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. 2015 Sep 10;9:59–80. doi: 10.4137/SART.S30120

Table 2.

Summary of findings for illicit opioid use outcome.

AUTHOR LAST NAME WAS ILLICIT OPIOID ABUSE AN OUTCOME? WAS ILLICIT OPIOID USE BEHAVIOR THE PRIMARY OUTCOME OF THE STUDY? HOW WAS ILLICIT OPIOID ABUSE MEASURED? DEFINITION OF ILLICIT OPIOID USE OUTCOMES BY CHRONIC PAIN STATUS STATISTICAL ANALYSIS PROPORTION OF OPIOID USE OUTCOMES SHOWING PAIN TO IMPACT ILLICIT OPIOID USE BEHAVIOR STUDY FINDINGS: DID PATIENTS CHARACTERIZED AS HAVING PAIN ALSO HAVE SIGNIFI-CANTLY HIGHER RATES OF ILLICIT OPIOID USE?
Peles Yes No Urine toxicology screening Participants were categorized as using opioids if ≥1 urine test in the month preceding the survey was positive. Chronic pain 15 (16%) positive, non-chronic pain 20 (26.3%) Chi-square 0 No
Dhingra Yes No Urine toxicology screening, Self-report A positive urine toxicology screen or indication by self-report as assessed by the ASI past 30 day drug use history. In univariate analyses, neither UDS nor self-reported drug use on the ASI was statistically associated with clinically significant pain. (report P-values) t-Test, Chi-square 0 No
Barry Yes No Self-report Participants reported any use in the past week, this was then analyzed as a binary variable. The pain groups reported comparable levels of psychoactive substance use, illegal drug use and non-medical use of prescription drug in the past week. No specific percentages are reported per group. ANOVA 0 No
Chakrabarti Yes No Urine toxicology screening Participants showing a single positive opioid urine screen were found to be a positive for illicit opioid use behaviour, confirmed by urinalysis. Opioid-positive urine (%)reported by Degree of pain Week 4 Week 8 Week 12
Extreme pain patients: 22.2% (2/9) 12.5% (1/8) 37.5% (3/8)
Some pain patients: 31.3% (10/32) 26.7% (8/30) 37.9% (11/29)
No pain: 21.4% (3/14) 20% (2/10) 66.7% (6/9)
Chi-square 0 No
Dennis Yes Yes Urine toxicology screening Continued opioid abuse (COA) was determined by calculating the percentage of positive opioid urine screens provided by participants (number of positive opioid urine screens/total number of opioid urine screens). High COA percentage is indicative of a high number of positive opioid urine screens or, alternatively, a higher rate of illicit opioid consumption. Mean percentage of positive opioid urine screens among pain patients: 23.99 (SD 27.14)
Mean percentage of positive opioid urine screens among non-pain patients: 15.82 (SD 20.11)
Univariate analysis using only COA outcome as the predictor of comorbid pain in a logistic regression model 1/1 Yes
Dreifuss Yes Yes Urine toxicology screening, self-report, addiction severity tool score The Substance Use Report, corroborated by weekly urine drug screens, was administered weekly during treatment and every two weeks during follow-up, and was used as the primary measure to determine “successful outcome.” Successful with chronic pain: 79 (44.6%)
Failure with chronic pain: 70 (38.3%)
Chi-square 0 No
Dunn Yes Yes Urine toxicology screening The mean percent of urine samples provided by each participant that tested positive for opioids, cocaine, or benzodiazepines were evaluated. Chronic pain: 9, No chronic pain: 11 Independent group t-tests were used to compare continuous variables 0 No
Fox Yes No Self-report Self-reported opioid use was obtained from the substance use survey administered at baseline and follow-up, which inquired as to substance use in the 30 days prior to baseline (heroin, methadone, opioid analgesics, cocaine, alcohol, sedatives, hypnotics, or tranquilizers) and follow-ups. These questions were adapted from the ASI. Not reported per pain status. However, they report that any opioid use decreased from 89% at baseline to 40% at 1 month, 33% at 3 months, and 26% at 6 months. Similar patterns were observed in those with and without baseline or persistent pain, and showed no significant association between any opioid use and baseline pain (AOR = 1.06, 95% CI: 0.27–4.17, P = 0.93) or persistent pain (AOR = 1.20, 95% CI: 0.31–4.63, P = 0.79), after adjusting for HIV status, depressive symptoms, history of IDU, history of incarceration, baseline opioid use, and time since initiating buprenorphine treatment. Determined whether pain was associated with use of any opioids during the 6-month follow-up period using nonlinear mixed effects (NLME) models with self-reported use of any opioids as the dependent variable. The NLME approach accounts for non-independence of repeated measures of opioid use within individuals. 0 0
Neumann Yes No Urine toxicology screening Report the number of patients (%) who have an opioid positive urine screen at 24 week follow-up Methadone: 2 (15.4%), buprenorphine: 5 (38.5%) P.0.05
Odds ratio: 0.280, 95% CI: 0.042–1.878, P = 0.371
Fishers exact test 0 No
Potter Yes No Urine toxicology screening, Addiction severity tool score Not described well or reported by pain status. Not reported by pain status n/a n/a n/a
Rosenblum Yes No Self-report A checklist was used to record drugs, including alcohol, that were used during the patient’s last week of active use. Drugs used in past 3 months (%) P = 0.05
None (reference for MMTP): CP 156 (42.9%) OR:1.00 1: CP:123 (27.6%) OR: 0.51 95%CI (0.31–0.84) 2: CP: 62 (38.7%) OR: 0.84 (0.46–1.53) $3: CP 49 (36.7%) 0.77 (0.40–1.50)
Mantel–Haenszel was used for ordinal variables with 3 or more categories 0 No
Trafton Yes Yes Addiction severity tool score Number of days of opioid use over last 30, as well as self-reported number of days of opioid use over lifetime. Opiates GP:1.6 days, 1.9 years; NP: 0.8 days, 0.9 years, P: 2.3 days, 2.9 years 0.03/0.005 The Kruskal–Wallis test was used to determine if variables significantly differed across pain severity ratings, followed by multiple t-tests to determine which levels of reported pain differed from the group reporting “none”. 2/3 Yes