ANI-Guided Anesthetic Desflurane Consumption

Analgesia/Nociception Index (ANI)-Guided Desflurane Titration Reduces Anesthetic Consumption in Laparoscopic Cholecystectomy: A Prospective Randomized Controlled Trial

General anesthesia requires precise titration of inhaled anesthetics like desflurane and opioids like remifentanil to balance sedation, analgesia, and hemodynamic stability. The Analgesia/Nociception Index (ANI), derived from heart rate variability (HRV), quantifies parasympathetic tone to assess nociception-antinociception balance on a 0-100 scale, with lower values indicating nociceptive stress. ANI analyzes high-frequency HRV components, reflecting parasympathetic inhibition during painful stimuli, making it a reliable indicator of intraoperative nociception. Studies validate the utility of ANI in detecting nociceptive events during laparoscopic surgery. ANI-guided opioid titration reduces opioid consumption and stabilizes hemodynamics, enhancing perioperative outcomes.

Study Overview

• Status: Completed
• Conditions: Postoperative Pain; General Anesthesia; Laparoscopic Cholecystectomy
• Intervention / Treatment: Device: Analgesia/Nociception Index (ANI)

Detailed Description

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).

• Study Type: Interventional
• Enrollment (Actual): 125
• Phase: Not Applicable

Contacts and Locations

Study Locations

• Korea, Republic of
  • Jeollabuk-do
    • Iksan, Jeollabuk-do, Korea, Republic of, 54538
      • Wonkwang University School of Medicine Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• aged 19-65 years, American Society of Anesthesiologists (ASA) physical status I-II, scheduled for elective laparoscopic cholecystectomy under general anesthesia.

Exclusion Criteria:

• chronic pain, preoperative opioid use, cardiac arrhythmias, autonomic dysfunction, or contraindications to desflurane or remifentanil.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: ANI-guided group; Desflurane started at 1 MAC (~6 Vol%), titrated in 0.1 MAC increments to maintain ANI 50-70 and BIS 40-60. ANI <50 prompted an increase; ANI >70 prompted a decrease	Device: Analgesia/Nociception Index (ANI); ANI was monitored using the ANI monitor (MetroDoloris, France) in both groups, but only guided adjustments in the ANI group
Active Comparator: Control group; Desflurane was titrated based on vital signs (heart rate, blood pressure) and BIS 40-60, per institutional protocol.	Device: Analgesia/Nociception Index (ANI); ANI was monitored using the ANI monitor (MetroDoloris, France) in both groups, but only guided adjustments in the ANI group

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mean End-Tidal Desflurane Concentration	The average end-tidal desflurane concentration (Vol%) during maintenance of general anesthesia, measured using continuous gas monitoring. Desflurane delivery is titrated based on ANI (Analgesia/Nociception Index) in the intervention group and based on vital signs in the control group.	From induction of anesthesia to end of surgery (approximately 60 minutes)

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Emergence Time	Time from discontinuation of anesthetics to eye opening upon verbal command, recorded in minutes.	At the end of surgery until eye opening (approximately 5-15 minutes)
Post-Anesthesia Care Unit (PACU) Length of Stay	Time from PACU admission to discharge readiness, measured in minutes.	From PACU entry to PACU discharge criteria fulfillment (approximately 30-90 minutes)
Additional Analgesic Requirement in PACU	Number of patients requiring additional analgesics in PACU and total morphine-equivalent dose administered.	During PACU stay (up to 2 hours after surgery)
Incidence of Postoperative Nausea and Vomiting (PONV)	Presence of nausea or vomiting events recorded within the first two postoperative hours.	Within 2 hours after surgery
Patient Satisfaction	Patient-reported satisfaction using a Visual Analog Scale (0-10) at PACU discharge and on postoperative day 1.	At PACU discharge and 24 hours postoperatively (POD1)

Collaborators and Investigators

• Sponsor: Wonkwang University Hospital
• Investigators: Principal Investigator: Cheol Lee, M.D.,Ph.D, Wonkwang University Hospital

Study record dates

Study Major Dates

• Study Start (Actual): February 5, 2024
• Primary Completion (Actual): April 30, 2024
• Study Completion (Actual): April 30, 2025

Study Registration Dates

• First Submitted: May 13, 2025
• First Submitted That Met QC Criteria: May 13, 2025
• First Posted (Actual): May 21, 2025

Study Record Updates

• Last Update Posted (Actual): May 21, 2025
• Last Update Submitted That Met QC Criteria: May 13, 2025
• Last Verified: May 1, 2025

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pain; Neurologic Manifestations; Postoperative Complications; Pathologic Processes; Pain, Postoperative
• Other Study ID Numbers: Wonkwang UH20

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No