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. 2020 Oct 16:28:100592.
doi: 10.1016/j.eclinm.2020.100592. eCollection 2020 Nov.

Risk factors for indicators of opioid-related harms amongst people living with chronic non-cancer pain: Findings from a 5-year prospective cohort study

Affiliations

Risk factors for indicators of opioid-related harms amongst people living with chronic non-cancer pain: Findings from a 5-year prospective cohort study

Gabrielle Campbell et al. EClinicalMedicine. .

Abstract

Background: The literature suggests patient characteristics and higher opioid doses and long-term duration are associated with problematic opioid behaviours but no one study has examined the role of all these factors simultaneously in a long-term prospective cohort study.

Methods: Five-year, community-based, prospective cohort of people prescribed opioids for chronic non-cancer pain (CNCP). Logistic mixed effect models with multiple imputation were used to address missing data. Oral morphine equivalent (OME) mg per day was categorised as: 0 mg OME/day, 1-49 mg OME/day (reference), 50-89 mg OME/day, 90-199 mg OME/day and 200mg+ OME/day. Patient risk factors included: age, gender, substance use, mental health history and pain-related factors. Main outcomes included: Prescribed Opioids Difficulties Scale (PODS), Opioid-Related Behaviours In Treatment (ORBIT) scale, and ICD-10 opioid dependence. Multiple confounders for problematic opioid behaviours were assessed.

Findings: Of 1,514 participants 44.4% were male (95%CI 41.9-46.9) and their mean age was 58 years (IQR 48-67). Participants had a mean duration of pain of 10 years (IQR 4.5-20.0) and had been taking strong opioids for a median of four years (IQR 1.0-10.0). At baseline, median OME/day was 73 (IQR 35-148). At 5-years, 85% were still taking strong opioids. PODS moderate-high scores reduced from 59.9% (95%CI 58.8-61.0) at baseline to 51.5% (95%CI 50.0-53.0) at 5-years. Around 9% met criteria for ICD-10 opioid dependence at each wave. In adjusted mixed effect models, the risk factors most consistently associated with problematic opioid use were: younger age, substance dependence, mental health histories and higher opioid doses.

Interpretation: Both patient risk factors and opioid dose are associated with problematic opioid use behaviours.

Keywords: Chronic non-cancer pain; Cohort; Dependence; Extra medical use; Pharmaceutical opioid.

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Conflict of interest statement

GC, LD, MF, RB, MC and SN report grants for the conduct of this study from the National Health and Medical Research Centre (NHMRC). The funder had no input into the design, conduct, data collection, analyses or publication of study findings In the past 36 months some authors have received investigator-driven untied educational grants for unrelated work from Indivior (LD, BL, MF, SN), Mundipharma (MF, RB, NL), Seqirus (LD, MF, BL, SN) and Camurus AB (NL). No company had input into the design, conduct, data collection, analyses or publication of study findings. All other authors have no conflicts of interest to declare.

Figures

Fig. 1
Fig. 1
STROBE flow diagram for the pain and opioids IN treatment (POINT) cohort.
Fig. 2
Fig. 2
Average daily opioid utilisation (oral morphine equivalent (OME) mg per day) in the POINT cohort. Note: coloured bands show 95% confidence interval around each point. Only data is presented on people who reported opioid use in the past week via the medication diary. Since all participants were prescribed opioids at baseline entry there is no participants on 0 OME at baseline (see Appendix A for details).
Fig. 3
Fig. 3
Prevalence of problematic outcomes according to average daily opioid utilisation (oral morphine equivalent (OME) per day) in the POINT cohort (non-imputed data) (95%CI). Notes: Opioid dependence are presented for lifetime for baseline and past 12 months for other waves. Opioid dependence not collected at 1-year. Since all participants were prescribed opioids at baseline entry there is no participants on 0 OME at baseline See Appendix C for details.

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