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Differences in the Analgesic Effect of Opioids on Pain in Cancer Patients With Spinal Metastases

BACKGROUND: Spinal metastasis pain includes both inflammatory and neuropathic pain, and opioids, which have only a μ-opioid receptor-stimulating effect, are generally less effective in neuropathic pain. However, no previous study has been conducted for the comparisons of the efficacy of opioids in t...

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Autores principales: Takemura, Miho, Niki, Kazuyuki, Okamoto, Yoshiaki, Tamura, Hiroshi, Kawamura, Tomohiro, Kohno, Makie, Matsuda, Yoshinobu, Ikeda, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457616/
https://www.ncbi.nlm.nih.gov/pubmed/37637760
http://dx.doi.org/10.1089/pmr.2023.0018
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author Takemura, Miho
Niki, Kazuyuki
Okamoto, Yoshiaki
Tamura, Hiroshi
Kawamura, Tomohiro
Kohno, Makie
Matsuda, Yoshinobu
Ikeda, Kenji
author_facet Takemura, Miho
Niki, Kazuyuki
Okamoto, Yoshiaki
Tamura, Hiroshi
Kawamura, Tomohiro
Kohno, Makie
Matsuda, Yoshinobu
Ikeda, Kenji
author_sort Takemura, Miho
collection PubMed
description BACKGROUND: Spinal metastasis pain includes both inflammatory and neuropathic pain, and opioids, which have only a μ-opioid receptor-stimulating effect, are generally less effective in neuropathic pain. However, no previous study has been conducted for the comparisons of the efficacy of opioids in treating spinal metastasis pain. OBJECTIVE: To compare the efficacy of tapentadol and methadone with other opioids for back pain caused by a metastatic spinal tumor. DESIGN: Retrospective cohort study. SETTING/SUBJECTS: A total of 274 patients were enrolled, who started a tapentadol extended-release tablet, methadone tablet, hydromorphone extended-release tablet, oxycodone extended-release tablet, or transdermal fentanyl patch for cancer pain due to spinal metastasis in Japan from January 1, 2013 to October 31, 2021. MEASUREMENTS: The primary endpoint, the difference in the numerical rating scale (NRS) scores before and seven days after each opioid administration, was compared among the five groups. RESULTS: In patients with numbness, a decrease of the NRS score on day seven compared with before starting each opioid was significantly higher in the tapentadol group than those in the hydromorphone, oxycodone, and fentanyl groups and comparable to that in the methadone group. In patients without numbness, no significant differences were observed in decreases of the NRS scores on day seven among the five groups. CONCLUSIONS: Tapentadol and methadone may be more effective than hydromorphone, oxycodone, and fentanyl for cancer pain due to spinal metastasis with numbness.
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spelling pubmed-104576162023-08-27 Differences in the Analgesic Effect of Opioids on Pain in Cancer Patients With Spinal Metastases Takemura, Miho Niki, Kazuyuki Okamoto, Yoshiaki Tamura, Hiroshi Kawamura, Tomohiro Kohno, Makie Matsuda, Yoshinobu Ikeda, Kenji Palliat Med Rep Original Article BACKGROUND: Spinal metastasis pain includes both inflammatory and neuropathic pain, and opioids, which have only a μ-opioid receptor-stimulating effect, are generally less effective in neuropathic pain. However, no previous study has been conducted for the comparisons of the efficacy of opioids in treating spinal metastasis pain. OBJECTIVE: To compare the efficacy of tapentadol and methadone with other opioids for back pain caused by a metastatic spinal tumor. DESIGN: Retrospective cohort study. SETTING/SUBJECTS: A total of 274 patients were enrolled, who started a tapentadol extended-release tablet, methadone tablet, hydromorphone extended-release tablet, oxycodone extended-release tablet, or transdermal fentanyl patch for cancer pain due to spinal metastasis in Japan from January 1, 2013 to October 31, 2021. MEASUREMENTS: The primary endpoint, the difference in the numerical rating scale (NRS) scores before and seven days after each opioid administration, was compared among the five groups. RESULTS: In patients with numbness, a decrease of the NRS score on day seven compared with before starting each opioid was significantly higher in the tapentadol group than those in the hydromorphone, oxycodone, and fentanyl groups and comparable to that in the methadone group. In patients without numbness, no significant differences were observed in decreases of the NRS scores on day seven among the five groups. CONCLUSIONS: Tapentadol and methadone may be more effective than hydromorphone, oxycodone, and fentanyl for cancer pain due to spinal metastasis with numbness. Mary Ann Liebert, Inc., publishers 2023-08-09 /pmc/articles/PMC10457616/ /pubmed/37637760 http://dx.doi.org/10.1089/pmr.2023.0018 Text en © Miho Takemura et al., 2023; Published by Mary Ann Liebert, Inc. https://creativecommons.org/licenses/by/4.0/This Open Access article is distributed under the terms of the Creative Commons License [CC-BY] (http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Takemura, Miho
Niki, Kazuyuki
Okamoto, Yoshiaki
Tamura, Hiroshi
Kawamura, Tomohiro
Kohno, Makie
Matsuda, Yoshinobu
Ikeda, Kenji
Differences in the Analgesic Effect of Opioids on Pain in Cancer Patients With Spinal Metastases
title Differences in the Analgesic Effect of Opioids on Pain in Cancer Patients With Spinal Metastases
title_full Differences in the Analgesic Effect of Opioids on Pain in Cancer Patients With Spinal Metastases
title_fullStr Differences in the Analgesic Effect of Opioids on Pain in Cancer Patients With Spinal Metastases
title_full_unstemmed Differences in the Analgesic Effect of Opioids on Pain in Cancer Patients With Spinal Metastases
title_short Differences in the Analgesic Effect of Opioids on Pain in Cancer Patients With Spinal Metastases
title_sort differences in the analgesic effect of opioids on pain in cancer patients with spinal metastases
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10457616/
https://www.ncbi.nlm.nih.gov/pubmed/37637760
http://dx.doi.org/10.1089/pmr.2023.0018
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