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  • 1
    In: Anesthesiology, Ovid Technologies (Wolters Kluwer Health), Vol. 108, No. 1 ( 2008-01-01), p. 63-70
    Abstract: The aim was to evaluate the performance of anesthesia depth monitors, Bispectral Index (BIS) and Entropy, during single-agent xenon anesthesia in 17 healthy subjects. Methods After mask induction with xenon and intubation, anesthesia was continued with xenon only. BIS, State Entropy and Response Entropy, and electroencephalogram were monitored throughout induction, steady-state anesthesia, and emergence. The performance of BIS, State Entropy, and Response Entropy were evaluated with prediction probability, sensitivity, and specificity analyses. The power spectrum of the raw electroencephalogram signal was calculated. Results The mean (SD) xenon concentration during anesthesia was 66.4% (2.4%). BIS, State Entropy, and Response Entropy demonstrated low prediction probability values at loss of response (0.455, 0.656, and 0.619) but 1 min after that the values were high (0.804, 0.941, and 0.929). Thereafter, equally good performance was demonstrated for all indices. At emergence, the prediction probability values to distinguish between steady-state anesthesia and return of response for BIS, State Entropy, and Response Entropy were 0.988, 0.892, and 0.992. No statistical differences between the performances of the monitors were observed. Quantitative electroencephalogram analyses showed generalized increase in total power (P & lt; 0.001), delta (P & lt; 0.001) and theta activity (P & lt; 0.001), and increased alpha activity (P = 0.003) in the frontal brain regions. Conclusions Electroencephalogram-derived depth of sedation indices BIS and Entropy showed a delay to detect loss of response during induction of xenon anesthesia. Both monitors performed well in distinguishing between conscious and unconscious states during steady-state anesthesia. Xenon-induced changes in electroencephalogram closely resemble those induced by propofol.
    Type of Medium: Online Resource
    ISSN: 0003-3022
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2008
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  • 2
    In: Anesthesiology, Ovid Technologies (Wolters Kluwer Health), Vol. 99, No. 3 ( 2003-09-01), p. 614-623
    Abstract: Animal experiments have demonstrated neuroprotection by ketamine. However, because of its propensity to increase cerebral blood flow, metabolism, and intracranial pressure, its use in neurosurgery or trauma patients has been questioned. Methods 15O-labeled water, oxygen, and carbon monoxide were used as positron emission tomography tracers to determine quantitative regional cerebral blood flow (rCBF), metabolic rate of oxygen (rCMRO2), and blood volume (rCBV), respectively, on selected regions of interest of nine healthy male volunteers at baseline and during three escalating concentrations of ketamine (targeted to 30, 100, and 300 ng/ml). In addition, voxel-based analysis for relative changes in rCBF and rCMRO2 was performed using statistical parametric mapping. Results The mean +/- SD measured ketamine serum concentrations were 37 +/- 8, 132 +/- 19, and 411 +/- 71 ng/ml. Mean arterial pressure was slightly elevated (maximally by 15.3%, P & lt; 0.001) during ketamine infusion. Ketamine increased rCBF in a concentration-dependent manner. In the region-of-interest analysis, the greatest absolute changes were detected at the highest ketamine concentration level in the anterior cingulate (38.2% increase from baseline, P & lt; 0.001), thalamus (28.5%, P & lt; 0.001), putamen (26.8%, P & lt; 0.001), and frontal cortex (25.4%, P & lt; 0.001). Voxel-based analysis revealed marked relative rCBF increases in the anterior cingulate, frontal cortex, and insula. Although absolute rCMRO2 was not changed in the region-of-interest analysis, subtle relative increases in the frontal, parietal, and occipital cortices and decreases predominantly in the cerebellum were detected in the voxel-based analysis. rCBV increased only in the frontal cortex (4%, P = 0.022). Conclusions Subanesthetic doses of ketamine induced a global increase in rCBF but no changes in rCMRO2. Consequently, the regional oxygen extraction fraction was decreased. Disturbed coupling of cerebral blood flow and metabolism is, however, considered unlikely because ketamine has been previously shown to increase cerebral glucose metabolism. Only a minor increase in rCBV was detected. Interestingly, the most profound changes in rCBF were observed in structures related to pain processing.
