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Quantitative EEG During Anesthesia Emergence in Children

Quantitative Frontal Electroencephalography (EEG) and Postoperative Emergence Delirium Following General Anesthesia in Children: a Prospective Observational Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03797274
Acronym
qEEG
Enrollment
60
Registered
2019-01-09
Start date
2019-02-08
Completion date
2019-06-01
Last updated
2019-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, General, Brain Waves, Child Behavior, Electroencephalography, Psychology, Children

Brief summary

Most drugs used in general anesthesia work on various receptors in the human brain, causing unconsciousness, loss of memory, and loss of reflection of the autonomic nervous system. After the anesthesia, baseline physiological function will be attained by administration of some reversal drugs or as the time goes by. In this process, various side effects may occur. Emergence delirium (ED) is a representative behavioral disturbance after general anesthesia in children and that can cause several problems during the recovery period. Previous EEG studies reported that this phenomenon is related to hyperexcitation of the brain, and occurrence of epileptiform discharges during anesthesia induction may indicate an increased vulnerability for the development of a functional brain disorder in these children. However, to the best of our knowledge, there is no studies concern evaluating quantitative EEG parameters for prediction of this postoperative negative behavior in children.

Interventions

None listed

Sponsors

Daegu Catholic University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

* Children aged between 2 and 10 years of American Society of Anesthesiologists physical status (ASA PS) I or II who are planned to receive surgery under general anesthesia

Exclusion criteria

* If the guardian and the subject are difficult to evaluate normally due to language barriers/language disorders/delay or autistic disorder * with developmental delay, neurological disorders or psychiatric diseases associated with symptoms of agitation, anxiety, attention deficit, sleep disturbances, etc * refusal of consent * Recent history (within a month) of received general anesthesia or surgery * presence of congenital or other genetic conditions thought to influence brain development

Design outcomes

Primary

MeasureTime frameDescription
Occurrence of Emergence deliriumDuring 60 minutes after PACU admissionOn arrival at post-anesthesia care unit (PACU), patients are checked post-anesthesia emergence delirium (PAED). The PAED scale is a validated observational measure of 5 aspects of child behavior (caregiver eye contact, purposeful movement, evidence of awareness of surroundings, restlessness, and inconsolability). Ratings are summed to produce a total score ranging from 0 to 20; greater scores indicate greater severity. If the PAED score is greater than 12, investigators define emergence delirium.
Relative power of each brain wavesFrom the cessation of sevoflurane inhalation to the extubation of airway devices such as tracheal tubes or laryngeal mask airwayOriginal frontal EEG segments are attained via 2 channel bispectral index monitoring (BIS VISTA™, Aspect Medical Systems, Inc. MA, USA) during the anesthesia period. The EEG is then segmented into 4 s epochs and fast Fourier transform (FFT) analysis is performed for each of these segments. FFT of all these selected EEG segments are computed in the following frequency bands: Delta: 1-4 Hz Theta: 4-8 Hz Alpha: 8-13 Hz Beta: 13-30 Hz And then, the relative power of each frequency bands to the total power of the sum is calculated.

Secondary

MeasureTime frameDescription
FLACC score on initial, 10, 20, and 30 minDuring 60 minutes after PACU admission]Face, legs, activity, cry, and consolability (FLACC) score is checked every 10min after PACU admission
Watcha scale on initial, 10, 20, and 30 minDuring 60 minutes after PACU admissionOn arrival and 10, 20, and 30 min after PACU admission, patients were checked Watcha scale as following 4-point scale 1. calm 2. crying, but can be consoled 3. Crying, cannot be consoled 4. Agitated and thrashing around Higher score indicates higher agitation.
modified Yale preoperative anxiety score (mYPAS)before anesthesia induction (about 30 min before the surgery)mYPAS is the assessment tool for measure the anxiety before induction. Higher score indicates higher anxiety.
Delta to alpha ratioFrom the cessation of sevoflurane inhalation to the extubation of airway devices such as tracheal tubes or laryngeal mask airwayFrom the relative power of each brain waves, the investigators calculated the ratio as follows: DAR = Delta wave / alpha wave
Theta to beta ratio (TBR)From the cessation of sevoflurane inhalation to the extubation of airway devices such as tracheal tubes or laryngeal mask airwayFrom the relative power of each brain waves, the investigators calculated the ratio as follows: TBR = Theta wave / beta wave
Delta-theta to alpha-beta ratio (DTABR)From the cessation of sevoflurane inhalation to the extubation of airway devices such as tracheal tubes or laryngeal mask airwayFrom the relative power of each brain waves, the investigators calculated the ratio as follows: DTABR = (Delta wave + Theta wave)/(alpha wave + beta wave)
PAED score during PACU stayDuring 60 min after PACU admissionOn arrival at post-anesthesia care unit (PACU) and every 10 min from then, patients were checked PAED. The PAED scale is a validated observational measure of 5 aspects of child behavior (caregiver eye contact, purposeful movement, evidence of awareness of surroundings, restlessness, and inconsolability). Ratings are summed to produce a total score ranging from 0 to 20; greater scores indicate greater severity.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026