Part 3: Delirium Assessment, Prevention, and Management

Complete delirium assessment tools (CAM-ICU flowsheet, ICDSC scoring), delirium subtypes, modifiable and non-modifiable risk factors, evidence-based non-pharmacologic prevention bundles, and pharmacologic management including haloperidol, quetiapine, and dexmedetomidine dosing.

guidelinesMar 2026guidelines

Delirium in the ICU: Overview

Delirium is an acute, fluctuating disturbance in attention and awareness, accompanied by additional cognitive dysfunction (disorientation, memory deficit, language disturbance, visuospatial impairment, or perceptual disturbance) that is not better explained by a pre-existing neurocognitive disorder and does not occur in the context of a severely reduced level of arousal (e.g., coma).1 2

Epidemiology

PopulationDelirium Prevalence
Mechanically ventilated patients60–80%
Non-ventilated medical ICU20–50%
Post-cardiac surgery30–50%
Post-operative (non-cardiac) ICU15–40%
Elderly (≥ 65) ICU patients50–70%

Consequences of ICU Delirium

OutcomeImpact
Mortality2–4× increased odds of death; each additional day of delirium increases 10-day mortality by 10%3
Duration of mechanical ventilationIncreased by 2–4 days
ICU length of stayIncreased by 5–10 days
Hospital length of stayIncreased by 5–8 days
Long-term cognitive impairment34% of survivors have cognitive impairment at 12 months (similar to moderate traumatic brain injury); 24% at 12 months similar to mild Alzheimer disease4
InstitutionalizationIncreased rate of discharge to long-term care facilities
Healthcare costsEstimated additional $16,000–$64,000 per patient per hospitalization
Post-traumatic stressHigher rates of PTSD, depression, and anxiety

Delirium Subtypes

SubtypePrevalence in ICUCharacteristicsRASS RangeDetection DifficultyPrognosis
Hyperactive1–2% (pure form)Agitation, restlessness, emotional lability, pulling at tubes, combativeness+1 to +4Easy — obvious behavioral changesBetter prognosis than other subtypes
Hypoactive40–50%Decreased alertness, lethargy, reduced motor activity, flat affect, withdrawal, inattention−1 to −3Difficult — often missed; may be mistaken for depression or over-sedationWorse prognosis; higher mortality; more associated with long-term cognitive impairment
Mixed45–55%Fluctuates between hyperactive and hypoactive features within same 24-hour periodVariesModerateIntermediate prognosis

Clinical Pearl: Hypoactive delirium is the most common subtype and the most frequently missed. It is associated with worse outcomes than hyperactive delirium. Routine screening with validated tools is essential to detect it.2


Delirium Assessment Tools

The Confusion Assessment Method for the ICU (CAM-ICU) — Complete Flowsheet

The CAM-ICU is the most widely used and validated bedside delirium assessment tool for ICU patients. It can be completed in 1–2 minutes by trained nurses, physicians, or other providers. Sensitivity is 80–95% and specificity is 89–100% when performed by trained assessors.2 5

Prerequisites before performing the CAM-ICU:

  • The patient must have a RASS score of −3 or higher (responsive to at least voice)
  • If RASS is −4 or −5 → patient is in coma → CAM-ICU cannot be assessed (record as “unable to assess — coma”)

CAM-ICU Flowsheet: Four Features

The CAM-ICU is POSITIVE (delirium present) if Feature 1 AND Feature 2 are present, PLUS either Feature 3 OR Feature 4.


Feature 1: Acute Onset or Fluctuating Course

QuestionSource
Is there an acute change in mental status from baseline?Medical record review; family or nursing report
Has the mental status fluctuated in the past 24 hours?Observation; serial RASS scores showing variability
Has the RASS score fluctuated in the past 24 hours?Nursing documentation

Scoring: If YES to any of the above → Feature 1 is POSITIVE → proceed to Feature 2. If NO to all → Feature 1 is NEGATIVE → CAM-ICU is NEGATIVE (no delirium). STOP.


