Fractional order impedance models as rising tools for quantification of unconscious analgesia

This research focuses on modeling the diffusion process that occurs in the human body when an analgesic drug is taken up, by using fractional-order impedance models (FOIMs). We discuss the measurement of a suitable feedback signal that can be used in a model-based control strategy. With this knowledge an early dawn concept of a pain sensor is presented. The major challenges that are encountered during this development consist of identification of the patient model, validation of the pain sensor and validation of the effect of the analgesic drug

CLOSED-LOOP CONTROLLED TOTAL INTRA VENOUS ANAESTHESIA

Anaesthesia is important for both surgery and intensive care and intravenous anaesthetics are widely used to provide rapid onset, stable maintenance, and rapid recovery compared with inhaled anaesthetics. The aim of the project on which this thesis is based was to investigate a reliable and safe methodology for delivering total intravenous anaesthesia using closed-loop control technology and bispectral analysis of human electroencephalogram (EEG) waveform. In comparison with Target Controlled Infusion (TCI), drug effect is measured during drug infusion in closed loop anaesthesia (CLAN). This may provide superior safety, better patient care, and better quality of anaesthesia whilst relieving the clinician of the need to make recurrent and minor alterations to drug administration. However, the development of a CLAN system has been hindered by the Jack of a 'gold standard' for anaesthetic states and difficulties with patient variability in pharmacokinetic and pharmacodynamic modelling, and a new and generic mathematical model of a closed-loop anaesthesia system was developed for this investigation. By using this CLAN model, investigations on pharmacokinetic and pharmacodynamic variability existing in patients were carried out. A new control strategy that combines a Proportional, Integral, Derivative (PID) controller, bispectral analysis of EEG waveform and pharmacokinetic/ pharmacodynamic models was investigated. Based on the mathematical model, a prototype CLAN system, the first CLAN system capable of delivering both hypnotics and analgesics simultaneously for total intravenous anaesthesia, was developed. A Bispectral Index (BIS), derived from power spectral and bispectral analysis on EEG waveform, is used to measure depth of anaesthesia. A supervision system with built-in digital signal processing techniques was developed to compensate the non-linear characteristics inherent in the system while providing a comprehensive protection mechanism for patient safety. The CLAN system was tested in 78125 virtual patients modelled using published data. Investigations on intravenous anaesthesia induction and maintenance with the CLAN system were carried out in various clinical settings on 21 healthy volunteers and 15 patients undergoing surgery. Anaesthesia targets were achieved quickly and well maintained in all volunteers/patients except for 2 patients with clinically satisfactory anaesthesia quality.Derriford Hospita

In vivo investigations of photoplethysmograms and arterial oxygen saturation from the auditory canal in conditions of compromised peripheral perfusion

Pulse oximeters rely on the technique of photoplethysmography (PPG) to estimate arterial oxygen saturation (SpO2). In conditions of poor peripheral perfusion such as hypotension, hypothermia, and vasoconstriction, the PPG signals detected are often small and noisy, or in some cases unobtainable. Hence, pulse oximeters produce erroneous SpO2 readings in these circumstances. The problem arises as most commercial pulse oximeter probes are designed to be attached to peripheral sites such as the finger or toes, which are easily affected by vasoconstriction. In order to overcome this problem, the ear canal was investigated as an alternative site for measuring reliable SpO2 on the hypothesis that blood flow to this central site is preferentially preserved. Novel miniature ear canal PPG sensors were developed along with a state of the art PPG processing unit and a data acquisition system to allow for PPG measurements from different depths and surfaces of the ear canal. A preliminary in vivo investigation on seven healthy volunteers has revealed that good quality PPG signals with high amplitude can be obtained from the posterior surface of the outer ear canal. Based on these observations, a second prototype probe suitable for acquisition of PPGs from the posterior surface of the outer ear canal was developed. A pilot study was then carried out on 15 healthy volunteers to validate the feasibility of measuring PPGs and SpO2 from the ear canal in conditions of induced local peripheral vasoconstriction (right hand immersion in ice water). The PPG signals acquired from the ear canal probe were compared with those obtained simultaneously from finger probes attached to the left and the right index fingers. Significant drop (p 45%) and right (> 50%) index fingers during the ice water immersion, while good quality PPG signals with relatively constant amplitude were obtained from the ear canal. Also, the SpO2 values showed that the ear canal pulse oximeter performed better than the two finger pulse oximeters (mean failure rate 30%). A second in vivo investigation was carried out in 15 healthy volunteers, where hypoperfusion was induced more naturally by exposing the volunteer to cold temperatures of 10C for 10min. Normalised Pulse Amplitude (NPA) and SpO2 was calculated from the PPG signals acquired from the ear canal, the finger and the earlobe. By the end of the cold exposure, a mean drop of > 80% was found in the NPA of finger PPGs. The % drop in the NPA of red and infrared earlobe PPG signals was 20% and 26% respectively. Contrarily to both these sites, the NPA of the ear canal PPGs had only dropped by 0.2% and 13% respectively. The SpO2 estimated from the finger sensor was below 90% in 5 volunteers (failure) by the end of the cold exposure. The earlobe pulse oximeter failed in 3 volunteers. The ear canal sensor on the other hand had only failed in 1 volunteer. These results strongly suggest that the ear canal may be used as a suitable alternative site for reliable monitoring of PPGs and SpO2 in cases of compromised peripheral perfusion

