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Stimulant use and opioid-related harm in patients on long-term opioids for chronic pain

There is lack of clarity regarding the impact of and optimal clinical response to stimulant use among people prescribed long-term opioid therapy (LTOT) for pain. To determine if a positive urine drug test (UDT) for stimulants was associated with subsequent opioid-related harm or discontinuation of L...

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Published in:Drug and alcohol dependence 2024-03, Vol.256, p.111065-111065, Article 111065
Main Authors: Appa, Ayesha, McMahan, Vanessa M., Long, Kyna, Shade, Starley B., Coffin, Phillip O.
Format: Article
Language:English
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Summary:There is lack of clarity regarding the impact of and optimal clinical response to stimulant use among people prescribed long-term opioid therapy (LTOT) for pain. To determine if a positive urine drug test (UDT) for stimulants was associated with subsequent opioid-related harm or discontinuation of LTOT. Retrospective cohort study. People living with and without HIV living in a major metropolitan area with public insurance, prescribed LTOT for chronic, non-cancer pain (n=600). UDT results from January 2012 to June 2019 were evaluated against 1) opioid-related emergency department (ED) visits (oversedation, constipation, infections associated with injecting opioids, and opioid seeking) or death in each 90-day period following a UDT, using logistic regression, and 2) LTOT discontinuation. There were no opioid overdose deaths within 90 days following a stimulant-positive UDT. A stimulant-positive UDT was not statistically significantly associated with opioid-related ED visits within 90 days (adjusted odds ratio [aOR] 1.39; 95% CI=0.88–2.21). Stimulant-positive UDT was independently associated with subsequent discontinuation of LTOT within 90 days (aOR 2.96; 95% CI=2.13 – 4.12). Living with HIV was independently associated with decreased odds of LTOT discontinuation (aOR 0.65; 95% CI 0.43 – 0.99). Despite no association between a stimulant-positive UDT and subsequent opioid-related harm, there was an association with subsequent LTOT discontinuation, with heterogeneity across clinical groups. Detection of stimulant use should result in a discussion of substance use and risk, rather than reflex LTOT discontinuation. •Odds of opioid-related harm among those with stimulant-positive urine tests while on long-term opioid therapy is unknown.•Stimulant-positive UDT was not statistically significantly associated with opioid-related ED visits or death within 90 days.•Results suggest that stimulant-positive UDT should trigger an LTOT discussion, not reflex discontinuation as was observed.
ISSN:0376-8716
1879-0046
DOI:10.1016/j.drugalcdep.2023.111065