Effect of Propfol Versus Sevoflurane on Auditory and Cognitive Function

Type and site of the study:

This study will be carried out at Beni-Suef university hospital, after approval by the department of Anaesthesiology, the local ethics and research committee and other involved departments, faculty of medicine, Beni-Suef University.

Date of the study:

The study will be performed starting from 1st of January 2021

Study design and population: This is a prospective randomized study that will be carried out on patients subjected to general anaesthesia.

Sampling Technique:

Patients will be randomly assigned into one of two equal groups Randomization will be carried out using a closed opaque envelope technique with the anesthetist will pick up a sealed envelope which contains a paper with the name of the group to which the patient will be randomized is written. Whichever the group written on the paper, the patient will be scheduled to it.

The patients will be subjected to the following:

• A routine preoperative check-up will be performed. Routine hematological and biochemical testing, along with electrocardiograms will be performed for patients. The procedure will be explained to the patients
• On arrival to the operating theatre, 18 G intravenous cannula will be inserted and IV crystalloid fluids will be infused, the monitor will be attached to the patients to take preoperative readings of heart rate, non-invasive arterial blood pressure, SpO2.
• The patients will be randomly divided to one of two groups:

Group 1:

• Induction of anesthesia will be done by injecting fentanyl 2 μg/kg, propofol1.5-2.5 mg/kg and atracurium 0.5 mg/kg for muscle relaxation. Laryngoscopy and endotracheal intubation will be performed using oral cuffed tube lubricated with lidocaine jelly 2 %.
• Maintenance of anaesthesia will be done using Propofol total intravenous anesthesia (TIVA) 6-12 mg/ kg/h by syringe pump, 100 % O2.

Group 2:

• Induction of anesthesia will be done by injecting fentanyl 2 μg/kg, propofol1.5-2.5 mg/kg and atracurium 0.5 mg/kg for muscle relaxation. Laryngoscopy and endotracheal intubation will be performed using oral cuffed tube lubricated with lidocaine jelly 2 %.
• Maintenance of anaesthesia will be done using sevoflorane1.5-2%, 100 % O2. The concentrations of propofol and sevoflorane will be adjusted according to patient's vital sign

Ventilation in both groups will be controlled artificially to maintain an end-tidal partial pressure of carbon dioxide of 33-35 mmHg.

At the end of surgery, neuromuscular blockade will be reversed with IV neostigmine 0.04mg/kg and atropine 0.02 mg/kg, the trachea will be extubated when the patient respond to commands, all patients will be transferred to PACU, where they receive oxygen via face mask 3-4 L/min and will be monitored.

The following parameters will be evaluated and recorded by senior anesthesiologist unaware of the study protocol:

• Demographic data: age and sex
• Operation type.
• Duration of anesthesia
• Hemodynamics of the patients: Mean arterial blood pressure and heart rate, SPO2, End tidal CO2: will be continuously monitored and recorded every 15 minutes

All included patients will be subjected to the following (preoperative and 1 week postoperative):

• Cognitive assessment:

Cognitive functions for the patients will be assessed using the following psychometric tests:

• Paired Associate Learning test (PALT) (9):

• Aim: to assess auditory verbal memory. The test uses the concept of semantic cueing
• Administration and scoring: In this test, the examiner says ten associated pairs in front of the candidate. These pairs contain 6 compatible semantically related pairs and 4 incompatible semantically unrelated pairs. After one minute, the candidate is given the first word of the pairs and is asked to recall the second word. The test is repeated three times. Each correct compatible pair takes a score 0.5, while each correct incompatible pair takes a score 1. The total score ranges from 0 to 21.
• Paced Auditory Serial Addition Test (PASAT) ( 10):

• Aim: Paced Auditory Serial Addition test is used for assessment of attention and auditory working memory

• Administration and scoring: In this test, a series of 61 single digit numbers are spoken on an audiotape (or CD) at a rate of one every 3 seconds. The subject is asked to add each number to the one immediately preceding it and not to give a running total. The subject has to report the sum orally. Total score is the sum of correct responses and it ranges from 0 to 60.

• Audiological assessment:

• Audiological evaluation: tonal audiometry in the frequency range 0.25 - 8 kHz. Using orbiter 922 in a sound treated room with a TDH 39 earphones. Speech audiometry including speech reception threshold (SRT) using arabic spondee words, (11) and word discrimination score (WDS), using, arabic phonetically balanced (PB) words. (11) Immittancemetry: will be done using AD 629 Interacoustic, calibrated according to the ISO standard, using single-component, single-frequency tympanometry with a probe tone of 226 Hz. Testing of the acoustic reflex threshold, for ipsilateral and contralateral elicited reflexes, using pure tones at 500, 1000, 2000 and 4000 Hz.
• Brainstem auditory evoked potentials (BAEPs): will be performed using (Interacoustic Eclipse ''EP25''). The reference electrodes will be placed on the right(A2) and left (Al) mastoids, the active is on the scalp at the vertex (Fz position of the 10-20 International System of EEG electrode placement) and the ground electrode is on the lower mid-frontal area (Fpz position). Ag/AgCl electrodes filled with conductive paste will be fixed to skin that will be abraded with a skin prepping gel. Electrode impedances will be less than 5 kΩ, and inter-electrode impedances will be less than 2 kΩ. The subject should be in relaxed state. Click is presented through TDH39 headphones. Click will be presented at a rate of 21.1 stimuli per second in rarefaction polarity at intensity of 80 dBHL. Averaged potentials to 1200 clicks will be obtained. Two recordings will be obtained to ensure the replicability of the waveforms. The latencies of waves I, III, V and interpeak latencies I-V, I- III, III-V (IPLs) will be studied with BAEPs.

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Inclusion criteria

• ASA I-II patients who are candidate for elective extra cranial surgery.
• Male and female patients with age between 20-60 years

Exclusion criteria

• Patients with a conductive or sensorineural hearing loss
• Patients with a history of ear infection
• Patients with a history of ear trauma
• Patients using ototoxic or neurotoxic drugs
• Patients with sternocleidomastoid muscle pathology (traumatic injury or weakness) that interfere with audiological assessment
• Patient subjected to gross hemodynamic or ventilatory fluctuations during the operation
• Patient who developed postoperative shock or major bleeding
• Patient with a history of neurodegenerative disease, concomitant medical or metabolic illness known to affect cognition
• Allergy to any drug used in the study.
• Pregnancy.