OBJECTIVE: The ability to monitor anesthetic states using automated approaches is expected to reduce inaccurate drug dosing and side-effects. Commercially available anesthetic state monitors perform poorly when ketamine is administered as an anesthetic-analgesic adjunct. Poor performance is likely because the models underlying these monitors are not optimized for the electroencephalogram (EEG) oscillations that are unique to the co-administration of ketamine. APPROACH: In this work, we designed two k-nearest neighbors algorithms for anesthetic state prediction. MAIN RESULTS: The first algorithm was trained only on sevoflurane EEG data, making it sevoflurane-specific. This algorithm enabled discrimination of the sevoflurane general anesthesia (GA) state from sedated and awake states (true positive rate = 0.87, [95% CI, 0.76, 0.97]). However, it did not enable discrimination of the sevoflurane-plus-ketamine GA state from sedated and awake states (true positive rate = 0.43, [0.19, 0.67]). In our second algorithm, we implemented a cross drug training paradigm by including both sevoflurane and sevoflurane-plus-ketamine EEG data in our training set. This algorithm enabled discrimination of the sevoflurane-plus-ketamine GA state from sedated and awake states (true positive rate = 0.91, [0.84, 0.98]). SIGNIFICANCE: Instead of a one-algorithm-fits-all-drugs approach to anesthetic state monitoring, our results suggest that drug-specific models are necessary to improve the performance of automated anesthetic state monitors.
OBJECTIVE: The ability to monitor anesthetic states using automated approaches is expected to reduce inaccurate drug dosing and side-effects. Commercially available anesthetic state monitors perform poorly when ketamine is administered as an anesthetic-analgesic adjunct. Poor performance is likely because the models underlying these monitors are not optimized for the electroencephalogram (EEG) oscillations that are unique to the co-administration of ketamine. APPROACH: In this work, we designed two k-nearest neighbors algorithms for anesthetic state prediction. MAIN RESULTS: The first algorithm was trained only on sevoflurane EEG data, making it sevoflurane-specific. This algorithm enabled discrimination of the sevoflurane general anesthesia (GA) state from sedated and awake states (true positive rate = 0.87, [95% CI, 0.76, 0.97]). However, it did not enable discrimination of the sevoflurane-plus-ketamine GA state from sedated and awake states (true positive rate = 0.43, [0.19, 0.67]). In our second algorithm, we implemented a cross drug training paradigm by including both sevoflurane and sevoflurane-plus-ketamine EEG data in our training set. This algorithm enabled discrimination of the sevoflurane-plus-ketamine GA state from sedated and awake states (true positive rate = 0.91, [0.84, 0.98]). SIGNIFICANCE: Instead of a one-algorithm-fits-all-drugs approach to anesthetic state monitoring, our results suggest that drug-specific models are necessary to improve the performance of automated anesthetic state monitors.
Authors: O Akeju; K J Pavone; J A Thum; P G Firth; M B Westover; M Puglia; E S Shank; E N Brown; P L Purdon Journal: Br J Anaesth Date: 2015-07 Impact factor: 9.166
Authors: Oluwaseun Akeju; Andrew H Song; Allison E Hamilos; Kara J Pavone; Francisco J Flores; Emery N Brown; Patrick L Purdon Journal: Clin Neurophysiol Date: 2016-03-16 Impact factor: 3.708
Authors: Oluwaseun Akeju; M Brandon Westover; Kara J Pavone; Aaron L Sampson; Katharine E Hartnack; Emery N Brown; Patrick L Purdon Journal: Anesthesiology Date: 2014-11 Impact factor: 7.892
Authors: Johanna M Lee; Oluwaseun Akeju; Kristina Terzakis; Kara J Pavone; Hao Deng; Timothy T Houle; Paul G Firth; Erik S Shank; Emery N Brown; Patrick L Purdon Journal: Anesthesiology Date: 2017-08 Impact factor: 7.892