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Psych MEQs / SAQsGeneral adult psychiatry — bipolar and related disorders

Psych MEQs / SAQs · General adult psychiatry — bipolar and related disorders

Mixed features crisis and rapid-cycling reformulation (MEQ)

FRANZCP-style MEQ on mixed features mania, rapid cycling, antidepressant monotherapy harm, lithium/SGA re-initiation, thyroid review, and STEP-BD/BALANCE-informed planning.

20 marks20 min2 min readVerification in progress

Target exams

FRANZCPMRCPsychABPNMD-DNB
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Target exams

FRANZCPMRCPsychABPNMD-DNB
Prompt
A 29-year-old woman with previously diagnosed bipolar I disorder is brought to ED by her partner. For 10 days she has slept 2–3 hours/night with high energy, spoken rapidly, spent excessively, and been irritable. Simultaneously she is tearful, says she is 'a failure who should die,' and has researched lethal means. She has been taking sertraline 150 mg monotherapy for 8 weeks after a GP diagnosis of 'depression.' Over the past year she has had two manias and three major depressions with incomplete recovery. TFT last year was normal; none repeated since lithium was stopped by the patient 14 months ago. Urine drug screen is negative; observations and bedside glucose are normal. (i) Formulate the current episode and 12-month course using operational specifiers. (ii) Outline acute risk management and legal status principles. (iii) Detail immediate pharmacotherapy changes with doses/monitoring and justify avoiding antidepressant monotherapy with evidence. (iv) Present a 12-month plan for rapid-cycling drivers, maintenance, and psychosocial care. (20 marks)

Model answer

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(i) Formulation of episode and course. Current episode: bipolar I disorder, current episode manic, with mixed features — full manic syndrome (decreased sleep need, pressure, irritability, spending) plus depressive cognitions and active suicidal ideation. Course specifier: rapid cycling is supported if the past-year count is at least four full episodes (here two manias + three depressions meets the bar). Sertraline monotherapy is a likely cycle accelerator and polarity-unsafe treatment. Negative UDS and normal observations reduce but do not eliminate medical differentials; still complete baseline bloods/ECG before re-starting lithium/SGA. Incomplete inter-episode recovery indicates high morbidity phenotype.[4][5]

(ii) Acute risk and legal principles. This is a high-risk mixed phenotype (depression + energy + means research). Same-day senior review; likely admission. Means restriction, continuous observation as indicated, no unescorted leave initially, partner involvement with consent. Assess capacity for treatment decisions; if incapacitous with serious risk, use least-restrictive involuntary pathway under local statute (do not invent foreign section numbers). Document risk formulation, not only a score.[4]

(iii) Pharmacotherapy. Stop sertraline (taper only if clinically needed to avoid discontinuation effects — in severe mixed mania, prompt cessation under cover is often appropriate). Start polarity-safe cover after baselines: e.g. olanzapine 10–15 mg oral at night (titrate toward 10–20 mg) plus lithium re-initiation at 450–900 mg/day with plan for 12-hour trough roughly 0.8–1.2 mmol/L in acute mania, level at 5–7 days; or add/substitute valproate if lithium unsuitable and pregnancy risk managed. Combination is reasonable in severe mixed mania. Short-term lorazepam for sleep/arousal per protocol. Monitor metabolic parameters, sedation, renal/thyroid/calcium for lithium. Do not replace sertraline with another antidepressant monotherapy. STEP-BD showed adjunctive antidepressants did not beat mood stabiliser plus placebo for durable recovery; monotherapy is even less defensible.[1][3][4]

(iv) 12-month plan. Confirm rapid-cycling chart prospectively. Re-check TFT and treat thyroid disease if present. Maintenance: continue effective acute regimen into early recovery then simplify toward lithium-first prevention when tolerated — BALANCE supports lithium over valproate monotherapy, with combination also effective.[2] Psychoeducation, sleep regularity, IPSRT or CBT-bipolar, substance review, written early-warning signs with partner, crisis contacts, contraceptive counselling if valproate ever considered, and structured outpatient follow-up with metabolic monitoring for SGA.[4][5]

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References5ShowHide
  1. [1]Sachs GS, Nierenberg AA, Calabrese JR, et al. Effectiveness of adjunctive antidepressant treatment for bipolar depression N Engl J Med, 2007.PMID 17392295
  2. [2]Geddes JR, Goodwin GM, Rendell J, et al. Lithium plus valproate combination therapy versus monotherapy for relapse prevention in bipolar I disorder (BALANCE): a randomised open-label trial Lancet, 2010.PMID 20092882
  3. [3]Tohen M, McIntyre RS, Kanba S, et al. Efficacy of olanzapine in the treatment of bipolar mania with mixed features defined by DSM-5 J Affect Disord, 2014.PMID 25046739
  4. [4]Malhi GS, Bell E, Bassett D, et al. The 2020 Royal Australian and New Zealand College of Psychiatrists clinical practice guidelines for mood disorders Aust N Z J Psychiatry, 2021.PMID 33353391
  5. [5]Kupka RW, Luckenbaugh DA, Post RM, et al. Comparison of rapid-cycling and non-rapid-cycling bipolar disorder based on prospective mood ratings in 539 outpatients Am J Psychiatry, 2005.PMID 15994709
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PreviousMissed bipolar II, antidepressant monotherapy, and polarity-safe rebuild (MEQ)General adult psychiatry — bipolar and related disordersNextSevere manic crisis: work-up, RT/seclusion, antimanic algorithm (MEQ)General adult psychiatry — bipolar and related disorders