    Type of Medium: Online Resource
    ISSN: 0003-3022
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2003
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  • 3
    In: Anesthesiology, Ovid Technologies (Wolters Kluwer Health), Vol. 100, No. 5 ( 2004-05-01), p. 1065-1071
    Abstract: The authors have recently shown with positron emission tomography that subanesthetic doses of racemic ketamine increase cerebral blood flow but do not affect oxygen consumption significantly. In this study, the authors wanted to assess the effects of racemic ketamine on regional glucose metabolic rate (rGMR) in similar conditions to establish whether ketamine truly induces disturbed coupling between cerebral blood flow and metabolism. Methods 18F-labeled fluorodeoxyglucose was used as a positron emission tomography tracer to quantify rGMR on 12 brain regions of interest of nine healthy male volunteers at baseline and during a 300-ng/ml ketamine target concentration level. In addition, voxel-based analysis was performed for the relative changes in rGMR using statistical parametric mapping. Results The mean +/- SD measured ketamine serum concentration was 326.4+/-86.3 ng/ml. The mean arterial pressure was slightly increased (maximally by 16.4%) during ketamine infusion (P & lt; 0.001). Ketamine increased absolute rGMR significantly in most regions of interest studied. The greatest increases were detected in the thalamus (14.6+/-15.9%; P = 0.029) and in the frontal (13.6+/-13.1%; P = 0.011) and parietal cortices (13.1+/-11.2%; P = 0.007). Absolute rGMR was not decreased anywhere in the brain. The voxel-based analysis revealed relative rGMR increases in the frontal, temporal, and parietal cortices. Conclusions Global increases in rGMR seem to parallel ketamine-induced increases in cerebral blood flow detected in the authors' earlier study. Therefore, ketamine-induced disturbance of coupling between cerebral blood flow and metabolism is highly unlikely. The previously observed decrease in oxygen extraction fraction may be due to nonoxidative glucose metabolism during ketamine-induced increase in glutamate release.
    Type of Medium: Online Resource
    ISSN: 0003-3022
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2004
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  • 4
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 1997
    In:  Anesthesiology Vol. 86, No. 5 ( 1997-05-01), p. 1055-1060
    In: Anesthesiology, Ovid Technologies (Wolters Kluwer Health), Vol. 86, No. 5 ( 1997-05-01), p. 1055-1060
    Abstract: alpha 2-Adrenergic agonists have been shown to reduce anesthetic requirements of other anesthetics, and they may even act as complete anesthetics by themselves at high doses in animal models. The present study was designed to define the interaction of intravenous infusion of dexmedetomidine, an alpha 2-adrenergic agonist, and isoflurane in patients having surgery by using the minimum alveolar concentration (MAC) of isoflurane as the measure of anesthetic potency. Methods Forty-nine women scheduled for abdominal hysterectomy were randomly allocated to receive either a placebo infusion (n = 16) or a two-stage infusion of dexmedetomidine with target plasma concentration of 0.3 ng/ml (n = 17) or 0.6 ng/ml (n = 16). The study drug infusion was commenced 15 min before induction of anesthesia with thiopental and alfentanil and was continued until skin incision. The end-tidal concentration of isoflurane for each patient was predetermined according to the "up-down" method of Dixon, and it was maintained for at least 15 min before the patient's response to skin incision was assessed. Results The MAC of isoflurane was 0.85% end-tidal in the control group, 0.55% end-tidal with the low dose of dexmedetomidine, and 0.45% end-tidal with the high dose of dexmedetomidine. Conclusions The MAC of isoflurane in the control group was lower than that reported previously in similar patients having surgery, probably due to anesthesia induction with thiopental and alfentanil. Nevertheless, with the high dose of dexmedetomidine, the MAC of isoflurane was still 47% less than that without dexmedetomidine.
    Type of Medium: Online Resource
    ISSN: 0003-3022
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 1997
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  • 5
    Online Resource
    Online Resource
    Elsevier BV ; 2000
    In:  Best Practice & Research Clinical Anaesthesiology Vol. 14, No. 2 ( 2000-06), p. 285-292
    In: Best Practice & Research Clinical Anaesthesiology, Elsevier BV, Vol. 14, No. 2 ( 2000-06), p. 285-292
    Type of Medium: Online Resource
    ISSN: 1521-6896
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2000
    detail.hit.zdb_id: 2028818-9
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  • 6
    Online Resource
    Online Resource
    Wiley ; 1991
    In:  Pharmacology & Toxicology Vol. 68, No. 5 ( 1991-05), p. 394-398
    In: Pharmacology & Toxicology, Wiley, Vol. 68, No. 5 ( 1991-05), p. 394-398
    Type of Medium: Online Resource
    ISSN: 0901-9928 , 1600-0773
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 1991
    detail.hit.zdb_id: 2151592-X
    detail.hit.zdb_id: 2027010-0
    SSG: 15,3
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  • 7
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2007
    In:  Anesthesiology Vol. 106, No. 6 ( 2007-06-01), p. 1128-1133
