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Delirium: non-drug and drug management

Treat delirium through urgent cause control and skilled non-drug care, de-escalate distress while preserving communication and mobility, and restrict sedating medicine to exceptional short-term safety indications with Parkinson and Lewy-body safeguards.

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Danger with an untreated cause

Severe agitation, pulling essential treatment, violence or inability to receive life-saving care may coexist with hypoxia, sepsis, pain, retention, withdrawal or intracranial disease; sedation can conceal deterioration and compromise airway or circulation.

Action: Call senior help, stabilise physiology, reduce stimulation and use one trained communicator, treat pain and reversible triggers, make the environment safe and use the lowest short medicine dose only when distress or risk remains and verbal de-escalation is ineffective or inappropriate.

Open the sections you need. The overview is shown first.
01OverviewDefinition, clinical context and the essential points that orientate the chapter.

Management begins by naming active causes and assigning actions. Correct oxygenation, glucose, circulation and metabolic disturbance; treat infection and pain; relieve retention and constipation; manage withdrawal; stop or reduce contributory medicines safely. Re-examine when behaviour changes because agitation can be the first sign of worsening physiology rather than failure of behavioural care.

De-escalation is skilled treatment. Approach from the front, identify yourself, use the person's preferred name and one instruction at a time, allow processing time and avoid arguing with a frightening misperception. Ask what they need, acknowledge emotion and offer food, drink, toilet, pain relief or a quieter space. Familiar carers can explain usual communication, but should never be compelled to provide constant supervision.

Create a therapeutic environment: stable bed space and staff where possible, daylight and ordinary daytime activity, low noise at night, visible clock and calendar, working sensory aids and personal objects. Mobilise with help and avoid bed rails or devices that increase climbing. Use enhanced observation focused on reassurance and needs, not silent surveillance or repeated confrontation.

Assess capacity for the immediate decision and use the least restrictive lawful response. A person may lack capacity to understand an essential infusion during severe delirium yet still express meaningful comfort and relationship preferences. Document why any restraint is necessary, proportionate, time-limited and reviewed. Physical restraint and rapid tranquillisation require local governance and senior oversight.

Medicine is exceptional. NICE advises short-term haloperidol when a delirious person is distressed or considered a risk to self or others and verbal and non-verbal de-escalation has failed or is inappropriate. The aim is the minimum reduction needed for safe essential care, not sleep or suppression of wandering. Explain off-label or protocol aspects and review after every dose.

MHRA advises a baseline ECG and correction of electrolyte disturbance, the lowest dose for the shortest possible time and close review for cardiac and extrapyramidal effects. In a frail adult, a local protocol may start 0.5 mg orally and reassess after one to two hours, avoiding repeated stacking. Oral treatment is preferable when accepted. Stop promptly when risk resolves and do not write routine discharge continuation.

Do not use haloperidol in Parkinson disease or dementia with Lewy bodies. Ask about parkinsonism, cognitive fluctuation, formed visual hallucinations, REM-sleep behaviour and previous severe antipsychotic reactions before prescribing. If medication is unavoidable, involve old-age psychiatry, geriatrics or neurology; low-dose quetiapine is sometimes selected off-label but has limited evidence and important sedation, hypotension and mortality risk.

Benzodiazepines can worsen disinhibition, falls and respiratory depression. Their main delirium roles are alcohol or benzodiazepine withdrawal under a specific symptom-triggered protocol and selected catatonia or palliative situations. Give parenteral sedatives only in a monitored environment with airway, reversal and escalation capability and never combine casually with opioids.

Review at least each shift: cause trajectory, distress, sleep, intake, mobility, bowel and bladder, sensory support, restrictive interventions and any medicine effect. Akathisia, rigidity or oversedation can look like ongoing delirium. If symptoms persist, reopen diagnosis and environmental delivery. Communicate any dose, indication and stop date across transitions.

