Synthetic cathinone toxicity
Background
- 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.
- ↑ National Center for Biotechnology Information. PubChem Compound Summary for CID 62258, Cathinone. https://pubchem.ncbi.nlm.nih.gov/compound/Cathinone. Accessed Nov. 26, 2020.
