期刊
BRITISH JOURNAL OF ANAESTHESIA
卷 107, 期 5, 页码 735-741出版社
OXFORD UNIV PRESS
DOI: 10.1093/bja/aer227
关键词
bispectral index; cerebral blood flow; cerebral oxygen saturation; laser-Doppler flowmetry; neuromonitoring; oximetry; propofol
资金
- German Society of Anaesthesiology and Intensive Care Medicine (Deutsche Gesellschaft fur Anasthesiologie und Intensivmedizin e.V., DGAI)
Background. Propofol reduces cerebral blood flow (CBF) secondary to cerebral metabolic depression. However, in vitro and in vivo studies demonstrate that propofol directly dilates the vascular smooth muscle. This study investigates the effects of propofol-induced changes in bispectral index (BIS) on cerebral microcirculation and oxygenation during craniotomies. Methods. In 21 craniotomy patients undergoing routine craniotomy, anaesthesia was maintained with propofol 4-10 mg kg(-1) h(-1) and remifentanil 0.1-0.4 mg kg(-1) min-1. Propofol concentration was adjusted to achieve higher BIS (target 40) or lower BIS (target 20). Regional measurements of capillary venous blood flow (rvCBF), oxygen saturation (srvO(2)), and haemoglobin amount (rvHb) at 2 mm (grey matter) and 8 mm (white matter) cerebral depth were randomly performed at higher and lower BIS by combined laser-Doppler flowmetry and spectroscopy. Calculations: approximated arteriovenous difference in oxygen content (avDO(2)) and cerebral metabolic rate of oxygen (aCMRO(2)). Results: mean values (SD). Statistics: Mann-Whitney test (*P<0.05). Results. Human cerebral microcirculation and oxygen saturation were assessed at propofol dosages 5.1 (2.3) mg kg(-1) h(-1) [BIS 40 (9)] and 7.8 (2.1) mg kg(-1) h(-1) [BIS-1 (7)]. Propofol-induced reduction in BIS resulted in increased srvO(2) (P=0.018), and decreased avDO(2) (P=0.025) and aCMRO(2) (P=0.022), in 2 mm cerebral depth, while rvCBF and rvHb remained unchanged. In 8 mm cerebral depth, srvO(2), rvCBF, rvHb, and also calculated parameters avDO(2) and aCMRO(2) remained unaltered. Conclusions. Findings suggest alteration of the CBF/CMRO(2) ratio by propofol in cortical brain regions; therefore, it might be possible that propofol affects coupling of flow and metabolism in the cerebral microcirculation.
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