Psych MEQs / SAQs · Addiction psychiatry — cannabis and psychosis
Cannabis use and psychosis — dual formulation to integrated care (MEQ)
FRANZCP-style MEQ on cannabis–psychosis dual diagnosis: classification, potency/frequency assessment, parallel treatment, SIP conversion risk, and family counselling.
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Target exams
Model answer
Reveal model answer
(i) Differential / working dual formulation. Not pure intoxication alone (symptoms span weeks with organised delusions and commentary). Working possibilities: cannabis-associated first presentation — cannabis-induced psychotic disorder versus primary first-episode psychosis with CUD comorbidity. Hold dual formulation until course after reduced use clarifies independence. Also exclude delirium/organic (currently low probability if alert and afebrile without red flags) and consider affective psychosis if mood becomes primary. Other substances on history. [1][5]
(ii) Assessment priorities. Risk (suicide, violence, vulnerability, driving, childcare); collateral and premorbid function; cannabis timeline — age of onset (15), frequency (most nights), high-THC potency, route, last use, withdrawal, CUD criteria; MSE with examples; capacity/legal status under local statute; baseline metabolic panel and ECG before antipsychotics; urine screen supports exposure but does not timestamp onset or measure potency. [1][5]
(iii) Management. Safety and least-restrictive setting that is still safe; do not withhold antipsychotics solely for positive UDS. Example start if psychosis warrants treatment: aripiprazole 10 mg orally daily after baselines, counsel akathisia, review within days, trial about 4–6 weeks with adherence support. Parallel CUD package: motivational interviewing, CBT for cannabis, family psychoeducation, contingency management if available — psychosocial interventions have the best evidence base for CUD. Address withdrawal (irritability, insomnia, craving) supportively. Refer early intervention / dual-diagnosis pathway. Relapse plan must name cannabis continuation as a risk amplifier. [3][4][5]
(iv) Family counselling. High-THC daily use is associated with increased psychotic disorder risk and contributes to incidence variation (EU-GEI framing); adolescent onset is a higher-risk window. Some substance-induced psychoses convert later to schizophrenia or bipolar disorder — resolution now does not mean zero follow-up. Continued use after onset raises relapse risk. Avoid fatalism ("schizophrenia forever on day one") and avoid minimisation ("just weed"). Crisis contacts, named review, education and study supports. [1][2][4]
Common errors
- Discharging as "drug-induced, no follow-up."
- Withholding antipsychotics until UDS clears.
- Asking only "do you use cannabis?" without frequency/potency/age of onset.
- Ignoring CUD psychosocial treatment.
- Inventing Mental Health Act section numbers for the wrong jurisdiction.
- Claiming CBD oil cures CUD or replaces antipsychotics. [2][3]
Examiner notes
Full marks require dual formulation language, potency/frequency assessment, named drug with dose and monitoring, parallel CUD psychosocial package, SIP conversion follow-up, and non-moralising family counselling grounded in Di Forti/Schoeler/Starzer-level evidence. [1][2][5]
References
- [1]Di Forti M, Quattrone D, Freeman TP, et al. The contribution of cannabis use to variation in the incidence of psychotic disorder across Europe (EU-GEI): a multicentre case-control study Lancet Psychiatry, 2019.PMID 30902669
- [2]Starzer MSK, Nordentoft M, Hjorthøj C Rates and Predictors of Conversion to Schizophrenia or Bipolar Disorder Following Substance-Induced Psychosis Am J Psychiatry, 2018.PMID 29179576
- [3]Gates PJ, Sabioni P, Copeland J, et al. Psychosocial interventions for cannabis use disorder Cochrane Database Syst Rev, 2016.PMID 27149547
- [4]Schoeler T, Petros N, Di Forti M, et al. Effects of continuation, frequency, and type of cannabis use on relapse in the first 2 years after onset of psychosis: an observational study Lancet Psychiatry, 2016.PMID 27567467
- [5]Galletly C, Castle D, Dark F, et al. Royal Australian and New Zealand College of Psychiatrists clinical practice guidelines for the management of schizophrenia and related disorders Aust N Z J Psychiatry, 2016.PMID 27106681