Evidence map›Paper›PMID 35976578›Full record

Trial reportJournal of clinical monitoring and computing2023

Reduced postoperative pain in patients receiving nociception monitor guided analgesia during elective major abdominal surgery: a randomized, controlled trial.

Rivka Fuica, Carlos Krochek, Rachel Weissbrod, Dimitri Greenman, Andres Freundlich, Yaacov Gozal

2 registry-linked trialsOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of clinical monitoring and computing, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 23 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 3 pooled it
8.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03970291 nacompletednot on this map

Impact of Nociceptive-Level (NOL) Intraoperative Guided Fentanyl Analgesia Versus Standard Clinical Care (SCC) for Elective Major Abdominal Surgery

TypeinterventionalSponsorMedasense Biometrics LtdRan2019 to 2021Enrolled95ConditionsAnesthesiaArmsPMD-200
NCT06522711 nanot yet recruitingnot on this mapstarted 2024, after this paper: background citation

Virtual Reality as a Strategy for Intra-operatory Anxiolysis and Pharmacological Sparing in Patients Undergoing Breast Surgeries : the V-RAPS Randomized Controlled Trial

TypeinterventionalSponsorCiusss de L'Est de l'Île de MontréalRan2024 to 2026Enrolled100ConditionsVirtual Reality, PropofolArmsVirtual reality headset, Standard of care
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 3 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  4. Trial
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  7. Pain monitoring in intensive care: How does the nociception level index affect treatment and prognosis? A randomized, controlled, double-blind trial.Ulusal travma ve acil cerrahi dergisi = Turkish journal of trauma & emergency surgery : TJTES · 2024
    Trial
  8. Trial
  9. Beyond the Numerical Rating Scale: Comprehensive Pain Assessment in the Post-Anesthesia Care Unit.Journal of perianesthesia nursing : official journal of the American Society of PeriAnesthesia Nurses · 2026
    Article
  10. Article
  11. Nociception level index response to pacemaker stimulation.Journal of clinical monitoring and computing · 2025
    Observational
  12. Review
  13. Observational
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  16. Review
  17. Article
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  20. Initial Validation of the NOL Nociception Level IndexMedical devices (Auckland, N.Z.) · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Rivka FuicaDepartment of Anesthesiology, Perioperative Medicine and Pain Treatment, Shaare Zedek Medical Center, PO Box 3235, Jerusalem, Israel.
Carlos KrochekDepartment of Anesthesiology, Perioperative Medicine and Pain Treatment, Shaare Zedek Medical Center, PO Box 3235, Jerusalem, Israel.
Rachel WeissbrodMedasense Biometrics Ltd, Ramat Gan, Israel.
Dimitri GreenmanDepartment of Anesthesiology, Perioperative Medicine and Pain Treatment, Shaare Zedek Medical Center, PO Box 3235, Jerusalem, Israel.
Andres FreundlichDepartment of Anesthesiology, Perioperative Medicine and Pain Treatment, Shaare Zedek Medical Center, PO Box 3235, Jerusalem, Israel.
Yaacov GozalDepartment of Anesthesiology, Perioperative Medicine and Pain Treatment, Shaare Zedek Medical Center, PO Box 3235, Jerusalem, Israel. gozaly@szmc.org.il.
Shaare Zedek Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Nociception Level index (NOL™) is a multiparameter index, based on artificial intelligence for the monitoring of nociception during anesthesia. We studied the influence of NOL-guided analgesia on postoperative pain scores in patients undergoing major abdominal surgery during sevoflurane/fentanyl anesthesia. This study was designed as a single-center, prospective randomized, controlled study. After Institutional Review Board approval and written informed consent, 75 ASA 1-3 adult patients undergoing major abdominal surgery, were randomized to NOL-guided fentanyl dosing (NOL) or standard care (SOC) and completed the study. The sevoflurane target MAC range was 0.8-1.2. In the NOL-guided group (N = 36), when NOL values were > 25 for at least 1 min, a weight adjusted fentanyl bolus was administered. In the control group (N = 39) fentanyl administration was based on hemodynamic indices and clinician judgement. After surgery, pain, was evaluated using the Numerical Rating Scale (NRS) pain scale, ranging from 0 to 10, at 15 min intervals for 180 min or until patient discharge from the PACU. Median postoperative pain scores reported were 3.0 [interquartile range 0.0-5.0] and 5.0 [3.0-6.0] at 90 min in NOL-guided and control groups respectively (Bootstrap corrected actual difference 1.5, 95% confidence interval 0.4-2.6). There was no difference in postoperative morphine consumption or intraoperative fentanyl consumption. Postoperative pain scores were significantly improved in nociception level index-guided patients. We attribute this to more objective fentanyl dosing when timed to actual nociceptive stimuli during anesthesia, contributing to lower levels of sympathetic activation and surgical stress. Clinicaltrials.gov identifier: NCT03970291 date of registration May 31, 2019.

Indexed as

AnalgesiaNociceptionAdultAnalgesics, OpioidArtificial IntelligenceFentanylHumansPostoperative PainProspective StudiesSevofluraneAnalgesics, OpioidFentanylSevofluraneArtificial IntelligenceNociceptionNociception level-guided analgesiaOpioidPersonalized AnesthesiaPostoperative pain

Identifiers

PMID35976578
PMCPMC9383658
OpenAlexW4292104153

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.