been extracted from photoplethysmography (PPG) with a good relativity with nociception, but without encouraging results in qualifying the balance of nociception-anti-nociception (NAN). The features of PPG have not been thoroughly depicted and more prospective univariate parameters deserve to be explored. The aim of this study was to investigate the ability of parameters derived from catacrotic phase of PPG to grade the level of analgesia. Methods: 45 patients with ASA I or II were randomized to receive a remifentanil effect-compartment target controlled infusion (Ce remi) of 0, 1, or 3 ng/ml, and a propofol effect-compartment target controlled infusion to maintain an acceptable level of hypnosis with state entropy (SE) at 40~60. Laryngeal mask airway (LMA) insertion was applied as a noxious stimulus. Five diastole-related parameters, namely diastolic interval (DI), diastolic slope (DS), the minimum slope during catacrotic phase (DSmin), the interval between DSmin and its nearest trough (DTI), and area difference ratio (ADR), were extracted. Pulse beat interval (PBI) was calculated as a reference parameter. Results: LMA insertion elicited a significant variation in all parameters except ADR during Ce remi of 0 and 1 ng/ml. Compared to PBI (prediction probability ( \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$\text{P}_{\text {K}}$ \end{document} ) = 0.796), the parameters of DI, DS, and DTI presented a better consistence with the level of anti-nociceptive medication, with \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{upgreek} \usepackage{mathrsfs} \setlength{\oddsidemargin}{-69pt} \begin{document} }{}$\text{P}_{\text {K}}$ \end{document} of 0.825, 0.822, and 0.822 respectively. Conclusion: The features extracted from catacrotic phase of PPG, including DI, DS, and DTI, could provide a promising potential to qualify the balance of NAN.

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          Most cited references39

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          Photoplethysmography and its application in clinical physiological measurement

          John Allen (2007)
          Physiological Measurement, 28(3), R1-R39
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            Studying sex and gender differences in pain and analgesia: a consensus report.

            In September 2006, members of the Sex, Gender and Pain Special Interest Group of the International Association for the Study of Pain met to discuss the following: (1) what is known about sex and gender differences in pain and analgesia; (2) what are the "best practice" guidelines for pain research with respect to sex and gender; and (3) what are the crucial questions to address in the near future? The resulting consensus presented herein includes input from basic science, clinical and psychosocial pain researchers, as well as from recognized experts in sexual differentiation and reproductive endocrinology. We intend this document to serve as a utilitarian and thought-provoking guide for future research on sex and gender differences in pain and analgesia, both for those currently working in this field as well as those still wondering, "Do I really need to study females?"
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              The influence of method of administration and covariates on the pharmacokinetics of propofol in adult volunteers.

              Unresolved issues with propofol include whether the pharmacokinetics are linear with dose, are influenced by method of administration (bolus vs. infusion), or are influenced by age. Recently, a new formulation of propofol emulsion, containing disodium edetate (EDTA), was introduced in the United States. Addition of EDTA was found by the manufacturer to significantly reduce bacterial growth. This study investigated the influences of method of administration, infusion rate, patient covariates, and EDTA on the pharmacokinetics of propofol. Twenty-four healthy volunteers aged 26-81 yr were given a bolus dose of propofol, followed 1 h later by a 60-min infusion. Each volunteer was randomly assigned to an infusion rate of 25, 50, 100, or 200 microg x kg(-1) x min(-1). Each volunteer was studied twice under otherwise identical circumstances: once receiving propofol without EDTA and once receiving propofol with EDTA. The influence of the method of administration and of the volunteer covariates was explored by fitting a three-compartment mamillary model to the data. The influence of EDTA was investigated by direct comparison of the measured concentrations in both sessions. The concentrations of propofol with and without EDTA were not significantly different. The concentration measurements after the bolus dose were significantly underpredicted by the parameters obtained just from the infusion data. The kinetics of propofol were linear within the infusion range of 25-200 microg x kg(-1) x min(-1). Age was a significant covariate for Volume2 and Clearance2, as were weight, height, and lean body mass for the metabolic clearance. These results demonstrate that method of administration (bolus vs. infusion), but not EDTA, influences the pharmacokinetics of propofol. Within the clinically relevant range, the kinetics of propofol during infusions are linear regarding infusion rate.
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                Author and article information

                Contributors
                Journal
                IEEE J Transl Eng Health Med
                IEEE J Transl Eng Health Med
                0063400
                JTEHM
                IJTEBN
                IEEE Journal of Translational Engineering in Health and Medicine
                IEEE
                2168-2372
                2020
                17 August 2020
                : 8
                : 2700609
                Affiliations
                [1 ]divisionCollege of Biomedical Engineering and Instrument Science, institutionZhejiang University, institutionringgold 12377; Hangzhou310027China
                [2 ]institutionZhejiang Provincial Key Laboratory of Cardio-Cerebral Vascular Detection Technology and Medicinal Effectiveness Appraisal; Hangzhou310027China
                [3 ]departmentDepartment of Anesthesia, divisionWomen’s Hospital, School of Medicine, institutionZhejiang University, institutionringgold 12377; Hangzhou310006China
                [4 ]divisionZhejiang Laboratory, institutionConnected Healthcare Big Data Research Center; Hangzhou311121China
                Article
                2700609
                10.1109/JTEHM.2020.3017368
                7647452
                80030dec-caa5-4e6d-bfa6-12ef6facaedb
                Copyright @ 2020

                This work is licensed under a Creative Commons Attribution 4.0 License. For more information, see https://creativecommons.org/licenses/by/4.0/

                History
                : 12 February 2020
                : 25 May 2020
                : 03 July 2020
                : 29 July 2020
                : 06 November 2020
                Page count
                Figures: 7, Tables: 5, Equations: 39, References: 39, Pages: 9
                Funding
                Funded by: National Natural Science Foundation of China, fundref 10.13039/501100001809;
                Award ID: 81870868
                Funded by: Major Scientific Project of Zhejiang Laboratory;
                Award ID: 2018DG0ZX01
                Funded by: China’s Natural Science Foundation, fundref 10.13039/501100001809;
                Award ID: #31627802
                This work was supported in part by the National Natural Science Foundation of China under Grant 81870868, in part by the Major Scientific Project of Zhejiang Laboratory under Grant 2018DG0ZX01, and in part by the China’s Natural Science Foundation under Grant #31627802.
                Categories
                Article

                balance of nociception-anti-nociception,catacrotic phase,photoplethysmography,wavelet de-noising

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