# Opioid dispensing prior to opioid toxicity hospitalizations and emergency department visits in Canada, 2018–2022

**Authors:** Bisola Hamzat, Grace Cheung, Dean T. Eurich, Jean-Luc Kaboré, Louis de Léséleuc, Zhaoyu Liu, Daniel McCormack, Houssem Missaoui, Jason R. Randall, Dana Shearer, David Stock, Tara Gomes

PMC · DOI: 10.1371/journal.pone.0339643 · PLOS One · 2026-01-12

## TL;DR

This study examines how prescription opioids contributed to opioid-related hospitalizations and emergency visits in Canada from 2018 to 2022, finding a decline in active opioid exposure overall except in British Columbia.

## Contribution

The study provides updated, province-level insights into prescription opioid use preceding opioid toxicity events in Canada, highlighting demographic and geographic variations.

## Key findings

- Active opioid exposure at hospital admissions declined in most provinces, except British Columbia, from 2018 to 2022.
- Opioid agonist treatment (OAT) exposure increased, while pain-related opioid exposure decreased during the study period.
- Emergency department visits showed more stable active opioid exposure rates compared to hospital admissions.

## Abstract

Both pharmaceutical and non-pharmaceutical opioids contribute to overdoses and other drug-related harms in Canada; however, the role of these sources of opioids have been dynamic over the past two decades and vary geographically. Therefore, we sought to examine trends in the prevalence of prescription opioid exposure at the time of opioid toxicity hospitalizations and emergency department (ED) visits across Canada over the past 5 years.

We conducted a population-based repeated cross-sectional study of yearly opioid toxicities treated in an inpatient hospital setting in 6 Canadian provinces―British Columbia, Alberta, Saskatchewan, Manitoba, Ontario, and Quebec―between January 2018 and December 2022. We linked hospitalization records with community pharmacy dispensing data to determine active exposure to prescribed opioids at the time of opioid toxicity, annually and stratified by patient characteristics and type of opioid dispensed. In a secondary analysis, we replicated these methods among opioid toxicities treated in EDs in 5 provinces where data were available.

We identified 23,876 opioid toxicity hospital admissions over the study period. Active opioid exposure at the time of hospital admission declined across provinces over time, apart from British Columbia (range, 20.0% in British Columbia to 47.5% in Quebec in 2018; 19.7% in British Columbia to 36.5% in Quebec in 2022). Generally, people ≥65 and females were proportionally more likely to have an active opioid exposure. When stratified by opioid type, we observed a shift towards active exposure to opioid agonist treatment (OAT), while active exposure to opioids for pain declined over time. Active opioid exposure was less common at the time of opioid toxicity ED visit but was more stable over time (range, 11.0% in British Columbia to 28.5% in Quebec in 2018; 14.9% in Alberta to 26.0% in Quebec in 2022), with only small declines in most provinces (Alberta, Ontario, and Quebec), and an increase in British Columbia (from 11.0% in 2018 to 16.8% in 2022), which was driven by a large increase in active OAT exposure.

Our findings highlight the increasing role of the potent unregulated drug supply in opioid toxicities across Canada, as well as important differences in the role of prescription opioids in harms across demographic groups, geography, and opioid indication.

## Full-text entities

- **Diseases:** drug-related harms (MESH:D000081015), SROM (MESH:D009021), drug toxicity (MESH:D064420), ED (MESH:D004630), death (MESH:D003643), OAT (MESH:D009293), overdose (MESH:D062787), pain (MESH:D010146)
- **Chemicals:** fentanyl (MESH:D005283), OAT (-), methadone (MESH:D008691), buprenorphine (MESH:D002047), hydromorphone (MESH:D004091), naloxone (MESH:D009270), morphine (MESH:D009020)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12795387/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12795387/full.md

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Source: https://tomesphere.com/paper/PMC12795387