´óÏóÊÓƵ

See also

Poisoning – acute guidelines for initial management
ResuscitationÌý
Anticholinergic Poisoning

Key points

1. The majority of antihistamine poisonings will only require supportive care.
2. Large overdoses of H1 Antihistamines are associated withÌýcardiac arrhythmia and may require close monitoring and specific treatment.
3. Consider investigating for common co-ingestions depending on the formulation, such as paracetamol levels.

For 24 hour advice, contact the Victorian Poisons Information Centre on 13 11 26

Background

Antihistamines are commonly recommended for the treatment of allergic symptoms. This guideline will only deal with H1 antagonists. H2 antagonists such as cimetidine and ranitidine are not covered by this guideline.

Antihistamines are divided into sedating and lesser sedating (previous called non-sedating) types. In general, the lesser sedating antihistamines have less serious toxicity in overdose.

Sedating antihistamines

As well as their H1 effect, sedating antihistamines can have alpha adrenergic, anticholinergic and serotonergic effects. As well as sedation, overdose often presents with anticholinergic symptoms (see Anticholinergic Syndrome). At higher doses, they can also cause sodium channel blockade with subsequent cardiovascular effects including QT prolongations and Torsades de Pointes.

Examples

• Cyproheptadine
• Dexchlorpheniramine
• Diphenhydramine
• Dimenhydrinate-used in combination with hyoscine/caffeine for travel
• Doxylamine
• Pheniramine
• Promethazine
• Trimeprazine
• Brompheniramine Ìý Ìý

Lesser sedating antihistamines

These medicines cause mostly peripheral H1 blockade with limited penetration into the CNS.Ìý In overdose symptoms can include dizziness, tachycardia, headache drowsiness or agitation. While the current generation of lesser sedating antihistamines do not affect the QT interval at normal doses (unlike the previous generation of medicines), there are concerns there may be some effect in overdose.Ìý

Examples

• Cetirizine
• Desloratadine
• Fexofenadine
• Loratadine

Children requiring assessment

• Acute ingestion of >3 X maximum daily dose
• All children or young people with intentional self-poisoning or significant accidental ingestion Ìý
• Any symptomatic child or young person Ìý
• Any child whose developmental age is inconsistent with accidental poisoning as non-accidental poisoning should be considered.

Risk Assessment

History:

Intentional poisoning or accidental

Dose:

• Stated or likely dose taken
• Presented as syrup, immediate or modified- release tablets
• If possible determine the exact name and tablet size.
• ÌýCalculate the maximum possible dose per kg

Ìý ÌýCo-ingestants eg paracetamol

Examination:

• CNS depression or confusion/delirium.
• CVS Tachycardia, arrhythmias, Hypotension

See Anticholinergic Poisoning

Investigations:

For those requiring further assessment:Ìý

• ECG: initially and repeat 4-6 hourly until normal. ÌýÌý
• Pathology: ÌýParacetamol level in all intentional overdoses

Acute Management

1. Resuscitation

Standard procedures and supportive careÌý

Sedating antihistamines

• In Adolescents, consider investigating for common co-ingestions (paracetamol, alcohol, etc.)
• Monitor level of consciousness and respiratory status and institute supportive measures for respiratory depression or depressed conscious state
• Decontamination - Consider activated charcoal after massive ingestion in older/sedating anti histamines, and within 1 hour / or after airway protection.Ìý Discuss with toxicologist.
• Seizures or severe agitation should be treated with benzodiazepines seeÌýSeizure
• Cardiac monitoring should be instituted and an initial 12 Lead ECG preformed and assessed for Long QT and arrhythmias. Consider repeat ECG at 6 hours if symptomatic.
• The use of anticholinesterases should be discussed with a toxicologist.

Lesser sedating antihistamines

• A 12 Lead ECG preformed and assessed for Long QT and arrhythmias.
• Cardiac monitoring may be necessary with large overdoses
• Treat any effects with symptomatic management.Ìý

When to admit/consult local paediatric teamÌý

Admission should be considered for all children or young people with an intentional poisoning.Ìý

Consult Contact Victorian Poisons Information Centre 13 11 26 for adviceÌýÌý Ìý Ìý

When to consider transfer to a tertiary centre

Consider transfer when:

• Significantly decreased conscious stage or conscious state not improving as expected.
• Need for respiratory supportÌý

For emergency advice and paediatric or neonatal ICU transfers, call the Paediatric Infant Perinatal Emergency Retrieval (PIPER) Service: 1300 137 650.ÌýÌý Ìý

Discharge Criteria

If features of poisoning have not developed at 6 hours post-ingestion
Normal GCS
Normal ECG
For intentional poisoning, a risk assessment should indicate that the child or young person is at low risk of further self harm in the discharge settingÌý

Discharge information and follow-upÌý

Accidental ingestion:ÌýÌýfrom Victorian Poisons Information centre on the prevention of poisoning:ÌýÌýÌýÌýÌýÌýÌýÌý

Intentional self–harm: Referral to local mental health services e.g. Orygen Youth Health:Ìý1800 888 320Ìý

Last updated August 2017