Evidence map›Paper›PMID 30605458›Full record

ArticlePloS one2019

A test of positive suggestions about side effects as a way of enhancing the analgesic response to NSAIDs.

Aurore Fernandez, Irving Kirsch, Louis Noël, Pierre Yves Rodondi, Ted J Kaptchuk, Marc R Suter, Isabelle Décosterd, Chantal Berna

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 2 pooled it
1.7field-weighted citation impact, top 17% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Changing Mindsets About Side Effects of the COVID-19 Vaccination: A Randomized Controlled Trial.Annals of behavioral medicine : a publication of the Society of Behavioral Medicine · 2023
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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

8 authors at 3 institutions in 2 countries.

Aurore FernandezPain Center, Department of Anesthesiology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.ORCID 0000-0001-9780-5152
Irving KirschProgram in Placebo Studies, Harvard Medical School, Boston, MA, United States of America.
Louis NoëlPain Center, Department of Anesthesiology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.ORCID 0000-0003-2387-060X
Pierre Yves RodondiFaculty of Biology and Medicine (FBM), University of Lausanne (UNIL), Lausanne, Switzerland.
Ted J KaptchukProgram in Placebo Studies, Harvard Medical School, Boston, MA, United States of America.
Marc R SuterPain Center, Department of Anesthesiology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Isabelle DécosterdPain Center, Department of Anesthesiology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
Chantal BernaPain Center, Department of Anesthesiology, Lausanne University Hospital (CHUV), Lausanne, Switzerland.
University of Lausanne · CHHarvard University · USInstitute of Social and Preventive Medicine · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Side effects are frequent in pharmacological pain management, potentially preceding analgesia and limiting drug tolerability. Discussing side effects is part of informed consent, yet can favor nocebo effects. This study aimed to test whether a positive suggestion regarding side effects, which could act as reminders of the medication having been absorbed, might favor analgesia in a clinical interaction model. Sixty-six healthy males participated in a study "to validate pupillometry as an objective measure of analgesia". Participants were unknowingly randomized double-blind to positive vs control information about side effects embedded in a video regarding the study drugs. Sequences of moderately painful heat stimuli applied before and after treatment with diclofenac and atropine served to evaluate analgesia. Atropine was deceptively presented as a co-analgesic, but used to induce side effects. Adverse events (AE) were collected with the General Assessment of Side Effects (GASE) questionnaire prior to the second induced pain sequence. Debriefing fully informed participants regarding the purpose of the study and showed them the two videos.The combination of medication led to significant analgesia, without a between-group difference. Positive information about side effects increased the attribution of AE to the treatment compared to the control information. The total GASE score was correlated with analgesia, i.e., the more AEs reported, the stronger the analgesia. Interestingly, there was a significant between-groups difference on this correlation: the GASE score and analgesia correlated only in the positive information group. This provides evidence for a selective link between AEs and pain relief in the group who received the suggestion that AEs could be taken as a sign "that help was on the way". During debriefing, 65% of participants said they would prefer to receive the positive message in a clinical context. Although the present results cannot be translated immediately to clinical pain conditions, they do indicate the importance of testing this type of modulation in a clinical context.

Indexed as

AdultAnalgesiaAnalgesicsAnti-Inflammatory Agents, Non-SteroidalAtropineDouble-Blind MethodHumansMaleNocebo EffectOptimismPain MeasurementPersuasive CommunicationPostoperative PainSuggestionAnalgesicsAnti-Inflammatory Agents, Non-SteroidalAtropine

Identifiers

PMID30605458
PMCPMC6317829
OpenAlexW2908127402

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.