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Celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain

INTRODUCTION: Celiac plexus neurolysis (CPN) has been verified for mitigating pancreatic cancer pain. However, information regarding CPN's use beyond this remains limited. OBJECTIVES: Identify which cancers benefit from CPN, which symptoms improve, and when symptoms improve. METHODS: Retrospect...

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Autores principales: Ambai, Vats T., Singh, Vinita, Boorman, David W., Neufeld, Nathan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546843/
https://www.ncbi.nlm.nih.gov/pubmed/34712884
http://dx.doi.org/10.1097/PR9.0000000000000930
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author Ambai, Vats T.
Singh, Vinita
Boorman, David W.
Neufeld, Nathan J.
author_facet Ambai, Vats T.
Singh, Vinita
Boorman, David W.
Neufeld, Nathan J.
author_sort Ambai, Vats T.
collection PubMed
description INTRODUCTION: Celiac plexus neurolysis (CPN) has been verified for mitigating pancreatic cancer pain. However, information regarding CPN's use beyond this remains limited. OBJECTIVES: Identify which cancers benefit from CPN, which symptoms improve, and when symptoms improve. METHODS: Retrospective analysis was conducted on 173 patients who received CPN for pain caused by various malignancies. Mean symptom changes on the MD Anderson Symptom Inventory (MDASI) from baseline to 2 weeks, 1 month, and 2 months after CPN were analyzed overall and then by cancer type: pancreatic (all stages and stages III–IV), hepatobiliary, and nonpancreatic, nonhepatobiliary gastrointestinal (NPNH-gastrointestinal). RESULTS: Eighty-two pancreatic, 43 NPNH-gastrointestinal, 14 hepatobiliary, and 34 patients with other cancers met inclusion criteria. Statistically significant changes included decrease in the pain score at 1 month by 1.01 points for all cancers, 1.65 points for all pancreatic cancers, and 1.88 points for late-stage pancreatic cancers. At 2 months, pain decreased by 1.50 points for all cancers, 1.68 points for all pancreatic cancers, 2.37 points for late-stage pancreatic cancers, and 1.50 points in NPNH-gastrointestinal cancers. At 2 months, quality of life improved by 1.07 points for all cancers and 1.53 points for all pancreatic cancers. Sleep improved at 2 months for all cancers by 0.73 points and 1.60 points in late-stage pancreatic cancers. At 2 months, pancreatic cancer patients improved in general activity by 0.93 points, walking by 1.00 points, and working by 1.12 points. CONCLUSION: Celiac plexus neurolysis can decrease cancer symptom burden beyond pain including quality of life and sleep for pancreatic and nonpancreatic cancers, as well as general activity for pancreatic cancers.
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spelling pubmed-85468432021-10-27 Celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain Ambai, Vats T. Singh, Vinita Boorman, David W. Neufeld, Nathan J. Pain Rep Cancer and Palliative INTRODUCTION: Celiac plexus neurolysis (CPN) has been verified for mitigating pancreatic cancer pain. However, information regarding CPN's use beyond this remains limited. OBJECTIVES: Identify which cancers benefit from CPN, which symptoms improve, and when symptoms improve. METHODS: Retrospective analysis was conducted on 173 patients who received CPN for pain caused by various malignancies. Mean symptom changes on the MD Anderson Symptom Inventory (MDASI) from baseline to 2 weeks, 1 month, and 2 months after CPN were analyzed overall and then by cancer type: pancreatic (all stages and stages III–IV), hepatobiliary, and nonpancreatic, nonhepatobiliary gastrointestinal (NPNH-gastrointestinal). RESULTS: Eighty-two pancreatic, 43 NPNH-gastrointestinal, 14 hepatobiliary, and 34 patients with other cancers met inclusion criteria. Statistically significant changes included decrease in the pain score at 1 month by 1.01 points for all cancers, 1.65 points for all pancreatic cancers, and 1.88 points for late-stage pancreatic cancers. At 2 months, pain decreased by 1.50 points for all cancers, 1.68 points for all pancreatic cancers, 2.37 points for late-stage pancreatic cancers, and 1.50 points in NPNH-gastrointestinal cancers. At 2 months, quality of life improved by 1.07 points for all cancers and 1.53 points for all pancreatic cancers. Sleep improved at 2 months for all cancers by 0.73 points and 1.60 points in late-stage pancreatic cancers. At 2 months, pancreatic cancer patients improved in general activity by 0.93 points, walking by 1.00 points, and working by 1.12 points. CONCLUSION: Celiac plexus neurolysis can decrease cancer symptom burden beyond pain including quality of life and sleep for pancreatic and nonpancreatic cancers, as well as general activity for pancreatic cancers. Wolters Kluwer 2021-05-12 /pmc/articles/PMC8546843/ /pubmed/34712884 http://dx.doi.org/10.1097/PR9.0000000000000930 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The International Association for the Study of Pain. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (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 Cancer and Palliative
Ambai, Vats T.
Singh, Vinita
Boorman, David W.
Neufeld, Nathan J.
Celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain
title Celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain
title_full Celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain
title_fullStr Celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain
title_full_unstemmed Celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain
title_short Celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain
title_sort celiac plexus neurolysis for abdominal cancers: going beyond pancreatic cancer pain
topic Cancer and Palliative
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8546843/
https://www.ncbi.nlm.nih.gov/pubmed/34712884
http://dx.doi.org/10.1097/PR9.0000000000000930
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