Understanding Other Phencyclidine-Induced Disorders: Symptoms, Identification, and Treatment

Understanding Other Phencyclidine-Induced Disorders: Symptoms, Identification, and Treatment | Emocare

Addiction Medicine • Psychiatry • Emergency Care

Understanding Other Phencyclidine‑Induced Disorders: Symptoms, Identification, and Treatment

Beyond acute PCP intoxication, dissociative substances (PCP, ketamine and related agents) may cause persistent psychiatric, neurological, urological and functional disorders. This guide summarises recognition, differential diagnosis and evidence‑informed management.

Spectrum of PCP/dissociative‑induced disorders

  • Persistent psychosis or substance‑induced psychotic disorder following repeated exposure.
  • Prolonged dissociative states and depersonalisation/derealisation beyond acute intoxication.
  • Ketamine‑related urological disease (cystitis, lower urinary tract symptoms) with chronic use.
  • Neurocognitive impairment after repeated or high‑dose exposure: memory, attention and executive function deficits.
  • Mood and anxiety disorders precipitated or worsened by dissociative use.

Recognition & assessment

  1. Detailed history: identify substance(s), frequency, dose, route, setting, onset and persistence of symptoms relative to last use.
  2. Screen for psychosis: hallucinations, delusions, thought disorder and assess duration — differentiate acute intoxication from a persisting psychotic disorder.
  3. Assess dissociative symptoms using structured questions (episodes of depersonalisation/derealisation, functional impact) and screen for PTSD or trauma history which may co‑occur.
  4. Investigate urinary symptoms thoroughly in suspected chronic ketamine users — urgency, frequency, haematuria, dysuria and reduced bladder capacity; refer to urology where indicated.

Differential diagnosis

  • Primary psychotic disorders (schizophrenia) — consider family history, premorbid functioning, and persistence after prolonged abstinence.
  • Primary dissociative or trauma‑related conditions — evaluate for PTSD and dissociative identity disorder where history suggests.
  • Neurological causes of cognitive impairment — consider neuroimaging and neuropsychological testing for atypical features or progressive course.

Investigations

  • Toxicology where available to confirm recent exposure; basic labs to exclude metabolic causes (electrolytes, thyroid, B12) and infection.
  • MRI brain if focal deficits, progressive cognitive decline or atypical features suggest structural pathology.
  • Urinalysis, ultrasound and urodynamic studies for suspected ketamine cystitis; refer early to urology for severe symptoms.
  • Neuropsychological testing for persistent cognitive complaints to guide rehabilitation planning.

Management principles

  • Encourage and support abstinence from dissociatives; counsel on risks of persistent symptoms and provide harm‑reduction advice for those not ready to stop.
  • Treat acute psychiatric symptoms: benzodiazepines for severe anxiety/agitation in the short term; antipsychotics for persistent psychosis under psychiatric supervision.
  • Address comorbid mood and anxiety disorders with evidence‑based therapies (CBT, SSRIs) while monitoring for interactions with substance use.
  • Coordinate multidisciplinary care — psychiatry, addiction services, neurology, urology (for ketamine cystitis), and rehabilitation services for cognitive deficits.

Specific management areas

Persistent psychosis

  • Consider a trial of antipsychotic medication when psychotic symptoms persist beyond intoxication and cause impairment; use lowest effective dose and monitor side effects.
  • Reassess diagnosis after a period of sustained abstinence — some cases resolve, while others may reveal a primary psychotic disorder.

Dissociative and depersonalisation states

  • Psychological therapies (trauma‑focused CBT, grounding, mindfulness) are first‑line; pharmacological options have limited evidence.
  • Provide safety planning for patients with high anxiety or self‑harm risk and consider specialist referral for complex dissociation.

Ketamine‑related uropathy

  • Mainstay is abstinence and urological management — anticholinergic agents, bladder instillations, and in severe cases surgical interventions may be needed.
  • Early referral to urology improves outcomes; manage comorbid infections and provide pain control and pelvic physiotherapy where appropriate.

Neurocognitive impairment

  • Cognitive rehabilitation, occupational therapy and structured psychosocial interventions support recovery; consider neurology referral for persistent or progressive deficits.

When to refer

  • Persistent psychosis, severe dissociation, ongoing suicidal ideation or functional decline — urgent psychiatric referral.
  • Severe lower urinary tract symptoms suggestive of ketamine cystitis — urology referral without delay.
  • Progressive cognitive impairment or focal neurological signs — neurology and neuropsychology referral.

Case vignette

Patient: K., 34, heavy recreational ketamine user with 2 years of daily use, presents with urinary frequency, severe bladder pain and reduced bladder capacity. After counselling and support for abstinence, urodynamic testing confirmed ketamine cystitis. K. received urological care, pelvic physiotherapy and joined a structured addiction treatment programme with gradual symptom improvement.

தமிழில் — சுருக்கம்

PCP மற்றும் கேடமைன் போன்ற நகல்களில் நீடித்த மனஅழுத்தம், மனஅசலின் நிலைகள் மற்றும் குறிப்பாக கேடமைனுக்கு பொதுவான சிறுநீரக பிரச்சினைகள் ஏற்படலாம். நீடித்த அறிகுறிகள் இருந்தால் சிறப்பு ஆலோசனை மற்றும் பல்துறை மேம்படுத்தப்பட்ட சிகிச்சை தேவை.

Key takeaways

  • Dissociative substances can cause long‑term psychiatric, cognitive and urological problems beyond acute intoxication.
  • Early identification, sustained abstinence and multidisciplinary care (psychiatry, addiction services, urology, neurology) improve outcomes.
  • Use presentations as opportunities to engage patients with tailored treatment plans and harm‑reduction strategies.

Clinical Lead: Seethalakshmi Siva Kumar • Phone / WhatsApp: +91-7010702114 • Email: emocare@emocare.co.in

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