Key points

  • Cause treatment and multicomponent non-drug care are first-line delirium management; no medicine cures the syndrome.
  • Use one calm communicator, introduce each action, validate fear, offer simple choices, restore glasses and hearing aids and involve familiar people when wanted.
  • Meet physical needs: oxygen when indicated, analgesia, hydration, nutrition, toilet, bowel care, temperature comfort, sleep and safe mobilisation.
  • Reduce noise, crowding, ward moves, alarms and unnecessary devices while maintaining daylight, clock, calendar and repeated orientation.
  • If the person is distressed or risks harm, attempt verbal and non-verbal de-escalation before medicine unless immediate danger makes this inappropriate.
  • NICE permits short-term haloperidol, usually one week or less, only when de-escalation fails or is inappropriate and distress or risk remains.
  • Before haloperidol, check Parkinson or DLB, cardiac history, QT-prolonging drugs, ECG and electrolytes and use the lowest dose for the shortest time.
  • A frail older-adult emergency regimen may begin haloperidol 0.5 mg orally once with reassessment; follow the local typed protocol and avoid automatic repeat dosing.
  • Avoid haloperidol in Parkinson disease and DLB. Seek specialist advice; medication alternatives are off-label and still carry sedation, stroke and mortality risk.
  • Benzodiazepines usually worsen ordinary delirium; reserve them for alcohol or benzodiazepine withdrawal, catatonia or a specialist indication.
02AetiologyUnderlying causes, associations and risk factors, with why each one matters.
01

Persisting medical driver

Infection, hypoxia, metabolic disturbance, pain, retention, constipation, organ failure or occult injury will sustain symptoms until specifically treated.

02

Iatrogenic perpetuation

Sedatives, anticholinergics, catheters, sleep interruption, immobility, ward moves and communication failure can convert a resolving insult into prolonged delirium.

03

Fear and unmet need

Hunger, thirst, toileting, sensory loss, unfamiliar care and misunderstood procedures may be expressed as shouting, striking or attempts to leave.

04

Withdrawal or drug toxicity

Alcohol, benzodiazepine or opioid withdrawal and accumulation of psychoactive or renally cleared medicines require distinct treatment rather than nonspecific sedation.

03PathophysiologyThe causal sequence from the underlying abnormality to symptoms and harm.
  1. 1
    Acute network dysregulation

    Attention and arousal networks fluctuate with the physiological insult, so behaviour can change rapidly and a medicine response does not prove psychiatric disease.

  2. 2
    Threat amplification

    Impaired interpretation turns touch, alarms and staff approach into perceived danger, activating sympathetic arousal and defensive behaviour.

  3. 3
    Sedation without resolution

    Antipsychotics may reduce visible movement without correcting hypoxia, inflammation or metabolic failure and can worsen swallowing and mobility.

  4. 4
    Dopamine-blockade vulnerability

    Nigrostriatal degeneration in Parkinson and Lewy-body disease makes D2 antagonism particularly likely to cause profound rigidity and deterioration.

  5. 5
    Functional cascade

    Bed rest, restraint and oversedation cause weakness, aspiration, pressure injury and sleep disruption that feed back into delirium.

04Clinical features and red flagsSymptoms, examination findings, patterns of presentation and time-critical warnings.
Distress with unmet need

Calling out, striking or leaving may lessen after pain, toileting, hunger, breathlessness, hearing or fear is addressed.

Immediate safety crisisRed flag

The person is about to cause serious harm or prevent essential life-saving treatment despite skilled de-escalation.

Neuroleptic sensitivityRed flag

After dopamine blockade, marked rigidity, somnolence, dysphagia or autonomic deterioration suggests DLB or Parkinson vulnerability.

Withdrawal phenotype

Tremor, sweating, tachycardia, insomnia, hallucination and exposure history point toward a specific withdrawal pathway.

Resolution without sedation

Attention and behaviour improve as causes, sleep, orientation, sensory support and mobility are restored.

Red flags requiring action

  • Never sedate agitation before checking oxygenation, glucose, pain, retention, constipation, withdrawal, medication toxicity and new neurological signs.
  • Parkinson disease or dementia with Lewy bodies creates marked neuroleptic sensitivity; haloperidol can cause rigidity, aspiration, reduced consciousness and death.
  • QT prolongation, bradycardia, electrolyte disturbance, cardiac disease or interacting medicines increases torsade risk and requires ECG-informed avoidance or correction.
  • Fever, severe rigidity, reduced consciousness and autonomic instability after an antipsychotic suggests neuroleptic malignant syndrome and requires immediate cessation and emergency care.
  • Alcohol or benzodiazepine withdrawal needs a specific benzodiazepine regimen and thiamine pathway rather than ordinary delirium sedation.
  • Restraint, repeated security presence or forced care can amplify fear and injury; any restriction requires immediate necessity, proportionality and frequent review.
05InvestigationsWhat to request, why it matters and how to interpret it.
Investigation order

Read from the initial assessment onwards. Tests may run in parallel in urgent care; first-line, preferred, confirmatory, definitive and gold-standard labels appear only when the chapter explicitly states them.

