Evidence map›Paper›PMID 25892658›Full record

Trial reportThe journal of pain2015

The Contribution of Differential Opioid Responsiveness to Identification of Opioid Risk in Chronic Pain Patients.

Stephen Bruehl, John W Burns, Steven D Passik, Rajnish Gupta, Asokumar Buvanendran, Melissa Chont, Erik Schuster, Daria Orlowska, Christopher R France

2 registry-linked trialsOpen access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The journal of pain, 2015. 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 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 15% 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.

NCT04034004 early_phase1completednot on this mapstarted 2021, after this paper: background citation

The Role of Endogenous Opioids in Mindfulness-based Chronic Pain Relief

TypeinterventionalSponsorUniversity of California, San DiegoRan2021 to 2022Enrolled88ConditionsPainArmsMindfulness, Naloxone, Saline, Meditation
NCT05142267 narecruitingnot on this mapstarted 2022, after this paper: background citation

Stress and Opioid Misuse Risk: The Role of Endogenous Opioid and Endocannabinoid Mechanisms

TypeinterventionalSponsorVanderbilt University Medical CenterRan2022 to 2026Enrolled120ConditionsOpioid Use Disorder, Back Pain, StressArmsPlacebo, Oxycodone, Naloxone
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Article
  7. Review
  8. Predicting Extent of Opioid Use Following Cardiac Surgery: A Pilot Study.Journal of cardiothoracic and vascular anesthesia · 2025
    Observational
  9. Review
  10. Review
  11. Article
  12. Article
  13. Opioids and Chronic Pain: Where Is the Balance?Current oncology reports · 2016
    Review
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

9 authors at 4 institutions in 1 country.

Stephen BruehlDepartment of Anesthesiology, Vanderbilt University School of Medicine, Nashville, Tennessee. Electronic address: Stephen.Bruehl@vanderbilt.edu.
John W BurnsDepartment of Behavioral Science, Rush University, Chicago, Illinois.
Steven D PassikMillennium Research Institute, San Diego, California.
Rajnish GuptaDepartment of Anesthesiology, Vanderbilt University School of Medicine, Nashville, Tennessee.
Asokumar BuvanendranDepartment of Anesthesiology, Rush University, Chicago, Illinois.
Melissa ChontDepartment of Anesthesiology, Vanderbilt University School of Medicine, Nashville, Tennessee.
Erik SchusterDepartment of Behavioral Science, Rush University, Chicago, Illinois.
Daria OrlowskaDepartment of Behavioral Science, Rush University, Chicago, Illinois.
Christopher R FranceDepartment of Psychology, Ohio University, Athens, Ohio.
Rush University · USVanderbilt University · USMillennium Engineering and Integration (United States) · USOhio University · US

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Predictors of Opioid Analgesic Responses and Common Endogenous Opioid MechanismsR01DA031726 · NIDA · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BRUEHL, STEPHEN, BURNS, JOHN W. · 2011 to 2015
$2.7M
NCATS NIH HHS UL1 TR000445NCATS NIH HHS UL1TR000445NIDA NIH HHS R01 DA031726NIDA NIH HHS R01-DA031726
6 · The paper itself

Abstract

unlabelledThe Screener and Opioid Assessment for Patients with Pain-Revised (SOAPP-R) predicts increased risk of opioid misuse in chronic pain patients. We evaluated whether higher SOAPP-R scores are associated with greater opioid reinforcing properties, potentially contributing to their predictive utility. Across 2 counterbalanced laboratory sessions, 55 chronic low back pain sufferers completed the SOAPP-R at baseline and measures of back pain intensity, evoked pain responsiveness (thermal, ischemic), and subjective opioid effects after receiving intravenous morphine (.08 mg/kg) or saline placebo. Morphine effect measures were derived for all outcomes, reflecting the difference between morphine and placebo condition values. Higher SOAPP-R scores were significantly associated with greater desire to take morphine again, less feeling down and feeling bad, and greater reductions in sensory low back pain intensity following morphine administration. This latter effect was due primarily to SOAPP-R content assessing medication-specific attitudes and behavior. Individuals exceeding the clinical cutoff (18 or higher) on the SOAPP-R exhibited significantly greater morphine liking, desire to take morphine again, and feeling sedated; less feeling bad; and greater reductions in sensory low back pain following morphine. The SOAPP-R may predict elevated opioid risk in part by tapping into individual differences in opioid reinforcing effects. PERSPECTIVE: Based on placebo-controlled morphine responses, associations were observed between higher scores on a common opioid risk screener (SOAPP-R) and greater desire to take morphine again, fewer negative subjective morphine effects, and greater analgesia. Opioids may provide the best analgesia in those patients at greatest risk of opioid misuse.

Indexed as

AdolescentAdultAnalgesics, OpioidCross-Over StudiesDouble-Blind MethodFemaleHumansLow Back PainMaleMiddle AgedMorphineNaloxoneNarcotic AntagonistsOpioid-Related DisordersPain MeasurementSeverity of Illness IndexAnalgesics, OpioidMorphineNaloxoneNarcotic Antagonistsabuse riskanalgesiachronic painmisuseOpioidpersonalized medicinescreening

Identifiers

PMID25892658
PMCPMC4486517
OpenAlexW2155728924

What OpenQuestion holds

Textmetadata
LicenceTDM
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.