TY - JOUR
T1 - A predictive risk model for nonfatal opioid overdose in a statewide population of buprenorphine patients
AU - Chang, Hsien Yen
AU - Krawczyk, Noa
AU - Schneider, Kristin E.
AU - Ferris, Lindsey
AU - Eisenberg, Matthew
AU - Richards, Tom M.
AU - Lyons, B. Casey
AU - Jackson, Kate
AU - Weiner, Jonathan P.
AU - Saloner, Brendan
N1 - Funding Information:
The Harold Rogers Grant from the US Department of Justice Bureau of Justice Assistance .
Publisher Copyright:
© 2019 Elsevier B.V.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Background: Predicting which individuals who are prescribed buprenorphine for opioid use disorder are most likely to experience an overdose can help target interventions to prevent relapse and subsequent consequences. Methods: We used Maryland prescription drug monitoring data from 2015 to identify risk factors for nonfatal opioid overdoses that were identified in hospital discharge records in 2016. We developed a predictive risk model for prospective nonfatal opioid overdoses among buprenorphine patients (N = 25,487). We estimated a series of models that included demographics plus opioid, buprenorphine and benzodiazepine prescription variables. We applied logistic regression to generate performance measures. Results: About 3.24% of the study cohort had ≥1 nonfatal opioid overdoses. In the model with all predictors, odds of nonfatal overdoses among buprenorphine patients were higher among males (OR = 1.39, 95% CI:1.21–1.62) and those with more buprenorphine pharmacies (OR = 1.19, 95% CI:1.11–1.28), 1+ buprenorphine prescription paid by Medicaid (OR = 1.21, 95% CI:1.02–1.48), Medicare (OR = 1.93, 95% CI:1.63–2.43), or a commercial plan (OR = 1.98, 95% CI:1.30–2.89), 1+ opioid prescription paid by Medicare (OR = 1.30, 95% CI:1.03–1.68), and more benzodiazepine prescriptions (OR = 1.04, 95% CI:1.02–1.05). The odds were lower among those with longer days of buprenorphine (OR = 0.64, 95% CI:0.60-0.69) or opioid (OR = 0.79, 95% CI:0.65-0.95) supply. The model had moderate predictive ability (c-statistic = 0.69). Conclusions: Several modifiable risk factors, such as length of buprenorphine treatment, may be targets for interventions to improve clinical care and reduce harms. This model could be practically implemented with common prescription-related information and allow payers and clinical systems to better target overdose risk reduction interventions, such as naloxone distribution.
AB - Background: Predicting which individuals who are prescribed buprenorphine for opioid use disorder are most likely to experience an overdose can help target interventions to prevent relapse and subsequent consequences. Methods: We used Maryland prescription drug monitoring data from 2015 to identify risk factors for nonfatal opioid overdoses that were identified in hospital discharge records in 2016. We developed a predictive risk model for prospective nonfatal opioid overdoses among buprenorphine patients (N = 25,487). We estimated a series of models that included demographics plus opioid, buprenorphine and benzodiazepine prescription variables. We applied logistic regression to generate performance measures. Results: About 3.24% of the study cohort had ≥1 nonfatal opioid overdoses. In the model with all predictors, odds of nonfatal overdoses among buprenorphine patients were higher among males (OR = 1.39, 95% CI:1.21–1.62) and those with more buprenorphine pharmacies (OR = 1.19, 95% CI:1.11–1.28), 1+ buprenorphine prescription paid by Medicaid (OR = 1.21, 95% CI:1.02–1.48), Medicare (OR = 1.93, 95% CI:1.63–2.43), or a commercial plan (OR = 1.98, 95% CI:1.30–2.89), 1+ opioid prescription paid by Medicare (OR = 1.30, 95% CI:1.03–1.68), and more benzodiazepine prescriptions (OR = 1.04, 95% CI:1.02–1.05). The odds were lower among those with longer days of buprenorphine (OR = 0.64, 95% CI:0.60-0.69) or opioid (OR = 0.79, 95% CI:0.65-0.95) supply. The model had moderate predictive ability (c-statistic = 0.69). Conclusions: Several modifiable risk factors, such as length of buprenorphine treatment, may be targets for interventions to improve clinical care and reduce harms. This model could be practically implemented with common prescription-related information and allow payers and clinical systems to better target overdose risk reduction interventions, such as naloxone distribution.
KW - Buprenorphine
KW - Opioid analgesics
KW - Opioid overdose
KW - Opioid use disorder
KW - Predictive risk model
KW - Prescription drug monitoring programs
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U2 - 10.1016/j.drugalcdep.2019.04.016
DO - 10.1016/j.drugalcdep.2019.04.016
M3 - Article
C2 - 31207453
AN - SCOPUS:85067255825
SN - 0376-8716
VL - 201
SP - 127
EP - 133
JO - Drug and alcohol dependence
JF - Drug and alcohol dependence
ER -