Feature 2: Inattention — Assessed Using the Attention Screening Examination (ASE)

Two methods are available; use whichever the patient can perform:

Method A — Auditory (Letters Test) (PREFERRED)

Read the following 10 letters slowly (one letter per second) in a monotone voice. Instruct the patient: “I am going to read you a series of 10 letters. Squeeze my hand whenever you hear the letter ‘A’.”

Letter sequence: S A V E A H A A R T

LetterCorrect Response
SDo NOT squeeze
ASQUEEZE
VDo NOT squeeze
EDo NOT squeeze
ASQUEEZE
HDo NOT squeeze
ASQUEEZE
ASQUEEZE
RDo NOT squeeze
TDo NOT squeeze

Errors = failing to squeeze on “A” OR squeezing on a non-“A” letter.

Method B — Visual (Pictures Test)

Show a set of 5 pictures. Then show a set of 10 pictures (the original 5 mixed with 5 new pictures). The patient must nod “yes” or “no” to indicate whether they have seen each picture before. Count errors (incorrect responses).

Scoring Feature 2:

  • 0–2 errors → Feature 2 is NEGATIVE (attention intact) → CAM-ICU is NEGATIVE. STOP.
  • > 2 errors → Feature 2 is POSITIVE (inattention present) → Proceed to Feature 3.

Feature 3: Altered Level of Consciousness

AssessmentResult
Current RASS scoreRecord the current RASS

Scoring:

  • RASS = 0 (alert and calm) → Feature 3 is NEGATIVE → Proceed to Feature 4
  • RASS ≠ 0 (any score other than 0) → Feature 3 is POSITIVE → CAM-ICU is POSITIVE (delirium present). STOP.

Feature 4: Disorganized Thinking

Ask the following Yes/No questions AND perform a simple command:

Set A (use on odd calendar days or first assessment):

QuestionCorrect Answer
Will a stone float on water?No
Are there fish in the sea?Yes
Does one pound weigh more than two pounds?No
Can you use a hammer to pound a nail?Yes

Set B (use on even calendar days or alternate assessments):

QuestionCorrect Answer
Will a leaf float on water?Yes
Are there elephants in the sea?No
Do two pounds weigh more than one pound?Yes
Can you use a hammer to cut wood?No

Command: “Hold up this many fingers” (examiner holds up 2 fingers). After the patient does this, say “Now do the same thing with the other hand” (the patient should hold up 2 fingers on the other hand without being shown again). If patient is unable to move both arms, substitute: “Add one more finger” (patient should hold up 3 fingers).

Scoring Feature 4:

  • Count errors from the questions (each incorrect answer = 1 error) and the command (inability to complete = 1 error)
  • 0–1 errors → Feature 4 is NEGATIVE → CAM-ICU is NEGATIVE
  • > 1 error → Feature 4 is POSITIVE → CAM-ICU is POSITIVE (delirium present)

CAM-ICU Summary Flowsheet

Step 1: Assess RASS
  ├── RASS −4 or −5 → COMA → Cannot assess CAM-ICU → Reassess later
  └── RASS ≥ −3 → Proceed to CAM-ICU

Step 2: Feature 1 — Acute onset or fluctuating course?
  ├── NO → CAM-ICU NEGATIVE (No Delirium)
  └── YES → Proceed to Feature 2

Step 3: Feature 2 — Inattention (ASE Letters or Pictures)?
  ├── ≤ 2 errors → CAM-ICU NEGATIVE (No Delirium)
  └── > 2 errors → Proceed to Feature 3

Step 4: Feature 3 — Altered level of consciousness (RASS ≠ 0)?
  ├── YES (RASS ≠ 0) → CAM-ICU POSITIVE (Delirium Present)
  └── NO (RASS = 0) → Proceed to Feature 4

Step 5: Feature 4 — Disorganized thinking?
  ├── > 1 error → CAM-ICU POSITIVE (Delirium Present)
  └── ≤ 1 error → CAM-ICU NEGATIVE (No Delirium)

