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1.
Acta Anaesthesiol Scand ; 58(8): 933-41, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24995461

ABSTRACT

BACKGROUND: The objective of the present study was to validate the qCON index of hypnotic effect and the qNOX index of nociception. Both indices are derived from the frontal electroencephalogram (EEG) and implemented in the qCON 2000 monitor (Quantium Medical, Barcelona, Spain). METHODS: The study was approved by the local ethics committee, including data from 60 patients scheduled for ambulatory surgery undergoing general anaesthesia with propofol and remifentanil, using TCI. The Bis (Covidien, Boulder, CO, USA) was recorded simultaneously with the qCON. Loss of eyelash reflex [loss of consciousness (LOC)] was recorded, and prediction probability for Bis and qCON was calculated. Movement as a response to noxious stimulation [laryngeal mask airway (LMA) insertion, laryngoscopy and tracheal intubation] was registered. The correlation coefficient between qCON and Bis was calculated. The patients were divided into movers/non-movers as a response to noxious stimulation. A paired t-test was used to assess significant difference for qCON and qNOX for movers/non-movers. RESULTS: The prediction probability (Pk) and the standard error (SE) for qCON and Bis for detecting LOC was 0.92 (0.02) and 0.94 (0.02) respectively (t-test, no significant difference). The R between qCON and Bis was 0.85. During the general anaesthesia (Ce propofol > 2 µg/ml, Ce remifentanil > 2 ng/ml), the mean value and standard deviation (SD) for qCON was 45 (8), while for qNOX it was 40 (6). The qNOX pre-stimuli values were significantly different (P < 0.05) for movers/non-movers as a response to LMA insertion [62.5 (24.0) vs. 45.5 (24.1)], tracheal intubation [58.7 (21.8) vs. 41.4 (20.9)], laryngoscopy [54.1 (21.4) vs. 41.0 (20.8)]. There were no significant differences in remifentanil or propofol effect-site concentrations for movers vs. non-movers. CONCLUSION: The qCON was able to reliably detect LOC during general anaesthesia with propofol and remifentanil. The qNOX showed significant overlap between movers and non-movers, but it was able to predict whether or not the patient would move as a response to noxious stimulation, although the anaesthetic concentrations were similar.


Subject(s)
Anesthesia, General , Electroencephalography , Monitoring, Intraoperative/methods , Nociception/physiology , Unconsciousness/physiopathology , Ambulatory Surgical Procedures/adverse effects , Analgesics/pharmacology , Anesthetics, General/pharmacology , Consciousness Monitors , Dyskinesias , Electroencephalography/instrumentation , Humans , Hypnotics and Sedatives/pharmacology , Intraoperative Awareness/diagnosis , Intraoperative Awareness/physiopathology , Intraoperative Awareness/prevention & control , Intubation, Intratracheal/adverse effects , Laryngeal Masks , Laryngoscopy/adverse effects , Monitoring, Intraoperative/instrumentation , Monitoring, Intraoperative/statistics & numerical data , Nociception/drug effects , Pain/etiology , Pain/physiopathology , Pain/prevention & control , Piperidines/pharmacology , Propofol/pharmacology , Reflex/drug effects , Remifentanil , Unconsciousness/chemically induced
2.
Anesth Analg ; 112(2): 331-9, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21131550

