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Impact of potential inappropriate NSAIDs use in chronic pain

Pain remains one of the main reasons for medical consultation worldwide: moderate- to severe-intensity pain occurs in 19% of adult Europeans, seriously affecting the quality of their social and working lives. Nonsteroidal anti-inflammatory drugs (NSAIDs) are not recommended for long-term use and a c...

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Autores principales: Ussai, S, Miceli, L, Pisa, F E, Bednarova, R, Giordano, A, Rocca, G Della, Petelin, R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403601/
https://www.ncbi.nlm.nih.gov/pubmed/25926717
http://dx.doi.org/10.2147/DDDT.S80686
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author Ussai, S
Miceli, L
Pisa, F E
Bednarova, R
Giordano, A
Rocca, G Della
Petelin, R
author_facet Ussai, S
Miceli, L
Pisa, F E
Bednarova, R
Giordano, A
Rocca, G Della
Petelin, R
author_sort Ussai, S
collection PubMed
description Pain remains one of the main reasons for medical consultation worldwide: moderate- to severe-intensity pain occurs in 19% of adult Europeans, seriously affecting the quality of their social and working lives. Nonsteroidal anti-inflammatory drugs (NSAIDs) are not recommended for long-term use and a careful surveillance to monitor for toxicity and efficacy is critical. This study aims to assess: 1) the pattern of use of NSAIDs and opioids in a population covered by a cloud-based pharmacovigilance surveillance system; and 2) potential inappropriate use. A retrospective 18-months systematic analysis on patients’ pain treatment was performed. The primary endpoint was evaluating the prevalence of NSAIDs and opioids use and the duration of therapy regimen. The secondary endpoint was to investigate the prevalence of NSAIDs taken for >21 consecutive days concomitant with drugs for peptic ulcer and gastroesophageal reflux disease (GORD) or antiplatelet drugs. The yearly cost for individual users of concomitant NSAIDs for more than 21 consecutive days and of GORD medications has been estimated. A total of 3,050 subjects with chronic pain were enrolled; 97% of them took NSAIDs for >21 consecutive days; about one-fourth of these users also received drugs for peptic ulcer and GORD (Anatomical Therapeutic Chemical code A02B). The yearly cost foran individual who uses NSAIDs for >21 consecutive days as well as concomitant GORD medications is 61.23 euros. In total, 238 subjects (8%) using NSAIDs for >21 days also received one antiplatelet agent. About 11% of subjects received opioids at least once and only 2% of them carried on the therapy for more than 90 consecutive days. In evaluating the escalation in dosage as a proxy of dependence risk, this study shows no dosage escalation in our cohort of chronic pain population - that is to say we show no risk of dependence.
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spelling pubmed-44036012015-04-29 Impact of potential inappropriate NSAIDs use in chronic pain Ussai, S Miceli, L Pisa, F E Bednarova, R Giordano, A Rocca, G Della Petelin, R Drug Des Devel Ther Original Research Pain remains one of the main reasons for medical consultation worldwide: moderate- to severe-intensity pain occurs in 19% of adult Europeans, seriously affecting the quality of their social and working lives. Nonsteroidal anti-inflammatory drugs (NSAIDs) are not recommended for long-term use and a careful surveillance to monitor for toxicity and efficacy is critical. This study aims to assess: 1) the pattern of use of NSAIDs and opioids in a population covered by a cloud-based pharmacovigilance surveillance system; and 2) potential inappropriate use. A retrospective 18-months systematic analysis on patients’ pain treatment was performed. The primary endpoint was evaluating the prevalence of NSAIDs and opioids use and the duration of therapy regimen. The secondary endpoint was to investigate the prevalence of NSAIDs taken for >21 consecutive days concomitant with drugs for peptic ulcer and gastroesophageal reflux disease (GORD) or antiplatelet drugs. The yearly cost for individual users of concomitant NSAIDs for more than 21 consecutive days and of GORD medications has been estimated. A total of 3,050 subjects with chronic pain were enrolled; 97% of them took NSAIDs for >21 consecutive days; about one-fourth of these users also received drugs for peptic ulcer and GORD (Anatomical Therapeutic Chemical code A02B). The yearly cost foran individual who uses NSAIDs for >21 consecutive days as well as concomitant GORD medications is 61.23 euros. In total, 238 subjects (8%) using NSAIDs for >21 days also received one antiplatelet agent. About 11% of subjects received opioids at least once and only 2% of them carried on the therapy for more than 90 consecutive days. In evaluating the escalation in dosage as a proxy of dependence risk, this study shows no dosage escalation in our cohort of chronic pain population - that is to say we show no risk of dependence. Dove Medical Press 2015-04-09 /pmc/articles/PMC4403601/ /pubmed/25926717 http://dx.doi.org/10.2147/DDDT.S80686 Text en © 2015 Ussai et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Ussai, S
Miceli, L
Pisa, F E
Bednarova, R
Giordano, A
Rocca, G Della
Petelin, R
Impact of potential inappropriate NSAIDs use in chronic pain
title Impact of potential inappropriate NSAIDs use in chronic pain
title_full Impact of potential inappropriate NSAIDs use in chronic pain
title_fullStr Impact of potential inappropriate NSAIDs use in chronic pain
title_full_unstemmed Impact of potential inappropriate NSAIDs use in chronic pain
title_short Impact of potential inappropriate NSAIDs use in chronic pain
title_sort impact of potential inappropriate nsaids use in chronic pain
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4403601/
https://www.ncbi.nlm.nih.gov/pubmed/25926717
http://dx.doi.org/10.2147/DDDT.S80686
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