Discontinuation of Buprenorphine Maintenance Therapy: Perspectives and Outcomes
Open accessAbstract
Buprenorphine maintenance therapy (BMT) is increasingly the preferred opioid maintenance agent due to its reduced toxicity and availability in an office-based setting in the United States. Although BMT has been shown to be highly efficacious, it is often discontinued soon after initiation. No current systematic review has yet investigated providers' or patients' reasons for BMT discontinuation or the outcomes that follow. Hence, provider and patient perspectives associated with BMT discontinuation after a period of stable buprenorphine maintenance and the resultant outcomes were systematically reviewed with specific emphasis on pre-buprenorphine-taper parameters predictive of relapse following BMT discontinuation. Few identified studies address provider or patient perspectives associated with buprenorphine discontinuation. Within the studies reviewed providers with residency training in BMT were more likely to favor long term BMT instead of detoxification, and providers were likely to consider BMT discontinuation in the face of medication misuse. Patients often desired to remain on BMT because of fear of relapse to illicit opioid use if they were to discontinue BMT. The majority of patients who discontinued BMT did so involuntarily, often due to failure to follow strict program requirements, and 1 month following discontinuation, rates of relapse to illicit opioid use exceeded 50% in every study reviewed. Only lower buprenorphine maintenance dose, which may be a marker for attenuated addiction severity, predicted better outcomes across studies. Relaxed BMT program requirements and frequent counsel on the high probability of relapse if BMT is discontinued may improve retention in treatment and prevent the relapse to illicit opioid use that is likely to follow BMT discontinuation.
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28% of physicians working in addiction cited difficulties with tapering opioids because of a lack of tablets at lower doses.
“Indeed, 28% of physicians working in addiction cited difficulties with tapering opioids because of a lack of tablets at lower doses. 36”
From Tapering and withdrawing opioids: guidance informed by fundamental principles to minimise withdrawal symptoms (2025) · cites this paper as [36]
In Results §3.2, the paper reports that 28% of surveyed physicians cited difficulty starting a buprenorphine taper because lower-dose tablets were unavailable. The claim broadens this finding to tapering opioids generally, which the passage does not establish. (LLM, conf=0.88)
Experimental — accuracy not yet measuredMore explicit application of these principles to tapering regimens might improve the ability of patients to achieve cessation, particularly during the challenging final dose reductions, especially given that fear of withdrawal symptoms is one of the most common barriers to discontinuation.
“More explicit application of these principles to tapering regimens might improve the ability of patients to achieve cessation, particularly during the challenging final dose reductions, especially given that fear of withdrawal symptoms is one of the most common barriers to discontinuation.6,36”
From Tapering and withdrawing opioids: guidance informed by fundamental principles to minimise withdrawal symptoms (2025) · cites this paper as [36]
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- Authors
- Bentzley, B. S., Barth, K. S., Back, S. E., & Book, S. W.
- Affiliations
- Medical University of South Carolina (US)
- Venue
- Journal of Substance Abuse Treatment
- Publisher
- Elsevier BV
- Published
- 2015-05
- Volume
- 52
- Pages
- 48-57
- ISSN
- 0740-5472 (ISSN-L)
- PMC
- PMC4382404
- OpenAlex
- W2022774038
- Cited by
- 176
- References
- 80
- Citations by year
- 2026: 12 · 2025: 18 · 2024: 18 · 2023: 24 · 2022: 19 · 2021: 22 · 2020: 21 · 2019: 16 · 2018: 10 · 2017: 7 · 2016: 4 · 2015: 5
- FWCI
- 0.83
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of Substance Abuse Treatment (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (F30 DA035065, T32 GM008716, K12 HD055885, R25 DA020537)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Opioid Use Disorder Treatment
- Health Sciences › Medicine › Epidemiology › Substance Abuse Treatment and Outcomes
- Health Sciences › Medicine › Anesthesiology and Pain Medicine › Pain Management and Opioid Use
- Keywords
- treatment discontinuation, opioid use disorder, relapse, provider perspectives, patient perspectives, medication misuse, treatment retention, addiction severity, office-based opioid treatment
- MeSH terms
- Analgesics, Opioid, Buprenorphine, Humans, Opioid-Related Disorders, Withholding Treatment
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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