CAM-ICU Assessment Frequency

SettingRecommended Frequency
All ICU patientsAt least every 8–12 hours (once per nursing shift), ideally every 8 hours
During SAT (sedation interruption)After awakening (RASS ≥ −3)
When clinical change notedImmediately
Post-operative (first 72 hours)Every 8 hours minimum

Intensive Care Delirium Screening Checklist (ICDSC) — Complete Scoring

The ICDSC is an 8-item checklist completed by the bedside nurse based on observations over an 8–24 hour period. Each item is scored 0 (absent) or 1 (present). Total score ranges from 0 to 8. A score ≥ 4 indicates delirium. Sensitivity is 74–99% and specificity is 64–82%.6

ICDSC — Complete Scoring Table

ItemAssessmentScore 0Score 1
1. Altered level of consciousnessAssess over the shift: Was there any period of altered consciousness?Normal wakefulness, or easily arousable throughout shiftAny of the following: (a) hypervigilance/agitation, (b) lethargy/drowsiness (awakens to mild-moderate stimulation), (c) difficult to arouse (awakens only to strong stimulation), (d) unarousable (score N/A if comatose entire shift)
2. InattentionDifficulty following commands or conversation; easily distracted; difficulty shifting attentionFollows commands and conversation consistentlyAny difficulty following commands; loses track of conversation; distracted by external stimuli
3. DisorientationDoes the patient recognize ICU staff? Is the patient oriented to the current situation?Oriented to person, place, and situationAny obvious misidentification of people or places; unaware of current situation
4. Hallucination, delusion, or psychosisClinical manifestation of hallucinations or behavior produced by hallucinations/delusions (including trying to remove non-existent objects)None observedHallucinations, delusions, or psychotic behavior observed
5. Psychomotor agitation or retardationHyperactivity requiring sedation or restraints OR hypoactivity (slowed, decreased movement — not due to sedation)Normal activityHyperactivity requiring additional intervention OR hypoactivity/slowness not attributable to sedation
6. Inappropriate speech or moodInappropriate, disorganized, or incoherent speech; inappropriate emotional displayNormal, appropriate speech and moodInappropriate, disorganized, or incoherent speech OR inappropriate mood/emotional display
7. Sleep/wake cycle disturbanceSleeping < 4 hours at night; frequent awakenings; sleeping during most of the dayNormal sleep/wake patternAny significant disruption: sleeping < 4 hours at night, waking frequently, sleeping most of day
8. Symptom fluctuationFluctuation of any of the above items (items 1–7) during the assessment periodSymptoms stable or absentAny fluctuation in the above manifestations over the 8–24 hour assessment period
ICDSC Total ScoreInterpretation
0No delirium
1–3Subsyndromal delirium (associated with worse outcomes than no delirium)
≥ 4Delirium (clinical delirium — initiate management)

Choosing Between CAM-ICU and ICDSC

FeatureCAM-ICUICDSC
Assessment typePoint-in-time bedside testObservation-based checklist over 8–24 h
Time to complete1–2 minutes2–5 minutes (based on shift observations)
Sensitivity80–95%74–99%
Specificity89–100%64–82%
Training requiredModerate (structured test)Low (observational)
Identifies subsyndromal deliriumNo (binary: positive or negative)Yes (scores 1–3)
Can assess in non-verbal patientsYesYes
Requires patient interactionYes (must perform tests)No (based on observation)

Recommendation: Both tools are acceptable. The CAM-ICU has higher specificity and is the most widely studied. The ICDSC may have higher sensitivity in some settings and captures subsyndromal delirium. An institution should select one tool and ensure consistent training and compliance.1


Delirium Risk Factors

Non-Modifiable Risk Factors

Risk FactorRelative Risk / Odds Ratio
Advanced age (≥ 65 years)OR 2.0–3.5
Pre-existing cognitive impairment / dementiaOR 2.5–6.3
History of deliriumOR 2.0–3.0
History of depressionOR 1.5–2.0
History of alcohol use disorderOR 2.0–4.0
Male sex (some studies)OR 1.2–1.5
Severity of illness (APACHE II ≥ 24)OR 1.5–3.0
Admission diagnosis of trauma or burnsOR 1.5–2.5
Surgical (vs. medical) admissionVariable
Genetic factors (APOE4 allele)OR 1.5–2.0 (limited evidence)

