Evidence map›Paper›PMID 42276321›Full record

ArticleJournal of substance use and addiction treatment2026

Healthcare provider approaches to managing the health harms of xylazine: A qualitative study.

Patrick J A Kelly, Amelia Bailey, Josiah D Rich, Katie B Biello, Brandon D L Marshall, Elizabeth S Chen, Jaclyn M W Hughto

Abstract read
In one paragraph

Article in Journal of substance use and addiction treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Patrick J A KellyDepartment of Behavioral and Social Sciences, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; Center for Health Promotion and Health Equity, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA. Electronic address: Patrick_kelly@brown.edu.
Amelia BaileyDepartment of Behavioral and Social Sciences, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; Center for Alcohol and Addiction Studies, Brown University School of Public Health, Providence, RI, 02903, USA.
Josiah D RichCenter of Biomedical Research Excellence on Opioids and Overdose, Rhode Island Hospital, 1125 North Main Street, Providence, RI, 02903, USA; The Warren Alpert School of Medicine of Brown University, 222 Richmond Street, Providence, RI, 02912, USA; Department of Epidemiology, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA.
Katie B BielloDepartment of Behavioral and Social Sciences, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; Department of Epidemiology, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; Center for Epidemiologic Research, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; The Fenway Institute, Fenway Health, 1340 Boylston St, Boston, MA, 02215, USA.
Brandon D L MarshallDepartment of Epidemiology, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA.
Elizabeth S ChenDepartment of Health Services Policy and Practice, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; Brown Center for Biomedical Informatics, Brown University Division of Biology and Medicine, 300 Richmond Street, Providence, RI, 02912, USA.
Jaclyn M W HughtoDepartment of Behavioral and Social Sciences, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; Center for Health Promotion and Health Equity, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; Center for Alcohol and Addiction Studies, Brown University School of Public Health, Providence, RI, 02903, USA; Center of Biomedical Research Excellence on Opioids and Overdose, Rhode Island Hospital, 1125 North Main Street, Providence, RI, 02903, USA; Department of Epidemiology, Brown University School of Public Health, 121 South Main Street, Providence, RI, 02903, USA; The Fenway Institute, Fenway Health, 1340 Boylston St, Boston, MA, 02215, USA.

Funding

Project 4: Neonatal Abstinence Syndrome (NAS): Fetus to First YearsP20GM125507 · NIGMS · RHODE ISLAND HOSPITAL · PI JOSIAH D RICH · 2018 to 2026
$23.4M
Community and big-data system approaches to identifying and understanding the health impact of xylazineF31DA061593 · NIDA · BROWN UNIVERSITY · PI Patrick John Kelly · 2024 to 2026
$149k
NIDA NIH HHS F31 DA061593NIGMS NIH HHS P20 GM125507
6 · The paper itself

Abstract

introductionXylazine-adulterated fentanyl use is associated with manifold negative health outcomes, including skin and soft tissue infections, intensified opioid withdrawal, and can complicate medication for opioid use disorder (MOUD) induction. This qualitative research aimed to explore how healthcare providers test for and treat xylazine-related health harms among people who use drugs (PWUD).

methodsFrom February-April 2025, twelve healthcare providers with expertise in managing the health harms of xylazine from three Northeastern states completed an approximately 45-min semi-structured interview to explore organizational capacity for xylazine toxicology screening and clinical management of xylazine-associated health harms. Rapid qualitative analysis was used to analyze transcripts and produce themes.

resultsParticipants worked in academic institutions (n = 7), free-standing clinics (n = 5), harm reduction organizations (n = 4), substance use treatment programs (n = 4), hospitals (n = 2), and a federally qualified health center (n = 1). Providers infer xylazine exposure based on clinical presentation and rarely order toxicology, which is often unavailable at some institutions. Providers noted three core clinical effects of xylazine use including overdose, xylazine-associated skin wounds, and withdrawal. Respiratory support and monitoring are essential when responding to xylazine-involved overdose. Additionally, wound chronicity, limited treatment guidelines, homelessness, and stigma complicate xylazine-associated skin wound healing. Withdrawal from xylazine typically co-occurs with opioid withdrawal and is worse than opioid-only withdrawal. Xylazine may be worsening experiences of precipitated withdrawal when inducting patients onto buprenorphine. Some physicians noted that medetomidine, a sedative more potent than xylazine, is associated with withdrawal worse than xylazine withdrawal, weakening the efficacy of recently developed xylazine withdrawal protocols and underscoring the volatility of the drug supply.

conclusionThe clinical effects of xylazine do not occur in isolation from the effects of other substances and often compound one another. Findings demonstrate the complexities of care coordination and management of xylazine-associated health harms. The high level of care coordination needed for xylazine-exposed PWUD is a result of the volatile drug supply, which is likely to become increasingly harmful as new sedative type adulterants, like medetomidine, emerge.

Indexed as

Health PersonnelOpioid-Related DisordersXylazineDrug ContaminationFemaleFentanylHumansHypnotics and SedativesQualitative ResearchSubstance Withdrawal SyndromeFentanylHypnotics and SedativesXylazineFentanylMedetomidineOverdoseQualitativeSkin woundTreatmentWithdrawalXylazine

Identifiers

PMID42276321
PMCPMC13344124

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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.