TY - JOUR
T1 - Usefulness of analgesia nociception index for guiding intraoperative opioid administration
T2 - a systematic review and meta-analysis
AU - Hung, Kuo Chuan
AU - Chang, Po Chih
AU - Hsu, Chih Wei
AU - Lan, Kuo Mao
AU - Liao, Shu Wei
AU - Lin, Yao Tsung
AU - Huang, Ping Wen
AU - Sun, Cheuk Kwan
N1 - Publisher Copyright:
© 2023 Edizioni Minerva Medica. All rights reserved.
PY - 2023/1
Y1 - 2023/1
N2 - INTRODUCTION: This study primarily aimed at investigating the efficacy of Analgesia Nociception Index (ANI) for guiding intraoperative opioid administration in patients receiving surgery under general anesthesia. eviDence acQUisition: the Medline, embase, google scholar, and the cochrane library databases were searched from inception to april 2022 for randomized controlled trials. the primary outcome was intraoperative opioid adminis-tration, while the secondary outcomes included postoperative opioid consumption, pain score, emergency time, risk of nausea/vomiting (PONV), and Postanesthesia Care Unit (PACU) stay. EVIDENCE SYNTHESIS: Six studies including 399 participants (published from 2015 to 2022) focused on non-cardiac surgery, including spine surgery (two trials), breast surgery (two trials), gynecologic surgery (one trial), and laparoscopic cholecystectomy (one trial) were included. Meta-analysis revealed no difference in intraoperative opioid administration with the use of ANI-guided analgesia compared to the control group that used conventional clinical measurements (e.g., heart rate) to guide opioid use [standardized mean difference (SMD)=-0.17, 95% CI: -0.56 to 0.22, P=0.39, I2=72%, six trials, 399 participants]. gender-based subgroup analysis showed effectiveness of ani for reducing opioid administration in female patients (SMD=-0.53, P=0.02). There were no differences in postoperative recovery characteristics including pain score [Mean difference (MD): -0.03, P=0.79], opioid consumption (SMD: -0.34, P=0.08), emergence time (MD=1.12, P=0.47), length of stay in the PACU (MD: -0.56, P=0.83), and risk of PONV [risk ratio(RR): 0.75, P=0.46] between the two groups. conclUsions: analgesia nociception index-guided analgesia was unable to reduce intraoperative opioid administra-tion compared to monitoring using conventional clinical parameters. Further studies are required to support our findings.
AB - INTRODUCTION: This study primarily aimed at investigating the efficacy of Analgesia Nociception Index (ANI) for guiding intraoperative opioid administration in patients receiving surgery under general anesthesia. eviDence acQUisition: the Medline, embase, google scholar, and the cochrane library databases were searched from inception to april 2022 for randomized controlled trials. the primary outcome was intraoperative opioid adminis-tration, while the secondary outcomes included postoperative opioid consumption, pain score, emergency time, risk of nausea/vomiting (PONV), and Postanesthesia Care Unit (PACU) stay. EVIDENCE SYNTHESIS: Six studies including 399 participants (published from 2015 to 2022) focused on non-cardiac surgery, including spine surgery (two trials), breast surgery (two trials), gynecologic surgery (one trial), and laparoscopic cholecystectomy (one trial) were included. Meta-analysis revealed no difference in intraoperative opioid administration with the use of ANI-guided analgesia compared to the control group that used conventional clinical measurements (e.g., heart rate) to guide opioid use [standardized mean difference (SMD)=-0.17, 95% CI: -0.56 to 0.22, P=0.39, I2=72%, six trials, 399 participants]. gender-based subgroup analysis showed effectiveness of ani for reducing opioid administration in female patients (SMD=-0.53, P=0.02). There were no differences in postoperative recovery characteristics including pain score [Mean difference (MD): -0.03, P=0.79], opioid consumption (SMD: -0.34, P=0.08), emergence time (MD=1.12, P=0.47), length of stay in the PACU (MD: -0.56, P=0.83), and risk of PONV [risk ratio(RR): 0.75, P=0.46] between the two groups. conclUsions: analgesia nociception index-guided analgesia was unable to reduce intraoperative opioid administra-tion compared to monitoring using conventional clinical parameters. Further studies are required to support our findings.
KW - analgesics, opioid
KW - nociception
KW - review
UR - https://www.scopus.com/pages/publications/85147536667
U2 - 10.23736/S0375-9393.22.16697-6
DO - 10.23736/S0375-9393.22.16697-6
M3 - 文献综述
C2 - 36282226
AN - SCOPUS:85147536667
SN - 0375-9393
VL - 89
SP - 74
EP - 84
JO - Minerva Anestesiologica
JF - Minerva Anestesiologica
IS - 1-2
ER -