Modifiable Risk Factors

Risk FactorRelative Risk / Odds RatioIntervention
Benzodiazepine useOR 2.0–4.0 per day of exposureAvoid benzodiazepines; use non-benzodiazepine sedation
Deep sedationOR 2.0–3.0Target light sedation (RASS 0 to −2)
Untreated painOR 1.5–2.5Routine pain assessment and analgesia
Physical restraintsOR 1.4–2.0Minimize restraint use; use alternatives
ImmobilityOR 1.5–2.5Early mobilization
Sleep deprivationOR 1.5–2.0Sleep promotion protocols
Anticholinergic medicationsOR 1.5–2.5Medication review; avoid high-anticholinergic drugs
Prolonged mechanical ventilationOR 1.5–3.0SAT/SBT protocols; early extubation
Metabolic derangements (acidosis, uremia, electrolyte abnormalities)VariableCorrect underlying metabolic disorder
Sepsis / infectionOR 2.0–5.0Early recognition and treatment of infections
DehydrationOR 1.5–2.0Adequate hydration
Sensory deprivation (no glasses, hearing aids)OR 1.5–2.0Provide assistive devices
Indwelling urinary catheterOR 1.5–2.5Remove as soon as possible

Delirium Prevention

Non-Pharmacologic Delirium Prevention Bundle

Non-pharmacologic, multicomponent prevention strategies are the cornerstone of delirium prevention and are recommended for all ICU patients (strong recommendation).1 7

DomainInterventionsEvidence Level
Cognitive stimulation / reorientationReorient to time, place, person at each interaction; provide clocks and calendars visible from bed; encourage family to bring familiar objects (photos, personal items); engage in conversation appropriate to cognitive level; TV/radio for orientation (not constant background noise)Moderate
Sleep promotionCluster care activities to minimize nighttime interruptions; reduce ambient light at night; provide earplugs and/or eye masks; minimize nighttime noise (target < 45 dB); maintain daytime light exposure; avoid sleep-disrupting medications at night (see Part 4)Moderate
Early mobilityBegin mobilization within 24–48 hours when safe; progressive activity (passive ROM → active ROM → sitting → standing → ambulation); see Part 4 for detailed protocolModerate
Sensory optimizationEnsure patients have their glasses and hearing aids; check hearing aid batteries; clean glasses daily; maximize communication abilityLow-Moderate
Pain managementRoutine pain assessment with validated tools; treat pain proactively; multimodal analgesia (see Part 1)Moderate
Medication reviewAvoid/minimize benzodiazepines, anticholinergics, antihistamines (diphenhydramine), meperidine; perform daily medication reconciliation to identify delirium-contributing medicationsModerate
Minimize sedationLight sedation target; daily SAT; nurse-driven sedation protocol; analgesia-first approach (see Part 2)Strong
Family engagementEncourage family presence and participation in care; structured family communication; family presence during SAT; family can assist with reorientationLow-Moderate
Environmental modificationReduce unnecessary alarms; single-patient rooms when possible; minimize patient transfers; maintain consistent nursing assignmentLow
Hydration and nutritionEnsure adequate hydration; early enteral nutrition; correct electrolyte abnormalitiesLow-Moderate
Catheter and restraint minimizationRemove unnecessary lines, tubes, and catheters; remove restraints when possible; provide alternatives to restraints (1:1 sitter, bed alarms, family presence)Low-Moderate

Pharmacologic Delirium Prevention

The 2018 guidelines do NOT recommend routine pharmacologic prophylaxis for delirium in most ICU patients. Specific findings:1