    In: Anesthesiology, Ovid Technologies (Wolters Kluwer Health), Vol. 106, No. 6 ( 2007-06-01), p. 1128-1133
    Abstract: Animal studies have demonstrated a strong neuroprotective property of xenon. Its usefulness in patients with cerebral pathology could be compromised by deleterious effects on regional cerebral blood flow (rCBF). Methods 15O-labeled water was used to determine rCBF in nine healthy male subjects at baseline and during 1 minimum alveolar concentration (MAC) of xenon (63%). Anesthesia was based solely on xenon. Absolute changes in rCBF were quantified using region-of-interest analysis and voxel-based analysis. Results Mean arterial blood pressure and arterial partial pressure for carbon dioxide remained unchanged. The mean (+/-SD) xenon concentration during anesthesia was 65.2+/-2.3%. Xenon anesthesia decreased absolute rCBF by 34.7+/-9.8% in the cerebellum (P & lt;0.001), by 22.8+/-10.4% in the thalamus (P=0.001), and by 16.2+/-6.2% in the parietal cortex (P & lt;0.001). On average, xenon anesthesia decreased absolute rCBF by 11.2+/-8.6% in the gray matter (P=0.008). A 22.1+/-13.6% increase in rCBF was detected in the white matter (P=0.001). Whole-brain voxel-based analysis revealed widespread cortical reductions and increases in rCBF in the precentral and postcentral gyri. Conclusions One MAC of xenon decreased rCBF in several areas studied. The greatest decreases were detected in the cerebellum, the thalamus and the cortical areas. Increases in rCBF were observed in the white matter and in the pre- and postcentral gyri. These results are in clear contradiction with ketamine, another N-methyl-D-aspartate antagonist and neuroprotectant, which induces a general increase in cerebral blood flow at anesthetic concentrations.
    Type of Medium: Online Resource
    ISSN: 0003-3022
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2007
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  • 8
    Online Resource
    Online Resource
    PAGEPress Publications ; 2014
    In:  Multidisciplinary Respiratory Medicine Vol. 9, No. 1 ( 2014-12)
    In: Multidisciplinary Respiratory Medicine, PAGEPress Publications, Vol. 9, No. 1 ( 2014-12)
    Type of Medium: Online Resource
    ISSN: 2049-6958
    Language: English
    Publisher: PAGEPress Publications
    Publication Date: 2014
    detail.hit.zdb_id: 2677839-7
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  • 9
    Online Resource
    Online Resource
    Wiley ; 2014
    In:  Scandinavian Journal of Caring Sciences Vol. 28, No. 4 ( 2014-12), p. 885-894
    In: Scandinavian Journal of Caring Sciences, Wiley, Vol. 28, No. 4 ( 2014-12), p. 885-894
    Abstract: The purpose of this study was to culturally validate three pain measurement instruments [ B ehavioral P ain S cale ( BPS ), the C ritical‐ C are P ain O bservation T ool ( CPOT ) and the N onverbal A dult P ain A ssessment S cale ( NVPS )] for sedated intensive care patients and in doing so to prepare the tools for psychometric testing in the F innish intensive care environment. Background Most patients feel pain during their stay in an intensive care unit. Pain recognition and assessment is the first step towards effective pain management. The BPS , CPOT and NVPS are the most valid and reliable pain assessment instruments developed to objectively assess pain in sedated intensive care patients. Method The translation and cultural adaptation of the instruments were done according to the guidelines of the I nternational S ociety for P harmacoeconomics and O utcomes ( ISPOR ). The process included 10 phases aiming to produce semantically correct F innish versions of the pain assessment instruments. This translation process was chosen due to its rigorousness and systematic approach. Results The 10‐step translation and cultural validation process were successfully conducted, although it was complex and time‐consuming. The resulting F innish versions of the three pain assessment instruments showed good evidence of content and conceptual equivalence. Although further work is needed to test these instruments in the F innish intensive care context, the current F innish versions are potential instruments for clinicians to use. Conclusion Deciding when this high‐quality process is needed requires thorough consideration. However, it is worthwhile to use it when implementing new instruments at a national level. We need a valid, reliable and feasible instrument for pain assessment in sedated intensive care patients in F inland. The next step in our process is conducting psychometric testing of these three instruments to choose the tool with the best properties to be implemented in clinical practice.
    Type of Medium: Online Resource
    ISSN: 0283-9318 , 1471-6712
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2014
    detail.hit.zdb_id: 2031090-0
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  • 10
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2012
    In:  Journal of Clinical Monitoring and Computing Vol. 26, No. 1 ( 2012-2), p. 37-43
    In: Journal of Clinical Monitoring and Computing, Springer Science and Business Media LLC, Vol. 26, No. 1 ( 2012-2), p. 37-43
    Type of Medium: Online Resource
    ISSN: 1387-1307 , 1573-2614
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2012
    detail.hit.zdb_id: 2010139-9
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