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. 2016 Oct 18;2016(10):CD007272. doi: 10.1002/14651858.CD007272.pub2

Summary of findings for the main comparison. Anaesthesia depth monitors (BIS and M‐entropy) versus standard clinical and electronic monitoring.

Anaesthesia depth monitors (BIS and M‐entropy) compared with standard clinical and electronic monitoring
Patient or population: patients with prevention of recall of events during surgery
Settings: All patients undergoing various surgical procedures in hospitals in Europe/Australia/Asia/Middle East/North America
Intervention: anaesthesia depth monitors (BIS, M‐Entropy)
Comparison: standard clinical and electronic monitoring
Outcomes Illustrative comparative risks* (95% CI) Relative effect
 (95% CI) No of participants
 (studies) Quality of the evidence
 (GRADE) Comments
Assumed risk Corresponding risk
Standard clinical and electronic monitoring Anaesthesia depth monitors
Awareness 
 Postoperative interview
 Follow‐up: 1 to 72 days 5 per 1000 5 per 1000
(3 to 7)
OR 0.98
(0.59 to 1.62)
34,744
(9 studies)
⊕⊕⊝⊝
 low1,2
Adverse effects of intraoperative wakefulness and/or postoperative awareness
(i.e. post‐traumatic stress syndrome, myocardial infarction, cardiac arrest, etc.)
Not defined or not identified
*The basis for the assumed risk (e.g. the median control group risk across studies) is provided in footnotes. The corresponding risk (and its 95% confidence interval) is based on the assumed risk in the comparison group and the relative effect of the intervention (and its 95% CI).
 BIS: Bispectral Index; CI: confidence interval; OR: odds ratio
GRADE Working Group grades of evidence
 High quality: Further research is very unlikely to change our confidence in the estimate of effect.
 Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate.
 Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate.
 Very low quality: We are very uncertain about the estimate.

1Inconsistency: downgraded one level for inconsistency of effect. Heterogeneity (I2) was moderate (49%). There were non‐overlapping 95% CIs.
 2Imprecision: downgraded one level for imprecision. Although the number of participants was large (34,744), the number of events was small (173) and the upper and lower bounds of the OR 95% CI did not exclude important effects.