14 Characterization of Xylazine-Related Overdose Deaths in Maryland (2020-2022)

OBJECTIVES/GOALS: Xylazine is a strong sedative and fentanyl contaminant which has been increasingly detected in drug overdose deaths in Maryland. The goal of this project is to analyze the demographic characteristics and time trends of xylazine-related overdose deaths (XROD) in Maryland from 2020-2...

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Main Authors: Erin Wang, Paul Nestadt
Format: Article
Language:English
Published: Cambridge University Press 2024-04-01
Series:Journal of Clinical and Translational Science
Online Access:https://www.cambridge.org/core/product/identifier/S2059866124000359/type/journal_article
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author Erin Wang
Paul Nestadt
author_facet Erin Wang
Paul Nestadt
author_sort Erin Wang
collection DOAJ
description OBJECTIVES/GOALS: Xylazine is a strong sedative and fentanyl contaminant which has been increasingly detected in drug overdose deaths in Maryland. The goal of this project is to analyze the demographic characteristics and time trends of xylazine-related overdose deaths (XROD) in Maryland from 2020-2022. METHODS/STUDY POPULATION: This cross-sectional study utilizes the Maryland medical examiner's autopsy reports from 2020-2022. These reports include every death in the state that was investigated by the medical examiner, with demographic and toxicological data showing the presence of various substances at the time of death. An XROD was defined as someone who died from drug overdose and had a positive serum xylazine test at time of death. Demographic characteristics and time trends for XROD were analyzed. Multivariable logistic regression modeled associations between demographic variables and the presence of other substances with XROD. RESULTS/ANTICIPATED RESULTS: A total of 1,509 people died from XROD, of which the mean age was 44.4 years and 73.3% were male. The majority were White (57.6%), 39.2% were Black, and 3.2% identified as another race. Over 99.9% of individuals who died from XROD tested positive for fentanyl. XROD peaked in January 2021 and has been trending downwards since then. Adjusted multivariable logistic regression revealed that White individuals had greater odds of XROD relative to Black individuals (OR=1.22, 95% CI=1.07-1.37), and adults aged 30-45 years had higher odds of XROD relative to adults over age 60 (OR=1.26, 95%CI=1.04-1.54). Individuals who used fentanyl had higher odds of XROD relative to those who did not use fentanyl (OR=327.4, 95%CI=46.0-2331.3). DISCUSSION/SIGNIFICANCE: This study demonstrates that middle age, White race, and fentanyl use are associated with xylazine-related overdose deaths in Maryland. Efforts to reduce xylazine-related mortality in the state should address the unique social and geographic factors that influence substance use in this population.
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spelling doaj.art-272017b6ce4a44b6b1266584b0fcd98a2024-04-03T02:00:21ZengCambridge University PressJournal of Clinical and Translational Science2059-86612024-04-0184410.1017/cts.2024.3514 Characterization of Xylazine-Related Overdose Deaths in Maryland (2020-2022)Erin Wang0Paul Nestadt1Johns Hopkins Bloomberg School of Public HealthJohns Hopkins Bloomberg School of Public Health Johns Hopkins University School of MedicineOBJECTIVES/GOALS: Xylazine is a strong sedative and fentanyl contaminant which has been increasingly detected in drug overdose deaths in Maryland. The goal of this project is to analyze the demographic characteristics and time trends of xylazine-related overdose deaths (XROD) in Maryland from 2020-2022. METHODS/STUDY POPULATION: This cross-sectional study utilizes the Maryland medical examiner's autopsy reports from 2020-2022. These reports include every death in the state that was investigated by the medical examiner, with demographic and toxicological data showing the presence of various substances at the time of death. An XROD was defined as someone who died from drug overdose and had a positive serum xylazine test at time of death. Demographic characteristics and time trends for XROD were analyzed. Multivariable logistic regression modeled associations between demographic variables and the presence of other substances with XROD. RESULTS/ANTICIPATED RESULTS: A total of 1,509 people died from XROD, of which the mean age was 44.4 years and 73.3% were male. The majority were White (57.6%), 39.2% were Black, and 3.2% identified as another race. Over 99.9% of individuals who died from XROD tested positive for fentanyl. XROD peaked in January 2021 and has been trending downwards since then. Adjusted multivariable logistic regression revealed that White individuals had greater odds of XROD relative to Black individuals (OR=1.22, 95% CI=1.07-1.37), and adults aged 30-45 years had higher odds of XROD relative to adults over age 60 (OR=1.26, 95%CI=1.04-1.54). Individuals who used fentanyl had higher odds of XROD relative to those who did not use fentanyl (OR=327.4, 95%CI=46.0-2331.3). DISCUSSION/SIGNIFICANCE: This study demonstrates that middle age, White race, and fentanyl use are associated with xylazine-related overdose deaths in Maryland. Efforts to reduce xylazine-related mortality in the state should address the unique social and geographic factors that influence substance use in this population.https://www.cambridge.org/core/product/identifier/S2059866124000359/type/journal_article
spellingShingle Erin Wang
Paul Nestadt
14 Characterization of Xylazine-Related Overdose Deaths in Maryland (2020-2022)
Journal of Clinical and Translational Science
title 14 Characterization of Xylazine-Related Overdose Deaths in Maryland (2020-2022)
title_full 14 Characterization of Xylazine-Related Overdose Deaths in Maryland (2020-2022)
title_fullStr 14 Characterization of Xylazine-Related Overdose Deaths in Maryland (2020-2022)
title_full_unstemmed 14 Characterization of Xylazine-Related Overdose Deaths in Maryland (2020-2022)
title_short 14 Characterization of Xylazine-Related Overdose Deaths in Maryland (2020-2022)
title_sort 14 characterization of xylazine related overdose deaths in maryland 2020 2022
url https://www.cambridge.org/core/product/identifier/S2059866124000359/type/journal_article
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