Xylazine spreads across the US: A growing component of the increasingly synthetic and polysubstance overdose crisis.


Journal

Drug and alcohol dependence
ISSN: 1879-0046
Titre abrégé: Drug Alcohol Depend
Pays: Ireland
ID NLM: 7513587

Informations de publication

Date de publication:
01 04 2022
Historique:
received: 14 12 2021
revised: 21 02 2022
accepted: 23 02 2022
pubmed: 6 3 2022
medline: 26 4 2022
entrez: 5 3 2022
Statut: ppublish

Résumé

Sharp exacerbations of the US overdose crisis are linked to polysubstance use of synthetic compounds. Xylazine is a veterinary tranquilizer, long noted in the street opioid supply of Puerto Rico, and more recently Philadelphia. Yet its national trends, geographic distribution, and health risks are poorly characterized. In this sequential mixed-methods study, xylazine was increasingly observed by ethnographers in Philadelphia among drug-sellers and people who inject drugs (PWID). Subsequently, we systematically searched for records describing xylazine-present overdose mortality across the US and assessed time trends and overlap with other drugs. In 10 jurisdictions - representing all four US Census Regions - xylazine was increasingly present in overdose deaths, rising from 0.36% of deaths in 015m 6.7% in 2020. The highest xylazine prevalence data was observed in Philadelphia, (25.8% of deaths), followed by Maryland (19.3%) and Connecticut (10.2%). Illicitly-manufactured-fentanyls were present in 98.4% of xylazine-present-overdose-deaths - suggesting a strong ecological link - as well as cocaine (45.4%), benzodiazepines (28.4%), heroin (23.3%), and alcohol (19.7%). PWID in Philadelphia described xylazine as a sought-after adulterant that lengthens the short duration of fentanyl injections. They also linked it to increased risk of soft tissue infection and naloxone-resistant overdose. Xylazine is increasingly present in overdose deaths, linked to the proliferation of illicitly-manufactured-fentanyls. Ethnographic accounts associate it with profound risks for PWID. Nevertheless, many jurisdictions do not routinely test for xylazine, and it is not comprehensively tracked nationally. Further efforts are needed to provide PWID with services that can help minimize additional risks associated with a shifting drug supply.

Sections du résumé

BACKGROUND
Sharp exacerbations of the US overdose crisis are linked to polysubstance use of synthetic compounds. Xylazine is a veterinary tranquilizer, long noted in the street opioid supply of Puerto Rico, and more recently Philadelphia. Yet its national trends, geographic distribution, and health risks are poorly characterized.
METHODS
In this sequential mixed-methods study, xylazine was increasingly observed by ethnographers in Philadelphia among drug-sellers and people who inject drugs (PWID). Subsequently, we systematically searched for records describing xylazine-present overdose mortality across the US and assessed time trends and overlap with other drugs.
RESULTS
In 10 jurisdictions - representing all four US Census Regions - xylazine was increasingly present in overdose deaths, rising from 0.36% of deaths in 015m 6.7% in 2020. The highest xylazine prevalence data was observed in Philadelphia, (25.8% of deaths), followed by Maryland (19.3%) and Connecticut (10.2%). Illicitly-manufactured-fentanyls were present in 98.4% of xylazine-present-overdose-deaths - suggesting a strong ecological link - as well as cocaine (45.4%), benzodiazepines (28.4%), heroin (23.3%), and alcohol (19.7%). PWID in Philadelphia described xylazine as a sought-after adulterant that lengthens the short duration of fentanyl injections. They also linked it to increased risk of soft tissue infection and naloxone-resistant overdose.
CONCLUSIONS
Xylazine is increasingly present in overdose deaths, linked to the proliferation of illicitly-manufactured-fentanyls. Ethnographic accounts associate it with profound risks for PWID. Nevertheless, many jurisdictions do not routinely test for xylazine, and it is not comprehensively tracked nationally. Further efforts are needed to provide PWID with services that can help minimize additional risks associated with a shifting drug supply.

Identifiants

pubmed: 35247724
pii: S0376-8716(22)00117-X
doi: 10.1016/j.drugalcdep.2022.109380
pmc: PMC9128597
mid: NIHMS1804518
pii:
doi:

Substances chimiques

Analgesics, Opioid 0
Xylazine 2KFG9TP5V8
Heroin 70D95007SX
Fentanyl UF599785JZ

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

109380

Subventions

Organisme : NIDA NIH HHS
ID : K08 DA048163
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA049644
Pays : United States
Organisme : NIDA NIH HHS
ID : T32 DA035165
Pays : United States
Organisme : NIDA NIH HHS
ID : K01 DA050771
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008042
Pays : United States

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

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Auteurs

Joseph Friedman (J)

Center for Social Medicine and Humanities, University of California, Los Angeles, CA, USA; Medical Informatics Home Area, University of California, Los Angeles, CA, USA. Electronic address: joseph.robert.friedman@gmail.com.

Fernando Montero (F)

Department of Anthropology, Columbia University, New York, NY, USA.

Phillippe Bourgois (P)

Center for Social Medicine and Humanities, University of California, Los Angeles, CA, USA. Electronic address: pbourgois@gmail.com.

Rafik Wahbi (R)

Fielding School of Public Health, University of California, Los Angeles, CA, USA.

Daniel Dye (D)

Department of Pathology, University of Alabama, Birmingham, AL, USA.

David Goodman-Meza (D)

Division of Infectious Diseases, University of California, Los Angeles, CA, USA.

Chelsea Shover (C)

Division of General Internal Medicine and Health Services Research, University of California, Los Angeles, CA, USA. Electronic address: CLShover@mednet.ucla.edu.

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Classifications MeSH