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Is Pregabalin Effective Against Acute Lumbar Radicular Pain ?

INTRODUCTION: Nonsteroidal anti-inflammatory drugs (NSAIDs) are the first-line treatment for acute lumbar radicular pain accompanying lumbar disc herniation (LDH), but their effects are minimal. The purpose of this study was to evaluate the efficacy and safety of pregabalin (PGB) as an alternative t...

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Autores principales: Nakashima, Hiroaki, Kanemura, Tokumi, Ando, Kei, Kobayashi, Kazuyoshi, Yoneda, Minoru, Ishiguro, Naoki, Imagama, Shiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society for Spine Surgery and Related Research 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690119/
https://www.ncbi.nlm.nih.gov/pubmed/31435553
http://dx.doi.org/10.22603/ssrr.2018-0003
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author Nakashima, Hiroaki
Kanemura, Tokumi
Ando, Kei
Kobayashi, Kazuyoshi
Yoneda, Minoru
Ishiguro, Naoki
Imagama, Shiro
author_facet Nakashima, Hiroaki
Kanemura, Tokumi
Ando, Kei
Kobayashi, Kazuyoshi
Yoneda, Minoru
Ishiguro, Naoki
Imagama, Shiro
author_sort Nakashima, Hiroaki
collection PubMed
description INTRODUCTION: Nonsteroidal anti-inflammatory drugs (NSAIDs) are the first-line treatment for acute lumbar radicular pain accompanying lumbar disc herniation (LDH), but their effects are minimal. The purpose of this study was to evaluate the efficacy and safety of pregabalin (PGB) as an alternative therapy for this condition. METHODS: Patients with acute lumbar radicular pain accompanying LDH were randomly administered either NSAIDs plus PGB (30 patients) or NSAIDs alone (30 patients) for up to 4 weeks. The primary outcome was leg pain at 2 and 4 weeks. Secondary outcomes were reduction in sleep disturbances and patient global impressions of change (PGIC) at 2 and 4 weeks. RESULTS: Four patients in the NSAIDs plus PGB group were deemed ineligible and excluded from the study. Fewer sleep disturbances were reported by patients administered NSAIDs plus PGB compared with the NSAID monotherapy group at both 2 and 4 weeks. Additionally, the NSAIDs plus PGB group showed greater improvement in pain than the NSAID monotherapy group at 4 weeks, although this difference was not significant. PGIC was also significantly better in the NSAIDs plus PGB group than in the NSAID monotherapy group at 4 weeks. The incidence of adverse events was significantly greater in the NSAIDs plus PGB group than in the NSAID monotherapy group. CONCLUSIONS: The combination of NSAIDs plus PGB is more effective against sleep disturbance than NSAIDs alone in patients with acute LDH, although the control of sciatic pain is minimal. Patients reported satisfactory recoveries could also be obtained, and thus, this combination therapy could be a good option for the conservative treatment of acute lumbar radicular pain, including LDH.
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spelling pubmed-66901192019-08-21 Is Pregabalin Effective Against Acute Lumbar Radicular Pain ? Nakashima, Hiroaki Kanemura, Tokumi Ando, Kei Kobayashi, Kazuyoshi Yoneda, Minoru Ishiguro, Naoki Imagama, Shiro Spine Surg Relat Res Original Article INTRODUCTION: Nonsteroidal anti-inflammatory drugs (NSAIDs) are the first-line treatment for acute lumbar radicular pain accompanying lumbar disc herniation (LDH), but their effects are minimal. The purpose of this study was to evaluate the efficacy and safety of pregabalin (PGB) as an alternative therapy for this condition. METHODS: Patients with acute lumbar radicular pain accompanying LDH were randomly administered either NSAIDs plus PGB (30 patients) or NSAIDs alone (30 patients) for up to 4 weeks. The primary outcome was leg pain at 2 and 4 weeks. Secondary outcomes were reduction in sleep disturbances and patient global impressions of change (PGIC) at 2 and 4 weeks. RESULTS: Four patients in the NSAIDs plus PGB group were deemed ineligible and excluded from the study. Fewer sleep disturbances were reported by patients administered NSAIDs plus PGB compared with the NSAID monotherapy group at both 2 and 4 weeks. Additionally, the NSAIDs plus PGB group showed greater improvement in pain than the NSAID monotherapy group at 4 weeks, although this difference was not significant. PGIC was also significantly better in the NSAIDs plus PGB group than in the NSAID monotherapy group at 4 weeks. The incidence of adverse events was significantly greater in the NSAIDs plus PGB group than in the NSAID monotherapy group. CONCLUSIONS: The combination of NSAIDs plus PGB is more effective against sleep disturbance than NSAIDs alone in patients with acute LDH, although the control of sciatic pain is minimal. Patients reported satisfactory recoveries could also be obtained, and thus, this combination therapy could be a good option for the conservative treatment of acute lumbar radicular pain, including LDH. The Japanese Society for Spine Surgery and Related Research 2018-06-29 /pmc/articles/PMC6690119/ /pubmed/31435553 http://dx.doi.org/10.22603/ssrr.2018-0003 Text en Copyright © 2019 by The Japanese Society for Spine Surgery and Related Research https://creativecommons.org/licenses/by-nc-nd/4.0/ Spine Surgery and Related Research is an Open Access journal distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Nakashima, Hiroaki
Kanemura, Tokumi
Ando, Kei
Kobayashi, Kazuyoshi
Yoneda, Minoru
Ishiguro, Naoki
Imagama, Shiro
Is Pregabalin Effective Against Acute Lumbar Radicular Pain ?
title Is Pregabalin Effective Against Acute Lumbar Radicular Pain ?
title_full Is Pregabalin Effective Against Acute Lumbar Radicular Pain ?
title_fullStr Is Pregabalin Effective Against Acute Lumbar Radicular Pain ?
title_full_unstemmed Is Pregabalin Effective Against Acute Lumbar Radicular Pain ?
title_short Is Pregabalin Effective Against Acute Lumbar Radicular Pain ?
title_sort is pregabalin effective against acute lumbar radicular pain ?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690119/
https://www.ncbi.nlm.nih.gov/pubmed/31435553
http://dx.doi.org/10.22603/ssrr.2018-0003
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