Surgical Pleth Index And Analgesia Nociception Index for intraoperative analgesia in patients undergoing neurosurgical spinal procedures, a comparative randomized study

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F19%3A10398843" target="_blank" >RIV/00179906:_____/19:10398843 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216208:11150/19:10398843

Výsledek na webu

<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=hkC0-UUPa8" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=hkC0-UUPa8</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.23736/S0375-9393.19.13765-0" target="_blank" >10.23736/S0375-9393.19.13765-0</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Surgical Pleth Index And Analgesia Nociception Index for intraoperative analgesia in patients undergoing neurosurgical spinal procedures, a comparative randomized study

Popis výsledku v původním jazyce

BACKGROUND: The Surgical Plethysmographic Index (SPI) and the Analgesia Nociception Index (ANI) have been suggested for the non-invasive intraoperative monitoring of nociception/anti-nociception balance. We aimed to compare patterns of intraoperative use of opioids, postoperative cortisol levels and postoperative pain scores after intraoperative analgesia guided either by ANI, SPI or anaesthesiologist&apos;s judgment. MATERIAL AND METHODS: Seventy two adult ASA I - III patients scheduled for elective neurosurgical spinal procedures were randomized into the ANI group, SPI group and control group. Anaesthesia and intraoperative use of opioids (sufentanil boluses based on body weight) were managed according to a strict protocol. The use of sufentanil was targeted to keep ANI value 50 - 70 in the ANI group, SPI value below individual postinduction baseline value plus 10 points in the SPI group. In the control group, the use of opioids was left at anaesthesiologist&apos;s discretion. RESULTS: Additional sufentanil boluses were administered earlier in the ANI and SPI groups in comparison to the control group (3rd dose after 51.8 +- 22.1 vs 52.7 +- 14.8 vs 84.5 +- 24.8 min respectively, p = 0.001; 4th dose after 61.3 +- 30.1 vs 57.2 +- 14.1 vs 120.0 +- 26.2 min, p = 0.003, and 5th dose after 78.8 +- 33.7 vs 74.0 +- 11.6 vs 146.7 +- 23.2 min respectively, p = 0.009). There were no differences in postoperative cortisol levels, time to spontaneous breathing at the end of anaesthesia and postoperative pain scores. CONCLUSIONS: Both ANI and SPI guidance significantly modified intraoperative opiod use, but no modification of postoperative cortisol levels and postoperative pain was observed.

Název v anglickém jazyce

Surgical Pleth Index And Analgesia Nociception Index for intraoperative analgesia in patients undergoing neurosurgical spinal procedures, a comparative randomized study

Popis výsledku anglicky

BACKGROUND: The Surgical Plethysmographic Index (SPI) and the Analgesia Nociception Index (ANI) have been suggested for the non-invasive intraoperative monitoring of nociception/anti-nociception balance. We aimed to compare patterns of intraoperative use of opioids, postoperative cortisol levels and postoperative pain scores after intraoperative analgesia guided either by ANI, SPI or anaesthesiologist&apos;s judgment. MATERIAL AND METHODS: Seventy two adult ASA I - III patients scheduled for elective neurosurgical spinal procedures were randomized into the ANI group, SPI group and control group. Anaesthesia and intraoperative use of opioids (sufentanil boluses based on body weight) were managed according to a strict protocol. The use of sufentanil was targeted to keep ANI value 50 - 70 in the ANI group, SPI value below individual postinduction baseline value plus 10 points in the SPI group. In the control group, the use of opioids was left at anaesthesiologist&apos;s discretion. RESULTS: Additional sufentanil boluses were administered earlier in the ANI and SPI groups in comparison to the control group (3rd dose after 51.8 +- 22.1 vs 52.7 +- 14.8 vs 84.5 +- 24.8 min respectively, p = 0.001; 4th dose after 61.3 +- 30.1 vs 57.2 +- 14.1 vs 120.0 +- 26.2 min, p = 0.003, and 5th dose after 78.8 +- 33.7 vs 74.0 +- 11.6 vs 146.7 +- 23.2 min respectively, p = 0.009). There were no differences in postoperative cortisol levels, time to spontaneous breathing at the end of anaesthesia and postoperative pain scores. CONCLUSIONS: Both ANI and SPI guidance significantly modified intraoperative opiod use, but no modification of postoperative cortisol levels and postoperative pain was observed.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

—

OECD FORD obor

30223 - Anaesthesiology

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2019

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Minerva Anestesiologica

ISSN

0375-9393

e-ISSN

—

Svazek periodika

85

Číslo periodika v rámci svazku

12

Stát vydavatele periodika

IT - Italská republika

Počet stran výsledku

8

Strana od-do

1265-1272

Kód UT WoS článku

000503499600005

EID výsledku v databázi Scopus

2-s2.0-85076179619