4.6 Article

Validation of Self-reported Opioid Agonist Treatment Among People Who Inject Drugs Using Prescription Dispensation Records

Journal

EPIDEMIOLOGY
Volume 33, Issue 2, Pages 287-294

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/EDE.0000000000001443

Keywords

Opioid agonist therapy; Opioid substitution treatment; Medication for opioid use disorder; Methadone; Buprenorphine-naloxone; Validation study

Funding

  1. Canadian Institutes of Health Research (CIHR)
  2. ICES - Ontario Ministry of Health and Long-Term Care
  3. Ontario Ministry of Research, Innovation and Science
  4. Program of Intervention, Research and Policy in Addictions Care from the St. Michael's Hospital Foundation

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This study assessed the validity of self-reported opioid agonist treatment measures among people who inject drugs (PWID). The results showed that the self-reported measures were fairly accurate, with some exceptions. Inaccurate recall and social desirability bias were identified as potential factors influencing the accuracy of the reports.
Background: Studies of people who inject drugs (PWID) commonly use questionnaires to determine whether participants are currently, or have recently been, on opioid agonist treatment for opioid use disorder. However, these previously unvalidated self-reported treatment measures may be susceptible to inaccurate reporting. Methods: We linked baseline questionnaire data from 521 PWID in the Ontario integrated Supervised Injection Services cohort in Toronto (November 2018-March 2020) with record-level health administrative data. We assessed the validity (sensitivity, specificity, positive and negative predictive value [PPV and NPV]) of self-reported recent (in the past 6 months) and current (as of interview) opioid agonist treatment with methadone or buprenorphine-naloxone relative to prescription dispensation records from a provincial narcotics monitoring system, considered the reference standard. Results: For self-reported recent opioid agonist treatment, sensitivity was 78% (95% CI = 72, 83), specificity was 90% (95% CI = 86, 94), PPV was 90% (95% CI = 85, 93), and NPV was 79% (95% CI = 74, 84). For self-reported current opioid agonist treatment, sensitivity was 84% (95% CI = 78, 90), specificity was 87% (95% CI = 83, 91), PPV was 74% (95% CI = 67, 81), and NPV was 93% (95% CI = 89, 95). Conclusions: Self-reported opioid agonist treatment measures were fairly accurate among PWID, with some exceptions. Inaccurate recall due to a lengthy lookback window may explain underreporting of recent treatment, whereas social desirability bias may have led to overreporting of current treatment. These validation data could be used in future studies of PWID to adjust for misclassification in similar self-reported treatment measures.

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