Bispectral index and propofol +/- ketamine anesthesia

Citation
T. Sakai et al., Bispectral index and propofol +/- ketamine anesthesia, INT CONGR S, 1168, 1998, pp. 123-128
Categorie Soggetti
Current Book Contents
ISSN journal
05315131
Volume
1168
Year of publication
1998
Pages
123 - 128
Database
ISI
SICI code
0531-5131(1998)1168:<123:BIAP+K>2.0.ZU;2-V
Abstract
Background. We studied the relationship between the clinical endpoints of u nresponsiveness to verbal commands (UVC), loss of eyelash reflex (LER), and inhibition of body movement response and/or sneezing to mechanical nasal m embrane stimulation (INBMR) vs. the processed EEG variables. Methods. A total of 48 patients were randomized to receive either propofol infusion, 30 mg . kg(-1). h(-1) (group P) or ketamine bolus, 0.25, 0.5 or 0 .75 mg i.v., followed by propofol infusion, 30 mg . kg(-1). h(-1) and varia ble dose ketamine infusion, 0.25, 0.5 or 0.75 mg . kg(-1). h(-1) (groups PK 0.25, PK0.5 and PK0.75) until UVC, LER and INBMR. Results. Propofol infusion, 30 mg . kg(-1). h(-1), induced UVC, LER and INB MR at bispectral index (BIS): 96.7 +/- 1.7, 63.1 +/- 9.1 and 33.3 +/- 7.2; 95% spectral edge frequency (SEF): 17.4 +/- 3.3, 16.8 +/- 3.9 and 13.9 +/- 2.7; and median frequency (MF) values of 4.8 +/- 2.4, 4.8 +/- 2.5 and 3.2 /- 1.6 (mean +/- SD), respectively. Ketamine supplementation in groups PK0. 5 and PK0.75 reduced the propofol dose requirement and achieved the clinica l endpoints at higher BIS and 95% SEF values with lower propofol concentrat ions as compared to groups P and PK0.25 (9.9 +/- 5.8 and 9.4 +/- 3.4 vs. 13 .4 +/- 4.5 and 14 +/- 5.8 mu g . ml(-1)). Conclusions. Our results suggest additive interaction between propofol and ketamine for achieving the clinical (hypnotic) endpoints. The paradoxically higher BIS and 95% SEF values at clinical endpoints with ketamine suppleme ntation of propofol may be due to either lower plasma propofol concentratio ns and/or excitatory effects of ketamine.