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. Author manuscript; available in PMC: 2019 Feb 1.
Published in final edited form as: J Subst Abuse Treat. 2017 Jul 3;85:90–96. doi: 10.1016/j.jsat.2017.07.001

Table 4.

Hazard of discontinuing medication therapy

Parameter Hazard Ratio 95% CI p-value
Medication at initiation
 Injectable naltrexone > 30 days 2.17 2.04–2.30 <0.001
 Oral naltrexone >30 days 2.54 2.45–2.64 <0.001
 Sublingual buprenorphine > 30 days 1.15 1.10–1.19 <0.001
 Transdermal buprenorphine* > 30 days 2.21 2.11–2.33 <0.001
 Sublingual or oromucosal buprenorphine/naloxone >30 days Reference
Age at initiation
 Younger than 30 1.25 1.22–1.28 <0.001
 30 or older Reference
Sex
 Male Reference
 Female 1.01 0.99–1.03 0.563
Substance use codes (indicators)
 Alcohol 1.15 1.08–1.22 <0.001
 Amphetamines 1.07 1.03–1.12 0.002
 Cannabis 1.10 1.07–1.13 <0.001
 Cocaine 1.13 1.09–1.17 <0.001
 Hallucinogens 1.02 0.93–1.12 0.698
 Sedative 1.16 1.13–1.19 <0.001
Ever seen in detox facility
 Yes 0.92 0.90–0.94 <0.001
 No Reference
Provider at initiation (indicators)
 Internal medicine 0.98 0.95–1.01 0.272
 Family practice 0.94 0.91–0.97 <0.001
 Pediatrics 0.88 0.78–0.99 0.028
 Psychiatry 0.94 0.91–0.97 <0.001
 Obstetrics and Gynecology 0.85 0.78–0.94 0.001
 Surgery 1.17 1.05–1.30 0.005
Place of initiation (indicators)
 Office visit 0.90 0.87–0.93 <0.001
 Outpatient clinic 1.08 1.05–1.12 <0.001
 ED 1.19 1.11–1.28 <0.001
 Inpatient 1.23 1.15–1.31 <0.001

CI = confidence interval; ED = emergency department

All variables in this table are included in one model. Model controls for region of residence, commercial insurance type, and the effect of medication type in the first 30 days of treatment.

*

Transdermal buprenorphine is FDA-approved for the treatment of chronic pain, not opioid use disorder.