Paeds SAQs · mental-behavioural-and-psychosomatic
Early-onset psychosis and mania — formative SAQs
Formative SAQs on running the psychosis-mania gate: organic exclusion before any psychiatric label, duration of untreated psychosis, TEOSS pharmacotherapy, distinguishing mania from chronic irritability and substance-induced states, and antipsychotic metabolic monitoring.
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SAQ 1 (10 marks)
A 15-year-old boy is brought to the emergency department after telling his mother that classmates have implanted a chip in his head. He has not slept for four nights, is guarded and frightened, and describes a voice telling him to run. His mother thinks it is "just cannabis and stress." He has smoked high-potency cannabis daily for six months. There is no fever, no fluctuating consciousness, no focal neurology and a normal physical examination, but his marks have fallen and he has lost two friendships over three months. [2] [5]
- State the immediate priorities in the first hour, including what must be excluded before any psychiatric label is applied. (3) [2]
- Outline the role of cannabis in this presentation and the evidence supporting your advice. (3) [5] [6]
- Describe first-line pharmacotherapy and how the TEOSS trial should inform the choice, plus the baseline and follow-up monitoring. (4) [1] [2] [4]
Model answer — SAQ 1
(1) Immediate priorities and organic exclusion (3). Safety first: assess suicide and self-harm risk with plan, intent and means, and apply means-restriction safety planning the same day; assess for acute behavioural disturbance and catatonia. Then exclude organic disease before any psychiatric label — full physical and neurological examination, full blood count, electrolytes, liver and renal function, thyroid function, inflammatory markers and a urine drug screen, with neuroimaging and an electroencephalogram if onset is acute, consciousness fluctuates, or focal neurology is present. A psychotic young person is a medical patient first and a psychiatric patient second; a collateral history from family and school is mandatory because he is an unreliable sole historian. [2]
(2) Cannabis and the evidence (3). Cannabis is a real, modifiable and dose-related risk factor for psychosis, not an aside. Moore's systematic review found cannabis use associated with a clear increase in psychotic outcomes, and Arseneault's longitudinal study showed adolescent cannabis use raised the risk of adult psychosis in a dose-related way, with earlier, more frequent and higher-potency use being worse. In this boy, daily high-potency use may have triggered or worsened the psychotic picture, so ask about potency, frequency and age of first use, counsel reduction, and arrange a period of supported abstinence and reassessment — persistent symptoms after abstinence warrant full assessment and treatment of a primary disorder. [5] [6]
(3) Pharmacotherapy, TEOSS and monitoring (4). After specialist assessment, first-line treatment for early-onset schizophrenia is an antipsychotic. The TEOSS trial compared second-generation drugs (risperidone, olanzapine) with the first-generation molindone and found efficacy was similar across groups with different side-effect burdens — so there is no clear efficacy advantage of second- over first-generation drugs, and the side-effect profile decides the choice. Risperidone or aripiprazole are common first-line options. Because duration of untreated psychosis drives long-term outcome, prompt specialist referral and early treatment are themselves the intervention. Baseline monitoring: weight, body-mass index, waist circumference, blood pressure, fasting glucose and lipids, prolactin and an electrocardiogram; then review at 4–6 weeks, 12 weeks and six-monthly, with extrapyramidal side effects, sedation and suicide risk assessed at every contact. [1] [4]
References10ShowHide
- [1]Sikich L, Frazier JA, McClellan J, Findling RL, Vitiello B, et al. Double-blind comparison of first- and second-generation antipsychotics in early-onset schizophrenia and schizo-affective disorder: findings from the Treatment of Early-Onset Schizophrenia Spectrum Disorders (TEOSS) study. American Journal of Psychiatry, 2008.PMID 18794207
- [2]McClellan J, Stock S Practice parameter for the assessment and treatment of children and adolescents with schizophrenia. Journal of the American Academy of Child and Adolescent Psychiatry, 2013.PMID 23972700
- [3]Cannon TD, Cadenhead K, Cornblatt B, Woods SW, Addington J, et al. Prediction of psychosis in youth at high clinical risk: a multisite longitudinal study in North America. Archives of General Psychiatry, 2008.PMID 18180426
- [4]Penttilä M, Jääskeläinen E, Hirvonen N, Isohanni M, Miettunen J Duration of untreated psychosis as predictor of long-term outcome in schizophrenia: systematic review and meta-analysis. British Journal of Psychiatry, 2014.PMID 25252316
- [5]Moore TH, Zammit S, Lingford-Hughes A, Barnes TR, Jones PB, et al. Cannabis use and risk of psychotic or affective mental health outcomes: a systematic review. Lancet, 2007.PMID 17662880
- [6]Arseneault L, Cannon M, Poulton R, Murray R, Caspi A, Moffitt TE Cannabis use in adolescence and risk for adult psychosis: longitudinal prospective study. BMJ, 2002.PMID 12446537
- [7]Geller B, Luby JL, Joshi P, Wagner KD, Emslie G, et al. A randomized controlled trial of risperidone, lithium, or divalproex sodium for initial treatment of bipolar I disorder, manic or mixed phase, in children and adolescents. Archives of General Psychiatry, 2012.PMID 22213771
- [8]Wagner KD, Kowatch RA, Emslie GJ, Findling RL, Wilens TE, et al. A double-blind, randomized, placebo-controlled trial of oxcarbazepine in the treatment of bipolar disorder in children and adolescents. American Journal of Psychiatry, 2006.PMID 16816222
- [9]Tohen M, Kryzhanovskaya L, Carlson G, Delbello M, Wozniak J, et al. Olanzapine versus placebo in the treatment of adolescents with bipolar mania. American Journal of Psychiatry, 2007.PMID 17898346
- [10]Haas M, Delbello MP, Pandina G, Kushner S, Van Hove I, et al. Risperidone for the treatment of acute mania in children and adolescents with bipolar disorder: a randomized, double-blind, placebo-controlled study. Bipolar Disorders, 2009.PMID 19839994