Front Lines of Thoracic Surgery

Front Lines of Thoracic Surgery collects up-to-date contributions on some of the most debated topics in today's clinical practice of cardiac, aortic, and general thoracic surgery,and anesthesia as viewed by authors personally involved in their evolution. The strong and genuine enthusiasm of the authors was clearly perceptible in all their contributions and I'm sure that will further stimulate the reader to understand their messages. Moreover, the strict adhesion of the authors' original observations and findings to the evidence base proves that facts are the best guarantee of scientific value. This is not a standard textbook where the whole discipline is organically presented, but authors' contributions are simply listed in their pertaining subclasses of Thoracic Surgery. I'm sure that this original and very promising editorial format which has and free availability at its core further increases this book's value and it will be of interest to healthcare professionals and scientists dedicated to this field

Separator fluid volume requirements in multi-infusion settings

INTRODUCTION. Intravenous (IV) therapy is a widely used method for the administration of medication in hospitals worldwide. ICU and surgical patients in particular often require multiple IV catheters due to incompatibility of certain drugs and the high complexity of medical therapy. This increases discomfort by painful invasive procedures, the risk of infections and costs of medication and disposable considerably. When different drugs are administered through the same lumen, it is common ICU practice to flush with a neutral fluid between the administration of two incompatible drugs in order to optimally use infusion lumens. An important constraint for delivering multiple incompatible drugs is the volume of separator fluid that is sufficient to safely separate them. OBJECTIVES. In this pilot study we investigated whether the choice of separator fluid, solvent, or administration rate affects the separator volume required in a typical ICU infusion setting. METHODS. A standard ICU IV line (2m, 2ml, 1mm internal diameter) was filled with methylene blue (40 mg/l) solution and flushed using an infusion pump with separator fluid. Independent variables were solvent for methylene blue (NaCl 0.9% vs. glucose 5%), separator fluid (NaCl 0.9% vs. glucose 5%), and administration rate (50, 100, or 200 ml/h). Samples were collected using a fraction collector until <2% of the original drug concentration remained and were analyzed using spectrophotometry. RESULTS. We did not find a significant effect of administration rate on separator fluid volume. However, NaCl/G5% (solvent/separator fluid) required significantly less separator fluid than NaCl/NaCl (3.6 ± 0.1 ml vs. 3.9 ± 0.1 ml, p <0.05). Also, G5%/G5% required significantly less separator fluid than NaCl/NaCl (3.6 ± 0.1 ml vs. 3.9 ± 0.1 ml, p <0.05). The significant decrease in required flushing volume might be due to differences in the viscosity of the solutions. However, mean differences were small and were most likely caused by human interactions with the fluid collection setup. The average required flushing volume is 3.7 ml. CONCLUSIONS. The choice of separator fluid, solvent or administration rate had no impact on the required flushing volume in the experiment. Future research should take IV line length, diameter, volume and also drug solution volumes into account in order to provide a full account of variables affecting the required separator fluid volume

Modern Developments in Transcranial Magnetic Stimulation (TMS) – Applications and Perspectives in Clinical Neuroscience

Transcranial magnetic stimulation (TMS) is being increasingly used in neuroscience and clinics. Modern advances include but are not limited to the combination of TMS with precise neuronavigation as well as the integration of TMS into a multimodal environment, e.g., by guiding the TMS application using complementary techniques such as functional magnetic resonance imaging (fMRI), electroencephalography (EEG), diffusion tensor imaging (DTI), or magnetoencephalography (MEG). Furthermore, the impact of stimulation can be identified and characterized by such multimodal approaches, helping to shed light on the basic neurophysiology and TMS effects in the human brain. Against this background, the aim of this Special Issue was to explore advancements in the field of TMS considering both investigations in healthy subjects as well as patients