3 Clinical psychopharmacology3.4 Therapeutics

3.4.7 Pharmacological management of psychiatric emergencies

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Written by Resident Doctor Committee · Published

Before any drug is given

  • The aim is calm wakefulness that allows assessment and care, not sleep.

  • Check airway, breathing, circulation, consciousness, vital signs and capillary glucose, and look for physical causes such as hypoxia, hypoglycaemia, infection, seizures and delirium.

  • Count every dose already given, including by ambulance and emergency staff, and ask about intoxication, allergies and pregnancy.

  • Use de-escalation first and offer oral medication before injection.

Choice of drug

Rapid tranquillisation usually means intramuscular (IM) medication when oral treatment is unsuitable. The National Institute for Health and Care Excellence (NICE) adult options are IM lorazepam alone or IM haloperidol with IM promethazine.

Situation

Choice

Active psychosis, tablets accepted

Oral newer antipsychotic

Respiratory disease

Avoid inhaled loxapine

No baseline electrocardiogram (ECG), cardiac disease or QT prolongation

Avoid haloperidol; NICE favours lorazepam

Stimulant toxicity

Benzodiazepine, with temperature and cardiovascular monitoring

Catatonia

Lorazepam; antipsychotics can worsen it

Alcohol or opioid intoxication

Benzodiazepines add to respiratory depression

Parkinson's disease, dementia with Lewy bodies

Haloperidol is contraindicated

Akathisia

Review the causative drug; more antipsychotic may worsen it

  • In psychotic agitation an antipsychotic calms and treats the cause, whereas a benzodiazepine or antihistamine only sedates.

  • In organic disinhibition, benzodiazepines are avoided because enhancing gamma-aminobutyric acid type A (GABA-A) receptors releases behaviour further when frontal control is already damaged.

  • Trazodone, selective serotonin reuptake inhibitors, valproate and beta-blockers have some evidence of reducing disinhibition or aggression.

  • Staff give a single dose and review it before repeating, because doses stacked before earlier ones take effect cause delayed respiratory depression.

Acute mania

UK licence

Drugs

Acute mania

Aripiprazole, quetiapine, olanzapine, risperidone, haloperidol

Relapse prevention

Carbamazepine, lamotrigine

Schizophrenia only

Clozapine, lurasidone

  • Benzodiazepines are used briefly for severe agitation or insomnia while a continuing antipsychotic or mood stabiliser plan is set up.

Complications of rapid tranquillisation

Finding

Action

Respiratory rate under 10 per minute or oxygen saturation under 90%

Give oxygen, raise the legs and keep the patient off their face; then intravenous (IV) flumazenil if a benzodiazepine is the cause

Postural fall in blood pressure over 30 mmHg, or diastolic under 50 mmHg

Lie the patient flat with the head of the bed lowered

Pulse under 50 per minute or irregular

Sinister sign, as haloperidol prolongs QT and causes arrhythmia; refer immediately to specialist medical care

Rising temperature

Possible early neuroleptic malignant syndrome (NMS); give no more antipsychotic and check creatine kinase (CK) urgently

Acute dystonia

Parenteral anticholinergic; airway support if the larynx is involved

Obstructed or noisy breathing

Open and clear the airway and call skilled help

The QT interval runs from the start of the QRS complex to the end of the T wave; haloperidol lengthens it, which is why a slow or irregular pulse after rapid tranquillisation is a sinister sign. PeaBrainC, CC BY-SA 4.0, via Wikimedia Commons
  • NICE observations after rapid tranquillisation are at least hourly, and every 15 minutes after high doses or when the person is asleep, sedated, or has used alcohol or drugs.

Flumazenil

  • Flumazenil acts at the benzodiazepine site of the GABA-A receptor.

  • Its half-life is about an hour, shorter than the benzodiazepines it reverses, so sedation can return and repeat doses may be needed.

  • It has no UK licence for benzodiazepine overdose.

  • It can provoke seizures and withdrawal, particularly in dependence or after proconvulsant co-ingestants.

Flumazenil binds the benzodiazepine (BZD) site between the alpha and gamma subunits, which is separate from the two GABA sites around the chloride pore. Chemgirl131 at English Wikipedia, public domain, via Wikimedia Commons

Drug-induced syndromes and catatonia

Syndrome

Recognition

Treatment

NMS

Rigidity, fever, autonomic instability, very high CK after antipsychotic exposure

Stop the drug, supportive care and cooling; bromocriptine, a dopamine agonist, reverses D2 blockade

Catatonia in depression

Mutism, posturing, staring; normal CK; no antipsychotic exposure

Lorazepam challenge first line, which usually works in affective catatonia

Serotonin syndrome

Rapid onset of clonus, hyperreflexia, dilated pupils, diarrhoea

Stop the drugs and give a benzodiazepine; cyproheptadine if it persists

Antipsychotic-induced syndrome of inappropriate antidiuretic hormone secretion (SIADH)

Low sodium, concentrated urine, normal volume status

If mild and asymptomatic, fluid restriction and regular sodium checks

Anticholinergic toxicity

Dry hot skin, dilated pupils, delirium, urinary retention

Supportive care; physostigmine only in selected specialist cases

  • Dantrolene is added when NMS is not controlled by stopping the drug and supportive care; it blocks calcium release inside muscle cells, cutting heat production and muscle breakdown.

  • Cyproheptadine is a 5-HT2A antagonist given by mouth or nasogastric tube.

  • Concentrated urine argues against primary polydipsia.

  • Malignant catatonia, with fever and autonomic instability, can overlap clinically with NMS.

  • A lorazepam response is not specific for catatonia, and electroconvulsive therapy is considered promptly when response is inadequate or life is threatened.

  • Muscle-generated hyperthermia needs active cooling, because antipyretics alone do not work.

Overdose and toxicity

Poison

Picture

Treatment

Reason

Salicylate

Level above 500 mg/L

Urinary alkalinisation to pH 7.5 to 8.5 with IV sodium bicarbonate

A weak acid ionises in the tubule, so excretion rises greatly

Lithium

Vomiting, coarse tremor, ataxia, confusion

Haemodialysis above 4.0 mmol/L with impaired kidney function, or at any level with reduced consciousness, seizures or arrhythmias

A small ion not bound to plasma proteins, so dialysis clears it efficiently

Amphetamine

Agitation, tachycardia, heat production

IV diazepam and active cooling

Diazepam calms, cuts heat generation and treats seizures

Opioid

Coma, respiratory rate of 5, pinpoint pupils

Naloxone, repeated as needed

Competitive opioid antagonist

Monoamine oxidase inhibitor with tyramine

Throbbing occipital headache, palpitations, severe hypertension

IV phentolamine, an alpha-adrenoceptor antagonist

Displaced noradrenaline acts on alpha-1 receptors

With MAO-A blocked, dietary tyramine displaces stored noradrenaline onto vascular alpha-1 receptors, causing the sudden rise in blood pressure that the alpha-adrenoceptor antagonist phentolamine reverses. Drawn for MRCPsychiatrist
  • Naloxone is short-acting, so the patient is observed for renarcotisation after waking.

  • Opioid tolerance falls within days of detoxification.

  • Suspected Wernicke's encephalopathy needs prompt parenteral thiamine, but emergency glucose for hypoglycaemia is not delayed while awaiting it.