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Clinical Atlas Prestige · Evidence-first

Psych MEQs / SAQsEmergency psychiatry

Psych MEQs / SAQs · Emergency psychiatry

Acute behavioural disturbance and contested excited delirium (MEQ)

FRANZCP-style MEQ on ABD-first framing, hyperthermia, prone restraint risk, droperidol/ketamine pathways, combination ban, capacity and disposition.

20 marks20 min
On this page & tools

Target exams

FRANZCPMRCPsychABPNMD-DNB

Target exams

FRANZCPMRCPsychABPNMD-DNB
Prompt
A 31-year-old man is brought by police after a 20-minute struggle in hot weather. Collateral suggests possible methamphetamine use. He is continuously thrashing, diaphoretic, HR 140, SpO2 96 percent on air, temperature 39.4 C, capillary glucose 6.1 mmol per litre. Staff are holding him prone. A registrar writes 'excited delirium' in the notes and proposes IM olanzapine 10 mg plus IM midazolam 5 mg together. (i) Critique the terminology and documentation plan. (ii) Outline immediate medical priorities including restraint positioning. (iii) Provide a safer parenteral sedation pathway with named doses, routes, monitoring and rescue options. (iv) List key investigations and differential drivers. (v) Address capacity, least-restrictive legal principles, and disposition. (20 marks)

Model answer

Reveal model answer

(i) Terminology and documentation. Prefer acute behavioural disturbance (ABD) / severe behavioural disturbance or hyperactive delirium with severe agitation. Excited delirium is not a DSM-5-TR or ICD-11 diagnosis; ACMT 2023 and critical reviews advise against using it as a diagnosis or sole cause of death. Document observed facts: continuous extreme agitation, hyperthermia, tachycardias, prolonged struggle, prone restraint, possible stimulant use. Avoid racialised or thought-terminating labels that skip investigation of restraint contribution and medical drivers.[1][2][6]

(ii) Immediate medical priorities. This is a medical resuscitation: ABCDE already partly captured; continue airway readiness, oxygen as needed, continuous observation. Stop prolonged prone hold as soon as control allows; reassess ventilation; prefer recovery-safe positioning. Active cooling for temperature 39.4 C. Large-bore IV access when safe; prepare for rhabdomyolysis and acidosis. Team roles; one lead communicator if any de-escalation window appears. Endpoint later is calm and rousable, not unconscious.[5][6]

(iii) Safer sedation pathway. Do not combine IM olanzapine with parenteral midazolam. In ANZ ED undifferentiated severe ABD, a common evidence-supported first-line is IM droperidol 5–10 mg with monitoring; IM midazolam 5–10 mg is an alternative with higher airway vigilance. If refractory and airway-skilled staff present, ketamine rescue under local protocol (commonly around 4–5 mg/kg IM). Post-dose: continuous observation; RR, SpO2, BP, HR, consciousness, temperature every 15 minutes for at least 1 hour. Never leave unmonitored.[3][4][5]

(iv) Investigations and differential. Immediate: serial vitals, glucose (done), ECG when practicable, CK, U&E, FBC, VBG/ABG if severe exertion/collapse risk. Do not delay sedation for urine drug screen. Differential: stimulant toxicity, primary psychosis/mania, delirium (sepsis, trauma, encephalitis), withdrawal, serotonin toxicity/NMS, head injury, hypoglycaemia/hypoxia already partly addressed. Targeted further tests for red flags.[5]

(v) Capacity, law, disposition. Capacity is decision-specific; extreme ABD with hyperthermia and continuous thrashing likely impairs capacity for remaining and treatment — document explicitly when feasible. Use emergency treatment principles and local Mental Health Act for ongoing psychiatric care without inventing section numbers; least-restrictive options when safer. Disposition: medical observation/ICU if deep sedation, ongoing hyperthermia, rhabdomyolysis, or airway need; psychiatric admission once medical risk controlled. Immediate discharge is inappropriate.[5]

Common errors

  • Reifying excited delirium as a validated diagnosis or sole cause of death
  • Continuing prolonged prone restraint
  • IM olanzapine + parenteral benzodiazepine
  • No named doses or no temperature-inclusive monitoring
  • Inventing Mental Health Act sections
[1] [5] [6]

Examiner notes

Full marks require ABD-first critique of ExDS, prone-restraint risk, a named safer parenteral pathway (droperidol ± ketamine rescue), combination ban, and capacity/disposition thinking. Vague “sedate for ExDS” fails. [1][2][5]

References

  1. [1]Stolbach AI, Dargan PI, Greller HA, et al. ACMT Position Statement: End the Use of the Term "Excited Delirium" J Med Toxicol, 2023.PMID 37349654
  2. [2]McGuinness T, Lipsedge M 'Excited Delirium', acute behavioural disturbance, death and diagnosis Psychol Med, 2022.PMID 35546291
  3. [3]Isbister GK, Calver LA, Page CB, et al. Randomized controlled trial of intramuscular droperidol versus midazolam for violence and acute behavioral disturbance: the DORM study Ann Emerg Med, 2010.PMID 20868907
  4. [4]Isbister GK, Calver LA, Downes MA, Page CB Ketamine as Rescue Treatment for Difficult-to-Sedate Severe Acute Behavioral Disturbance in the Emergency Department Ann Emerg Med, 2016.PMID 26899459
  5. [5]Patel MX, Sethi FN, Barnes TR, et al. Joint BAP NAPICU evidence-based consensus guidelines for the clinical management of acute disturbance: De-escalation and rapid tranquillisation J Psychopharmacol, 2018.PMID 29882463
  6. [6]Weedn V, Steinberg A, Speth P Prone restraint cardiac arrest in in-custody and arrest-related deaths J Forensic Sci, 2022.PMID 35869602