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Clinical Atlas Prestige · Evidence-first

Psych MEQs / SAQsConsultation-liaison psychiatry

Psych MEQs / SAQs · Consultation-liaison psychiatry

Cardiac psychiatry — post-ACS depression, trials, safety (MEQ)

FRANZCP-style MEQ on post-ACS depression, AHA risk framing, SADHART/CREATE/ENRICHD literacy, SSRI dosing with dual antiplatelets, and beta-blocker myth correction.

20 marks20 min
On this page & tools

Target exams

FRANZCPMRCPsychABPNMD-DNB

Target exams

FRANZCPMRCPsychABPNMD-DNB
Prompt
A 64-year-old man is 10 days after NSTEMI treated with stents. He is on dual antiplatelet therapy, a beta-blocker, ACE inhibitor, and statin. Ward staff report tearfulness, anhedonia, early waking, and passive suicidal ideation; he has refused cardiac rehab, saying 'the next one will kill me anyway.' A junior doctor wants amitriptyline 'because it helps sleep' and to stop the beta-blocker 'which always causes depression.' Another junior asks whether starting an SSRI will prevent reinfarction based on 'the big American trial.' (i) Formulate the psychiatric issues and prognosis framing. (ii) Outline assessment and investigations relevant to psychotropic start. (iii) Give an evidence-informed treatment plan with named agents/doses, trial literacy (SADHART, ENRICHD, CREATE), and rehab/collaborative care. (iv) Address the beta-blocker request, suicide risk, and disposition. (20 marks)

Model answer

Reveal model answer

(i) Formulation and prognosis. Concurrent post-ACS major depression (depressive disorder due to another medical condition when the ACS is the aetiological context): anhedonia, insomnia, passive SI, rehab refusal with fatalistic cognitions at day 10.[1][2] Depression after MI is linked to worse early prognosis (classic Frasure-Smith signal) and is framed by AHA as a risk factor for poor prognosis after ACS.[2][3] Also consider comorbid anxiety/ACS-PTSD symptoms driving rehab avoidance.[8]

(ii) Assessment and investigations. Cardiac dossier (NSTEMI, stents, dual antiplatelets, beta-blocker/ACE/statin, EF if known), full MSE and structured suicide risk, collateral, substance/sleep, PHQ-type screen if helpful.[1] Before SSRI: ECG/QTc, electrolytes (Na), renal/hepatic function; review bleeding risk with dual antiplatelets.[1][4]

(iii) Treatment and trial literacy. Multimodal: clinical management, behavioural activation toward cardiac rehab, smoking cessation, adherence support; collaborative care models (MOSAIC) improve depression/anxiety after recent cardiac events.[1][7] First-line SSRI: sertraline 25–50 mg oral daily, titrate toward 50–200 mg as tolerated (SADHART safety/efficacy anchor for post-ACS depression), monitoring GI effects, hyponatraemia, bleeding, sexual side effects.[4] CREATE: citalopram effective vs placebo in CAD with clinical management, but IPT did not beat clinical management alone — and high-dose citalopram needs QTc caution, so sertraline is often preferred here.[6] ENRICHD honesty: treating depression/low social support with CBT (± antidepressant) improved psychosocial outcomes but did not reduce death or recurrent MI — do not promise reinfarction prevention as the reason to treat.[5] Avoid amitriptyline first-line post-ACS (arrhythmia/overdose risk).[1]

(iv) Beta-blocker, risk, disposition. Do not stop evidence-based beta-blocker solely for a universal "causes depression" myth; treat depression while protecting secondary prevention unless cardiology agrees a switch is needed for a clear reason.[1] Suicide safety plan, observation as indicated, least-restrictive legal pathway if risk escalates. Disposition: stepwise rehab re-engagement, GP/CL follow-up, collaborative care if available, review response in 2–4 weeks, document bleeding counselling.[1][7]

Common errors

Promising SSRI will prevent reinfarction after ENRICHD; starting TCA first-line post-MI; stopping beta-blocker automatically; ignoring dual-antiplatelet bleeding; omitting suicide risk and rehab integration.[4][5][1]

References

  1. [1]Lichtman JH, Bigger JT Jr, Blumenthal JA, et al. Depression and coronary heart disease: recommendations for screening, referral, and treatment Circulation, 2008.PMID 18824640
  2. [2]Lichtman JH, Froelicher ES, Blumenthal JA, et al. Depression as a risk factor for poor prognosis among patients with acute coronary syndrome Circulation, 2014.PMID 24566200
  3. [3]Frasure-Smith N, Lespérance F, Talajic M Depression following myocardial infarction. Impact on 6-month survival JAMA, 1993.PMID 8411525
  4. [4]Glassman AH, O'Connor CM, Califf RM, et al. Sertraline treatment of major depression in patients with acute MI or unstable angina (SADHART) JAMA, 2002.PMID 12169073
  5. [5]Berkman LF, Blumenthal J, Burg M, et al. Effects of treating depression and low perceived social support on clinical events after myocardial infarction (ENRICHD) JAMA, 2003.PMID 12813116
  6. [6]Lespérance F, Frasure-Smith N, Koszycki D, et al. Effects of citalopram and interpersonal psychotherapy on depression in patients with coronary artery disease (CREATE) JAMA, 2007.PMID 17244833
  7. [7]Huffman JC, Mastromauro CA, Beach SR, et al. Collaborative care for depression and anxiety disorders in patients with recent cardiac events (MOSAIC) JAMA Intern Med, 2014.PMID 24733277
  8. [8]Edmondson D, Richardson S, Falzon L, et al. Posttraumatic stress disorder prevalence and risk of recurrence in acute coronary syndrome patients PLoS One, 2012.PMID 22745687