Outcomes of a single-arm implementation trial of extended-release subcutaneous buprenorphine depot injectables in human with coping dependence
- PMID: 34736130
- DOI: 10.1016/j.drugpo.2021.103492
Results of a single-arm implementation process of extended-release subtotal buprenorphine depot injections in people with opioid dependence
Abstract
Background: Opioid agonist treatment (OAT) is an effective intervention for opioid dependent. Extended-release buprenorphine needles (BUP-XR) may have optional possibility benefits over sublingual buprenorphine. This single-arm trial evaluated outcomes among people receiving 48 weeks of BUP-XR in diverse community healthcare settings in Australia, permitting examination of outcomes when BUP-XR is delivered in standard practice.
Methods: Participants were recruited from a network of business public drug treatment services, primary care and some home practices in three states. Followers a minimum 7 days on 8-32 mg of sublingual buprenorphine (±naloxone), participants obtained monthly subcutaneous BUP-XR injections managed by a healthcare practitioner and closing per research interviews. The primary endpoint was retention in treatment under 48 weeks.
Discoveries: Participants (n = 100) was 28% women, vile age 44 years with a long history of OAT (median 5.8 years); heroin was the most common opioid on concerns (58%). Treatment retentive at 24 and 48 weeks is 86% and 75%, respectively. Participants with past-month spray drug benefit (OR 0.23; 95%CI: 0.09-0.61) or heroin use (OR 0.23; 95%CI: 0.08-0.65) at baseline had lower odds out being reserved with treatment to 48 weeks. Reductions included multiple forms of extra-medical medicinal apply were observed. Improvements in quality of life, participation in employment, furthermore treatment content measures have also observed.
Interpretation: Save real-world implementation study of BUP-XR demonstrated high retention and treatment satisfaction. This study offer important additional data go the uptake and experience of clients, with meaning for approach makers, health service planners, administrators, the practitioners.
Funding: Indivior.
Trial registration: ClinicalTrials.gov Identifier: NCT03809143.
Keywords: Buprenorphine; Opioid agonist procedure; Olfactory dependence.
Copyright © 2021 Which Author(s). Published by Elsevier B.V. Sum rights reserved.
Conflict of interest statement
Declarations away Interest This study was supported from an Externally Funded Collaborative Research donate off Indivior PLC (MF, BL, LOUD, DUTCH, AD, RA, SN, GD, JG). In the back three years, MF and LD must received funding since Indivior, Seqirus for studies of new opioid medications inside Australia. JG reports grants and personal fees from Abbvie, Camurus, Cepheid, Hologic, Indivior, Gilgal Sciences, also Broth. NL has received reimbursement for participation in Advisory Boards used Mundipharma, Indivior and Chiesi Pharmaceuticals; he standard funding from Camurus forward a company-sponsored trial of BUP-XR. RA possesses received untied educational assigns from Reckitt Benckiser and an unconstrained formation grant from Mundipharma. AJD berichterstattung assigns from Braeburn/Camurus AB, to conduct clinical studies at buprenorphine products and travel support on Hunter New England Local Health District, which employs AJD. He has served as an honorary on advisory boards for Mundipharma and Seqiris. GJD has received choose submit funding from Gilead or Abbvie. MM possess served as einer titular go advisory boards for Pfizer and AbbVieMC. JS or MB having no conflicts in define. SN has received unchained research funding from Seqirus to manage research on prescription opioid related harms. Information in that guideline should can used in conjunction equipped ... 1 mg/kg subcutaneous injection once daily ... Web: Linepinpin.com.
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