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Emergence of new psychoactive substance 2-fluorodeschloroketamine: Toxicology and urinary analysis in a cluster of patients exposed to ketamine and multiple analogues.

M. H. Tang, Terence C. Li, C. Lai, Y. Chong, C. Ching, T. Mak

Forensic Science International May 7, 2020 DOI: 10.1016/j.forsciint.2020.110327 (opens in new tab) via Semantic Scholar

Summary

AI-generated from the abstract

A new ketamine-like drug called 2-fluorodeschloroketamine (2F-DCK) has been identified in patients, often alongside other similar substances. Between January and July 2019, 20 cases of confirmed 2F-DCK exposure were reported, with 19 involving at least one other ketamine-type drug, most commonly ketamine (90%), deschloroketamine (50%), and 2-oxo-PCE (45%). Six patients had four different ketamine-type drugs in their urine. Clinical effects were primarily neurological (impaired consciousness, agitation, abnormal behavior) and cardiovascular (hypertension, tachycardia); five patients experienced loss of consciousness or convulsions. All patients recovered with supportive care. This is the first clinical case series of 2F-DCK, highlighting the need for awareness of this expanding class of drugs and frequent co-ingestion of multiple analogues.

Study at a glance

Characteristics Case series Case report Peer reviewed
Sample size 20
Population Patients with analytically confirmed 2F-DCK exposure
Keywords Medicine Chemistry
Key finding 2F-DCK is a newly identified ketamine analogue frequently co-ingested with other ketamine-type drugs, causing neurological and cardiovascular effects, but all patients recovered with supportive care.

Abstract

New psychoactive substances (NPS) emerge continually, amongst which is a growing class of ketamine analogues with an arylcyclohexylamine backbone. Recently we reported a poisoning outbreak associated with 2-oxo-PCE (deschloro-N-ethyl-ketamine). The present report describes the emergence of another ketamine analogue, 2-fluorodeschloroketamine (2F-DCK). The compound was first detected in a patient's urine, its identity confirmed by accurate mass analysis and comparison with reference standard. Four putative metabolites were identified, including nor-2F-DCK, dehydronor-2F-DCK (major metabolite) and two hydroxylated derivatives of nor-2F-DCK. Between January and July 2019, 20 cases of analytically confirmed 2F-DCK exposure were encountered. In 19 out of 20 cases, at least one more ketamine-type drug was detected concurrently with 2F-DCK, including ketamine (90%), deschloroketamine (DCK, 50%), 2-oxo-PCE (45%) and tiletamine (10%). In particular, six of the cases showed the presence of 4 ketamine-type drugs in the same urine sample. The clinical effects observed in patients exposed to 2F-DCK are predominantly neurological (impaired consciousness, agitation, abnormal behaviour) and cardiovascular (hypertension, tachycardia); five patients had loss of consciousness or convulsion. Management was mainly supportive; all patients recovered uneventfully. This is the first clinical case series involving 2F-DCK and frontline medical personnel are urged to be aware of this rapidly expanding class of NPS, in particular the co-ingestion of multiple ketamine analogues.

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