Expectations and positive emotional feelings accompany reductions in ongoing and evoked neuropathic pain following placebo interventions

Large placebo but not nocebo effects were seen in ongoing and evoked neuropathic pain, and patients’ expectations about these treatments coexisted with emotional feelings. Research on placebo analgesia and nocebo hyperalgesia has primarily included healthy subjects or acute pain patients, and it is...

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Published inPain (Amsterdam) Vol. 155; no. 12; pp. 2687 - 2698
Main Authors Petersen, Gitte L., Finnerup, Nanna B., Grosen, Kasper, Pilegaard, Hans K., Tracey, Irene, Benedetti, Fabrizio, Price, Donald D., Jensen, Troels S., Vase, Lene
Format Journal Article
LanguageEnglish
Published Philadelphia, PA Elsevier B.V 01.12.2014
International Association for the Study of Pain
Elsevier
Subjects
Online AccessGet full text
ISSN0304-3959
1872-6623
1872-6623
DOI10.1016/j.pain.2014.09.036

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Abstract Large placebo but not nocebo effects were seen in ongoing and evoked neuropathic pain, and patients’ expectations about these treatments coexisted with emotional feelings. Research on placebo analgesia and nocebo hyperalgesia has primarily included healthy subjects or acute pain patients, and it is unknown whether these effects can be obtained in ongoing pain in patients with chronic pain caused by an identifiable nerve injury. Eighteen patients with postthoracotomy neuropathic pain were exposed to placebo and nocebo manipulations, in which they received open and hidden administrations of pain-relieving (lidocaine) or pain-inducing (capsaicin) treatment controlled for the natural history of pain. Immediately after the open administration, patients rated their expected pain levels on a mechanical visual analogue scale (M-VAS). They also reported their emotional feelings via a quantitative/qualitative experiential method. Subsequently, patients rated their ongoing pain levels on the M-VAS and underwent quantitative sensory testing of evoked pain (brush, pinprick, area of hyperalgesia, wind-up-like pain). There was a significant placebo effect on both ongoing (P=.009 to .019) and evoked neuropathic pain (P=.0005 to .053). Expected pain levels accounted for significant amounts of the variance in ongoing (53.4%) and evoked pain (up to 34.5%) after the open lidocaine administration. Furthermore, patients reported high levels of positive and low levels of negative emotional feelings in the placebo condition compared with the nocebo condition (P⩽.001). Pain increases during nocebo were nonsignificant (P=.394 to 1.000). To our knowledge, this is the first study to demonstrate placebo effects in ongoing neuropathic pain. It provides further evidence for placebo-induced reduction in hyperalgesia and suggests that patients’ expectations coexist with emotional feelings about treatments.
AbstractList Large placebo but not nocebo effects were seen in ongoing and evoked neuropathic pain, and patients’ expectations about these treatments coexisted with emotional feelings. Research on placebo analgesia and nocebo hyperalgesia has primarily included healthy subjects or acute pain patients, and it is unknown whether these effects can be obtained in ongoing pain in patients with chronic pain caused by an identifiable nerve injury. Eighteen patients with postthoracotomy neuropathic pain were exposed to placebo and nocebo manipulations, in which they received open and hidden administrations of pain-relieving (lidocaine) or pain-inducing (capsaicin) treatment controlled for the natural history of pain. Immediately after the open administration, patients rated their expected pain levels on a mechanical visual analogue scale (M-VAS). They also reported their emotional feelings via a quantitative/qualitative experiential method. Subsequently, patients rated their ongoing pain levels on the M-VAS and underwent quantitative sensory testing of evoked pain (brush, pinprick, area of hyperalgesia, wind-up-like pain). There was a significant placebo effect on both ongoing (P=.009 to .019) and evoked neuropathic pain (P=.0005 to .053). Expected pain levels accounted for significant amounts of the variance in ongoing (53.4%) and evoked pain (up to 34.5%) after the open lidocaine administration. Furthermore, patients reported high levels of positive and low levels of negative emotional feelings in the placebo condition compared with the nocebo condition (P⩽.001). Pain increases during nocebo were nonsignificant (P=.394 to 1.000). To our knowledge, this is the first study to demonstrate placebo effects in ongoing neuropathic pain. It provides further evidence for placebo-induced reduction in hyperalgesia and suggests that patients’ expectations coexist with emotional feelings about treatments.
