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Intraoperative Fentanyl Consumption Guided by Analgesia Nociception Index

Not Applicable
Completed
Conditions
Postoperative Pain
Postoperative Complications
Interventions
Procedure: Standard protocol
Procedure: ANI protocol
Registration Number
NCT03716453
Lead Sponsor
Khon Kaen University
Brief Summary

Balanced anesthesia needs optimization of hypnotic, relaxant, and narcotic. Administration of hypnotic drugs can be monitored by bispectral index score (BIS), while the dosage of muscle relaxants can be guided by train-of four (TOF). However, administration of narcotics lacks objective monitor. Overdosage of narcotic may lead to delayed awakening, while underdosage may lead to high degree of postoperative pain. Recently, there is a monitor, Analgesic Nociceptive Index (ANI) monitor, designed to guide the administration of narcotics. There are many descriptive studies supporting the correlation of ANI score and pain score but there are still very few randomized control studies which report the efficacy of ANI in clinical practice.

Detailed Description

Objective: To evaluate the efficacy of ANI to guide the administration of intraoperative fentanyl.

Methods: Sixty female patients undergoing breast surgery with balanced anesthesia will be randomized into 2 groups. The first group will receive fentanyl according to standard practice of attending anesthesiologists. The second group will receive fentanyl according to ANI score protocol.

Primary outcome: Postoperative pain numeric rating scale (NRS) score during 60 minutes in postanesthetic care unit (PACU).

Secondary outcomes: Total intraoperative dose of fentanyl and postoperative nausea/vomiting and sedation score in PACU.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
60
Inclusion Criteria
  • Adults female undergoing elective breast surgery
  • American Society of Anesthesiologists (ASA) classification I-III
  • Body mass index (BMI) 18.5-35 kg/m2
Exclusion Criteria
  • Implanted pacemaker
  • Cardiac arrythmia
  • Autonomic nervous system (ANS) disorder, e.g. epilepsy, stroke
  • Chronic opioid use
  • Chronic pain
  • On beta-blocker, calcium channel blocker, or other drugs to control arrythmia
  • Previous mastectomy
  • Pregnancy
  • On Nsaids

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control groupStandard protocolIntraoperative fentanyl administration will be guided by standard protocol
ANI groupANI protocolIntraoperative fentanyl administration will be guided by ANI protocol
Primary Outcome Measures
NameTimeMethod
Postoperative pain: NRSduring 60 minutes in PACU

Measure pain numeric rating scale (NRS) every 15 minutes. NRS has a range from 0 to 10 with 0 indicates no pain while 10 indicates worst pain. NRS of 0-3 is mild, 4-6 is moderate, and 7-10 is severe pain.

Secondary Outcome Measures
NameTimeMethod
Intraoperative fentanyl consumptionDuring intraoperative period

Cumulative fentanyl used intraoperatively of both groups

Intraoperative ANI scoreDuring intraoperative period

Intraoperative ANI score of both groups. ANI has a range from 0 to 100 with 0 indicates worst pain while 100 indicates no pain. ANI 0-49 suggests that more opioid is needed. ANI 50-70 indicate optimal analgesic and no opioid is needed. ANI \> 70 indicates excessive effect of opioid and opioid should be withheld.

Postoperative nausea/vomitingDuring 24 hours postoperatively

Nausea/vomiting score (PONV score) every 4 hours. PONV score has a range of 0 to 3. N/V scores 0= none, 1= mild, 2= moderate, and 3= severe PONV.

Postoperative sedation scoreDuring 24 hours postoperatively

Sedation score every 4 hours. Sedation score has a range of 0 to 3 with 0= fully alert, 1= mild sedation, easy to rouse, 2= moderate sedation, arousable with gentle shaking, and 3= deep sedation, not aroused by speaking or gentle shaking.

Trial Locations

Locations (1)

Srinagarind Hospital, Faculty of Medicine, Khon Kaen University

🇹🇭

Khon Kaen, Thailand

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