Supervised Consumption and Drug Related Harm

  • Research type

    Research Study

  • Full title

    Natural Experiment of the impact of supervised Opiate Agonist Therapy (OAT) consumption on drug related harm and treatment outcomes

  • IRAS ID

    327396

  • Contact name

    Matthew Hickman

  • Contact email

    Matthew.Hickman@bristol.ac.uk

  • Sponsor organisation

    University of Bristol

  • Duration of Study in the UK

    1 years, 5 months, 29 days

  • Research summary

    Opioid Agonist Treatment (OAT) is used to treat opioid dependence/opioid drug use disorders. Before the COVID-19 lockdown, daily supervised prescription and consumption at pharmacies or community drug agencies was the norm, although there is limited evidence on benefits, both economic or for patients. The COVID-19 led to patients being supplied with weekly or fortnightly supplies of OAT; in the UK this was well-received by patients but there is mixed evidence on the safety and success of this change in practice. This observational cohort study will determine and compare rates of drug related harm (hospital admission, non-fatal overdose, self-harm, drug related deaths), suicide death and all-cause mortality during periods of supervised and unsupervised OAT (methadone or buprenorphine) and off OAT, before, during and after the COVID-19 pandemic. It will also assess duration and retention on supervised compared with unsupervised OAT, before, during and after the COVID-19 pandemic.

    We will use data from a community drug agency, linked with hospital and mortality data, to identify patients prescribed either methadone or buprenorphine by a community drug agency and assess associations between OAT supervision and suspension and drug-related harm outcomes in multilevel regression models, adjusting for patient-related factors.

  • REC name

    London - Harrow Research Ethics Committee

  • REC reference

    23/PR/0763

  • Date of REC Opinion

    21 Aug 2023

  • REC opinion

    Favourable Opinion