Patient-maintained propofol sedation using reaction time monitoring: a volunteer safety study

被引:8
|
作者
Allam, S. [1 ]
Anderson, K. J. [2 ]
O'Brien, C. [3 ]
Macpherson, J. A. [4 ]
Gambhir, S. [5 ]
Leitch, J. A. [6 ]
Kenny, G. N. C. [7 ]
机构
[1] Forth Valley Royal Hosp, Dept Anaesthesia, Larbert, Scotland
[2] Foothills Med Ctr, Dept Anaesthesia, Calgary, AB, Canada
[3] Univ Glasgow, Sch Dent, Glasgow, Lanark, Scotland
[4] Liverpool Univ Dent Hosp, Liverpool, Merseyside, England
[5] Hairmyres Hosp, E Kilbride, Lanark, Scotland
[6] Scottish Govt, Qual Unit, Edinburgh, Midlothian, Scotland
[7] Univ Glasgow, Glasgow Royal Infirm, Dept Anaesthesia, Glasgow G31 2ER, Lanark, Scotland
关键词
UPPER GASTROINTESTINAL ENDOSCOPY; TARGET-CONTROLLED INFUSION; CONTROLLED SYSTEM; PREMEDICATION; MIDAZOLAM; SURGERY; OXYGEN;
D O I
10.1111/anae.12036
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Previous volunteer studies of an effect-site controlled, patient-maintained sedation system using propofol have demonstrated a risk of over-sedation. We have incorporated a reaction-time monitor into the handset of the patient-maintained sedation system to add an individualised patient-feedback mechanism. This study assessed if such reaction-time feedback modification would reduce the risk of over-sedation in 20 healthy volunteers deliberately attempting to over-administer themselves propofol. All the volunteers successfully sedated themselves without reaching any unsafe endpoints. All volunteers maintained verbal contact throughout, in accordance with the definition of conscious sedation. The mean (SD) lowest SpO2 was 97 (1.7) % when breathing room air and no volunteer required supplementary oxygen. The mean (SD) maximum effect-site propofol concentration reached was 1.7 (0.4) mu g center dot ml-1. The present system was found to be safer than its predecessors, allowing conscious sedation, but preventing over-sedation.
引用
收藏
页码:154 / 158
页数:5
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