Abstract
Background and Objectives
Extended-release injectable naltrexone (XR-naltrexone) is an effective relapse prevention treatment of patients with opioid use disorder (OUD), but retention remains a problem. Previous trials have either only calculated the association of one or two predictors or used claims-based datasets with only limited data to identify these characteristics. This analysis tested multiple baseline and clinical predictors for association with early retention on XR-naltrexone using combined data from five consecutive studies enrolling patients with active opioid use.
Methods
Bivariate associations between patients’ demographic and clinical characteristics at baseline and during the weeks after the first XR-naltrexone injection, and receipt of a second injection were calculated (n = 200). Significant factors were included in a multivariable logistic regression model.
Results
148/200 participants (74%) received the second injection. Lower Hamilton-Depression Scale (HAM-D) scores after the first injection were significantly associated with receiving a second injection in univariate and multivariable analysis. The following factors were significantly associated with receipt of the second injection in the univariate but not in the multivariable model: longest period of abstinence 1–11 months, use of cocaine in the 7 days before enrollment, use of alcohol or cocaine in the week after first injection, lower severity of cravings for opioids after first injection, lower self-report withdrawal scores after the first injection.
Conclusions and Scientific Significance
Depressive symptoms after first XR-naltrexone injection are associated with nonreceipt of a second injection. Clinicians should educate patients about this risk and monitor for possible depression symptoms after the first injection.