Literature DB >> 28802882

Chronic Opioid Therapy Modifies QST Changes After Ketamine Infusion in Chronic Pain Patients.

Dermot P Maher1, Yi Zhang2, Shihab Ahmed2, Tina Doshi3, Charlene Malarick2, Kristin Stabach2, Jianren Mao2, Lucy Chen2.   

Abstract

The long-term effects of opioids on sensitization processes are believed to be mediated through the N-methyl-D-aspartate receptor. Quantitative sensory testing (QST) changes observed after a ketamine infusion have been previously described but the effect that chronic opioids will have is not known. The results of this prospective randomized factorial trial compared the thermal QST changes observed after a .05 mg/kg ketamine infusion or a saline placebo in chronic pain subjects who were either opioid-naive or were chronically using opioids for chronic noncancer pain are presented. No baseline QST differences were noted between the 4 groups at baseline. Comparison of changes preinfusion with postinfusion QST measurements resulted in decreased average change in temporal summation response between opioid subjects who received a placebo compared with those who received a ketamine infusion (-5.22, SD = 9.96 vs 13.81, SD = 19.55; P = .004). Additionally, the average change in temporal summation was decreased among subjects who received a ketamine infusion and were not chronically using opioids compared with subjects who were using chronic opioids and received a placebo infusion (-1.91, SD = 13.25 vs 13.81, SD = 19.55; P = .007). The results indicate that low-dose ketamine infusions produce subtle changes in QST phenotypes that are modified by the chronic use of opioids. This illustrates the potential diagnostic and therapeutic value of ketamine in the setting of chronic opioid use. PERSPECTIVE: The presented data further our understanding of modulation of sensory perception in the setting of chronic opioid use and the role of the N-methyl-D-aspartate receptor. The use of low-dose ketamine infusions may be useful for the treatment as well as diagnosis of opioid-related neuropathic conditions.
Copyright © 2017 American Pain Society. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Ketamine; N-methyl-D-aspartate receptor; opioid receptor; quantitative sensory testing; temporal summation

Mesh:

Substances:

Year:  2017        PMID: 28802882      PMCID: PMC5729746          DOI: 10.1016/j.jpain.2017.07.008

Source DB:  PubMed          Journal:  J Pain        ISSN: 1526-5900            Impact factor:   5.820


  31 in total

Review 1.  Opioid-induced abnormal pain sensitivity: implications in clinical opioid therapy.

Authors:  Jianren Mao
Journal:  Pain       Date:  2002-12       Impact factor: 6.961

2.  The effect of target-controlled infusion of low-dose ketamine on heat pain and temporal summation threshold.

Authors:  Joon-Ho Lee; Sung-Hwan Cho; Sang-Hyun Kim; Won-Soek Chae; Hee-Cheol Jin; Jeong-Seok Lee; Yong-Ik Kim
Journal:  J Anesth       Date:  2011-04-22       Impact factor: 2.078

3.  Increased pain sensitivity in chronic pain subjects on opioid therapy: a cross-sectional study using quantitative sensory testing.

Authors:  Yi Zhang; Shihab Ahmed; Trang Vo; Kristin St Hilaire; Mary Houghton; Abigail S Cohen; Jianren Mao; Lucy Chen
Journal:  Pain Med       Date:  2014-11-06       Impact factor: 3.750

4.  Concentration-effect relationship of intravenous alfentanil and ketamine on peripheral neurosensory thresholds, allodynia and hyperalgesia of neuropathic pain.

Authors:  A Leung; M S Wallace; B Ridgeway; T Yaksh
Journal:  Pain       Date:  2001-03       Impact factor: 6.961

5.  Altered quantitative sensory testing outcome in subjects with opioid therapy.

Authors:  Lucy Chen; Charlene Malarick; Lindsey Seefeld; Shuxing Wang; Mary Houghton; Jianren Mao
Journal:  Pain       Date:  2009-02-23       Impact factor: 6.961

6.  Experimental mononeuropathy reduces the antinociceptive effects of morphine: implications for common intracellular mechanisms involved in morphine tolerance and neuropathic pain.

Authors:  Jianren Mao; Donald D Price; David J Mayer
Journal:  Pain       Date:  1995-06       Impact factor: 6.961

7.  The N-methyl-D-aspartate receptor antagonist dextromethorphan selectively reduces temporal summation of second pain in man.

Authors:  Donald D Price; Jianren Mao; Hanan Frenk; David J Mayer
Journal:  Pain       Date:  1994-11       Impact factor: 6.961

8.  Neuropathic pain phenotyping as a predictor of treatment response in painful diabetic neuropathy: data from the randomized, double-blind, COMBO-DN study.

Authors:  Didier Bouhassira; Stefan Wilhelm; Alexander Schacht; Serge Perrot; Eva Kosek; Giorgio Cruccu; Rainer Freynhagen; Solomon Tesfaye; Alberto Lledó; Ernest Choy; Paolo Marchettini; Juan Antonio Micó; Michael Spaeth; Vladimir Skljarevski; Thomas Tölle
Journal:  Pain       Date:  2014-08-27       Impact factor: 6.961

9.  Thermal QST Phenotypes Associated with Response to Lumbar Epidural Steroid Injections: A Pilot Study.

Authors:  Dermot P Maher; Weihua Ding; Sarabdeep Singh; Arissa Opalacz; Claire Fishman; Mary Houghton; Shihab Ahmed; Lucy Chen; Jianren Mao; Yi Zhang
Journal:  Pain Med       Date:  2017-08-01       Impact factor: 3.750

10.  Ketamine coadministration attenuates morphine tolerance and leads to increased brain concentrations of both drugs in the rat.

Authors:  T O Lilius; V Jokinen; M S Neuvonen; M Niemi; E A Kalso; P V Rauhala
Journal:  Br J Pharmacol       Date:  2015-06       Impact factor: 8.739

View more
  2 in total

1.  Increased Experimental Pain Sensitivity in Chronic Pain Patients Who Developed Opioid Use Disorder.

Authors:  Peggy A Compton; Thomas E Wasser; Martin D Cheatle
Journal:  Clin J Pain       Date:  2020-09       Impact factor: 3.423

2.  Low mechano-afferent fibers reduce thermal pain but not pain intensity in CRPS.

Authors:  Heidrun H Krämer; Susann Seddigh; Kathrin Habig; Gothje Lautenschläger; Hagen Maxeiner; Frank Birklein
Journal:  BMC Neurol       Date:  2021-07-09       Impact factor: 2.474

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.