Nonpharmacologic and supportive care
›Supportive measures
›Environment
›Low stimulation room
›Remove restraints as soon as safe
›Analgesia when pain suspected
›Nonopioid analgesics when appropriate
›Opioids with close monitoring when indicated
›Hydration and cooling
›IV fluids for dehydration and rhabdomyolysis risk
›Active cooling for hyperthermia syndromes
Physical restraint and monitoring
›Restraint principles
›Indications
›Immediate danger to staff or patient
›Failed de-escalation and unsafe to delay sedation
›Technique
›Least restrictive effective method
›Supine positioning with head elevation when feasible
›Monitoring
›Continuous pulse oximetry
›End-tidal CO2 when deep sedation risk
›Medical risks
›Positional asphyxia risk
›Rhabdomyolysis risk with prolonged struggling
Pharmacologic strategy selection
›Medication approach
›Primary psychiatric agitation without delirium
›Antipsychotic first-line consideration
›Add benzodiazepine for severe agitation or stimulant co-use
›Delirium or medical agitation
›Antipsychotic preferred over benzodiazepine in most cases
›Benzodiazepine reserved for withdrawal and selected toxidromes
›Withdrawal states
›Benzodiazepine first-line for alcohol withdrawal
›Phenobarbital protocols per local practice when appropriate
›Excited delirium like severe hyperadrenergic state
›Rapid dissociative sedation pathway when immediate control required
›Aggressive cooling and complication prevention
Oral options when cooperative
›Oral medications
›Antipsychotics
›Olanzapine PO 5 to 10 mg
›Avoid combined IM olanzapine and parenteral benzodiazepine within short interval
›Sedation monitoring for respiratory depression risk
›Risperidone PO 1 to 2 mg
›Useful for psychosis with cooperation
›Add lorazepam PO for anxiety component when appropriate
›Benzodiazepines
›Lorazepam PO 1 to 2 mg
›Higher risk of delirium worsening in older adults
›Add monitoring when combined with other sedatives
Intramuscular and intravenous options
›Antipsychotics
›Haloperidol IM 5 mg
›Repeat dosing 5 mg every 15 to 30 minutes as needed
›Typical max total dose 20 to 30 mg in ED with monitoring
›EPS risk higher than atypicals
›Droperidol IM 5 mg
›Repeat dosing 2.5 to 5 mg every 10 to 15 minutes as needed
›QT prolongation risk and ECG consideration in high-risk patients
›Rapid onset for severe agitation
›Olanzapine IM 10 mg
›Repeat dosing 5 to 10 mg after 2 hours as needed
›Avoid concomitant parenteral benzodiazepine near in time
›Lower EPS risk than haloperidol
›Benzodiazepines
›Midazolam IM 5 mg
›Repeat dosing 2.5 to 5 mg every 5 to 10 minutes as needed
›Faster onset than lorazepam
›Higher respiratory depression risk when combined with opioids or alcohol
›Lorazepam IM 2 mg
›Repeat dosing 1 to 2 mg every 15 to 30 minutes as needed
›Longer duration and slower onset than midazolam
›Combination therapy
›Haloperidol plus benzodiazepine
›Haloperidol IM 5 mg plus lorazepam IM 2 mg
›Useful for severe psychosis with agitation
›Increased sedation risk requiring monitoring
Dissociative sedation for uncontrolled violence
›Ketamine pathway
›Ketamine IM 4 mg/kg
›Typical range 3 to 5 mg/kg
›Onset often within minutes
›Airway readiness and monitoring required
›Ketamine IV 1 to 2 mg/kg
›Titrate in small boluses when IV access secure
›Higher apnea risk with rapid IV push
›Post-ketamine care
›Treat hypersalivation with suction and anticholinergic if needed
›Emergence reaction management with benzodiazepine when clinically appropriate
Syndrome-specific treatments
›Alcohol withdrawal agitation
›Benzodiazepines
›Diazepam IV 10 mg
›Repeat dosing every 5 to 10 minutes to symptom control
›Longer half-life and active metabolites
›Lorazepam IV 2 mg
›Repeat dosing every 10 to 20 minutes to symptom control
›Preferred in liver dysfunction
›Thiamine
›Thiamine IV 100 mg before glucose when malnutrition risk
›Higher dose protocols per local practice for Wernicke concern
›Stimulant intoxication agitation
›Benzodiazepines first-line
›Midazolam IM 5 mg or IV 2.5 mg
›Titrate to calm without apnea
›Hyperthermia management
›Active cooling and IV fluids
›Avoid physical struggle and prolonged restraint
›Neuroleptic malignant syndrome concern
›Supportive care and stop dopamine blockers
›Cooling and IV fluids
›ICU consultation for severe rigidity and hyperthermia
›Serotonin toxicity concern
›Benzodiazepines and supportive care
›Cyproheptadine PO when moderate symptoms and able to take oral
›ICU consultation for severe hyperthermia or rigidity
Medication safety and monitoring
›Monitoring bundle after parenteral sedation
›Continuous pulse oximetry
›Early detection of hypoxia
›Escalation trigger with persistent desaturation
›End-tidal CO2 when deep sedation risk
›Early detection of hypoventilation
›Assisted ventilation escalation trigger
›ECG considerations
›QT risk factors review before QT-prolonging antipsychotics when feasible
›Electrolyte correction for hypokalemia and hypomagnesemia when present
›Evidence grading anchors
›ACEP Level B style recommendation for benzodiazepines in stimulant intoxication
›Strong clinical consensus and supportive evidence base
›Primary goal rapid sedation and complication prevention
›Class IIa style recommendation for antipsychotic use in primary psychosis agitation
›Benefit outweighs risk with monitoring
›Choice individualized to QT and EPS risk profile