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Natural history of pain associated with melanoma surgery
INTRODUCTION: After excision of a primary malignant melanoma (MM), treatment of stage IB or higher MM consists of sentinel lymph node biopsy (SLNB). If malignant cells are identified, a complete lymph node dissection (CLND) can be performed. OBJECTIVE: To determine the natural history of pain and se...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344134/ https://www.ncbi.nlm.nih.gov/pubmed/30706034 http://dx.doi.org/10.1097/PR9.0000000000000689 |
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author | Slagelse, Charlotte Munch, Troels Glazer, Clara Greene, Kaitlin Finnerup, Nanna Brix Kashani-Sabet, Mohammed Leong, Stanley P. Petersen, Karin Lottrup Rowbotham, Michael C. |
author_facet | Slagelse, Charlotte Munch, Troels Glazer, Clara Greene, Kaitlin Finnerup, Nanna Brix Kashani-Sabet, Mohammed Leong, Stanley P. Petersen, Karin Lottrup Rowbotham, Michael C. |
author_sort | Slagelse, Charlotte |
collection | PubMed |
description | INTRODUCTION: After excision of a primary malignant melanoma (MM), treatment of stage IB or higher MM consists of sentinel lymph node biopsy (SLNB). If malignant cells are identified, a complete lymph node dissection (CLND) can be performed. OBJECTIVE: To determine the natural history of pain and sensory changes after MM surgery. METHODS: We prospectively followed 39 patients (29 SLNB-only, 2 CLND-only, and 8 CLND preceded by SLNB) from before inguinal or axillary surgery through 6 months after surgery on measures of pain intensity, sensory symptoms, allodynia, and questionnaires of anxiety, depression, and catastrophizing. RESULTS: No patient had pain preoperatively. Ten days after surgery, 35% had surgical site pain after SLNB-only compared with 90% after CLND (P < 0.003); clinically meaningful pain (Visual Analogue Scale ≥ 30 mm/100 mm) was reported by 3% of patients after SLNB-only compared with 40% after CLND (P < 0.001). At 6 months, all SLNB-only patients were pain-free. By contrast, 4 of 7 in the SLNB + CLND group still had pain (P < 0.002). At 6 months, symptoms of altered sensation or numbness were reported by 32% and 42% of SLNB-only patients, and by 67% and 67% of patients undergoing CLND surgery (both P > 0.05). CONCLUSION: Acute pain is more common after CLND surgery. Undergoing SLNB followed by more invasive CLND surgery may increase the likelihood of pain at 6 months. Persistent sensory symptoms typical of those associated with nerve injury are more common after CLND. Surgery for MM is a good model for studying the natural history of postsurgical pain and sensory changes. |
format | Online Article Text |
id | pubmed-6344134 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer |
record_format | MEDLINE/PubMed |
spelling | pubmed-63441342019-01-31 Natural history of pain associated with melanoma surgery Slagelse, Charlotte Munch, Troels Glazer, Clara Greene, Kaitlin Finnerup, Nanna Brix Kashani-Sabet, Mohammed Leong, Stanley P. Petersen, Karin Lottrup Rowbotham, Michael C. Pain Rep Cancer and Palliative INTRODUCTION: After excision of a primary malignant melanoma (MM), treatment of stage IB or higher MM consists of sentinel lymph node biopsy (SLNB). If malignant cells are identified, a complete lymph node dissection (CLND) can be performed. OBJECTIVE: To determine the natural history of pain and sensory changes after MM surgery. METHODS: We prospectively followed 39 patients (29 SLNB-only, 2 CLND-only, and 8 CLND preceded by SLNB) from before inguinal or axillary surgery through 6 months after surgery on measures of pain intensity, sensory symptoms, allodynia, and questionnaires of anxiety, depression, and catastrophizing. RESULTS: No patient had pain preoperatively. Ten days after surgery, 35% had surgical site pain after SLNB-only compared with 90% after CLND (P < 0.003); clinically meaningful pain (Visual Analogue Scale ≥ 30 mm/100 mm) was reported by 3% of patients after SLNB-only compared with 40% after CLND (P < 0.001). At 6 months, all SLNB-only patients were pain-free. By contrast, 4 of 7 in the SLNB + CLND group still had pain (P < 0.002). At 6 months, symptoms of altered sensation or numbness were reported by 32% and 42% of SLNB-only patients, and by 67% and 67% of patients undergoing CLND surgery (both P > 0.05). CONCLUSION: Acute pain is more common after CLND surgery. Undergoing SLNB followed by more invasive CLND surgery may increase the likelihood of pain at 6 months. Persistent sensory symptoms typical of those associated with nerve injury are more common after CLND. Surgery for MM is a good model for studying the natural history of postsurgical pain and sensory changes. Wolters Kluwer 2018-10-19 /pmc/articles/PMC6344134/ /pubmed/30706034 http://dx.doi.org/10.1097/PR9.0000000000000689 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain. This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Cancer and Palliative Slagelse, Charlotte Munch, Troels Glazer, Clara Greene, Kaitlin Finnerup, Nanna Brix Kashani-Sabet, Mohammed Leong, Stanley P. Petersen, Karin Lottrup Rowbotham, Michael C. Natural history of pain associated with melanoma surgery |
title | Natural history of pain associated with melanoma surgery |
title_full | Natural history of pain associated with melanoma surgery |
title_fullStr | Natural history of pain associated with melanoma surgery |
title_full_unstemmed | Natural history of pain associated with melanoma surgery |
title_short | Natural history of pain associated with melanoma surgery |
title_sort | natural history of pain associated with melanoma surgery |
topic | Cancer and Palliative |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6344134/ https://www.ncbi.nlm.nih.gov/pubmed/30706034 http://dx.doi.org/10.1097/PR9.0000000000000689 |
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