Abstract

BackgroundExhaled propofol concentrations correlate with propofol concentrations in adult human blood and the brain tissue of rats, as well as with electroencephalography (EEG) based indices of anesthetic depth. The pharmacokinetics of propofol are however different in children compared to adults. The value of exhaled propofol measurements in pediatric anesthesia has not yet been investigated. Breathing system filters and breathing circuits can also interfere with the measurements. In this study, we investigated correlations between exhaled propofol (exP) concentrations and the Narkotrend Index (NI) as well as calculated propofol plasma concentrations.MethodsA multi-capillary-column (MCC) combined with ion mobility spectrometry (IMS) was used to determine exP. Optimal positioning of breathing system filters (near-patient or patient-distant) and sample line (proximal or distal to filter) were investigated. Measurements were taken during induction (I), maintenance (M) and emergence (E) of children under total intravenous anesthesia (TIVA). Correlations between ExP concentrations and NI and predicted plasma propofol concentrations (using pediatric pharmacokinetic models Kataria and Paedfusor) were assessed using Pearson correlation and regression analysis.ResultsNear-patient positioning of breathing system filters led to continuously rising exP values when exP was measured proximal to the filters, and lower concentrations when exP was measured distal to the filters. The breathing system filters were therefore subsequently attached between the breathing system tubes and the inspiratory and expiratory limbs of the anesthetic machine. ExP concentrations significantly correlated with NI and propofol concentrations predicted by pharmacokinetic models during induction and maintenance of anesthesia. During emergence, exP significantly correlated with predicted propofol concentrations, but not with NI.ConclusionIn this study, we demonstrated that exP correlates with calculated propofol concentrations and NI during induction and maintenance in pediatric patients. However, the correlations are highly variable and there are substantial obstacles: Without patient proximal placement of filters, the breathing circuit tubing must be changed after each patient, and furthermore, during ventilation, a considerable additional loss of heat and moisture can occur. Adhesion of propofol to plastic parts (endotracheal tube, breathing circle) may especially be problematic during emergence.Trial RegistrationThe study was registered in the German registry of clinical studies (DRKS-ID: DRKS00015795).

Highlights

  • Total intravenous anesthesia (TIVA) has over the years been demonstrated to have many advantages in pediatric anesthesia, with decreased postoperative emergence agitation compared to volatile anesthetics, and a major reduction in postoperative nausea and vomiting [1, 2]

  • We investigated the correlation between exhaled propofol (exP) and EEG-based monitoring as well as propofol plasma concentrations calculated using pediatric pharmacokinetic models in pediatric anesthesia

  • We studied the impact of three different sizes of filters

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Summary

Introduction

Total intravenous anesthesia (TIVA) has over the years been demonstrated to have many advantages in pediatric anesthesia, with decreased postoperative emergence agitation compared to volatile anesthetics, and a major reduction in postoperative nausea and vomiting [1, 2]. Electroencephalography (EEG) based monitoring can provide cerebral pharmacodynamic feedback of the hypnotic effect, but drug concentrations may only be estimated from pharmacokinetic models. Exhaled propofol (exP) measurements may reflect a real-time estimation of plasma concentration and can be useful in the clinical setting. It has been demonstrated that there is a good correlation between EEG-based anesthesia depth and exP concentrations in adults [3]. We investigated the correlation between exP and EEG-based monitoring as well as propofol plasma concentrations calculated using pediatric pharmacokinetic models in pediatric anesthesia. Exhaled propofol concentrations correlate with propofol concentrations in adult human blood and the brain tissue of rats, as well as with electroencephalography (EEG) based indices of anesthetic depth. We investigated correlations between exhaled propofol (exP) concentrations and the Narkotrend Index (NI) as well as calculated propofol plasma concentrations

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