Comparison of Target-Controlled and Manual Total Intravenous Anesthesia in Supratentorial Surgery

This study will be conducted following approval by the Istanbul University-Cerrahpaşa Medical Research Ethics Committee (Approval No: 1504004) in patients scheduled for supratentorial craniotomy at the operating rooms of the Department of Neurosurgery, Cerrahpaşa Faculty of Medicine, Istanbul University-Cerrahpaşa, after obtaining written informed consent. The study is designed as a prospective, randomized controlled trial with two groups: a manually controlled total intravenous anesthesia group (Manual group) and a target-controlled infusion group (TCI group).

Sample size calculation was performed based on the delirium rates reported in the study by Varsha, as no direct comparison between target-controlled infusion and manual total intravenous anesthesia in terms of delirium was identified in the available literature. In that study, the incidence of postoperative delirium was reported as 34.2% (12/35) in the inhalational anesthesia group and 8.8% (3/34) in the propofol total intravenous anesthesia group. Based on these proportions, an a priori power analysis was conducted using G*Power version 3.1.9.7 for comparison of proportions between two independent groups. Assuming a one-sided test, an alpha level of 0.05, power of 80% (1-β = 0.80), and a group allocation ratio of N2/N1 = 0.97, a minimum of 32 patients in the first group and 31 patients in the second group were required, resulting in a total sample size of 63 patients.

Adult male and female patients aged 18-60 years undergoing supratentorial surgery and classified as American Society of Anesthesiologists (ASA) physical status I or II will be included. Exclusion criteria include refusal to provide consent, ASA physical status III or higher, pregnancy, emergency surgery, presence of brain herniation, anticipated or documented difficult airway, inability to communicate (non-Turkish speaking or hearing impairment), preoperative risk factors for delirium (substance abuse, use of neuropsychiatric medications, preoperative hemoglobin concentration below 8 g/dL, malnutrition, electrolyte or thyroid hormone abnormalities), intraoperative deviations from the study protocol (changes in surgical or anesthetic technique, severe intraoperative complications), and contraindications to propofol or remifentanil use.

Eligible patients will be randomized into either the Manual Total Intravenous Anesthesia group or the Target-Controlled Infusion group using the sealed-envelope method. Patient evaluation will begin during routine preoperative anesthesia assessment, including screening for delirium using the Confusion Assessment Method (CAM). In the operating room, in addition to standard monitoring, bispectral index monitoring (BIS™, Covidien/Medtronic, USA), invasive arterial blood pressure monitoring, and bladder catheterization will be applied to all patients. Demographic data and baseline hemodynamic measurements (blood pressure and heart rate) will be recorded prior to induction of anesthesia.

Anesthesia induction will be performed using remifentanil, propofol, and rocuronium. To reduce injection pain associated with propofol, 40 mg intravenous lidocaine will be administered using a tourniquet technique. In the Manual group, after initiation of remifentanil infusion at 0.1 µg/kg/min, propofol will be administered in 20-mg boluses guided by electroencephalographic changes observed on the BIS monitor. In the TCI group, automatic induction will be performed using an infusion pump (BeneFusion nSP, Mindray Bio-Medical Electronics Co., China) with target concentrations of 2-3 ng/mL for remifentanil and 3-3.5 µg/mL for propofol. For both drugs, the Eleveld pharmacokinetic model with effect-site targeting will be used, and opioid co-infusion mode will be enabled for propofol administration. In both groups, rocuronium at a dose of 0.6-0.9 mg/kg will be administered intravenously once delta waves are observed on the raw EEG display of the BIS monitor, followed by tracheal intubation.

During the induction period, induction time, total propofol dose, immediate post-intubation monitoring data, and burst suppression duration will be recorded. Induction time will be defined as the interval between initiation of propofol administration and the appearance of delta waves on the BIS monitor. Following intubation, scalp block using 15-20 mL of 0.5% bupivacaine, intravenous dexketoprofen 50 mg, and antibiotic prophylaxis will be administered when not contraindicated. Mechanical ventilation will be provided using a volume-controlled mode with AutoFlow enabled (VC-AF) via an anesthesia workstation (Perseus A500, Dräger, Lübeck, Germany), with tidal volumes of 4-8 mL/kg and positive end-expiratory pressure of 5-8 cmH₂O.

Anesthesia maintenance in both groups will be achieved using propofol-remifentanil total intravenous anesthesia. In patients not undergoing intraoperative neuromonitoring, rocuronium infusion at 20-30 mg/h will be administered. Propofol and remifentanil doses will be titrated by the attending anesthesiologist to maintain BIS values between 40 and 60 and to achieve normotension. Total propofol and remifentanil consumption and burst suppression durations will be recorded at the 1st, 2nd, and 4th intraoperative hours and at the end of surgery. At the conclusion of surgery, patients will receive intravenous tramadol (50-100 mg), ondansetron (8 mg), and sugammadex (200 mg). Patients who are not clinically suitable for extubation will be transferred to the intensive care unit intubated and excluded from the study.

During the extubation period, time to awakening, extubation time, post-extubation monitoring data, total drug consumption, total burst suppression duration, and surgical and anesthesia durations will be recorded. Awakening time will be defined as the interval between discontinuation of infusions and the patient's response to verbal commands, and extubation time as the interval between infusion cessation and tracheal extubation.

The recovery period will be defined as the first postoperative hour. Hemodynamic measurements, pain intensity assessed using the Numeric Rating Scale (NRS), presence of nausea and vomiting, recovery profile assessed using the Aldrete score, and additional analgesic requirements will be recorded at 15, 30, and 60 minutes postoperatively. Patients in both groups will be followed for postoperative delirium for three days. Delirium assessments will be performed using CAM at postoperative hour 6, at 08:00 on the first postoperative day, and at 24, 48, and 72 hours postoperatively. For patients discharged before 72 hours, the final assessment will be conducted at discharge.

Due to the nature of the study, the attending anesthesiologist will be aware of group allocation during the intraoperative period. However, postoperative recovery and delirium assessments will be performed by a nurse and/or physician blinded to group assignment.