Trajectories of dispensed prescription opioids among beneficiaries enrolled in a Medicaid controlled substance “lock-in” program
Supporting Files
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1 2019
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File Language:
English
Details
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Alternative Title:Pharmacoepidemiol Drug Saf
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Personal Author:
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Description:Purpose:
“Lock-in” programs (LIPs) are used by health insurers to address potential substance (e.g., opioid) misuse among beneficiaries. We sought to (1) examine heterogeneity in trajectories of dispensed opioids (in terms of average daily morphine milligram equivalents (MMEs)) over time: prior to, during, and following release from a LIP; and (2) assess associations between trajectory patterns and beneficiary characteristics.
Methods:
Medicaid claims were linked to Prescription Drug Monitoring Program records for a cohort of beneficiaries enrolled in the North Carolina Medicaid LIP (n=2,701). Using latent class growth analyses, we estimated trajectories of average daily MMEs of opioids dispensed to beneficiaries across specific time periods of interest.
Results:
Five trajectory patterns appeared to sufficiently describe underlying heterogeneity. Starting values and slopes varied across the five trajectory groups, which followed these overall patterns: (1) start at a high level of MMEs, end at a high level of MMEs (13.1% of cohort); (2) start medium, end medium (13.2%); (3) start medium, end low (21.5%); (4) start low, end medium (22.6%); and (5) start low, end low (29.6%). We observed strong associations between patterns and beneficiaries’ demographics, substance use-related characteristics, comorbid conditions, and healthcare utilization.
Conclusions:
In its current form, the Medicaid “lock-in” program (LIP) appeared to have limited impact on beneficiaries’ opioid trajectories. However, strong associations between trajectory patterns and beneficiary characteristics provide insight into potential LIP design modifications that might improve program impact (e.g., LIP integration of substance use disorder assessment and referral to treatment, assessment and support for alternate pain therapies).
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Keywords:
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Source:Pharmacoepidemiol Drug Saf. 28(1):16-24
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Pubmed ID:29700904
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Pubmed Central ID:PMC7482140
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Document Type:
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Funding:K12 CA120780/CA/NCI NIH HHSUnited States/ ; U01 CE002160-01/CE/NCIPC CDC HHSUnited States/ ; R49-CE001495/CE/NCIPC CDC HHSUnited States/ ; K01 DA035153/NH/NIH HHSUnited States/ ; U01 CE002160/CE/NCIPC CDC HHSUnited States/ ; K01 DA035153/DA/NIDA NIH HHSUnited States/ ; R49 CE001495/CE/NCIPC CDC HHSUnited States/ ; K12CA120780/CA/NCI NIH HHSUnited States/
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Volume:28
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Issue:1
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Collection(s):
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Main Document Checksum:urn:sha256:b23fcc990106ba0225651126aaa5cd13ed3249fcaa56dc03fb3adc4f9f236c72
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Download URL:
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File Type:
Supporting Files
File Language:
English
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