ANI-Guided Anesthetic Desflurane Consumption

Study Design This prospective, single-center, randomized controlled trial receives approval from the \[Institutional Review Board Name\] (Approval No. 2024-01-05-21-004). Written informed consent is obtained from all participants.

Participants Eligible patients are aged 19-65 years, American Society of Anesthesiologists (ASA) physical status I-II, and are scheduled for elective laparoscopic cholecystectomy under general anesthesia. Exclusion criteria include chronic pain, preoperative opioid use, cardiac arrhythmias, autonomic dysfunction, or contraindications to desflurane or remifentanil.

Randomization and Blinding Patients are randomized (1:1) to Analgesia/Nociception Index (ANI)-guided or standard care groups using a computer-generated sequence in blocks of four. Group allocation is concealed in opaque, sealed envelopes, which are opened before induction. Anesthesiologists remain unblinded due to ANI monitoring requirements, but patients and postoperative outcome assessors remain blinded to reduce bias.

Anesthesia Protocol Anesthesia is induced with propofol (2 mg/kg) and rocuronium (0.6 mg/kg). Maintenance includes desflurane and remifentanil (0.1 µg/kg/min continuous infusion). Ventilation maintains normocapnia (end-tidal Carbon dioxide: 35-40 mmHg). Bispectral index (BIS) is monitored to ensure hypnotic depth (target: 40-60).

Novel Metrics

In addition to standard intraoperative management, the following novel physiological and recovery-related metrics are assessed to enhance the evaluation of ANI-guided anesthesia:

* ∆ANI (Dynamic Change of ANI): The percentage change in ANI at specific surgical stimuli (e.g., skin incision, trocar insertion) is recorded as: ∆ANI = (ANI\_post - ANI\_pre) / ANI\_pre × 100. * Autonomic Nervous System Indicators: * Heart Rate Variability (HRV): High Frequency (HF) and Low Frequency (LF)/HF ratio are calculated at baseline, mid-surgery, and end-surgery. Continuous beat-to-beat blood pressure (BP) and lead II electrocardiogram (ECG) are recorded noninvasively for 5 minutes using the equipment. HRV parameters are extracted using Software. * Baroreflex Sensitivity (BRS): BRS is assessed pre-induction and intraoperatively. It is quantified using the spontaneous sequence method with regression analysis between Blood Pressure and respiratory rate intervals, measured with the equipment and analyzed with HRV Software.

Recovery Room Metrics

* Post-Anesthesia Care Unit (PACU) Length of Stay (LOS): Time from PACU entry to discharge readiness is recorded. * Additional Analgesic Requirement: Any supplemental pain medication and dosage are recorded during PACU stay. * Postoperative Nausea and Vomiting (PONV): Incidence is recorded within the first two postoperative hours.

Patient-Reported Outcomes

* Satisfaction Scores (Visual analogue scale \[VAS\]0-10): Are assessed at PACU discharge and on postoperative day 1 (POD1). * ANI Group: Desflurane starts at 1 Minimum Alveolar Concentration (MAC) (\~6 Vol%) and is titrated in 0.1 MAC increments to maintain ANI 50-70 and BIS 40-60. ANI \<50 prompts an increase; ANI \>70 prompts a decrease. * Control Group: Desflurane is titrated based on vital signs and BIS 40-60 per institutional protocol.

ANI is monitored using the ANI monitor in both groups, but only guides adjustments in the ANI group. Hemodynamic data are recorded every 5 minutes.

Emergence and Recovery At the end of the surgery, desflurane and remifentanil are discontinued. Neuromuscular blockade is monitored using Train-of-Four (TOF) stimulation. When TOF count reaches ≥2, sugammadex (2 mg/kg) is administered to reverse rocuronium. Extubation occurs when TOF ratio \>0.9, with adequate spontaneous breathing and responsiveness to verbal commands. Emergence time is recorded as time from anesthetic cessation to eye opening.

Outcome Measures

* Primary Outcome: Mean end-tidal desflurane concentration (Vol%). * Secondary Outcomes: * Emergence time (min). * Postoperative pain (VAS, 0-10) at 30 min post-extubation. * Intraoperative hemodynamic stability (hypertension \[Mean arterial pressure \> 100 mmHg\] or tachycardia \[HR \>100 bpm\]). * ∆ANI at surgical stimuli. * HRV metrics (HF, LF/HF ratio). * Baroreflex Sensitivity (BRS). * PACU LOS. * Requirements and dosage of additional analgesics in PACU. * Incidence of PONV within 2 hours post-op. * Patient satisfaction (PACU discharge and postoperative day 1).

• Emergence Time [Срок оценки: At the end of surgery until eye opening (approximately 5-15 minutes)]
• Post-Anesthesia Care Unit (PACU) Length of Stay [Срок оценки: From PACU entry to PACU discharge criteria fulfillment (approximately 30-90 minutes)]
• Additional Analgesic Requirement in PACU [Срок оценки: During PACU stay (up to 2 hours after surgery)]
• Incidence of Postoperative Nausea and Vomiting (PONV) [Срок оценки: Within 2 hours after surgery]
• Patient Satisfaction [Срок оценки: At PACU discharge and 24 hours postoperatively (POD1)]