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Clinical Atlas Prestige · Evidence-first

Psych VivasGeneral adult psychiatry — bipolar and related disorders

Psych Vivas · General adult psychiatry — bipolar and related disorders

Bipolar depression and polarity-safe treatment — structured clinical viva

Fellowship viva covering bipolar depression, antidepressant monotherapy pitfalls (STEP-BD), quetiapine/lurasidone/OFC/lamotrigine choices with doses, suicide risk, and shared decision-making.

clinical
On this page & tools

Target exams

FRANZCPMRCPsychABPNMD-DNB

Target exams

FRANZCPMRCPsychABPNMD-DNB
Prompt
You are the psychiatry registrar in clinic. A 35-year-old woman with previously diagnosed bipolar II disorder presents with a 6-week major depressive episode, MADRS 32, passive death wishes without plan, sleeping 12 hours/day, and marked anhedonia. She has been taking sertraline 150 mg monotherapy for 3 months started in primary care. She asks for 'a stronger antidepressant.' Discuss your assessment, risks of current treatment, evidence-based options for bipolar depression, and a monitoring plan.

Interpretation

Reveal interpretation

This is bipolar depression on antidepressant monotherapy, which is a polarity-safety problem even in bipolar II. Assessment must cover suicide risk in detail (intent, plan, means, protective factors, mixed features such as racing thoughts or decreased sleep need, alcohol), current hypomanic symptoms, medication adherence, thyroid status, substance use, and psychosocial stressors. Passive death wishes still require a safety plan and follow-up intensity decision; admission if risk escalates or support is inadequate.[4]

Do not simply escalate the SSRI. STEP-BD showed adjunctive antidepressants did not outperform mood stabiliser plus placebo for durable recovery in bipolar depression; monotherapy is even harder to defend.[1] Plan a switch toward polarity-safe treatment: e.g. taper sertraline while introducing quetiapine titrated toward 300–600 mg at night with metabolic monitoring (BOLDER evidence includes bipolar II depression), or consider lurasidone 20–120 mg with food where available, lithium, or carefully titrated lamotrigine for longer-term depression prevention.[2][3][4]

Explain metabolic, sedation, and rash (lamotrigine) risks; agree review timing; involve supports with consent; document early warning signs for switch into hypo/mania if any antidepressant cover remains briefly during transition.[4]

Key points

Antidepressant monotherapy is the trap

In known bipolar illness, 'stronger antidepressant alone' is usually the wrong answer.

Name doses and monitoring

Quetiapine 300–600 mg pathway needs metabolic monitoring; lurasidone needs food and akathisia vigilance.

STEP-BD is examinable by name

Adjunctive AD did not beat mood stabiliser plus placebo for durable recovery.
[1]

References

  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]Calabrese JR, Keck PE Jr, Macfadden W, et al. A randomized, double-blind, placebo-controlled trial of quetiapine in the treatment of bipolar I or II depression Am J Psychiatry, 2005.PMID 15994719
  3. [3]Loebel A, Cucchiaro J, Silva R, et al. Lurasidone monotherapy in the treatment of bipolar I depression: a randomized, double-blind, placebo-controlled study Am J Psychiatry, 2014.PMID 24170180
  4. [4]Yatham LN, Kennedy SH, Parikh SV, et al. Canadian Network for Mood and Anxiety Treatments (CANMAT) and International Society for Bipolar Disorders (ISBD) 2018 guidelines for the management of patients with bipolar disorder Bipolar Disord, 2018.PMID 29536616