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Cystitis due to the use of ketamine as a recreational drug: a case report
© Colebunders and Van Erps; licensee BioMed Central Ltd. 2008
Received: 02 January 2008
Accepted: 26 June 2008
Published: 26 June 2008
Ketamine is a derivative of phencyclidine and is a dissociative anaesthetic. Its use as a recreational drug is on the increase among young adults attending clubs and parties.
We describe the case of a 20-year-old man who presented with a 7-month history of urinary frequency, nocturia, urgency, suprapubic discomfort during micturition and episodes of severe haematuria shortly after commencing weekly recreational ketamine use. Complementary examinations were negative except for a thickened bladder wall on ultrasound examination and mild inflammatory changes on cystoscopy. So far only nine cases of ketamine-associated ulcerative cystitis have been described.
We expect that in the future an increasing number of cases of cystitis caused by ketamine use will be seen in young adults.
Ketamine is a derivative of phencyclidine, a popular street drug which is known as 'PCP' or 'angel dust'. Ketamine is less potent and shorter acting compared with phencyclidine and is used as a dissociative anaesthetic in humans . Ketamine, known as 'Special K', is becoming more widely used among young adults attending clubs and parties, including raves . It is labelled a 'club drug' by the National Institute on Drug Abuse (NIDA) of the United States. The effects of ketamine include profound changes in consciousness and psychotomimetic symptoms, such as out-of-body experiences . It can also induce a state of virtual helplessness and a pronounced lack of coordination . Negative effects include increased heart and respiratory rates, nausea and vomiting, convulsions, temporary paralysis and hallucinations . So far only one report has described the effect of ketamine on the urinary system: nine patients were found to have developed a ketamine-associated ulcerative cystitis . We report an additional case.
We describe the case of a 20-year-old man who presented with a 7-month history of urinary frequency, nocturia, urgency, suprapubic discomfort during micturition and episodes of severe haematuria shortly after commencing weekly recreational ketamine use. The patient occasionally works as a disk jockey at 'hardstyle' and 'jump' parties. His past medical history was significant for nose polyps and asthma, for which he was treated with montelukast (Singulair®) and fluticasone propionate in combination with salmeterol (Seretide®). He had never travelled outside of Europe.
After 2 months of symptoms he had been treated with antibiotics for 5 days and anticholinergics for several weeks without any improvement. Routine urine analysis and urine cytology were negative and a urine culture was sterile. An ultrasound examination revealed a thickened bladder wall and a small bladder capacity but normal kidneys. Cystoscopy showed mild inflammatory changes, although there was no visual blood in the urine. Bladder biopsies were negative; however, they were not taken during an episode of active cystitis. We advised the patient to stop ketamine use.
Characteristics of 10 patients with ketamine-associated cystitis reported in the literature.
Duration of symptoms
Mild squamous metaplasia, ulcerated patches
Epithelial denudation, inflammation, eosinophilic infiltrate
In three patients, similar to patient 1
Benefited from cessation of ketamine
In our case cystoscopy showed only mild signs of inflammation and biopsies were negative. However, our patient used ketamine only on a weekly basis, whereas the patients described in the literature were daily users. This could explain the difference between our patient's cystoscopy and biopsy findings with those of the nine cases reported in the literature. Moreover, in our patient the biopsies were not taken during an episode of active cystitis. We suspect, however, that ketamine was the cause of the patient's complaints, as the timing of the onset of symptoms correlated strongly with the commencement of ketamine use. In addition, the evidence shows our case to be consistent in many ways with the nine other cases described in the literature (Table 1).
The mechanism by which ketamine induces cystitis is not clear. Ketamine and its metabolites norketamine and hydroxynorketamine can be measured in high quantities in the urine of patients using ketamine . It is possible that ketamine and its active metabolites cause significant bladder irritation.
As ketamine is being used increasingly as a recreational drug we expect ketamine-associated cystitis to become more prevalent in young adults. Health care workers should be aware of the problem and patients should be informed about the possible side effects of ketamine. The long-term sequelae of ketamine on the bladder remain unknown.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
- Ivani G, Vercillino C, Tonetti F: Ketamine: a new look to an old drug. Minerva Anestesiol. 2003, 69: 468-471.PubMedGoogle Scholar
- Dillon P, Copeland J, Jansen K: Patterns of use and harm associated with non-medical ketamine use. Drug Alcohol Depend. 2003, 69: 23-28. 10.1016/S0376-8716(02)00243-0.View ArticlePubMedGoogle Scholar
- Schnoll SH, Weaver MF: Phencyclidine and ketamine. Textbook of Substance Abuse Treatment. Edited by: Galanter M, Klebert HD. 2004, Washington, DC: American Psychiatric Press, 211-3Google Scholar
- Jansen KLR: Non-medical use of ketamine. BMJ. 1993, 306: 601-602.View ArticlePubMedPubMed CentralGoogle Scholar
- Shahani R, Streutker C, Dickson B, Stewart RJ: Ketamine-associated ulcerative cystitis: a new clinical entity. Urology. 2007, 69: 810-812. 10.1016/j.urology.2007.01.038.View ArticlePubMedGoogle Scholar
- Moore KA, Sklerov J, Levine B, Jacobs AJ: Urine concentrations of ketamine and norketamine following illegal consumption. J Anal Toxicol. 2001, 25: 583-588.View ArticlePubMedGoogle Scholar
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