AgentRecommendation for Prevention
HaloperidolNOT recommended for delirium prevention (no benefit in RCTs)
Atypical antipsychoticsNOT recommended for delirium prevention
DexmedetomidineConditional recommendation for use as a sedative that is associated with lower delirium incidence compared to benzodiazepines (this is a sedation choice, not a prophylactic intervention)
StatinsNOT recommended for delirium prevention
KetamineInsufficient evidence for delirium prevention
Melatonin / RamelteonInsufficient evidence; some promising data; not formally recommended

Exception — Perioperative dexmedetomidine: In cardiac and non-cardiac surgical populations, perioperative dexmedetomidine has shown delirium-preventive effects in some trials. This may be considered for high-risk surgical ICU patients (conditional recommendation based on limited evidence).8


Delirium Management

Step 1: Identify and Treat Underlying Causes

When delirium is identified, the first priority is to identify and treat reversible precipitating factors. The mnemonic “THINK” can be used:1 9

LetterDomainSpecific Causes to Investigate
TToxic / medicationsBenzodiazepines, anticholinergics, opioids (accumulation), corticosteroids, antihistamines, fluoroquinolones; new medication review; drug interactions
HHypoxemia / metabolicHypoxia (check SpO2, ABG); hypercapnia; hepatic encephalopathy; uremia; hypo/hyperglycemia; hypo/hypernatremia; hypercalcemia; thyroid dysfunction; adrenal insufficiency; acidosis
IInfection / InflammationNew or worsening infection (UTI, pneumonia, line infection, wound, Clostridioides difficile, meningitis); sepsis; pancreatitis
NNon-pharmacologic interventionsIs the bundle being applied? Check sleep, mobility, reorientation, sensory aids, restraint minimization
KK+ and electrolytesHypokalemia, hypomagnesemia, hypophosphatemia, hypo/hypernatremia, hypercalcemia

Step 2: Non-Pharmacologic Management

All non-pharmacologic prevention strategies (see prevention bundle above) should be continued and intensified during active delirium.1 7

InterventionApplication in Active Delirium
ReorientationIncrease frequency; have family assist; use simple, calm language
MobilityContinue/initiate if safe — exercise may reduce delirium duration
Sleep promotionIntensify nighttime sleep protection
Minimize noxious stimuliReduce alarms, lights, noise; limit nighttime interventions
Pain controlRe-assess pain; ensure adequate analgesia
Remove deliriogenic medicationsStop or reduce benzodiazepines, anticholinergics, unnecessary opioids
Remove unnecessary devicesFoley catheters, unnecessary IV lines, restraints
Music therapyMay reduce anxiety and delirium severity

Step 3: Pharmacologic Management of Delirium

The 2018 guidelines recommend AGAINST the routine use of haloperidol or atypical antipsychotics for the treatment of ICU delirium (conditional recommendation), based on the MIND-USA and AID-ICU trials which found no significant benefit on delirium duration, ventilator-free days, or mortality.1 10 11

However, antipsychotics may be considered in the following circumstances:

  • Patients with severe agitation that poses an immediate safety risk to the patient or staff
  • Hyperactive delirium with distressing symptoms (hallucinations, severe agitation) refractory to non-pharmacologic measures
  • As a bridge while treating reversible underlying causes
  • Patients with delirium and significant psychological distress

Haloperidol

ParameterDetails
MechanismD2 dopamine receptor antagonist (typical/first-generation antipsychotic)
RouteIV preferred in ICU (faster onset, fewer EPS than IM); also IM, PO
IV dose — mild agitation0.5–2 mg IV q 4–6 h PRN
IV dose — moderate agitation2–5 mg IV q 2–4 h PRN
IV dose — severe agitation5–10 mg IV q 30–60 min until calm; max ~20 mg/day (some protocols up to 40 mg/day with close monitoring)
Onset (IV)3–20 minutes
Duration4–8 hours
QTc monitoringMandatory — obtain baseline ECG before starting; monitor QTc q 12–24 h; HOLD if QTc > 500 ms or increases by > 25% from baseline
Torsades de pointes riskDose-dependent; risk increases with hypokalemia, hypomagnesemia, concurrent QT-prolonging drugs
Extrapyramidal symptoms (EPS)Less common with IV than IM/PO; includes akathisia, dystonia, parkinsonism; treat acute dystonia with diphenhydramine 25–50 mg IV or benztropine 1–2 mg IV
Neuroleptic malignant syndrome (NMS)Rare but life-threatening; fever, rigidity, autonomic instability, elevated CK; discontinue immediately; dantrolene and supportive care
ContraindicationsQTc > 500 ms; history of torsades; Parkinson disease; Lewy body dementia; active NMS
NoteIV haloperidol is used off-label (FDA-approved routes are IM and PO only)

