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Hallucinogen Persisting Perception Disorder Following Therapeutic Ketamine: A Case Report

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Intravenous ketamine, a dissociative anaesthetic, has been reported to alleviate major depression [1] and chronic pain [2] with minimal adverse effects [3,4], although perceptual disturbances are not uncommon [5]. Hallucinogen persisting perception disorder (HPPD)is an illness arising from the abuse of hallucinogens in which individuals suffer visual pseudohallucinations for months to years following exposure to LSD and similar drugs [6]. We now report a case of HPPD in a young man who received medically administered intravenous ketamine for treatment of a complex regional pain syndrome (CRPS).

Case Report

A 13 year old male piano student developed CRPS following a sacral injury. He had no history of substance use. At 15, chronic pain was treated with two continuous intravenous infusions of ketamine, each lasting a week, with maximal doses of 50 mg per hour. During each treatment he vomited and had visual and synesthetic hallucinations.Six months later he suffered the progressive onset of an array of visual pseudohallucinations and hypersensitivity to light and sound. Imagery included particles in the entire visual field seen in the air and on surfaces; large moving coloured blobs on surfaces; afterimages; trails of objects moving through his visual field, such as a tennis ball; objects changing their shape; and difficulty reading and playing the piano. He also suffered the incessant sensation of the euphoria he felt when given ketamine. These symptoms were reported as daily and constant on multiple follow-up visits over a three year period.A psychiatric evaluation found no evidence of psychosis or depression. The mental status examination confirmed a deficit in short term memory. The patient described continual visual disturbances during the examination. Reality testing was intact.There were no auditory hallucinations or delusions. Psychological testing confirmed a reading disorder. A quantitative EEG found evidence of an auditory processing disorder with irritability in the left temporal and occipital regions, including activation of the auditory system by visual stimuli, a putative marker for drug-induced synaesthesia.Medications including divalproex sodium, several SSRIs, gabapentin and pregabalin were unsuccessful. Lorazepam 2 mg twice daily reduced, but did not ablate, his symptoms for two months. In that time he returned to the piano and was admitted to a university music program. Relapse followed as the patient apparently developed tolerance to the treatment. A similar pattern followed use of diazepam10 mg a day. At the age of 18, he developed complex partial seizures which have been controlled with topiramate. However, the perceptual symptoms and ketamine euphoria have continued.

Discussion and Conclusion

Studies in subjects with HPPD suggest that the pathophysiology of the disorder involves either a slowly reversible or permanent disruption in the inhibition of visual information processing. This has been described from the use of LSD, MDMA, psychostimulants and a variety of botanical preparations of hallucinogens [7]. Evidence for visual disinhibition following LSD includes persisting after imagery [8],abnormal flicker fusion testing, impaired dark adaptation [9],electrophysiological measures of cortical disinhibition [10] and increased measures of cerebral coherence, a putative measure of increased cortical activation [11]. To the best of our knowledge this report is the first association between ketamine and HPPD.The mechanism by which ketamine antagonism of the NMDA receptor induces perceptual or psychotic symptoms is not known.Consistent in both animal and human studies, however, is the observation that ketamine increases activity of brain waves in the gamma (30 to 60 Hz) range. De la Salle et al. reported such an increase in gamma current density in the default mode network implicated ins chizophrenia, as well as activation of gamma frequencies across the cerebrum [12]. This finding supports a disinhibition model of HPPD.In addition, GABA-A agonists such as midazolam reduce HPPD symptoms [13].HPPD also appears to be associated with increased cerebral coherence, a measure of cortical connectivity [14]. Similarly, temporal lobe epilepsy involving the neocortex has been associated with increased coherence [15]. The role of ketamine in the generation or control of seizures is not known. But in our case, enhancement of cortical coherence with neurofeedback resulted in an exacerbation of HPPD.Ketamine, a schedule III drug which is an anaesthetic agent, can be prescribed by any physician. Enthusiasm for its use in treatment of refractory depression has yet to be tempered by a body of research establishing safety and efficacy [16]. The history of LSD in the 1960sfollowed such a course over time, in which a period of rising enthusiasm was followed by one of sober reconsideration as the risks and benefits were identified [17]. This report adds a note of caution to the process.



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  • 4 weeks later...

Interesting that he eventually develops seizures. You see kids, doctors are fucking stupid, case in point. Now hes on topiramate, Im not sure about that one specifically but  most anti seizure meds long term cause neuronal loss, and after about 20 years most patients so significant signs of reduced brain size.

But as I have said I do believe that HPPD, migraines, and seizures are closely related.

Edited by Fawkinchit
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