# The impact of changes in opioid dependency treatment upon COVID-19 transmission in Sydney, Australia: a retrospective longitudinal observational study

**Authors:** Benjamin T. Trevitt, Victoria Hayes, Rachel Deacon, Llewellyn Mills, Apo Demirkol, Nicholas Lintzeris

PMC · DOI: 10.1186/s12889-024-17827-0 · BMC Public Health · 2024-02-02

## TL;DR

A study in Sydney found that opioid treatment clients were more likely to get COVID-19, and reducing dosing frequency and using pharmacies helped lower the risk.

## Contribution

This study identifies specific treatment modifications that can reduce COVID-19 transmission among opioid dependency treatment clients.

## Key findings

- Clients in opioid dependency treatment had 13.6 times higher odds of acquiring COVID-19 compared to the general NSW population.
- Pharmacy dosing and vaccination were associated with significantly lower odds of acquiring COVID-19.
- Each additional day of required attendance increased the odds of infection by 5%.

## Abstract

In April 2020, in response to the COVID-19 public health emergency, South Eastern Sydney Local Health District (SESLHD) Drug and Alcohol services modified their delivery of opioid dependency treatment (ODT) to reduce spread of COVID-19 and maintain continuity of care by increasing use of takeaway doses (TADs), transferring clients to local community pharmacies for dosing and encouraging the use of long-acting depot buprenorphine (LADB) which enabled once a month dosing.

This study was a retrospective longitudinal case–control study conducted from August 1st, to November 30th, 2021. Eligible clients were those admitted for treatment with SESLHD ODT Services prior to August 1st,2021 and who remained in treatment beyond November 30th, 2021. COVID-19 diagnoses were determined by a COVID-19 PCR and extracted from the electronic Medical Records (eMR) Discern Reporting Portal. Demographic, clinical and dosing related data were collected from eMR and the Australian Immunisation Register (AIR).

Clients attending SESLHD ODT services had significantly greater odds of acquiring COVID-19 than the NSW adult population at large (OR: 13.63, 95%CI: 9.64,18.88). Additionally, amongst SESLHD ODT clients, being of Aboriginal and Torres Strait Islander origin was associated with greater odds of acquiring COVID-19 (OR = 2.18, CI: 1.05,4.53); whilst being employed (OR = 0.06, CI:0.01,0.46), receiving doses at pharmacy (OR = 0.43, CI: 0.21,0.89), and being vaccinated (OR = 0.12, CI: 0.06,0.26) were associated with lower odds. Every additional day of attendance required for dosing was associated with a 5% increase in odds of acquiring COVID-19 (OR = 1.05, CI: 1.02,1.08).

Clients attending SESLHD ODT services are significantly more likely to acquire COVID-19 than the NSW population at large. Promoting vaccination uptake, transferring clients to pharmacy, and reducing the frequency of dosing (by use of takeaway doses or long-acting depot buprenorphine) are all potential methods to reduce this risk.

## Linked entities

- **Diseases:** COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** chronic obstructive pulmonary disease (MESH:D029424), diabetes (MESH:D003920), ODT (MESH:D009293), Torres (MESH:D055653), eMR (MESH:D000069279), respiratory illnesses (MESH:D012140), trauma (MESH:D014947), ATOP (MESH:D011248), anxiety (MESH:D001007), sleep difficulty (MESH:D012893), COVID (MESH:D000086382), palpitations (MESH:D006331), Coronavirus (MESH:D018352), depression (MESH:D003866), SESLHD (OMIM:603663), SUDs (MESH:D019966), infection (MESH:D007239), hepatitis C (MESH:D019698), fatigue (MESH:D005221), PHU (MESH:C000719203), infectious disease (MESH:D003141), anosmia (MESH:D000857), myalgia (MESH:D063806), dizziness (MESH:D004244), chronic kidney disease (MESH:D051436), LADB (MESH:D000094024), hair-loss (MESH:D000505), SL-BPN (MESH:D013362), NCIMS (MESH:D020763)
- **Chemicals:** buprenorphine (MESH:D002047), methadone (MESH:D008691), Alcohol (MESH:D000438), BPN (MESH:D001977), Drug and Alcohol (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

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## References

53 references — full list in the complete paper: https://tomesphere.com/paper/PMC10835853/full.md

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Source: https://tomesphere.com/paper/PMC10835853