  1. 01
    Repeat physiological assessmentFirst step
    Why
    Detect a new or untreated medical driver.
    Interpretation and limitations
    Recheck ABCDE, glucose, observations, pain, hydration, bladder, bowel, injury and neurological signs whenever behaviour changes.
  2. 02
    Medication and withdrawal review
    Why
    Identify toxicity and specific withdrawal syndromes.
    Interpretation and limitations
    Verify recent starts, stops, PRN doses, renal function, alcohol and sedative exposure and anticholinergic or dopaminergic burden.
  3. 03
    Distress and communication assessment
    Why
    Find unmet need before sedating.
    Interpretation and limitations
    Use familiar communication, sensory aids, behavioural observation and carer knowledge to test pain, fear, thirst, toilet and environment.
  4. 04
    Antipsychotic safety check
    Why
    Reduce preventable cardiac and neurological harm.
    Interpretation and limitations
    Before haloperidol assess Parkinson or DLB, ECG and QT, potassium and magnesium, cardiac disease, interactions and prior sensitivity.
  5. 05
    Post-dose reassessment
    Why
    Determine whether benefit exceeds harm.
    Interpretation and limitations
    Record target behaviour, dose, effect, arousal, swallow, rigidity, posture and ECG concern before considering any repeat.
  6. 06
    Persistent-delirium review
    Why
    Reopen causes and alternative diagnoses.
    Interpretation and limitations
    Repeat examination and targeted tests for occult infection, injury, stroke, seizure, abdominal disease, withdrawal and medicine reaction.
06Differential diagnosisRealistic alternatives and the features that help distinguish them.
01

Uncontrolled pain or distress

Fracture, urinary retention, constipation, breathlessness and fear can cause resistance while attention may be relatively preserved.

02

Withdrawal syndrome

Autonomic activation, tremor, hallucinations and exposure history suggest alcohol or sedative withdrawal needing protocol-based therapy. Distinguish it through chronology, examination and targeted testing.

03

Lewy-body fluctuation

Chronic cognitive fluctuation, visual hallucinations, REM-sleep behaviour and parkinsonism suggest DLB, although acute illness can still cause superimposed delirium.

04

Primary psychiatric illness

Mania, psychosis and severe depression are possible but new late-life symptoms require organic and medication assessment first.

05

Akathisia or medicine reaction

Restlessness after dopamine blockade can be misread as worse agitation and provoke harmful dose escalation. Distinguish it through chronology, examination and targeted testing.

Additional chapter-specific clues

Akathisia mimic

New motor restlessness follows antipsychotic exposure and is misread as persistent agitation requiring more drug.

07ManagementImmediate care, first-line treatment, alternatives and escalation.
01First-line non-drug managementTreat causes and reduce threatFirst stepFirst lineDelirium is recognised with distress, disorientation or unsafe behaviour.
  1. 1Correct physiological and medical drivers and provide pain, hydration, nutrition, bowel, bladder and sensory care.
  2. 2Use one calm communicator, familiar support, orientation, low-stimulation space, sleep protection and safe mobilisation.
  3. 3Review response and capacity frequently and remove unnecessary devices and restrictions.
02Exceptional medicine routeUse the least dose for the narrowest indicationEscalationDistress or serious risk persists after de-escalation or immediate danger makes it inappropriate.
  1. 1Define the target and check Parkinson or DLB, ECG, electrolytes, interactions and prior antipsychotic reaction.
  2. 2Give the lowest protocol-approved oral dose, monitor closely and avoid dose stacking or treatment for staff convenience.
  3. 3Reassess after every dose, stop once risk resolves and never continue automatically at discharge.
03Neuroleptic-sensitive routeAvoid dopamine blockade and obtain expertiseParkinson disease, DLB features or a prior severe reaction is present.
  1. 1EscalationIntensify cause control, pain treatment, environment, familiar support and one-to-one de-escalation.
  2. 2Avoid haloperidol and seek urgent geriatric, neurology or old-age psychiatry advice if medication remains unavoidable.
  3. 3Monitor swallow, rigidity, consciousness and autonomic function and treat any severe reaction as an emergency.
04Restriction reviewRestore freedom as soon as possibleEnhanced observation, restraint or emergency medication has been used.
  1. 1Document capacity, immediate harm, alternatives attempted and why the intervention was necessary and proportionate.
  2. 2Review physical and psychological effect continuously and meet the need that triggered the behaviour.
  3. 3Remove the restriction at the earliest safe moment and debrief the person, carer and team.
Key medicines and prescribing safety3 treatments · regimens, roles and cautions
Exceptional short-term symptom control only after de-escalation fails or is inappropriate; it does not treat the underlying delirium.

Haloperidol

For a severely distressed or dangerous frail older adult, a typed local protocol commonly starts 0.5 mg orally once, reassesses after one to two hours and limits total exposure; NICE advises treatment usually for one week or less.

