Synthetic cathinone toxicity

Revision as of 21:53, 26 November 2020 by Rossdonaldson1 (talk | contribs) (Rossdonaldson1 moved page Synthetic Cathinones to Synthetic cathinone toxicity)

Background

Chemical structure of cathinone[1]
  • Cathinone is naturally occurring β-ketone analog of amphetamine found in the leaves of the “khat” plant (Catha edulis) consumed recreationally in Arabian peninsula and northeast Africa
  • Methcathinone first synthesized in 1928
  • Sharp increase in exposures around 2007-2011 due to products sold as “bath salts” and labelled “not for human consumption”
  • Common synthetic versions found today include mephedrone, methylone, MDPV, and many others

Bupropion is only cathinone derivative used medically in the US and Europe

Mechanism of Action

  • Thought to be similar to MOA of amphetamines and MDMA (increase of NE, dopamine and serotonin concentrations in synapses)
    • Inhibition of monoamine uptake transporters
    • Release of neurotransmitters from intracellular stores
  • Beta-ketone group decreases ability to penetrate BBB

Clinical Features

  • Presents similar to other sympathomimetics
  • Patient experiences euphoria, increased energy, agitation, psychosis, hallucinations
  • Case reports suggest tachycardia tends to be more severe than hypertension (HR >150 and SBP<150)
  • Can lead to psychosis, agitated delirium, seizures, hyperthermia, rhabdo, cardiovascular collapse, renal failure, hepatic dysfunction, DIC and death
    • Retrospective review showed OR of 3.09 and 7.98 for rhabdomyolysis and severe rhabdomyolysis compared to other sympathomimetics

Differential Diagnosis

  • Sympathomimetic toxicity
    • Methamphetamines
    • Cocaine
  • Anticholinergic toxicity

Evaluation

Workup

EKG, CBC, CMP, PT/INR, CK, APAP, ASA, ethanol

Diagnosis

UDS does not detect synthetic cathinones; must use GCMS

Management

  • In general, care is supportive
  • IVF for dehydration/rhabdo/AKI
  • Benzodiazepines for agitation

Disposition

  • If persistently altered, admission for observation
  • Otherwise if workup unremarkable and patient alert and oriented, discharge

References

1. Prosser JM, Nelson LS. The toxicology of bath salts: a review of synthetic cathinones. J Med Toxicol. 2012;8(1):33-42. doi:10.1007/s13181-011-0193-z

2. Baumann MH, Partilla JS, Lehner KR. Psychoactive "bath salts": not so soothing. Eur J Pharmacol. 2013 Jan 5;698(1-3):1-5. doi: 10.1016/j.ejphar.2012.11.020. Epub 2012 Nov 23. PMID: 23178799; PMCID: PMC3537229.

3. O’Connor AD, Padilla-Jones A, Gerkin RD, Levine M. Prevalence of rhabdomyolysis in sympathomimetic toxicity: a comparison of stimulants. J Med Toxicol 2015 Jun;11(2):195-200.

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 62258, Cathinone. https://pubchem.ncbi.nlm.nih.gov/compound/Cathinone. Accessed Nov. 26, 2020.