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Clinical Atlas Prestige · Evidence-first

Psych MEQs / SAQsConsultation-liaison psychiatry

Psych MEQs / SAQs · Consultation-liaison psychiatry

Dementia and major NCD — assessment, BPSD, and pharmacotherapy (MEQ)

FRANZCP-style MEQ on major NCD/DLB phenotype, delirium superimposition, antipsychotic caution, AChEI/memantine, and Appelbaum capacity.

20 marks20 min
On this page & tools

Target exams

FRANZCPMRCPsychABPNMD-DNB

Target exams

FRANZCPMRCPsychABPNMD-DNB
Prompt
An 78-year-old woman is referred from the medical ward. She has a two-year history of progressive forgetfulness and now needs help with shopping and medications. Three days after a UTI she became more confused, pulled out her IV, and struck a nurse. Staff request 'regular olanzapine and a depot'. Collateral reveals dream-enactment behaviour for years, fluctuating alertness, and well-formed visions of children in the room even before this admission. MoCA is 18/30 with marked attentional and visuospatial errors. She is not on cognitive enhancers. (i) Formulate the neurocognitive diagnosis and acute problem, with key discriminators. (ii) Outline immediate management of agitation including what not to do. (iii) Discuss longer-term cognitive and BPSD pharmacotherapy with named evidence and doses where appropriate. (iv) Outline how you would assess capacity for discharge destination decisions. (20 marks)

Model answer

Reveal model answer

(i) Formulation. Working diagnosis: major neurocognitive disorder with a probable dementia with Lewy bodies (DLB) phenotype — progressive functional decline plus core features of cognitive fluctuations, recurrent well-formed visual hallucinations, and REM sleep behaviour disorder (dream enactment). Acute problem: delirium superimposed on dementia, precipitated by UTI and hospital environment, with secondary aggression. Discriminators: not pure late-onset primary psychosis (progressive multi-domain decline and RBD); not typical amnestic-only AD as the sole explanation (early fluctuations/hallucinations/RBD). Still complete medical work-up and consider mixed pathology.[1][3]

(ii) Immediate agitation management. Treat as medical emergency of behaviour: ABCDE, treat UTI and other delirium drivers, orientation, low-stimulus environment, pain/constipation/retention check, family presence if helpful. Do not start regular olanzapine or depot. In DLB, antipsychotics risk severe neuroleptic sensitivity. If imminent danger persists after non-drug measures, any psychotropic is last-line, lowest dose, shortest time, with mortality counselling (Schneider meta-analysis increased death risk; CATIE-AD modest efficacy/high adverse effects; DART-AD withdrawal often safer long-term). Prefer specialist advice before antipsychotics in DLB.[1][2][3][7][8]

(iii) Longer-term pharmacotherapy. After delirium clears, consider a cholinesterase inhibitor. Rivastigmine has pivotal evidence in related Lewy body disease (PDD — Emre): titrate carefully (e.g. oral start around 1.5 mg twice daily with stepwise increases, or transdermal 4.6 then 9.5 mg/24 h per product information), monitor GI effects and heart rate. Donepezil 5 mg daily for 4 weeks then 10 mg is the AD backbone and may be used depending on phenotype and local pathways; DOMINO-AD supports continuation benefit in moderate–severe AD contexts. Memantine (titrate 5 mg daily by 5 mg weekly to 10 mg twice daily) is primarily moderate–severe AD evidence (Reisberg/Tariot/Cochrane) — optional if AD-mixed features. BPSD: DICE-style non-drug plan first; antipsychotics not for maintenance wandering.[4][5][3]

(iv) Capacity for discharge destination. Decision-specific assessment using Appelbaum abilities: understand options (home with package vs residential care), appreciate personal risks (night wandering, falls), reason comparatively, communicate a consistent choice. Optimise hearing, language, timing (not at peak delirium). If lacking capacity for that decision, use jurisdiction-specific substitute decision-maker / guardianship pathways — name the principle of least restriction without inventing section numbers. Document process.[6]

Common errors

Common fails: starting depot antipsychotic on a DLB phenotype; ignoring delirium and treating only "behavioural dementia"; claiming AChEIs are disease-modifying cures; equating low MMSE with global incapacity; inventing Mental Health Act sections for residential placement.[1][2][6]

Examiner notes

High-scoring answers integrate subtype + delirium + black-box antipsychotic caution + named trials (Emre, Schneider, CATIE-AD, DART-AD, DOMINO) + Appelbaum.[1][2][5][6]

References

  1. [1]McKeith IG, Boeve BF, Dickson DW, et al. Diagnosis and management of dementia with Lewy bodies: Fourth consensus report of the DLB Consortium Neurology, 2017.PMID 28592453
  2. [2]Schneider LS, Dagerman KS, Insel P Risk of death with atypical antipsychotic drug treatment for dementia: meta-analysis of randomized placebo-controlled trials JAMA, 2005.PMID 16234500
  3. [3]Kales HC, Gitlin LN, Lyketsos CG Assessment and management of behavioral and psychological symptoms of dementia BMJ, 2015.PMID 25731881
  4. [4]Emre M, Aarsland D, Albanese A, et al. Rivastigmine for dementia associated with Parkinson's disease N Engl J Med, 2004.PMID 15590953
  5. [5]Howard R, McShane R, Lindesay J, et al. Donepezil and memantine for moderate-to-severe Alzheimer's disease N Engl J Med, 2012.PMID 22397651
  6. [6]Appelbaum PS, Grisso T Assessing patients' capacities to consent to treatment N Engl J Med, 1988.PMID 3200278
  7. [7]Ballard C, Hanney ML, Theodoulou M, et al. The dementia antipsychotic withdrawal trial (DART-AD): long-term follow-up of a randomised placebo-controlled trial Lancet Neurol, 2009.PMID 19138567
  8. [8]Schneider LS, Tariot PN, Dagerman KS, et al. Effectiveness of atypical antipsychotic drugs in patients with Alzheimer's disease N Engl J Med, 2006.PMID 17035647