Characterizing the Association Between Traumatic Brain Injury and Discontinuation of Medications for Opioid Use Disorder in a Commercially Insured Adult Population.
Jake R Morgan, Sharon Reif, Maureen T Stewart and 2 others
PMID 39019485WHAT IT FOUND
Adults with a traumatic brain injury were 13% more likely to stop taking medications for opioid use disorder compared to those without.
Type of medication mattered more: oral naltrexone had a 63% higher risk of discontinuation than buprenorphine.
Key findings
01Individuals with a TBI diagnosis were 13% more likely to discontinue MOUD at a given time compared to those without TBI.
02Oral naltrexone products were associated with a 63% increased risk of discontinuing treatment compared to buprenorphine.
03People with TBI were disproportionately prescribed naltrexone rather than buprenorphine, by nearly 10 percentage points compared to individuals without TBI.
STILL TO COME
How it was doneWhat they foundWhat it means for SLPs
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What it does not show
TBI status was determined by insurance diagnosis codes, which likely underestimates prevalence, especially for mild injuries where patients did not seek medical attention. The study only looked at TBI diagnoses within two years prior to starting treatment, so it may miss older injuries. Methadone was excluded because it is rarely covered by commercial insurance, so findings do not apply to patients on methadone. The sample was limited to adults with employer-sponsored insurance, so results may not generalize to Medicaid, Medicare, or uninsured populations. The study did not account for TBI severity or specific cognitive deficits, only the presence of a diagnosis.
Declared interests
The authors declared no known competing financial interests or personal relationships. The study was supported by the National Institutes of Health.
The easy way to misread this
Do not assume TBI is the primary driver of treatment failure. While TBI increased risk by 13%, the choice of medication (oral naltrexone vs. buprenorphine) had a much larger impact on discontinuation rates (63% increased risk for oral naltrexone).