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Zhongguo Wei Zhong Bing Ji Jiu Yi Xue · Apr 2011
Randomized Controlled Trial Comparative Study[A comparison of bispectral index and sedation agitation scale in guiding sedation therapy: a randomized controlled study in patients undergoing short term mechanical ventilation].
- Dong Zhao, Yuan Xu, Wei He, Tong Li, and Yin He.
- Department of Intensive Care Unit, Beijing Tongren Hospital, Capital Medical University , Beijing 100730, China.
- Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2011 Apr 1;23(4):220-3.
ObjectiveTo compare the value of bispectral index (BIS) monitoring and sedation agitation scale (SAS) in guiding intensive care unit (ICU) sedation therapy for the patients undergoing short term mechanical ventilation.MethodsOne hundred and five patients aged 18-60 years after operation receiving mechanical ventilation for longer than 12 hours in ICU were enrolled in this study. The patients were randomly divided into two groups: BIS guided group (n=42) and SAS guided group (n=63). All of them received protocolized continuous sedation and analgesia by using fentanyl for analgesia and propofol plus midazolam to sedate intravenously. The effect of sedation was assessed every hour till BIS reaching 50-70 or SAS reaching grade 3-4. Sedatives and analgesics were suspended at 6:00 am on next day after ICU admission , and BIS and the SAS were recorded every hour, sedation time, time to wake up, duration of mechanical ventilation, daily dosage of midazolam and propofol, and the incidence of adverse events including restlessness after suction, endotracheal tube resistance, pain tolerance during sedation, and delirium after extubation were all recorded accordingly.ResultsDosages of midazolam and propofol were found higher in BIS guided group than the SAS guided group [midazolam (mg×kg(-1) ×h(-1) ): 0.10±0.02 vs. 0.09±0.02, propofol (mg×kg(-1) ×h(-1) ): 0.95±0.23 vs. 0.86±0.20, both P<0.05]. The total time (D t) of patients under sedative control was significantly longer in BIS guided group compared with SAS guided group, and also in first three hours [D 1, D 2, D 3, D t: 75.2% (507) vs. 52.8% (421), D 1: 78.6% (33) vs. 22.2% (14), D 2: 88.1% (37) vs. 20.6% (13), D 3: 81.0% (34) vs. 31.7% (20), all P<0.01]. The time to wake up (minutes) was significantly shorter in BIS guided group compared with SAS guided group [0 (0, 20) vs. 15 (0, 47), P<0.05]. No significant difference in acute physiology and chronic health evaluation II (APACHE II) score (3.57±2.60 vs. 4.19±2.30), duration of mechanical ventilation [hours: 16.5 (14.5, 19.0) vs. 17.0 (15.0, 19.0)], sedation time [hours: 14.0 (12.9, 17.1) vs. 16.0 (13.0, 18.0)] and incidence of adverse events including restlessness after suction (81.0% vs. 79.4%), endotracheal tube resistance (71.4% vs. 74.6%), pain tolerance during sedation (92.8% vs. 93.6%) and delirium after extubation (4.8% vs. 1.6%) was found between BIS guided group and SAS guided group (all P>0.05).ConclusionBIS monitoring is better in sedative control than SAS assessment for ICU patients undergoing short term mechanical ventilation.
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