Evidence map›Paper›PMID 42380718›Full record

ArticleNeurocritical care2026

Low-Dose Buprenorphine Initiations During Opioid and Sedative Weaning in Mechanically Ventilated Neurocritical Care Patients: A Retrospective Pilot Cohort Study.

David K Carroll, Andrew M King, Brandtly Yakey, Mark K Greenwald, Eric A Woodcock, Andrew R Isaacson, Bram A Dolcourt, Arun Sherma, Maria Muzammil

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Article in Neurocritical care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

9 authors.

David K CarrollDetroit Medical Center, Detroit, MI, USA. hj7218@wayne.edu.ORCID http://orcid.org/0009-0000-9349-0261
Andrew M KingDetroit Medical Center, Detroit, MI, USA.
Brandtly YakeyDetroit Medical Center, Detroit, MI, USA.
Mark K GreenwaldDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, USA.
Eric A WoodcockDepartment of Psychiatry and Behavioral Neurosciences, Wayne State University School of Medicine, Detroit, MI, USA.
Andrew R IsaacsonDetroit Medical Center, Detroit, MI, USA.
Bram A DolcourtDetroit Medical Center, Detroit, MI, USA.
Arun ShermaDetroit Medical Center, Detroit, MI, USA.
Maria MuzammilDetroit Medical Center, Detroit, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIatrogenic opioid dependence, withdrawal, and opioid accumulation can impede neurologic assessment and delay liberation from invasive mechanical ventilation (IMV) in neurocritical care. We evaluated whether low-dose buprenorphine (BUP) initiation was associated with improved sedation and ventilator outcomes.

methodsWe conducted a retrospective matched cohort/case-control study of adults in the neurocritical care unit (NCCU) receiving parenteral opioids while on IMV ≥ 24 h. Patients receiving low-dose BUP initiation (≤ 2 mg cumulative in the first 8 h with ≥ 1 sublingual dose; n = 19) were matched by demographics and diagnosis to patients not receiving BUP (NO-BUP; n = 18). Outcomes included ventilator days/time to liberation, daily intravenous (IV) morphine milligram equivalents (MME), time-in-target range Richmond Agitation-Sedation Scale (RASS - 2 to 0), continuous sedative infusion exposure, opioid withdrawal, and BUP-attributable adverse events [precipitated opioid withdrawal (POW) or respiratory depression].

resultsBUP patients had fewer ventilator days than NO-BUP patients (17.7 ± 13.9 vs. 29.3 ± 13.9 days; mean difference - 11.65, 95% CI - 20.9 to - 2.4; Cohen's d = 0.84; p = 0.008) and earlier median liberation (16.0 vs. 23.5 days; p = 0.021). After BUP initiation, daily IV MME decreased (597.6 ± 617.5 to 6.8 ± 18.3 mg; p = 0.001), target RASS time increased (63.9 ± 27.8% to 81.6 ± 22.0%; p = 0.0001), and continuous sedative infusions declined (73.7% to 31.6%; p = 0.021). No BUP patient experienced POW or respiratory depression temporally related to BUP; opioid withdrawal occurred in 0/19 BUP vs. 6/18 NO-BUP patients (33.3%; p = 0.008). The intensive care unit (ICU) length of stay was similar (30.2 ± 18.6 vs. 31.8 ± 14.9 days; p = 0.385).

conclusionsIn this pilot retrospective matched cohort study, low-dose BUP initiation as part of an opioid/sedative-weaning strategy was feasible and associated with higher documented time-in-target RASS, reduced opioid/sedative exposure, and faster IMV liberation without documented POW. Given the small sample size, co-interventions, retrospective design, and residual confounding, these findings should be considered hypothesis-generating and require prospective validation.

Indexed as

BuprenorphineIntensive care unitsOpioid-related disordersSubstance withdrawal syndromeVentilator weaning

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.