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Low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the Norwegian prescription database

PURPOSE: Low‐dose naltrexone (LDN) is used in a wide range of conditions, including chronic pain and fibromyalgia. Because of the opioid antagonism of naltrexone, LDN users are probably often warned against concomitant use with opioids. In this study, based on data from the Norwegian prescription da...

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Detalles Bibliográficos
Autores principales: Raknes, Guttorm, Småbrekke, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485080/
https://www.ncbi.nlm.nih.gov/pubmed/28370746
http://dx.doi.org/10.1002/pds.4201
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author Raknes, Guttorm
Småbrekke, Lars
author_facet Raknes, Guttorm
Småbrekke, Lars
author_sort Raknes, Guttorm
collection PubMed
description PURPOSE: Low‐dose naltrexone (LDN) is used in a wide range of conditions, including chronic pain and fibromyalgia. Because of the opioid antagonism of naltrexone, LDN users are probably often warned against concomitant use with opioids. In this study, based on data from the Norwegian prescription database, we examine changes in opioid consumption after starting LDN therapy. METHODS: We included all Norwegian patients (N = 3775) with at least one recorded LDN prescription in 2013 and at least one dispensed opioid prescription during the 365 days preceding the first LDN prescription. We allocated the patients into three subgroups depending on the number of collected LDN prescriptions and recorded the number of defined daily doses (DDDs) on collected prescriptions on opioids, nonsteroidal anti‐inflammatory drugs and other analgesics and antipyretics from the same patients. RESULTS: Among the patients collecting ≥4 LDN prescriptions, annual average opioid consumption was reduced by 41 DDDs per person (46%) compared with that of the previous year. The reduction was 12 DDDs per person (15%) among users collecting two to three prescriptions and no change among those collecting only one LDN prescription. We observed no increase in the number of DDDs in nonsteroidal anti‐inflammatory drugs or other analgesics and antipyretics corresponding to the decrease in opioid use. CONCLUSIONS: Possibly, LDN users avoided opioids because of warnings on concomitant use or the patients continuing on LDN were less opioid dependent than those terminating LDN. Therapeutic effects of LDN contributing to lower opioid consumption cannot be ruled out. © 2017 The Authors. Pharmacoepidemiology & Drug Safety Published by John Wiley & Sons Ltd.
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spelling pubmed-54850802017-07-11 Low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the Norwegian prescription database Raknes, Guttorm Småbrekke, Lars Pharmacoepidemiol Drug Saf Original Reports PURPOSE: Low‐dose naltrexone (LDN) is used in a wide range of conditions, including chronic pain and fibromyalgia. Because of the opioid antagonism of naltrexone, LDN users are probably often warned against concomitant use with opioids. In this study, based on data from the Norwegian prescription database, we examine changes in opioid consumption after starting LDN therapy. METHODS: We included all Norwegian patients (N = 3775) with at least one recorded LDN prescription in 2013 and at least one dispensed opioid prescription during the 365 days preceding the first LDN prescription. We allocated the patients into three subgroups depending on the number of collected LDN prescriptions and recorded the number of defined daily doses (DDDs) on collected prescriptions on opioids, nonsteroidal anti‐inflammatory drugs and other analgesics and antipyretics from the same patients. RESULTS: Among the patients collecting ≥4 LDN prescriptions, annual average opioid consumption was reduced by 41 DDDs per person (46%) compared with that of the previous year. The reduction was 12 DDDs per person (15%) among users collecting two to three prescriptions and no change among those collecting only one LDN prescription. We observed no increase in the number of DDDs in nonsteroidal anti‐inflammatory drugs or other analgesics and antipyretics corresponding to the decrease in opioid use. CONCLUSIONS: Possibly, LDN users avoided opioids because of warnings on concomitant use or the patients continuing on LDN were less opioid dependent than those terminating LDN. Therapeutic effects of LDN contributing to lower opioid consumption cannot be ruled out. © 2017 The Authors. Pharmacoepidemiology & Drug Safety Published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2017-03-29 2017-06 /pmc/articles/PMC5485080/ /pubmed/28370746 http://dx.doi.org/10.1002/pds.4201 Text en © 2017 The Authors. Pharmacoepidemiology & Drug Safety Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Reports
Raknes, Guttorm
Småbrekke, Lars
Low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the Norwegian prescription database
title Low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the Norwegian prescription database
title_full Low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the Norwegian prescription database
title_fullStr Low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the Norwegian prescription database
title_full_unstemmed Low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the Norwegian prescription database
title_short Low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the Norwegian prescription database
title_sort low‐dose naltrexone and opioid consumption: a drug utilization cohort study based on data from the norwegian prescription database
topic Original Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485080/
https://www.ncbi.nlm.nih.gov/pubmed/28370746
http://dx.doi.org/10.1002/pds.4201
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