Large placebo but not nocebo effects were seen in ongoing and evoked neuropathic pain, and patients’ expectations about these treatments coexisted with emotional feelings. Research on placebo analgesia and nocebo hyperalgesia has primarily included healthy subjects or acute pain patients, and it is unknown whether these effects can be obtained in ongoing pain in patients with chronic pain caused by an identifiable nerve injury. Eighteen patients with postthoracotomy neuropathic pain were exposed to placebo and nocebo manipulations, in which they received open and hidden administrations of pain-relieving (lidocaine) or pain-inducing (capsaicin) treatment controlled for the natural history of pain. Immediately after the open administration, patients rated their expected pain levels on a mechanical visual analogue scale (M-VAS). They also reported their emotional feelings via a quantitative/qualitative experiential method. Subsequently, patients rated their ongoing pain levels on the M-VAS and underwent quantitative sensory testing of evoked pain (brush, pinprick, area of hyperalgesia, wind-up-like pain). There was a significant placebo effect on both ongoing (P = .009 to .019) and evoked neuropathic pain (P = .0005 to .053). Expected pain levels accounted for significant amounts of the variance in ongoing (53.4%) and evoked pain (up to 34.5%) after the open lidocaine administration. Furthermore, patients reported high levels of positive and low levels of negative emotional feelings in the placebo condition compared with the nocebo condition (P ≤ .001). Pain increases during nocebo were nonsignificant (P = .394 to 1.000). To our knowledge, this is the first study to demonstrate placebo effects in ongoing neuropathic pain. It provides further evidence for placebo-induced reduction in hyperalgesia and suggests that patients’ expectations coexist with emotional feelings about treatments.
Research on placebo analgesia and nocebo hyperalgesia has primarily included healthy subjects or acute pain patients, and it is unknown whether these effects can be obtained in ongoing pain in patients with chronic pain caused by an identifiable nerve injury. Eighteen patients with postthoracotomy neuropathic pain were exposed to placebo and nocebo manipulations, in which they received open and hidden administrations of pain-relieving (lidocaine) or pain-inducing (capsaicin) treatment controlled for the natural history of pain. Immediately after the open administration, patients rated their expected pain levels on a mechanical visual analogue scale (M-VAS). They also reported their emotional feelings via a quantitative/qualitative experiential method. Subsequently, patients rated their ongoing pain levels on the M-VAS and underwent quantitative sensory testing of evoked pain (brush, pinprick, area of hyperalgesia, wind-up-like pain). There was a significant placebo effect on both ongoing (P=.009 to .019) and evoked neuropathic pain (P=.0005 to .053). Expected pain levels accounted for significant amounts of the variance in ongoing (53.4%) and evoked pain (up to 34.5%) after the open lidocaine administration. Furthermore, patients reported high levels of positive and low levels of negative emotional feelings in the placebo condition compared with the nocebo condition (P⩽.001). Pain increases during nocebo were nonsignificant (P=.394 to 1.000). To our knowledge, this is the first study to demonstrate placebo effects in ongoing neuropathic pain. It provides further evidence for placebo-induced reduction in hyperalgesia and suggests that patients' expectations coexist with emotional feelings about treatments.Research on placebo analgesia and nocebo hyperalgesia has primarily included healthy subjects or acute pain patients, and it is unknown whether these effects can be obtained in ongoing pain in patients with chronic pain caused by an identifiable nerve injury. Eighteen patients with postthoracotomy neuropathic pain were exposed to placebo and nocebo manipulations, in which they received open and hidden administrations of pain-relieving (lidocaine) or pain-inducing (capsaicin) treatment controlled for the natural history of pain. Immediately after the open administration, patients rated their expected pain levels on a mechanical visual analogue scale (M-VAS). They also reported their emotional feelings via a quantitative/qualitative experiential method. Subsequently, patients rated their ongoing pain levels on the M-VAS and underwent quantitative sensory testing of evoked pain (brush, pinprick, area of hyperalgesia, wind-up-like pain). There was a significant placebo effect on both ongoing (P=.009 to .019) and evoked neuropathic pain (P=.0005 to .053). Expected pain levels accounted for significant amounts of the variance in ongoing (53.4%) and evoked pain (up to 34.5%) after the open lidocaine administration. Furthermore, patients reported high levels of positive and low levels of negative emotional feelings in the placebo condition compared with the nocebo condition (P⩽.001). Pain increases during nocebo were nonsignificant (P=.394 to 1.000). To our knowledge, this is the first study to demonstrate placebo effects in ongoing neuropathic pain. It provides further evidence for placebo-induced reduction in hyperalgesia and suggests that patients' expectations coexist with emotional feelings about treatments.
Research on placebo analgesia and nocebo hyperalgesia has primarily included healthy subjects or acute pain patients, and it is unknown whether these effects can be obtained in ongoing pain in patients with chronic pain caused by an identifiable nerve injury. Eighteen patients with postthoracotomy neuropathic pain were exposed to placebo and nocebo manipulations, in which they received open and hidden administrations of pain-relieving (lidocaine) or pain-inducing (capsaicin) treatment controlled for the natural history of pain. Immediately after the open administration, patients rated their expected pain levels on a mechanical visual analogue scale (M-VAS). They also reported their emotional feelings via a quantitative/qualitative experiential method. Subsequently, patients rated their ongoing pain levels on the M-VAS and underwent quantitative sensory testing of evoked pain (brush, pinprick, area of hyperalgesia, wind-up-like pain). There was a significant placebo effect on both ongoing (P=.009 to .019) and evoked neuropathic pain (P=.0005 to .053). Expected pain levels accounted for significant amounts of the variance in ongoing (53.4%) and evoked pain (up to 34.5%) after the open lidocaine administration. Furthermore, patients reported high levels of positive and low levels of negative emotional feelings in the placebo condition compared with the nocebo condition (P⩽.001). Pain increases during nocebo were nonsignificant (P=.394 to 1.000). To our knowledge, this is the first study to demonstrate placebo effects in ongoing neuropathic pain. It provides further evidence for placebo-induced reduction in hyperalgesia and suggests that patients' expectations coexist with emotional feelings about treatments.
