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LibraryPsychiatry

MBBS viva · Psychiatry

Depression — clinical viva (SIGECAPS, suicide risk, SSRI and ECT)

Final-prof viva on major depressive disorder: diagnostic threshold, severity, suicide assessment, first-line SSRI + CBT, monitoring, and ECT indications.

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Exam tags

NEET-PGINICETUSMLE

Exam tags

NEET-PGINICETUSMLE

Opening stem

"A 28-year-old woman reports 3 weeks of low mood, anhedonia, early-morning wakening, weight loss, and thoughts that she would be better off dead. How do you approach her?" [1]

Q1: Diagnosis and classification (2 min)

  • Define MDD: ≥5 of 9 symptoms for ≥2 weeks, including depressed mood or anhedonia, with impairment, not better explained by substance/medical illness, and no prior mania.[1]
  • Recite SIGECAPS (Sleep, Interest, Guilt, Energy, Concentration, Appetite, Psychomotor, Suicide + Mood).
  • Classify by severity (mild / moderate / severe), course (single vs recurrent), and specifier (melancholic, atypical, psychotic, catatonic, peripartum, seasonal).
  • Name key differentials: bipolar depression, adjustment disorder, grief, hypothyroidism, anaemia, substance-induced, dementia (elderly), schizoaffective disorder.

Q2: Risk assessment and organic work-up (2 min)

  • Structure suicide assessment: ideation → plan → intent → means → protective factors → prior attempts → access to means.
  • Red flags for urgent admission: active plan/intent, psychosis, catatonia/refusal of food, severe self-neglect, postpartum infant-harm thoughts.
  • Baseline investigations: FBC, U&E, glucose, TFT, B12/folate, LFT; urine drug screen if indicated; pregnancy test in women of childbearing age.
  • Always screen for prior hypomania/mania before antidepressants (DIGFAST). [1]

Q3: Management ladder (3 min)

  • Mild: active monitoring, guided self-help, CBT; consider medication if persistent.
  • Moderate–severe: SSRI first-line — e.g. sertraline 50 mg OD (or escitalopram 10 mg, fluoxetine 20 mg) plus CBT.[2]
  • Counsel: delayed benefit 4–6 weeks; early side effects; review within 1–2 weeks for suicidality (especially under 25 years).
  • Continuation: treat ≥6–9 months after remission (first episode); longer if recurrent.
  • Inadequate response: check adherence → optimise dose → switch class → augment (e.g. lithium, atypical antipsychotic in specialist care).
  • ECT indications: severe/psychotic/catatonic depression, high suicide risk, life-threatening refusal of intake, treatment resistance, preference in pregnancy for severe illness.

Q4: Special populations and pitfalls (1–2 min)

  • Pregnancy/postpartum: prefer psychological therapy first if mild–moderate; sertraline often preferred if drug needed; always assess infant-harm thoughts and bonding.
  • Elderly: start low, go slow; watch hyponatraemia (SIADH with SSRIs); somatic presentation common; exclude dementia/delirium.
  • Adolescents: irritability may dominate; combine psychotherapy; close early review for activation/suicidality.
  • Pitfalls: missing bipolar switch; prescribing TCA in high-risk overdose patient; discharging without a safety plan; stopping antidepressant abruptly (discontinuation syndrome, especially paroxetine/venlafaxine). [1]

Key phrases examiners want

  • "Five of nine for two weeks, including mood or anhedonia."
  • "Suicide risk is dynamic — reassess every contact."
  • "Sertraline 50 mg daily, review in one to two weeks, full effect at four to six weeks."
  • "ECT for psychotic, catatonic, or life-threatening depression." [1]

References

  1. [1]McCarron RM, Shapiro B, Rawles J, Luo J. Depression. Ann Intern Med, 2021.PMID 33971098
  2. [2]Mutz J, Vipulananthan V, Carter B, Hurlemann R, Fu CHY, Young AH. Comparative efficacy and acceptability of non-surgical brain stimulation for the acute treatment of major depressive episodes in adults: systematic review and network meta-analysis. BMJ, 2019.PMID 30917990
  3. [3]Cipriani A, Furukawa TA, Salanti G, et al. Comparative efficacy and acceptability of 21 antidepressant drugs for the acute treatment of adults with major depressive disorder: a systematic review and network meta-analysis. Lancet, 2018.PMID 29477251