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Management of breakthrough pain due to cancer

Breakthrough pain is defined as the transient exacerbation of pain occurring in a patient with otherwise stable, persistent pain. It is estimated to affect over 50% of patients, particularly those with moderate to severe background pain. Breakthrough pain is one of the most difficult pain syndromes...

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Detalles Bibliográficos
Autor principal: Rudowska, Joanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687475/
https://www.ncbi.nlm.nih.gov/pubmed/23788935
http://dx.doi.org/10.5114/wo.2012.32481
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author Rudowska, Joanna
author_facet Rudowska, Joanna
author_sort Rudowska, Joanna
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description Breakthrough pain is defined as the transient exacerbation of pain occurring in a patient with otherwise stable, persistent pain. It is estimated to affect over 50% of patients, particularly those with moderate to severe background pain. Breakthrough pain is one of the most difficult pain syndromes to treat. There are several types of breakthrough cancer pain: incidental type involves flares of pain associated with movement or activity; idiopathic type is transitory pain unrelated to a specific activity; and in end-of-dose failure pain occurs when blood levels of medications fall below an analgesic threshold at the end of a dosing interval. Persistent and breakthrough pain are distinct components of cancer pain and require separate management. Successful management of breakthrough pain may require a combination of pharmacological and non-pharmacological treatment strategies. Supplemental analgesia, known as rescue medication, is a common pharmacological treatment option. Breakthrough pain is treated with supplemental short-acting opioid use, as needed, e.g. short-acting morphine, intranasal fentanyl and buccal tablets of fentanyl.
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spelling pubmed-36874752013-06-20 Management of breakthrough pain due to cancer Rudowska, Joanna Contemp Oncol (Pozn) Review Breakthrough pain is defined as the transient exacerbation of pain occurring in a patient with otherwise stable, persistent pain. It is estimated to affect over 50% of patients, particularly those with moderate to severe background pain. Breakthrough pain is one of the most difficult pain syndromes to treat. There are several types of breakthrough cancer pain: incidental type involves flares of pain associated with movement or activity; idiopathic type is transitory pain unrelated to a specific activity; and in end-of-dose failure pain occurs when blood levels of medications fall below an analgesic threshold at the end of a dosing interval. Persistent and breakthrough pain are distinct components of cancer pain and require separate management. Successful management of breakthrough pain may require a combination of pharmacological and non-pharmacological treatment strategies. Supplemental analgesia, known as rescue medication, is a common pharmacological treatment option. Breakthrough pain is treated with supplemental short-acting opioid use, as needed, e.g. short-acting morphine, intranasal fentanyl and buccal tablets of fentanyl. Termedia Publishing House 2013-01-04 2012 /pmc/articles/PMC3687475/ /pubmed/23788935 http://dx.doi.org/10.5114/wo.2012.32481 Text en Copyright © 2012 Termedia http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Rudowska, Joanna
Management of breakthrough pain due to cancer
title Management of breakthrough pain due to cancer
title_full Management of breakthrough pain due to cancer
title_fullStr Management of breakthrough pain due to cancer
title_full_unstemmed Management of breakthrough pain due to cancer
title_short Management of breakthrough pain due to cancer
title_sort management of breakthrough pain due to cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687475/
https://www.ncbi.nlm.nih.gov/pubmed/23788935
http://dx.doi.org/10.5114/wo.2012.32481
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