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Intrathecal betamethasone for cancer pain: A study of its analgesic efficacy and safety
BACKGROUND: A preliminary study has shown effective cancer pain relief by intrathecal betamethasone (ITB). However, further evidence is needed to support this new approach. METHODS: Cancer patients with opioid‐resistant pain received lumbar intrathecal administration of betamethasone 2 or 3 mg once...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587555/ https://www.ncbi.nlm.nih.gov/pubmed/30536525 http://dx.doi.org/10.1111/aas.13305 |
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author | Taguchi, Hitoshi Oishi, Keiko Shingu, Koh Matsumoto, Hideo Masuzawa, Munehiro |
author_facet | Taguchi, Hitoshi Oishi, Keiko Shingu, Koh Matsumoto, Hideo Masuzawa, Munehiro |
author_sort | Taguchi, Hitoshi |
collection | PubMed |
description | BACKGROUND: A preliminary study has shown effective cancer pain relief by intrathecal betamethasone (ITB). However, further evidence is needed to support this new approach. METHODS: Cancer patients with opioid‐resistant pain received lumbar intrathecal administration of betamethasone 2 or 3 mg once a week for 28 days. Immediate and short‐term analgesia (using a percentage pain reduction scale and a numerical rating scale, NRS) and long‐term analgesia (using NRS) were assessed. Patients were classified into two groups according to the most painful site of metastasis: vertebral column and/or surrounding nerve plexus metastases (group A) and other metastases distal from the vertebral column (group B). RESULTS: A total of 104 patients received ITB. Pain relief was observed not only in the lower half but also in the upper half of the body. The proportion of group A patients who experienced immediate analgesia was 81% (47/58), which was significantly greater than that of group B (P < 0.001). A decrease in NRS scores 1 day after ITB administration was observed in significantly more patients in group A than in group B (P < 0.001). Long‐term analgesia was also recorded in a greater proportion of patients in group A than in group B in the 7‐day (59%, 38/64 vs 6%, 2/33) and 28‐day periods (71%, 40/56 vs 31%, 8/26) (P < 0.001). No adverse effects related to neurotoxicity were recorded. CONCLUSION: Intrathecal injection of betamethasone produced analgesia for opioid‐resistant cancer pain, and may be a potent therapeutic option for intolerable pain from vertebral column and/or surrounding nerve plexus metastases. |
format | Online Article Text |
id | pubmed-6587555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65875552019-07-02 Intrathecal betamethasone for cancer pain: A study of its analgesic efficacy and safety Taguchi, Hitoshi Oishi, Keiko Shingu, Koh Matsumoto, Hideo Masuzawa, Munehiro Acta Anaesthesiol Scand Regional Anaesthesia and Pain Therapy BACKGROUND: A preliminary study has shown effective cancer pain relief by intrathecal betamethasone (ITB). However, further evidence is needed to support this new approach. METHODS: Cancer patients with opioid‐resistant pain received lumbar intrathecal administration of betamethasone 2 or 3 mg once a week for 28 days. Immediate and short‐term analgesia (using a percentage pain reduction scale and a numerical rating scale, NRS) and long‐term analgesia (using NRS) were assessed. Patients were classified into two groups according to the most painful site of metastasis: vertebral column and/or surrounding nerve plexus metastases (group A) and other metastases distal from the vertebral column (group B). RESULTS: A total of 104 patients received ITB. Pain relief was observed not only in the lower half but also in the upper half of the body. The proportion of group A patients who experienced immediate analgesia was 81% (47/58), which was significantly greater than that of group B (P < 0.001). A decrease in NRS scores 1 day after ITB administration was observed in significantly more patients in group A than in group B (P < 0.001). Long‐term analgesia was also recorded in a greater proportion of patients in group A than in group B in the 7‐day (59%, 38/64 vs 6%, 2/33) and 28‐day periods (71%, 40/56 vs 31%, 8/26) (P < 0.001). No adverse effects related to neurotoxicity were recorded. CONCLUSION: Intrathecal injection of betamethasone produced analgesia for opioid‐resistant cancer pain, and may be a potent therapeutic option for intolerable pain from vertebral column and/or surrounding nerve plexus metastases. John Wiley and Sons Inc. 2018-12-07 2019-05 /pmc/articles/PMC6587555/ /pubmed/30536525 http://dx.doi.org/10.1111/aas.13305 Text en © 2018 The Authors. Acta Anaesthesiologica Scandinavica published by John Wiley & Sons Ltd on behalf of Acta Anaesthesiologica Scandinavica Foundation This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Regional Anaesthesia and Pain Therapy Taguchi, Hitoshi Oishi, Keiko Shingu, Koh Matsumoto, Hideo Masuzawa, Munehiro Intrathecal betamethasone for cancer pain: A study of its analgesic efficacy and safety |
title | Intrathecal betamethasone for cancer pain: A study of its analgesic efficacy and safety |
title_full | Intrathecal betamethasone for cancer pain: A study of its analgesic efficacy and safety |
title_fullStr | Intrathecal betamethasone for cancer pain: A study of its analgesic efficacy and safety |
title_full_unstemmed | Intrathecal betamethasone for cancer pain: A study of its analgesic efficacy and safety |
title_short | Intrathecal betamethasone for cancer pain: A study of its analgesic efficacy and safety |
title_sort | intrathecal betamethasone for cancer pain: a study of its analgesic efficacy and safety |
topic | Regional Anaesthesia and Pain Therapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587555/ https://www.ncbi.nlm.nih.gov/pubmed/30536525 http://dx.doi.org/10.1111/aas.13305 |
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