Prevalence of fentanyl in methamphetamine and cocaine samples collected by community-based drug checking services.


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 11 2023
Historique:
received: 07 08 2023
revised: 19 09 2023
accepted: 28 09 2023
pmc-release: 01 11 2024
medline: 30 10 2023
pubmed: 13 10 2023
entrez: 12 10 2023
Statut: ppublish

Résumé

Overdose deaths involving stimulants and opioids simultaneously have raised the specter of widespread contamination of the stimulant supply with fentanyl. We quantified prevalence of fentanyl in street methamphetamine and cocaine, stratified by crystalline texture, analyzing samples sent voluntarily to a public mail-in drug checking service (May 2021-June 2023). Samples from 77 harm reduction programs and clinics originated in 25 US states. Sample donors reported expected drug and physical descriptions. Substances were identified by gas chromatography-mass spectrometry. Negative binomial models were used to calculate fentanyl prevalence, adjusting for potential confounders related to sample selection. We also examined if xylazine changed donors' accuracy of detecting fentanyl. We analyzed 718 lab-confirmed samples of methamphetamine (64%) and cocaine (36%). The adjusted prevalence of fentanyl was 12.5% (95% CI: 2.2%, 22.9%) in powder methamphetamine and 14.8% (2.3%, 27.2%) in powder cocaine, with notable geographic variation. Crystalline forms of both methamphetamine (Chisq=57, p<0.001) and cocaine (Chisq=18, p<0.001) were less likely to contain fentanyl: less than 1% of crystal methamphetamine (2/276) and no crack cocaine (0/53). Heroin was present in 6.6% of powder cocaine samples. Xylazine reduced donors' ability to detect fentanyl, with correct classification dropping from 92% to 42%. Fentanyl was detected primarily in powder forms of methamphetamine and cocaine. Recommended interventions include expanding community-based drug checking, naloxone and fentanyl test strip distribution for people who use stimulants , and supervised drug consumption sites. New strategies to dampen variability in street drug composition are needed to reduce inadvertent fentanyl exposure.

Sections du résumé

BACKGROUND
Overdose deaths involving stimulants and opioids simultaneously have raised the specter of widespread contamination of the stimulant supply with fentanyl.
METHODS
We quantified prevalence of fentanyl in street methamphetamine and cocaine, stratified by crystalline texture, analyzing samples sent voluntarily to a public mail-in drug checking service (May 2021-June 2023). Samples from 77 harm reduction programs and clinics originated in 25 US states. Sample donors reported expected drug and physical descriptions. Substances were identified by gas chromatography-mass spectrometry. Negative binomial models were used to calculate fentanyl prevalence, adjusting for potential confounders related to sample selection. We also examined if xylazine changed donors' accuracy of detecting fentanyl.
RESULTS
We analyzed 718 lab-confirmed samples of methamphetamine (64%) and cocaine (36%). The adjusted prevalence of fentanyl was 12.5% (95% CI: 2.2%, 22.9%) in powder methamphetamine and 14.8% (2.3%, 27.2%) in powder cocaine, with notable geographic variation. Crystalline forms of both methamphetamine (Chisq=57, p<0.001) and cocaine (Chisq=18, p<0.001) were less likely to contain fentanyl: less than 1% of crystal methamphetamine (2/276) and no crack cocaine (0/53). Heroin was present in 6.6% of powder cocaine samples. Xylazine reduced donors' ability to detect fentanyl, with correct classification dropping from 92% to 42%.
CONCLUSIONS
Fentanyl was detected primarily in powder forms of methamphetamine and cocaine. Recommended interventions include expanding community-based drug checking, naloxone and fentanyl test strip distribution for people who use stimulants , and supervised drug consumption sites. New strategies to dampen variability in street drug composition are needed to reduce inadvertent fentanyl exposure.

Identifiants

pubmed: 37826988
pii: S0376-8716(23)01223-1
doi: 10.1016/j.drugalcdep.2023.110985
pmc: PMC10688611
mid: NIHMS1937998
pii:
doi:

Substances chimiques

Fentanyl UF599785JZ
Cocaine I5Y540LHVR
Methamphetamine 44RAL3456C
Xylazine 2KFG9TP5V8
Powders 0
Analgesics, Opioid 0
Crack Cocaine 0
Central Nervous System Stimulants 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

110985

Subventions

Organisme : NCATS NIH HHS
ID : UL1TR001449
Pays : United States
Organisme : CDC HHS
ID : R01CE003356
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001449
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35GM118055
Pays : United States
Organisme : NIGMS NIH HHS
ID : R35 GM118055
Pays : United States
Organisme : NCIPC CDC HHS
ID : R01 CE003356
Pays : United States

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest ND serves on the Scientific Advisory Board of the non-profit RADARS System of Denver Health and Hospitals Authority, which had no knowledge of or involvement in this manuscript. ND is also on the Board of Directors of the non-profit organization Remedy Alliance For The People. The remaining authors have no conflicts of interest to declare.

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Auteurs

Karla D Wagner (KD)

Department of Health Behavior, Policy, and Administration Sciences, School of Public Health, University of Nevada, Reno, NV 89557, USA. Electronic address: karlawagner@unr.edu.

Phillip Fiuty (P)

The Mountain Center, Española, NM 87606, USA. Electronic address: phillip@pfhrsnm.com.

Kimberly Page (K)

Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA. Electronic address: Pagek@salud.unm.edu.

Erin C Tracy (EC)

Injury Prevention Research Center, University of North Carolina, CB 7505, 725 Martin Luther King Jr. Blvd, Chapel Hill, NC 27599, USA. Electronic address: ectracy@unc.edu.

Maryalice Nocera (M)

Injury Prevention Research Center, University of North Carolina, CB 7505, 725 Martin Luther King Jr. Blvd, Chapel Hill, NC 27599, USA. Electronic address: mnocera@unc.edu.

Colin W Miller (CW)

Injury Prevention Research Center, University of North Carolina, CB 7505, 725 Martin Luther King Jr. Blvd, Chapel Hill, NC 27599, USA. Electronic address: cwm@unc.edu.

Lina J Tarhuni (LJ)

Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque, NM 87131, USA; Department of Pharmacy, University of Washington, Seattle, WA 98195, USA. Electronic address: LTarhuni@salud.unm.edu.

Nabarun Dasgupta (N)

Injury Prevention Research Center, University of North Carolina, CB 7505, 725 Martin Luther King Jr. Blvd, Chapel Hill, NC 27599, USA. Electronic address: nab@unc.edu.

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Classifications MeSH