Author Benedetti, Fabrizio
Petersen, Gitte L.
Pilegaard, Hans K.
Jensen, Troels S.
Price, Donald D.
Vase, Lene
Tracey, Irene
Finnerup, Nanna B.
Grosen, Kasper
AuthorAffiliation Department of Psychology and Behavioural Sciences, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital, Skejby, Denmark Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, UK Department of Neuroscience, Clinical and Applied Physiology Program, University of Turin Medical School, Turin, Italy Division of Neuroscience, Department of Oral and Maxillofacial Surgery, University of Florida, Gainesville, FL, USA
AuthorAffiliation_xml – name: Department of Psychology and Behavioural Sciences, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital, Skejby, Denmark Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, UK Department of Neuroscience, Clinical and Applied Physiology Program, University of Turin Medical School, Turin, Italy Division of Neuroscience, Department of Oral and Maxillofacial Surgery, University of Florida, Gainesville, FL, USA
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  givenname: Nanna B.
  surname: Finnerup
  fullname: Finnerup, Nanna B.
  organization: Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark
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  givenname: Hans K.
  surname: Pilegaard
  fullname: Pilegaard, Hans K.
  organization: Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital, Skejby, Denmark
– sequence: 5
  givenname: Irene
  surname: Tracey
  fullname: Tracey, Irene
  organization: Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB), Nuffield Department of Clinical Neurosciences, University of Oxford, John Radcliffe Hospital, UK
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  surname: Benedetti
  fullname: Benedetti, Fabrizio
  organization: Department of Neuroscience, Clinical and Applied Physiology Program, University of Turin Medical School, Turin, Italy
– sequence: 7
  givenname: Donald D.
  surname: Price
  fullname: Price, Donald D.
  organization: Division of Neuroscience, Department of Oral and Maxillofacial Surgery, University of Florida, Gainesville, FL, USA
– sequence: 8
  givenname: Troels S.
  surname: Jensen
  fullname: Jensen, Troels S.
  organization: Danish Pain Research Center, Aarhus University Hospital, Aarhus, Denmark
– sequence: 9
  givenname: Lene
  surname: Vase
  fullname: Vase, Lene
  organization: Department of Psychology and Behavioural Sciences, School of Business and Social Sciences, Aarhus University, Aarhus, Denmark
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IsScholarly true
Issue 12
Keywords Emotional feelings
Expectation
Placebo analgesia
Nocebo hyperalgesia
Neuropathic pain
Affect affectivity
Analgesia
Nervous system diseases
Treatment
Placebo
Emotion emotionality
Hyperalgesia
Language English
License CC BY 4.0
Copyright © 2014 International Association for the Study of Pain. Published by Elsevier B.V. All rights reserved.
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Snippet Large placebo but not nocebo effects were seen in ongoing and evoked neuropathic pain, and patients’ expectations about these treatments coexisted with...
Research on placebo analgesia and nocebo hyperalgesia has primarily included healthy subjects or acute pain patients, and it is unknown whether these effects...
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SubjectTerms Adult
Aged
Anesthetics, Local - therapeutic use
Biological and medical sciences
Capsaicin - administration & dosage
Emotional feelings
Emotions
Expectation
Female
Humans
Lidocaine - therapeutic use
Male
Medical sciences
Middle Aged
Nervous system (semeiology, syndromes)
Nervous system as a whole
Nervous system involvement in other diseases. Miscellaneous
Neuralgia - psychology
Neuralgia - therapy
Neurology
Neuropathic pain
Nocebo Effect
Nocebo hyperalgesia
Pain Measurement
Physical Stimulation
Placebo analgesia
Placebo Effect
Postoperative Complications - drug therapy
Postoperative Complications - psychology
Psychological Tests
Sensory System Agents - administration & dosage
Thoracostomy - adverse effects
Title Expectations and positive emotional feelings accompany reductions in ongoing and evoked neuropathic pain following placebo interventions
URI https://dx.doi.org/10.1016/j.pain.2014.09.036
https://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00006396-201412000-00033
https://www.ncbi.nlm.nih.gov/pubmed/25281929
https://www.proquest.com/docview/1629587057
https://www.proquest.com/docview/1717242619
Volume 155
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