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Clinical Atlas Prestige · Evidence-first

Psych MEQs / SAQsGeneral adult psychiatry — mood disorders

Psych MEQs / SAQs · General adult psychiatry — mood disorders

Melancholic vs atypical features — diagnosis and treatment (MEQ)

FRANZCP-style MEQ contrasting melancholic and atypical feature specifiers: criteria hinge, differentials, ECT for severe melancholia, MAOI historical evidence and safety, pitfalls.

20 marks20 min
On this page & tools

Target exams

FRANZCPMRCPsychABPNMD-DNB

Target exams

FRANZCPMRCPsychABPNMD-DNB
Prompt
A 42-year-old nurse presents with a 10-week major depressive episode. Case A (same day clinic): near-total anhedonia, no mood lift to family visits, early waking, 7 kg weight loss, marked psychomotor retardation, excessive guilt. Case B (same clinic list): mood brightens briefly when friends visit, hypersomnia, 5 kg weight gain, leaden heaviness in limbs, lifelong interpersonal rejection sensitivity impairing work. Neither has psychosis. Bipolar screen negative so far. (i) Assign the correct DSM-5-TR feature specifier to each case and list the mandatory hinge criterion that separates them. (ii) List three priority differentials for Case B with discriminators. (iii) Outline first-line management for Case A including when you would choose ECT, with named evidence framing. (iv) Outline stepped pharmacotherapy and psychotherapy for Case B, including historical MAOI evidence and one concrete safety rule if phenelzine is later used. (v) State two common examiner pitfalls when coding or treating these specifiers. (20 marks)

Model answer

Reveal model answer

(i) Specifiers and hinge. Case A: major depressive episode with melancholic features (near-total anhedonia/nonreactivity, early waking, weight loss, psychomotor retardation, excessive guilt). Case B: major depressive episode with atypical features (mood reactivity present; reverse vegetative cluster; leaden paralysis; rejection sensitivity). Hinge: mood reactivity is required for atypical features and absent/near-absent for melancholia — do not dual-code conflicting reactivity. [5][7]

(ii) Differentials for Case B. (1) Bipolar depression — prior hypo/mania, mixed features, family history; reverse vegetative atypical features are common in bipolar depression. (2) Medical/sleep mimic — hypothyroidism, OSA (hypersomnia + weight gain), substances/medications. (3) Personality/anxiety overlap — trait rejection sensitivity and social anxiety can coexist; still require full MDE criteria rather than labelling only "personality." [5][7]

(iii) Case A management / ECT. Measurement-based adequate antidepressant trial with secondary-care intensity; suicide-risk and intake monitoring. Early ECT if food/fluid refusal, catatonia, psychosis, uncontainable risk, prior excellent ECT response, or too slow on medicines — UK ECT Review Group supports strong efficacy in severe depressive disorders; RANZCP frames early biological intensity for severe melancholia. Name agents if pharmacotherapy first (e.g. venlafaxine XR start 75 mg oral daily titrating; sertraline 50 mg oral daily titrating) with monitoring. [4][5]

(iv) Case B management. Start modern first-line antidepressant and/or evidence-based psychotherapy (CBT/IPT; behavioural activation); Jarrett supports cognitive therapy as active treatment versus placebo alongside phenelzine. Historical Columbia evidence: phenelzine preferential versus imipramine/placebo in atypical depression (Liebowitz; Quitkin). If phenelzine later used: start low (e.g. 15 mg oral daily building toward often 45–90 mg/day divided), tyramine diet, pharmacy flag, never combine with SSRI/SNRI/clomipramine/tramadol; respect washouts (about 5 weeks after fluoxetine). [1][2][3][6][7]

(v) Pitfalls. Coding both melancholic and atypical when reactivity conflicts; treating atypical as mild/low-risk; delaying ECT in food-refusing melancholia; starting MAOI without diet/washout plan; missing bipolarity; using DST as a modern diagnostic gate. [5][6]

Common errors

  • Dual-coding melancholic and atypical on conflicting reactivity.
  • Omitting rejection sensitivity or leaden paralysis from atypical criteria.
  • Jumping to MAOI for every reverse vegetative outpatient without first-line steps.
  • Forgetting ECT thresholds in severe melancholia.
  • Inventing Mental Health Act section numbers. [1][4][5]

Examiner notes

Full marks require opposite-pole criteria, three differentials with discriminators, named ECT evidence framing, Columbia/Jarrett MAOI–therapy evidence, and at least one concrete MAOI safety rule. [1][2][3][4]

References

  1. [1]Quitkin FM, Stewart JW, McGrath PJ, et al. Phenelzine versus imipramine in the treatment of probable atypical depression: defining syndrome boundaries of selective MAOI responders Am J Psychiatry, 1988.PMID 3278631
  2. [2]Liebowitz MR, Quitkin FM, Stewart JW, et al. Antidepressant specificity in atypical depression Arch Gen Psychiatry, 1988.PMID 3276282
  3. [3]Jarrett RB, et al. Treatment of atypical depression with cognitive therapy or phenelzine: a double-blind, placebo-controlled trial Arch Gen Psychiatry, 1999.PMID 10232298
  4. [4]UK ECT Review Group Efficacy and safety of electroconvulsive therapy in depressive disorders: a systematic review and meta-analysis Lancet, 2003.PMID 12642045
  5. [5]Malhi GS, 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
  6. [6]Van den Eynde V, et al. The prescriber's guide to classic MAO inhibitors (phenelzine, tranylcypromine, isocarboxazid) for treatment-resistant depression CNS Spectr, 2023.PMID 35837681
  7. [7]Stewart JW Treating depression with atypical features J Clin Psychiatry, 2007.PMID 17348764