Xylazine poisoning: a systematic review

Clin Toxicol (Phila). 2022 Aug;60(8):892-901. doi: 10.1080/15563650.2022.2063135. Epub 2022 Apr 20.

Abstract

Purpose: Xylazine is an alpha-2-adrenergic agonist used for its sedative and analgesic properties in veterinary medicine. While not approved by the Food and Drug Administration for use in humans, anecdotal evidence suggests that exposures in humans is on the rise. We sought to systematically review and synthesize the evidence on xylazine exposure in humans focusing on the clinical presentation, management, and outcomes.

Methods: We conducted a systematic review of the literature including PubMed, Embase, and Scopus from their inception to September 9, 2021. We searched abstracts from selected emergency medicine and toxicology conferences from 2011 through 2021. We included clinical reports of xylazine exposure in humans. We excluded animal studies, in vitro studies, laboratory studies, or articles in a language other than English. From each included article, we extracted subjective and objective data that focused on clinical presentation, management, and outcomes of patients exposed to xylazine.

Results: We evaluated a total of 1409 records, rendering a final set of 17 articles and 2 abstracts meeting inclusion criteria. We identified a total of 98 patients amongst reports ranging from 1979 to 2020 and across nine countries. The most common types of xylazine exposures reported were unintentional exposure and intentional misuse/abuse. Common symptoms on presentation included hypotension, bradycardia, drowsiness, lethargy, while apnea with intubation and death were less frequently reported.

Conclusion: Human exposure to xylazine appears to be a rising concern within the prehospital and emergency medicine setting. Although a standardized treatment algorithm cannot be recommended at this time, further research is needed to improve the care of patients exposed to xylazine.

Keywords: Xylazine; poisoning; toxicity; systematic review.

Publication types

  • Systematic Review

MeSH terms

  • Adrenergic Agonists
  • Bradycardia
  • Humans
  • Hypnotics and Sedatives
  • Hypotension*
  • United States
  • Xylazine*

Substances

  • Adrenergic Agonists
  • Hypnotics and Sedatives
  • Xylazine