Abstract:Background
The prevalence of psychoactive medications (PAMs) use in patients enrolled in Office Based Opioid Treatment (OBOT) and its association with engagement in this care is largely unknown.
Objective
To describe the use of PAMs, including those medications with emerging evidence of misuse (“emerging PAMs” - gabapentin, clonidine and promethazine) among patients on buprenorphine, and its association with disengagement from OBOT.
Methods
This is a retrospective cohort study of adults on buprenorphine fr… Show more
“…People with cooccurring mental disorders and drug use disorders are more likely to seek treatment than those with a single disorder alone [43,44]. Furthermore, psychiatric diagnosis among those receiving buprenorphine has been associated with improved treatment retention [45,46]. Thus, people who receive benzodiazepines may have a more severe underlying mental disorder, and it may be the underlying mental disorder that leads them to seek and remain in buprenorphine treatment rather than receiving the benzodiazepine prescription.…”
Background and Aims Benzodiazepines are commonly prescribed to patients with opioid use disorder receiving buprenorphine treatment, yet may increase overdose risk. However, prescribed benzodiazepines may improve retention in care by reducing buprenorphine discontinuation and thus may prevent relapse to illicit opioid use. We aimed to test the association between benzodiazepine prescription and fatal opioid overdose, non-fatal opioid overdose, all-cause mortality and buprenorphine discontinuation. Design and Setting This was a retrospective cohort study using five individually linked data sets from Massachusetts, United States government agencies. Participants We studied 63 389 Massachusetts residents aged 18 years or older who received buprenorphine treatment between January 2012 and December 2015. Measurements Filled benzodiazepine prescription during buprenorphine treatment was the main independent variable. The primary outcome was time to fatal opioid overdose. Secondary outcomes were time to non-fatal opioid overdose, all-cause mortality and buprenorphine discontinuation. We defined buprenorphine discontinuation as having a 30day gap without another prescription following the end date of the previous prescription. We used Cox proportional hazards models to calculate hazards ratios that tested the association between receipt of benzodiazepines and all outcomes, restricted to periods during buprenorphine treatment. Findings Of the 63 345 individuals who received buprenorphine, 24% filled at least one benzodiazepine prescription during buprenorphine treatment. Thirty-one per cent of the 183 deaths from opioid overdose occurred when individuals received benzodiazepines during buprenorphine treatment. Benzodiazepine receipt during buprenorphine treatment was associated with an increased risk of fatal opioid overdose adjusted hazard ratio (HR) = 2.92, 95% confidence interval (CI) = 2.10-4.06, non-fatal opioid overdose, adjusted HR = 2.05, 95% CI, 1.68-2.50, all-cause mortality, adjusted HR = 1.90, 95% CI, 1.48-2.44 and a decreased risk of buprenorphine discontinuation, adjusted HR = 0.87, 95% CI, 0.85-0.89. Conclusions Benzodiazepine receipt appears to be associated with both increased risk of opioid overdose and all-cause mortality and decreased risk of buprenorphine discontinuation among people receiving buprenorphine.
“…People with cooccurring mental disorders and drug use disorders are more likely to seek treatment than those with a single disorder alone [43,44]. Furthermore, psychiatric diagnosis among those receiving buprenorphine has been associated with improved treatment retention [45,46]. Thus, people who receive benzodiazepines may have a more severe underlying mental disorder, and it may be the underlying mental disorder that leads them to seek and remain in buprenorphine treatment rather than receiving the benzodiazepine prescription.…”
Background and Aims Benzodiazepines are commonly prescribed to patients with opioid use disorder receiving buprenorphine treatment, yet may increase overdose risk. However, prescribed benzodiazepines may improve retention in care by reducing buprenorphine discontinuation and thus may prevent relapse to illicit opioid use. We aimed to test the association between benzodiazepine prescription and fatal opioid overdose, non-fatal opioid overdose, all-cause mortality and buprenorphine discontinuation. Design and Setting This was a retrospective cohort study using five individually linked data sets from Massachusetts, United States government agencies. Participants We studied 63 389 Massachusetts residents aged 18 years or older who received buprenorphine treatment between January 2012 and December 2015. Measurements Filled benzodiazepine prescription during buprenorphine treatment was the main independent variable. The primary outcome was time to fatal opioid overdose. Secondary outcomes were time to non-fatal opioid overdose, all-cause mortality and buprenorphine discontinuation. We defined buprenorphine discontinuation as having a 30day gap without another prescription following the end date of the previous prescription. We used Cox proportional hazards models to calculate hazards ratios that tested the association between receipt of benzodiazepines and all outcomes, restricted to periods during buprenorphine treatment. Findings Of the 63 345 individuals who received buprenorphine, 24% filled at least one benzodiazepine prescription during buprenorphine treatment. Thirty-one per cent of the 183 deaths from opioid overdose occurred when individuals received benzodiazepines during buprenorphine treatment. Benzodiazepine receipt during buprenorphine treatment was associated with an increased risk of fatal opioid overdose adjusted hazard ratio (HR) = 2.92, 95% confidence interval (CI) = 2.10-4.06, non-fatal opioid overdose, adjusted HR = 2.05, 95% CI, 1.68-2.50, all-cause mortality, adjusted HR = 1.90, 95% CI, 1.48-2.44 and a decreased risk of buprenorphine discontinuation, adjusted HR = 0.87, 95% CI, 0.85-0.89. Conclusions Benzodiazepine receipt appears to be associated with both increased risk of opioid overdose and all-cause mortality and decreased risk of buprenorphine discontinuation among people receiving buprenorphine.
“…Although discontinuing therapy with methadone or buprenorphine/naloxone may be a personal goal for many patients, family members, and addiction treatment staff, there are discouraging odds of completing a taper and remaining abstinent from illicit opioids. Weinstein et al 28 conclude that, though many patients want to discontinue, few are successful, and the medical community “should direct its efforts to overcome the barriers to long-term maintenance.” Robert Newman went further, challenging the significance of attempting to build interventions to make patients medication-free when they are already doing well on a maintenance medication. Newman asked, “to what end?” (p.1429) 29 .…”
This paper offers a review and recommendations for clinicians working with patients interested in discontinuing opioid agonist treatment. As buprenorphine/naloxone has gained widespread acceptance for opioid addiction, many treatment providers and patients have a range of hopes and expectations about its optimal use. A surprising number assume buprenorphine/naloxone is primarily useful as a medication to transition off illicit opioid use, and success is partially defined by discontinuing the medication. Despite accumulating evidence that a majority of patients will need to remain on medication to preserve their gains, clinicians often have to address a patient's fervent desire to taper. Using the concept of “recovery capital,” our review addresses (1) the appropriate duration of opioid agonist treatment, (2) risks associated with discontinuing, (3) a checklist that guides the patient through self-assessment of the wisdom of discontinuing opioid agonist treatment, and (4) shared decision making about how to proceed.
“…Discontinuation of treatment can occur for a variety of reasons related to patient (e.g., relapse), provider (e.g., quality of care), and system factors (e.g., arbitrary limits of duration of care). [21][22][23][24][25][26] Research priorities include understanding how to implement chronic disease management for MOUD, understanding factors leading to MOUD discontinuation, and re-engaging patients who discontinue care. 27 Finally, studying interventions to link patients who have a non-fatal overdose to MOUD treatment was deemed a high priority.…”
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