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Safety Events Associated with Tramadol Use Among Older Adults with Osteoarthritis

Tramadol is a low-level opioid increasingly recommended to treat moderate-to-severe acute and chronic pain. Although characterized as having fewer opioid-related adverse events, the longer term safety of tramadol use among older adults has not been thoroughly documented. Thus, the primary objective...

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Autores principales: Musich, Shirley, Wang, Shaohung S., Schaeffer, James A., Slindee, Luke, Kraemer, Sandra, Yeh, Charlotte S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7875128/
https://www.ncbi.nlm.nih.gov/pubmed/32119805
http://dx.doi.org/10.1089/pop.2019.0220
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author Musich, Shirley
Wang, Shaohung S.
Schaeffer, James A.
Slindee, Luke
Kraemer, Sandra
Yeh, Charlotte S.
author_facet Musich, Shirley
Wang, Shaohung S.
Schaeffer, James A.
Slindee, Luke
Kraemer, Sandra
Yeh, Charlotte S.
author_sort Musich, Shirley
collection PubMed
description Tramadol is a low-level opioid increasingly recommended to treat moderate-to-severe acute and chronic pain. Although characterized as having fewer opioid-related adverse events, the longer term safety of tramadol use among older adults has not been thoroughly documented. Thus, the primary objective was to examine the risk of safety events associated with chronic tramadol use compared to other chronic opioid use or no opioids among older adults with osteoarthritis. Safety events considered included: ≥3 emergency room (ER) visits, falls/hip fractures, cardiovascular (CVD) hospitalization, composite safety event hospitalization, and all-cause mortality. The study population included older adults ages ≥65 years diagnosed with osteoarthritis and classified into new or continuing tramadol use, new or continuing other opioid use, or nonuse. Inclusion criteria included: 6-month pre period and up to 33 months post period. Tramadol, other opioid, and no opioid users were 1:1 propensity-matched providing study populations of 25,899 within each category; 72% were new chronic opioid users. Multiple logistic regression or Cox proportional hazard ratios were used to document risk. Generally, tramadol users had fewer adverse event risks compared to other opioid users but higher risks than nonusers. New users of tramadol or other opioids had higher risks than continuing users. Tramadol use was associated with increased risk of multiple ER utilizations, falls/fractures, CVD hospitalizations, safety event hospitalizations, and mortality (new users only) compared to nonuse. Thus, although tramadol use may be appropriately recommended within a pain management strategy for older adults with osteoarthritis, careful monitoring for adverse safety events is warranted.
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spelling pubmed-78751282021-02-11 Safety Events Associated with Tramadol Use Among Older Adults with Osteoarthritis Musich, Shirley Wang, Shaohung S. Schaeffer, James A. Slindee, Luke Kraemer, Sandra Yeh, Charlotte S. Popul Health Manag Original Articles Tramadol is a low-level opioid increasingly recommended to treat moderate-to-severe acute and chronic pain. Although characterized as having fewer opioid-related adverse events, the longer term safety of tramadol use among older adults has not been thoroughly documented. Thus, the primary objective was to examine the risk of safety events associated with chronic tramadol use compared to other chronic opioid use or no opioids among older adults with osteoarthritis. Safety events considered included: ≥3 emergency room (ER) visits, falls/hip fractures, cardiovascular (CVD) hospitalization, composite safety event hospitalization, and all-cause mortality. The study population included older adults ages ≥65 years diagnosed with osteoarthritis and classified into new or continuing tramadol use, new or continuing other opioid use, or nonuse. Inclusion criteria included: 6-month pre period and up to 33 months post period. Tramadol, other opioid, and no opioid users were 1:1 propensity-matched providing study populations of 25,899 within each category; 72% were new chronic opioid users. Multiple logistic regression or Cox proportional hazard ratios were used to document risk. Generally, tramadol users had fewer adverse event risks compared to other opioid users but higher risks than nonusers. New users of tramadol or other opioids had higher risks than continuing users. Tramadol use was associated with increased risk of multiple ER utilizations, falls/fractures, CVD hospitalizations, safety event hospitalizations, and mortality (new users only) compared to nonuse. Thus, although tramadol use may be appropriately recommended within a pain management strategy for older adults with osteoarthritis, careful monitoring for adverse safety events is warranted. Mary Ann Liebert, Inc., publishers 2021-02-01 2021-02-02 /pmc/articles/PMC7875128/ /pubmed/32119805 http://dx.doi.org/10.1089/pop.2019.0220 Text en © Shirley Musich et al. 2021; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons License (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 Original Articles
Musich, Shirley
Wang, Shaohung S.
Schaeffer, James A.
Slindee, Luke
Kraemer, Sandra
Yeh, Charlotte S.
Safety Events Associated with Tramadol Use Among Older Adults with Osteoarthritis
title Safety Events Associated with Tramadol Use Among Older Adults with Osteoarthritis
title_full Safety Events Associated with Tramadol Use Among Older Adults with Osteoarthritis
title_fullStr Safety Events Associated with Tramadol Use Among Older Adults with Osteoarthritis
title_full_unstemmed Safety Events Associated with Tramadol Use Among Older Adults with Osteoarthritis
title_short Safety Events Associated with Tramadol Use Among Older Adults with Osteoarthritis
title_sort safety events associated with tramadol use among older adults with osteoarthritis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7875128/
https://www.ncbi.nlm.nih.gov/pubmed/32119805
http://dx.doi.org/10.1089/pop.2019.0220
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