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Pharmacist-led DE-eSCALation of opioids post-surgical dischargE (DESCALE) – A multi-centre, non-randomised, feasibility study protocol [Version 1]

Veale, Emma L. and Theron, Johanna and Rees-Roberts, Melanie and Hedayioglu, Julie H. and Santer, Ellie and Hulbert, Sabina and Short, Vanessa J. (2024) Pharmacist-led DE-eSCALation of opioids post-surgical dischargE (DESCALE) – A multi-centre, non-randomised, feasibility study protocol [Version 1]. [Preprint] (doi:10.3310/nihropenres.13716.1) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:109763)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
https://doi.org/10.3310/nihropenres.13716.1

Abstract

Background

Opioids are frequently prescribed for short-term acute pain following surgery. Used appropriately, opioids deliver extremely favourable pain relief. Used longer than 90-days, however, can result in health complications, including unintentional overdose and addiction. Globally, >40 million people are dependent on opioids and annually >100,000 die from opioid misuse. With >4.7 million surgical procedures occurring annually in the United Kingdom it is imperative that opioid-use is managed upon discharge. A declining General Practitioner (GP) workforce and increased patient numbers, however, means gaps in healthcare during transfer of care. Here we report a mixed-methods protocol to understand the feasibility, and acceptability of a clinical pharmacist (CP)-led early opioid deprescribing intervention for discharged surgical patients.

Methods

DESCALE is a multicentre, non-randomised, pragmatic feasibility study. Participants aged ≥18 years who have undergone a surgical procedure at a single NHS trust in Southeast England and discharged with opioids and without a history of long-term opioid use, cancer diagnosis or study contraindications will be offered a Medicines Use Review (MUR) within 7-10 days of discharge. The MUR will be delivered by CPs at participating GP practices. Feasibility outcomes will focus on recruitment, fidelity of CPs to deliver the MUR, and barriers within primary care that affect delivery of the intervention, with a maximum sample size of 100. Clinical outcomes will focus on the number of participants that reduce or stop opioid use within 91 days. Prescribing, medical, surgical, and demographic data for individual participants will be collected and analysed to inform future trial design. Qualitative interviews with participants and associated healthcare professionals will explore acceptability and implementation of the intervention.

Conclusion

Data collected with respect to opioid use post-surgery, feasibility and acceptability of the intervention, patient experience and outcome data will inform the design of future research and larger clinical trials.

Item Type: Preprint
DOI/Identification number: 10.3310/nihropenres.13716.1
Refereed: No
Name of pre-print platform: NIHR Open Research
Uncontrolled keywords: Opioids, deprescribing, surgery, dependence, clinical pharmacists, Medicines Use Review, primary care, secondary care
Subjects: H Social Sciences
R Medicine
Institutional Unit: Schools > Medway School of Pharmacy
Schools > School of Social Sciences > Centre for Health Services Studies
Former Institutional Unit:
Divisions > Division of Natural Sciences > Medway School of Pharmacy
Divisions > Division for the Study of Law, Society and Social Justice > School of Social Policy, Sociology and Social Research > Centre for Health Services Studies
Funders: National Institute for Health Research (https://ror.org/0187kwz08)
Depositing User: Emma Veale
Date Deposited: 25 Apr 2025 09:23 UTC
Last Modified: 20 May 2025 09:57 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/109763 (The current URI for this page, for reference purposes)

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