Quetiapine

ParameterDetails
MechanismAtypical antipsychotic; D2, 5-HT2A, H1, alpha-1 antagonist
RoutePO/NG only (no IV formulation)
Starting dose25–50 mg PO/NG q 12 h (12.5–25 mg in elderly)
TitrationIncrease by 25–50 mg per dose every 24 h as tolerated
Usual effective dose50–200 mg PO q 12 h
Maximum dose400 mg/day (ICU use)
AdvantagesSedating (useful for sleep in hypoactive/mixed delirium); lower EPS risk than haloperidol; anxiolytic
DisadvantagesPO only (requires enteral access); sedating (may worsen hypoactive delirium); hypotension (alpha-1 blockade); hyperglycemia; QTc prolongation (less than haloperidol)
QTc monitoringRecommended; same thresholds as haloperidol
Use in ICUMay be considered when PO route available; some evidence suggests faster delirium resolution when added to haloperidol; useful for nighttime sedation in delirious patients

Olanzapine

ParameterDetails
MechanismAtypical antipsychotic; D2, 5-HT2A, muscarinic, H1 antagonist
RoutePO, IM (no IV)
Dose2.5–5 mg PO/IM q 12–24 h; max 20 mg/day
AdvantagesAvailable IM; less hypotension than quetiapine
DisadvantagesAnticholinergic properties (may worsen delirium paradoxically); metabolic effects; sedation; limited ICU-specific evidence

Dexmedetomidine is NOT an antipsychotic but is the preferred sedative for patients with delirium who require sedation, based on its lower delirium-promoting profile compared to benzodiazepines and its potential to facilitate delirium resolution.1 10 12

ParameterDetails
Indication in deliriumSedation for agitated delirious patients who remain on mechanical ventilation; facilitation of extubation in delirious patients; nocturnal sedation for sleep promotion in delirious patients
Dose0.2–1.5 mcg/kg/h IV infusion (no loading dose in this context to avoid hypotension/bradycardia)
EvidenceDahLIA trial: dexmedetomidine vs. placebo for ventilated patients with agitated delirium — faster delirium resolution (median 23.3 vs. 40.0 h), more ventilator-free hours12
AdvantagesDoes not worsen delirium; produces arousable sedation; no respiratory depression
LimitationDoes not treat delirium per se — provides a delirium-friendly form of sedation

Pharmacologic Treatment Algorithm for ICU Delirium

Step 1: Identify and treat underlying causes (THINK)
        ↓
Step 2: Implement/intensify non-pharmacologic bundle
        ↓
Step 3: Assess delirium subtype and severity
        ├── Hypoactive delirium (calm, inattentive)
        │   → Non-pharmacologic interventions are PRIMARY
        │   → Remove sedatives if possible
        │   → Optimize sleep (quetiapine 25–50 mg PO qHS may help with sleep cycle)
        │   → Pharmacologic treatment NOT routinely recommended
        │   → Do NOT use haloperidol (may worsen sedation)
        │
        ├── Hyperactive delirium (agitated, hallucinations, combative)
        │   → Non-pharmacologic interventions FIRST
        │   → If safety concern or significant distress:
        │       → Haloperidol 2–5 mg IV q 30 min–4 h PRN (check QTc)
        │       → OR quetiapine 25–50 mg PO/NG q 12 h if enteral route available
        │   → If on mechanical ventilation requiring sedation:
        │       → Dexmedetomidine preferred sedative
        │       → AVOID benzodiazepines (worsen delirium)
        │
        └── Mixed delirium
            → Combine approaches based on predominant symptoms
            → Reassess subtype at each assessment