Avoid Parkinson disease and DLB, prolonged QT and major cardiac risk; obtain ECG and correct electrolytes, monitor rigidity, akathisia, dysphagia and sedation, and stop promptly.

Protocol-based alcohol or benzodiazepine withdrawal, selected catatonia or another specialist-defined indication where benzodiazepine benefit outweighs risk.

Lorazepam

For ordinary delirium avoid routine use; when a specialist identifies catatonia or a specific withdrawal indication, a cautious older-adult test dose may be 0.5 mg orally or parenterally with monitored reassessment.

Can cause paradoxical agitation, falls, aspiration and respiratory depression; reduce in frailty and never combine casually with opioids or repeat without response assessment.

Rare specialist alternative when immediate severe psychosis or distress threatens safety and intensive non-drug measures are insufficient.

Quetiapine

If Parkinson or DLB creates an unavoidable specialist antipsychotic decision, off-label treatment may begin 12.5 mg orally once, commonly at night, with slow individual titration.

Evidence in delirium is limited; causes sedation, postural hypotension, QT effects and increased stroke and mortality risk in dementia and still may worsen parkinsonism.

08ComplicationsImportant consequences, why they occur and why they matter clinically.
01

Aspiration and respiratory compromise

Sedation, rigidity and impaired swallow increase pneumonia and airway risk, especially after repeated parenteral dosing. Anticipatory multidisciplinary prevention and review are therefore important.

02

Cardiac arrhythmia

QT prolongation, electrolyte disturbance and interacting drugs can produce malignant ventricular arrhythmia with haloperidol and other antipsychotics.

03

Falls and loss of function

Postural effects, sedation and restraint accelerate immobility, fracture, pressure injury and new dependence. Anticipatory multidisciplinary prevention and review are therefore important.

04

Neurological toxicity

Extrapyramidal effects, neuroleptic malignant syndrome and profound DLB sensitivity can cause life-threatening decline. Anticipatory multidisciplinary prevention and review are therefore important.

05

Moral and psychological injury

Coercive care and frightening hallucinations distress the person, relatives and staff and may persist as traumatic memories.

09Monitoring and follow-upTreatment response, safety checks and longer-term review.
  • Review underlying causes and non-drug bundle each shift and after every move, procedure or sudden behavioural change.
  • After any sedating medicine record the target, dose, alertness, respiration, posture, swallow, rigidity, akathisia and actual benefit.
  • Repeat ECG or electrolytes according to baseline risk, exposure and symptoms and stop immediately for concerning cardiac or neurological toxicity.
  • Count and challenge every restraint, security call, catheter and observation restriction and record the earliest removal plan.
  • At discharge remove routine antipsychotic prescriptions unless a separately justified specialist indication exists and communicate any stop plan.
10Special situationsVariants, exceptions and circumstances that change the usual approach.

Calm is not resolution

A sedated patient may look better while hypoxia, sepsis or retention continues unseen.

Behaviour communicates need

Resistance often reflects pain, fear, toilet, sensory loss or misunderstood touch rather than psychiatric aggression.

DLB changes the risk calculus

A single dopamine-blocking dose can produce disproportionate rigidity, swallow failure and reduced consciousness.

Dose stacking causes harm

Delirium fluctuates naturally; repeating before the first dose peaks can create delayed oversedation.

Restrictions perpetuate delirium

Restraint and crowding increase perceived threat, immobility and sleep disruption.

Discharge prescriptions persist

An emergency antipsychotic can be copied indefinitely unless indication and stop date are explicit.

11Common pitfallsFrequent interpretation and management errors.
  1. 01

    Using medication because wandering or calling out inconveniences the ward.

  2. 02

    Giving haloperidol before checking Parkinson disease, DLB, ECG, electrolytes and interacting drugs.

  3. 03

    Treating sedation as clinical improvement without reassessing attention and the underlying cause.

  4. 04

    Repeating doses rapidly during natural fluctuation and causing delayed aspiration or hypotension.

  5. 05

    Using benzodiazepines for ordinary delirium without withdrawal, catatonia or specialist indication.

  6. 06

    Continuing an emergency antipsychotic on discharge without target, review or stop date.

Practice

Two practice questions

Question 1 of 20 correct
Medicine of older adultsOriginal SBA

Medicine threshold in delirium

A delirious patient repeatedly tries to climb from bed but settles when taken to the toilet and given analgesia. Which management is most appropriate?

Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateComplete draftClinical stateAwaiting reviewJurisdictionUnited Kingdom