TY - JOUR
T1 - Characteristics and time course of benzodiazepine-type new psychoactive substance detections in Australia
T2 - results from the Emerging Drugs Network of Australia - Victoria project 2020-2022
AU - Syrjanen, Rebekka
AU - Greene, Shaun L.
AU - Weber, Courtney
AU - Smith, Jennifer L.
AU - Hodgson, Sarah E.
AU - Abouchedid, Rachelle
AU - Gerostamoulos, Dimitri
AU - Maplesden, Jacqueline
AU - Knott, Jonathan
AU - Hollerer, Hans
AU - Rotella, Joe Anthony
AU - Graudins, Andis
AU - Schumann, Jennifer L.
AU - on behalf of the EDNAV Project Research Group
N1 - Funding Information:
The authors acknowledge funding from the Victorian Department of Health and the National Health and Medical Research Council ( GNT2001107 ).
Publisher Copyright:
© 2023
PY - 2023/12
Y1 - 2023/12
N2 - Introduction: The emergence of benzodiazepine-type new psychoactive substances (NPSs) are a growing international public health concern, with increasing detections in drug seizures and clinical and coronial casework. This study describes the patterns and nature of benzodiazepine-type NPS detections extracted from the Emerging Drugs Network of Australia – Victoria (EDNAV) project, to better characterise benzodiazepine-type NPS exposures within an Australian context. Methods: EDNAV is a state-wide illicit drug toxicosurveillance project collecting data from patients presenting to an emergency department with illicit drug-related toxicity. Patient blood samples were screened for illicit, pharmaceutical and NPSs utilising liquid chromatography-tandem mass spectrometry. Demographic, clinical, and analytical data was extracted from the centralised registry for cases with an analytical confirmation of a benzodiazepine-type NPS(s) between September 2020–August 2022. Results: A benzodiazepine-type NPS was detected in 16.5 % of the EDNAV cohort (n = 183/1112). Benzodiazepine-type NPS positive patients were predominately male (69.4 %, n = 127), with a median age of 24 (range 16-68) years. Twelve different benzodiazepine-type NPSs were detected over the two-year period, most commonly clonazolam (n = 82, 44.8 %), etizolam (n = 62, 33.9 %), clobromazolam (n = 43, 23.5 %), flualprazolam (n = 42, 23.0 %), and phenazepam (n = 31, 16.9 %). Two or more benzodiazepine-type NPSs were detected in 47.0 % of benzodiazepine-type NPS positive patients. No patient referenced the use of a benzodiazepine-type NPS by name or reported the possibility of heterogenous product content. Conclusion: Non-prescription benzodiazepine use may be an emerging concern in Australia, particularly amongst young males. The large variety of benzodiazepine-type NPS combinations suggest that consumers may not be aware of product heterogeneity upon purchase or use. Continued monitoring efforts are paramount to inform harm reduction opportunities.
AB - Introduction: The emergence of benzodiazepine-type new psychoactive substances (NPSs) are a growing international public health concern, with increasing detections in drug seizures and clinical and coronial casework. This study describes the patterns and nature of benzodiazepine-type NPS detections extracted from the Emerging Drugs Network of Australia – Victoria (EDNAV) project, to better characterise benzodiazepine-type NPS exposures within an Australian context. Methods: EDNAV is a state-wide illicit drug toxicosurveillance project collecting data from patients presenting to an emergency department with illicit drug-related toxicity. Patient blood samples were screened for illicit, pharmaceutical and NPSs utilising liquid chromatography-tandem mass spectrometry. Demographic, clinical, and analytical data was extracted from the centralised registry for cases with an analytical confirmation of a benzodiazepine-type NPS(s) between September 2020–August 2022. Results: A benzodiazepine-type NPS was detected in 16.5 % of the EDNAV cohort (n = 183/1112). Benzodiazepine-type NPS positive patients were predominately male (69.4 %, n = 127), with a median age of 24 (range 16-68) years. Twelve different benzodiazepine-type NPSs were detected over the two-year period, most commonly clonazolam (n = 82, 44.8 %), etizolam (n = 62, 33.9 %), clobromazolam (n = 43, 23.5 %), flualprazolam (n = 42, 23.0 %), and phenazepam (n = 31, 16.9 %). Two or more benzodiazepine-type NPSs were detected in 47.0 % of benzodiazepine-type NPS positive patients. No patient referenced the use of a benzodiazepine-type NPS by name or reported the possibility of heterogenous product content. Conclusion: Non-prescription benzodiazepine use may be an emerging concern in Australia, particularly amongst young males. The large variety of benzodiazepine-type NPS combinations suggest that consumers may not be aware of product heterogeneity upon purchase or use. Continued monitoring efforts are paramount to inform harm reduction opportunities.
KW - Benzodiazepine-type NPS
KW - Early warning system
KW - NPS
KW - Toxicosurveillance
UR - http://www.scopus.com/inward/record.url?scp=85175793101&partnerID=8YFLogxK
U2 - 10.1016/j.drugpo.2023.104245
DO - 10.1016/j.drugpo.2023.104245
M3 - Article
C2 - 37944339
AN - SCOPUS:85175793101
SN - 0955-3959
VL - 122
JO - International Journal of Drug Policy
JF - International Journal of Drug Policy
M1 - 104245
ER -