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Reduction of Intraoperative EEG Burst Suppression (BsR)

T

Technical University of Munich

Status

Completed

Conditions

Postoperative Delirium
EEG With Abnormally Slow Frequencies
Burst Suppression

Treatments

Other: Treatment of hypotension and/or reduction of anesthetics

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Burst suppression (BS) is a not physiological pattern in the electroencephalogram (EEG). BS during general anesthesia is mainly seen as a sign for too deep hypnosis and may increase the risk of postoperative delirium (POD), a disturbance of consciousness arising within 24 hours after surgery. This monocentric, simple masked randomized study aims primarily to investigate, whether particular anesthesiological interventions reduce the occurrence of intraoperative burst suppression. The investigator initiated trial includes 66 patients (male and female) aged ≥ 60 years in two groups (intervention and control group). Secondary aims will be the correlation of burst suppression and mean arterial pressure, concentration of anesthetics and postoperative delirium.

Full description

Intraoperative burst suppression represents a non physiological EEG pattern. According to the literature and scientific knowledge, intraoperative burst suppression patterns might be caused either by hypotension resulting in a reduced cerebral circulation or by an oversedation of anesthetics correlating with a very deep level of hypnosis.

Some publications exist that discuss the occurrence of intraoperative burst suppression especially in elderly people (aged ≥ 60 years) as a predictor of postoperative delirium and postoperative cognitive dysfunction.

None of the studies however was able to prove a causal relationship between burst suppression and postoperative delirium. Contrary it might simply be an epiphenomenon.

Conducting this interventional trail primarily aims to prove whether specific anesthesiological interventions, such as the treatment of intraoperative hypotension in first line and/or the reduction of the concentration of anesthetics in second line, reduce intraoperative burst suppression. Hence it might be possible to investigate a possible casualty between burst suppression and postoperative delirium in a second trial.

Enrollment

106 patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥ 60 years
  • Surgical interventions in general anesthesia (volatile or total intravenous anesthesia)
  • expected surgery duration ≥ 1h
  • American Society of Anesthesiologists (ASA) 1-4
  • written informed consent prior to study participation

Exclusion criteria

  • Neurological or psychiatric disorders
  • hearing difficulty
  • deafness
  • neurosurgical (intra)cranial surgery
  • pregnancy
  • expected continuous mandatory ventilation after surgery

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

106 participants in 2 patient groups

1 - Blinded
No Intervention group
Description:
EEG and Entropy will be blinded. The anesthesiological management will be performed by the anesthetist according to clinical standard operations.
2 - Unblinded
Active Comparator group
Description:
EEG and Entropy will be unblinded. The intervention starts with the start of a positive burst suppression rate. In the case of a concurrent hypotension the anesthetist treats the hypotension according to clinical standard operations in the first step. Hypotension means blood pressure values blow the baseline value which is defined by the lowest, preoperatively measured value. If after this treatment and a reevaluation of the BSR, BSR remains positive, the anesthetist is going to reduce the concentration of anesthetics in a second step. In case of positive BSR and a blood pressure value ≥ the baseline value, the concentration of anesthetics will be reduced as a first measure. The aim is to figure out whether one or both of these interventions can reduce to total, cumulative BSR.
Treatment:
Other: Treatment of hypotension and/or reduction of anesthetics

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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