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Lookup NU author(s): Dr Simon Hill, Dr Michael Dunn, Professor Simon ThomasORCiD
This is the authors' accepted manuscript of an article that has been published in its final definitive form by Taylor and Francis Inc., 2019.
For re-use rights please refer to the publisher's terms and conditions.
Objective: Use of the New Psychoactive Substance (NPS) methiopropamine was first reported in 2011, but there are limited data on its acute toxicity. We report 11 patients presenting with analytically confirmed methiopropamine use.Methods: Adults presenting to 26 hospitals in the UK with severe acute toxicity after suspected NPS use were recruited from March 2015 to April 2018. Clinical features were recorded and biological samples analysed using tandem mass-spectrometry.Results: Methiopropamine was detected in 11 of 414 patients, with the last detection in August 2016. It was the only substance detected in one patient; other substances detected included other NPS in nine and conventional drugs of misuse in five. Common features included tachycardia (10/11), agitation (7/11), confusion (7/11), reduced level of consciousness (5/11), hallucinations (5/11) and a raised creatine kinase (7/11). Median length of hospital-stay was 17hours; ten were discharged without sequelae and one was transferred for in-patient psychiatric treatment.Conclusions: Methiopropamine was only detected during 2015 and 2016; most patients had other drugs detected, particularly other NPS. Raised CK was common but it is not possible to determine the degree to which this and other features could be contributed to by co-use of other substances.
Author(s): White JC, Wood DM, Hill SL, Eddleston M, Officer J, Dargan PI, Dunn M, Thomas SHL
Publication type: Article
Publication status: Published
Journal: Clinical Toxicology
Year: 2019
Volume: 57
Issue: 7
Pages: 663-667
Online publication date: 24/01/2019
Acceptance date: 14/10/2018
Date deposited: 22/10/2018
ISSN (print): 1556-3650
ISSN (electronic): 1556-9519
Publisher: Taylor and Francis Inc.
URL: https://doi.org/10.1080/15563650.2018.1538519
DOI: 10.1080/15563650.2018.1538519
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