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The relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis

BACKGROUND: Euphoria is a complex, multifactorial problem that is reported as an adverse event in clinical trials of analgesics including pregabalin. The relationship between the reporting of euphoria events and pregabalin early treatment responses was examined in this exploratory post-hoc analysis....

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Autores principales: Parsons, Bruce, Freynhagen, Rainer, Schug, Stephan, Whalen, Ed, Ortiz, Marie, Bhadra Brown, Pritha, Knapp, Lloyd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709807/
https://www.ncbi.nlm.nih.gov/pubmed/31686899
http://dx.doi.org/10.2147/JPR.S199203
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author Parsons, Bruce
Freynhagen, Rainer
Schug, Stephan
Whalen, Ed
Ortiz, Marie
Bhadra Brown, Pritha
Knapp, Lloyd
author_facet Parsons, Bruce
Freynhagen, Rainer
Schug, Stephan
Whalen, Ed
Ortiz, Marie
Bhadra Brown, Pritha
Knapp, Lloyd
author_sort Parsons, Bruce
collection PubMed
description BACKGROUND: Euphoria is a complex, multifactorial problem that is reported as an adverse event in clinical trials of analgesics including pregabalin. The relationship between the reporting of euphoria events and pregabalin early treatment responses was examined in this exploratory post-hoc analysis. METHODS: Data were from patients with neuropathic or non-neuropathic chronic pain enrolled in 40 randomized clinical trials, who received pregabalin (75–600 mg/day) or placebo. Reports of treatment-emergent euphoria events were based on the Medical Dictionary of Regulatory Activities preferred term “euphoric mood”. Prevalence rates of euphoria events overall and by indication were assessed. Post-treatment endpoints included ≥30% improvements in pain and sleep scores up to 3 weeks as well as a ≥1-point improvement in daily pain score up to 11 days after treatment. RESULTS: 13,252 patients were analyzed; 8,501 (64.1%) and 4,751 (35.9%) received pregabalin and placebo, respectively. Overall, 1.7% (n=222) of patients reported euphoria events. Among pregabalin-treated patients, a larger proportion who reported euphoria events achieved an early pain response compared with those who did not report euphoria (30% pain responders in week 1 with euphoria events [43.0%], without euphoria events [24.2%]). Results were similar for weeks 2 and 3. For Days 2–11, a larger proportion of pregabalin-treated patients with (relative to without) euphoria events were 1-point pain responders. Findings were similar in pregabalin-treated patients for sleep endpoints (30% sleep responders in week 1 with euphoria events [50.7%], without euphoria events [36.1%]). Similar results were found for weeks 2 and 3. Patients who received placebo showed similar patterns, although the overall number of them who reported euphoria events was small (n=13). CONCLUSION: In patients who received pregabalin for neuropathic or non-neuropathic chronic pain, those who experienced euphoria events may have better early treatment responses than those who did not report euphoria events.
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spelling pubmed-67098072019-11-04 The relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis Parsons, Bruce Freynhagen, Rainer Schug, Stephan Whalen, Ed Ortiz, Marie Bhadra Brown, Pritha Knapp, Lloyd J Pain Res Original Research BACKGROUND: Euphoria is a complex, multifactorial problem that is reported as an adverse event in clinical trials of analgesics including pregabalin. The relationship between the reporting of euphoria events and pregabalin early treatment responses was examined in this exploratory post-hoc analysis. METHODS: Data were from patients with neuropathic or non-neuropathic chronic pain enrolled in 40 randomized clinical trials, who received pregabalin (75–600 mg/day) or placebo. Reports of treatment-emergent euphoria events were based on the Medical Dictionary of Regulatory Activities preferred term “euphoric mood”. Prevalence rates of euphoria events overall and by indication were assessed. Post-treatment endpoints included ≥30% improvements in pain and sleep scores up to 3 weeks as well as a ≥1-point improvement in daily pain score up to 11 days after treatment. RESULTS: 13,252 patients were analyzed; 8,501 (64.1%) and 4,751 (35.9%) received pregabalin and placebo, respectively. Overall, 1.7% (n=222) of patients reported euphoria events. Among pregabalin-treated patients, a larger proportion who reported euphoria events achieved an early pain response compared with those who did not report euphoria (30% pain responders in week 1 with euphoria events [43.0%], without euphoria events [24.2%]). Results were similar for weeks 2 and 3. For Days 2–11, a larger proportion of pregabalin-treated patients with (relative to without) euphoria events were 1-point pain responders. Findings were similar in pregabalin-treated patients for sleep endpoints (30% sleep responders in week 1 with euphoria events [50.7%], without euphoria events [36.1%]). Similar results were found for weeks 2 and 3. Patients who received placebo showed similar patterns, although the overall number of them who reported euphoria events was small (n=13). CONCLUSION: In patients who received pregabalin for neuropathic or non-neuropathic chronic pain, those who experienced euphoria events may have better early treatment responses than those who did not report euphoria events. Dove 2019-08-22 /pmc/articles/PMC6709807/ /pubmed/31686899 http://dx.doi.org/10.2147/JPR.S199203 Text en © 2019 Parsons et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Parsons, Bruce
Freynhagen, Rainer
Schug, Stephan
Whalen, Ed
Ortiz, Marie
Bhadra Brown, Pritha
Knapp, Lloyd
The relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis
title The relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis
title_full The relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis
title_fullStr The relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis
title_full_unstemmed The relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis
title_short The relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis
title_sort relationship between the reporting of euphoria events and early treatment responses to pregabalin: an exploratory post-hoc analysis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6709807/
https://www.ncbi.nlm.nih.gov/pubmed/31686899
http://dx.doi.org/10.2147/JPR.S199203
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