ABSTRACT

BACKGROUND: The increasing demand for anesthetic procedures in the gastrointestinal endoscopy area has not been followed by a similar increase in the methods to provide and control sedation and analgesia for these patients. In this study, we evaluated different combinations of propofol and remifentanil, administered through a target-controlled infusion system, to estimate the optimal concentrations as well as the best way to control the sedative effects induced by the combinations of drugs in patients undergoing ultrasonographic endoscopy. METHODS: One hundred twenty patients undergoing ultrasonographic endoscopy were randomized to receive, by means of a target-controlled infusion system, a fixed effect-site concentration of either propofol or remifentanil of 8 different possible concentrations, allowing adjustment of the concentrations of the other drug. Predicted effect-site propofol (C(e)pro) and remifentanil (C(e)remi) concentrations, parameters derived from auditory evoked potential, autoregressive auditory evoked potential index (AAI/2) and electroencephalogram (bispectral index [BIS] and index of consciousness [IoC]) signals, as well as categorical scores of sedation (Ramsay Sedation Scale [RSS] score) in the presence or absence of nociceptive stimulation, were collected, recorded, and analyzed using an Adaptive Neuro Fuzzy Inference System. The models described for the relationship between C(e)pro and C(e)remi versus AAI/2, BIS, and IoC were diagnosed for inaccuracy using median absolute performance error (MDAPE) and median root mean squared error (MDRMSE), and for bias using median performance error (MDPE). The models were validated in a prospective group of 68 new patients receiving different combinations of propofol and remifentanil. The predictive ability (P(k)) of AAI/2, BIS, and IoC with respect to the sedation level, RSS score, was also explored. RESULTS: Data from 110 patients were analyzed in the training group. The resulting estimated models had an MDAPE of 32.87, 12.89, and 8.77; an MDRMSE of 17.01, 12.81, and 9.40; and an MDPE of -1.86, 3.97, and 2.21 for AAI/2, BIS, and IoC, respectively, in the absence of stimulation and similar values under stimulation. P(k) values were 0.82, 0.81, and 0.85 for AAI/2, BIS, and IoC, respectively. The model predicted the prospective validation data with an MDAPE of 34.81, 14.78, and 10.25; an MDRMSE of 16.81, 15.91, and 11.81; an MDPE of -8.37, 5.65, and -1.43; and P(k) values of 0.81, 0.8, and 0.8 for AAI/2, BIS, and IoC, respectively. CONCLUSION: A model relating C(e)pro and C(e)remi to AAI/2, BIS, and IoC has been developed and prospectively validated. Based on these models, the (C(e)pro, C(e)remi) concentration pairs that provide an RSS score of 4 range from (1.8 µg·mL(-1), 1.5 ng·mL(-1)) to (2.7 µg·mL(-1), 0 ng·mL(-1)). These concentrations are associated with AAI/2 values of 25 to 30, BIS of 71 to 75, and IoC of 72 to 76. The presence of noxious stimulation increases the requirements of C(e)pro and C(e)remi to achieve the same degree of sedative effects.


Subject(s)
Analgesics, Opioid/administration & dosage , Endoscopy, Gastrointestinal , Endosonography , Fuzzy Logic , Hypnotics and Sedatives/administration & dosage , Piperidines/administration & dosage , Propofol/administration & dosage , Adult , Aged , Aged, 80 and over , Consciousness/drug effects , Consciousness Monitors , Dose-Response Relationship, Drug , Drug Dosage Calculations , Electroencephalography , Endoscopy, Gastrointestinal/adverse effects , Endosonography/adverse effects , Evoked Potentials, Auditory/drug effects , Female , Humans , Infusion Pumps , Male , Middle Aged , Pain Threshold/drug effects , Predictive Value of Tests , Prospective Studies , Remifentanil , Reproducibility of Results , Spain , Young Adult
3.
Article in English | MEDLINE | ID: mdl-18003368

ABSTRACT

Subjects with ischemic dilated cardiomiopathy tend to suffer episodes of sudden cardiac death, thus risk stratification is essential to establish an adequate therapy for the patients. In this work, a new methodology was proposed for the study of the heart rate variability by using a multiscale analysis based on the concept of entropy rates, for improving risk prediction in cardiac patients. Symbolic dynamics were applied to RR time series and sets of words in several scales were constructed. The multiscale regularity analysis was proposed by comparing the entropies, calculated using Shannon and Renyi definitions, of the series of words in different scales. The study considered the selection of the best parameters for the length of the words (l) and the order of the entropies (q). Statistical analysis with repeated measures and discriminant analysis revealed statistically significant differences (p-value<0.05) and a high percentage of well classified subjects in their different risk groups, with sensitivity, specificity and positive predictive values of 100%.


Subject(s)
Arrhythmias, Cardiac/diagnosis , Arrhythmias, Cardiac/mortality , Cardiomyopathy, Dilated/diagnosis , Cardiomyopathy, Dilated/mortality , Death, Sudden, Cardiac/epidemiology , Heart Rate , Risk Assessment/methods , Comorbidity , Death, Sudden, Cardiac/prevention & control , Diagnosis, Computer-Assisted/methods , Electrocardiography, Ambulatory/methods , Female , Humans , Male , Proportional Hazards Models , Reproducibility of Results , Risk Factors , Sensitivity and Specificity , Spain/epidemiology , Survival Analysis , Survival Rate
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