Table 2

Results of a zero-inflated negative binomial regression analysis of the association between early drug class(es) dispensed and strength of opioid received in the first 8 weeks after injury and days on benefits and benefit status after the 8-week exposure window up to 1 year after injury

PredictorDays on benefits after 8-week exposure windowOn benefits after 8-week exposure window
Number of days on benefits after 8-week exposure window, mean (SD), medianIRR (95% CI)Receiving benefits after 8-week exposure window, n (%)OR (95% CI)
UnadjustedAdjustedUnadjusted
Adjusted
Drug class(es) dispensed in first 8 weeks (n=55 571)
 NSAIDs and/or SMRs (n=29 104)19.5 (46.9), 0.01.001.00*10 817 (37.2)1.001.00*
 Opioids only (n=7730)24.9 (56.3), 0.01.22 (1.17 to 1.28)1.09 (1.04 to 1.14)3030 (39.2)1.08 (1.02 to 1.14)0.99 (0.93 to 1.05)
 Opioids with NSAIDs and/or SMRs (n=18 737)38.3 (67.0), 3.01.40 (1.35 to 1.45)1.26 (1.22 to 1.30)9889 (52.8)1.89 (1.82 to 1.96)1.61 (1.54 to 1.69)
Strength of opioids dispensed in first 8 weeks (n=26 467)
 Weak opioid(s) only (n=23 271)31.1 (60.7), 0.01.001.00†10 903 (46.9)1.001.00†
 Strong opioid(s) only (n=1711)47.0 (75.8), 6.01.30 (1.20 to 1.40)1.21 (1.12 to 1.30)941 (55.0)1.39 (1.25 to 1.54)1.18 (1.05 to 1.32)
 Weak and strong opioids (n=1485)70.5 (87.3), 32.01.48 (1.37 to 1.59)1.29 (1.20 to 1.39)1075 (72.4)3.13 (2.70 to 3.45)2.27 (2.00 to 2.63)
  • *Adjusted for sex, age, year of injury, income, diagnosis code, health authority, pain specialist visit within first 8 weeks, cumulative days of opioids in previous year, sedative hypnotic dispense within first 8 weeks, spinal X-ray within first 8 weeks, hospital contact within first 8 weeks, back/neck pain in prior 2 years, cumulative days of NSAIDs in previous year.

  • †Adjusted for sex, age, year of injury, income, diagnosis code, pain specialist visit within first 8 weeks, sedative hypnotic dispense within first 8 weeks, back/neck pain comorbidity within prior 2 years.

  • IRR, incidence rate ratio; NSAID, non-steroidal anti-inflammatory drug; SMR, skeletal muscle relaxant.