Evaluation of opioid use disorder treatment outcomes in patients receiving split daily versus once daily dosing of buprenorphine-naloxone.


Journal

Journal of substance use and addiction treatment
ISSN: 2949-8759
Titre abrégé: J Subst Use Addict Treat
Pays: United States
ID NLM: 9918541186406676

Informations de publication

Date de publication:
Jan 2024
Historique:
received: 21 02 2023
revised: 29 09 2023
accepted: 24 10 2023
medline: 4 12 2023
pubmed: 9 11 2023
entrez: 8 11 2023
Statut: ppublish

Résumé

In clinical practice, sublingual (SL) buprenorphine-naloxone is prescribed as once daily or split daily dosing for the management of opioid use disorder (OUD). Evidence is lacking that assesses how split daily buprenorphine-naloxone affects OUD outcomes. This study aims to evaluate how the dosing frequency of SL buprenorphine-naloxone impacts therapy effectiveness when treating patients with OUD. This retrospective analysis included adult outpatients prescribed treatment with SL buprenorphine-naloxone for OUD between July 1, 2016, and March 1, 2020. The study excluded patients with sickle cell disease, recent methadone treatment, or pregnancy. We characterized study groups by dosing frequency, either once daily or split dosing. The study compared retention in treatment, medication adherence, adherence to treatment program, and hospital encounters between groups. The study screened eight-hundred and seven patients, and included 250 patients newly prescribed SL buprenorphine-naloxone. Fifty-seven patients (22.8 %) were prescribed once daily dosing and 193 patients (77.2 %) were prescribed split daily dosing. The study found no significant differences noted in 12-month rates of treatment retention (52.6 % vs. 45.6 %, p = .35). These outcomes remained similar when assessed at three and six months. Within a year of buprenorphine-naloxone initiation, the study found no differences in the percentage of patients with hospitalizations (26.3 % vs. 38.3 %, p = .10), median number of hospitalizations (2 vs. 2), or proportion of days covered by a prescription ≥80 % (93.3 % vs. 92.0 %, p = .82). In this study, patients receiving once daily buprenorphine-naloxone had similar treatment outcomes to patients receiving split dosing. Further controlled studies are necessary to evaluate which patients are more likely to benefit from split dosing.

Identifiants

pubmed: 37939905
pii: S2949-8759(23)00260-6
doi: 10.1016/j.josat.2023.209209
pii:
doi:

Substances chimiques

Buprenorphine, Naloxone Drug Combination 0
Buprenorphine 40D3SCR4GZ
Narcotic Antagonists 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

209209

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest None.

Auteurs

Joshua B Borris (JB)

Johns Hopkins Bayview Medical Center, Department of Pharmacy, 4940 Eastern Ave, Baltimore, MD 21224, United States of America. Electronic address: jborris@umaryland.edu.

Caitlin Dowd-Green (C)

The Johns Hopkins Hospital, Department of Pharmacy, 600 N Wolfe St, Baltimore, MD 21287, United States of America. Electronic address: cdowd2@jhmi.edu.

Lindsay A Bowman (LA)

The Johns Hopkins Hospital, Department of Pharmacy, 600 N Wolfe St, Baltimore, MD 21287, United States of America. Electronic address: ljablon2@jhmi.edu.

Suzanne A Nesbit (SA)

The Johns Hopkins Hospital, Department of Pharmacy, 600 N Wolfe St, Baltimore, MD 21287, United States of America. Electronic address: snesbit1@jhmi.edu.

Michael Fingerhood (M)

Johns Hopkins University School of Medicine, Department of Medicine, 5200 Eastern Ave, Baltimore, MD 21224, United States of America. Electronic address: mifinger@jhmi.edu.

Rosalyn W Stewart (RW)

Johns Hopkins University School of Medicine, Department of Medicine, 5200 Eastern Ave, Baltimore, MD 21224, United States of America. Electronic address: rstewart@jhmi.edu.

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Classifications MeSH