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. 2018;44(4):488-496.
doi: 10.1080/00952990.2018.1458234. Epub 2018 Apr 19.

Sex differences in opioid use and medical issues during buprenorphine/naloxone treatment

Affiliations

Sex differences in opioid use and medical issues during buprenorphine/naloxone treatment

Celestina Barbosa-Leiker et al. Am J Drug Alcohol Abuse. 2018.

Abstract

Background: There are sex differences in buprenorphine/naloxone clinical trials for opioid use. While women have fewer opioid-positive urine samples, relative to men, a significant decrease in opioid-positive samples was found during treatment for men, but not women. In order to inform sex-based approaches to improve treatment outcomes, research is needed to determine if opioid use, and predictors of opioid use, differs between men and women during treatment.

Objectives: To test for sex differences in opioid use during a buprenorphine/naloxone clinical trial and determine if sex differences exist in the associations between addiction-related problem areas and opioid use over the course of the trial.

Method: This secondary data analysis of the National Drug Abuse Treatment Clinical Trials Network (CTN) 0003 examined sex differences (men = 347, women = 169) in opioid-positive samples in a randomized clinical trial comparing 7-day vs. 28-day buprenorphine/naloxone tapering strategies. Addiction-related problem areas were defined by Addiction Severity-Lite (ASI-L) domain composite scores.

Results: Women were more likely than men to use opioids during the course of the buprenorphine/naloxone clinical trial (B = .33, p = .01) and medical issues were positively related to submitting an opioid-positive sample during treatment for women (B = 1.67, p = .01). No ASI-L domain composite score was associated with opioid-positive samples during treatment for men.

Conclusion: Women were more likely than men to use opioids during the course of the buprenorphine/naloxone clinical trial, and medical issues predicted opioid use during treatment for women but not men. Complementary treatment for medical problems during opioid replacement therapy may benefit women.

Keywords: Opioid dependence; addiction severity index; buprenorphine/naloxone; sex differences.

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Figures

Figure 1.
Figure 1.
Percent of opioid-positive urine samples for the total sample and by sex.
Figure 2.
Figure 2.
Schematic representation of the linear latent growth model of opioid-positive urinalysis (opioid+UA) over time in a randomized clinical trial that compared buprenorphine/naloxone tapering strategies (7-day and 28-day). Intercept and slope parameters are constrained to indicate the linear model.
Figure 3.
Figure 3.
Schematic representation or primary results of the linear latent growth model of opioid-positive urinalysis (opioid+UA) over time in a randomized clinical trial that compared buprenorphine/naloxone tapering strategies (7-day and 28-day) in the female sample. Unstandardized regression coefficients are reported. ASI-L = Addiction Severity Index-Lite; *p<.05; ns statistically non-significant.
Figure 4.
Figure 4.
Schematic representation or primary results of the linear latent growth model of opioid-positive urinalysis (opioid+UA) over time in a randomized clinical trial that compared buprenorphine/naloxone tapering strategies (7-day and 28-day) in the male sample. Unstandardized regression coefficients are reported. ASI-L = Addiction Severity Index-Lite; *p<.05; ns statistically non-significant.

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