SURGICAL STIMULATION INDUCES CHANGES IN BRAIN ELECTRICAL-ACTIVITY DURING ISOFLURANE NITROUS-OXIDE ANESTHESIA - A TOPOGRAPHIC ELECTROENCEPHALOGRAPHIC ANALYSIS

被引:101
作者
KOCHS, E
BISCHOFF, P
PICHLMEIER, U
AMESCH, JS
机构
[1] UNIV HAMBURG, HOSP EPPENDORF, DEPT ANESTHESIOL, W-2000 HAMBURG, GERMANY
[2] UNIV HAMBURG, HOSP EPPENDORF, DEPT MATH & COMP SCI, W-2000 HAMBURG, GERMANY
关键词
ANESTHETICS; GASES; NITROUS OXIDE; VOLATILE; ISOFLURANE; MONITORING; ELECTROENCEPHALOGRAPHY BRAIN ELECTRICAL ACTIVITY MAPPING; SURGERY; ABDOMINAL;
D O I
10.1097/00000542-199405000-00012
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: The aim of this study was to investigate topographic changes hn electroencephalographic (EEG) power and frequency Induced by abdominal surgery during anesthesia with 0.6% or 1.2% isoflurane in 66% nitrous oxide. Methods: Forty-six patients (aged 41+/-13 yr) scheduled for elective abdominal surgery were studied. The trachea of each patient was intubated and the lungs ventilated. patients were randomly assigned to one of four groups: anesthesia was maintained with 0.6% (group 1, n=12; group 2, n=11) or 1.2% end-tidal isoflurane (group 3, n=12; group 4, n=11) in 66% nitrous oxide. Data were recorded over 20 min. Groups 1 and 3 were studied without surgery (as controls). In groups 2 and 4 recording was started 6 min before skin incision. The EEG was acquired via 17 scalp electrodes placed in standard International 10-20 locations (reference C-2). Absolute and relative power densities were calculated hn selected frequency bands. EEG maps of spectral power densities were coded according to a continuous color spectrum. Results:During baseline recordings, alpha activity was dominant at frontal areas In groups 1 and 2. In comparison, in groups 3 and 4, delta and theta activities were dominant at frontal leads. In group 2, the start of surgery resulted in Increases In delta activity and decreases In alpha activity that were most dominant frontally (delta +181% and alpha -61%, 4). The delta shift was attenuated at 1.2% isoflurane (group 4, delta +44%, F-3), but decreases hn alpha activity (-53%, F,) were comparable to those Ln group 2. The EEG response in all frequency bands was attenuated at parietotemporal recording sites at both isoflurane concentrations. Conclusions: The current data demonstrate graded EEG responses induced by abdominal surgery during anesthesia with 0.6% or 1.2% isoflurane in 66% nitrous oxide. Spatial heterogeneities In absolute spectral power densities were reflected by color changes in the EEG maps. The topographic EEG analysis indicates that these changes were most dominant at frontal areas. The increases in delta and decreases hn alpha activities may be related to intraoperative ''paradoxical'' electrophysiologic arousal phenomena.
引用
收藏
页码:1026 / 1034
页数:9
相关论文
共 36 条
[11]   BRAIN ELECTRICAL-ACTIVITY MAPPING (BEAM) - METHOD FOR EXTENDING THE CLINICAL UTILITY OF EEG AND EVOKED-POTENTIAL DATA [J].
DUFFY, FH ;
BURCHFIEL, JL ;
LOMBROSO, CT .
ANNALS OF NEUROLOGY, 1979, 5 (04) :309-321
[12]   ELECTROENCEPHALOGRAPHIC MAPPING DURING ISOFLURANE ANESTHESIA FOR TREATMENT OF MENTAL DEPRESSION [J].
ENGELHARDT, W ;
CARL, G ;
DIERKS, T ;
MAURER, K .
JOURNAL OF CLINICAL MONITORING, 1991, 7 (01) :23-29
[13]   PATTERNS OF AROUSAL IN COMATOSE PATIENTS [J].
EVANS, BM .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1976, 39 (04) :392-402
[14]   EVALUATION OF THE TRADITIONAL SIGNS AND STAGES OF ANESTHESIA - AN ELECTROENCEPHALOGRAPHIC AND CLINICAL STUDY [J].
GALLA, SJ ;
ROCCO, AG ;
VANDAM, LD .
ANESTHESIOLOGY, 1958, 19 (03) :328-338
[15]   THIOPENTAL PHARMACODYNAMICS .2. QUANTITATION OF CLINICAL AND ELECTROENCEPHALOGRAPHIC DEPTH OF ANESTHESIA [J].
HUNG, OR ;
VARVEL, JR ;
SHAFER, SL ;
STANSKI, DR .
ANESTHESIOLOGY, 1992, 77 (02) :237-244
[16]   EEG SYNCHRONIZATION INDUCED BY HIGH FREQUENCY MIDBRAIN RETICULAR STIMULATION IN ANESTHETIZED CATS [J].
KAADA, BR ;
THOMAS, F ;
ALNAES, E ;
WESTER, K .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1967, 22 (03) :220-+
[17]  
KIERSEY D K, 1951, Br J Anaesth, V23, P141, DOI 10.1093/bja/23.3.141
[18]  
KING EE, 1956, J PHARMACOL EXP THER, V116, P404
[19]  
Lehmann D, 1987, HDB ELECTROENCEPHALO, P309