Duration of Antipsychotic Therapy

  • If antipsychotics are initiated for delirium, plan for taper and discontinuation
  • Reassess need at least daily
  • Once delirium resolves (CAM-ICU negative for ≥ 24 hours), taper and discontinue antipsychotics over 2–5 days
  • Do NOT continue antipsychotics at ICU discharge unless the patient had a pre-existing psychiatric indication
  • Document the indication, planned duration, and taper plan in the medical record

Benzodiazepines and Delirium

Benzodiazepines are a major risk factor for ICU delirium and should be avoided whenever possible.1 2

EvidenceFinding
Every additional day of benzodiazepine exposure4–7% increased odds of delirium transition the following day
Midazolam vs. dexmedetomidine (SEDCOM)Higher delirium prevalence with midazolam (76.6% vs. 54%)13
Lorazepam vs. dexmedetomidine (MENDS)More delirium-free and coma-free days with dexmedetomidine14
Midazolam infusion > 48 hUnpredictable wake-up time; accumulation of active metabolite

When benzodiazepines are appropriate:

  • Active seizures (first-line)
  • Alcohol or sedative/hypnotic withdrawal (specific benzodiazepine protocols — see Part 5)
  • Procedural anxiolysis/sedation (single dose)
  • Refractory agitation not responding to non-benzodiazepine agents (rescue)
  • Patients on chronic benzodiazepine therapy (continue at prior dose to avoid withdrawal)
  • Anxiety disorders with documented benzodiazepine dependence

Medications That Increase Delirium Risk

The following medications should be reviewed and minimized in ICU patients at risk for delirium:1

ClassHigh-Risk ExamplesAlternatives
BenzodiazepinesMidazolam, lorazepam, diazepamDexmedetomidine, propofol for sedation
AnticholinergicsDiphenhydramine, promethazine, scopolamine, hydroxyzine, oxybutynin, atropine (systemic)Ondansetron (for nausea); non-anticholinergic alternatives
Opioids (high dose / accumulation)Meperidine (active metabolite normeperidine), morphine in renal failureFentanyl, hydromorphone; dose optimization
Corticosteroids (high dose)Dexamethasone, methylprednisolone (pulse dose)Use lowest effective dose; consider steroid taper
FluoroquinolonesCiprofloxacin, levofloxacinAlternative antibiotic classes when possible
H2 receptor antagonistsFamotidine, ranitidineProton pump inhibitors (if acid suppression needed)

Delirium Documentation and Communication

ElementDetails
Tool usedCAM-ICU or ICDSC
ResultPositive, Negative, or Unable to Assess (coma)
RASS at time of assessmentDocument actual score
Delirium subtypeHyperactive, hypoactive, or mixed
Likely contributing factorsMedications, metabolic, infection, sleep deprivation, etc.
Interventions initiatedNon-pharmacologic and pharmacologic (with doses)
Response to interventionsImproved, unchanged, worsened

Handoff Communication for Delirium

Include in every nurse-to-nurse and nurse-to-provider handoff:

  1. Current delirium status (CAM-ICU/ICDSC result)
  2. Trend over past 24–48 hours
  3. Identified contributing factors
  4. Current management plan
  5. Outstanding workup (pending labs, imaging, medication review)

References


  1. Devlin JW, Skrobik Y, Gélinas C, et al. “Clinical Practice Guidelines for the Prevention and Management of Pain, Agitation/Sedation, Delirium, Immobility, and Sleep Disruption in Adult Patients in the ICU.” Crit Care Med. 2018;46(9):e825-e873. DOI: 10.1097/CCM.0000000000003299 ↩︎ ↩︎ ↩︎ ↩︎ ↩︎ ↩︎ ↩︎ ↩︎ ↩︎ ↩︎

  2. Ely EW, Inouye SK, Bernard GR, et al. “Delirium in Mechanically Ventilated Patients: Validity and Reliability of the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU).” JAMA. 2001;286(21):2703-2710. DOI: 10.1001/jama.286.21.2703 ↩︎ ↩︎ ↩︎ ↩︎

  3. Ely EW, Shintani A, Truman B, et al. “Delirium as a Predictor of Mortality in Mechanically Ventilated Patients in the Intensive Care Unit.” JAMA. 2004;291(14):1753-1762. DOI: 10.1001/jama.291.14.1753 ↩︎

  4. Pandharipande PP, Girard TD, Jackson JC, et al. “Long-Term Cognitive Impairment After Critical Illness.” N Engl J Med. 2013;369(14):1306-1316. DOI: 10.1056/NEJMoa1301372 ↩︎

  5. Ely EW, Margolin R, Francis J, et al. “Evaluation of Delirium in Critically Ill Patients: Validation of the Confusion Assessment Method for the Intensive Care Unit (CAM-ICU).” Crit Care Med. 2001;29(7):1370-1379. DOI: 10.1097/00003246-200107000-00012 ↩︎

  6. Bergeron N, Dubois MJ, Dumont M, Dial S, Skrobik Y. “Intensive Care Delirium Screening Checklist: Evaluation of a New Screening Tool.” Intensive Care Med. 2001;27(5):859-864. DOI: 10.1007/s001340100909 ↩︎

  7. Inouye SK, Bogardus ST Jr, Charpentier PA, et al. “A Multicomponent Intervention to Prevent Delirium in Hospitalized Older Patients.” N Engl J Med. 1999;340(9):669-676. DOI: 10.1056/NEJM199903043400901 ↩︎ ↩︎

  8. Duan X, Coburn M, Rossaint R, Sanders RD, Waesberghe JV, Kowark A. “Efficacy of Perioperative Dexmedetomidine on Postoperative Delirium: Systematic Review and Meta-Analysis with Trial Sequential Analysis of Randomised Controlled Trials.” Br J Anaesth. 2018;121(2):384-397. DOI: 10.1016/j.bja.2018.04.046 ↩︎

  9. DAS-Taskforce 2015, Baron R, Binder A, et al. “Evidence and Consensus Based Guideline for the Management of Delirium, Analgesia, and Sedation in Intensive Care Medicine (DAS-Guideline 2015).” Ger Med Sci. 2015;13:Doc19. DOI: 10.3205/000223 ↩︎

  10. Girard TD, Exline MC, Carson SS, et al. “Haloperidol and Ziprasidone for Treatment of Delirium in Critical Illness.” N Engl J Med. 2018;379(26):2506-2516. DOI: 10.1056/NEJMoa1808217 ↩︎ ↩︎

  11. Andersen-Ranberg NC, Poulsen LM, Perner A, et al. “Haloperidol for the Treatment of Delirium in ICU Patients.” N Engl J Med. 2022;387(26):2425-2435. DOI: 10.1056/NEJMoa2211868 ↩︎

  12. Reade MC, Eastwood GM, Bellomo R, et al. “Effect of Dexmedetomidine Added to Standard Care on Ventilator-Free Time in Patients with Agitated Delirium: A Randomized Clinical Trial.” JAMA. 2016;315(14):1460-1468. DOI: 10.1001/jama.2016.2707 ↩︎ ↩︎

  13. Riker RR, Shehabi Y, Bokesch PM, et al. “Dexmedetomidine vs Midazolam for Sedation of Critically Ill Patients: A Randomized Trial.” JAMA. 2009;301(5):489-499. DOI: 10.1001/jama.2009.56 ↩︎

  14. Pandharipande PP, Pun BT, Herr DL, et al. “Effect of Sedation with Dexmedetomidine vs Lorazepam on Acute Brain Dysfunction in Mechanically Ventilated Patients: The MENDS Randomized Controlled Trial.” JAMA. 2007;298(22):2644-2653. DOI: 10.1001/jama.298.22.2644 ↩︎