atropine
antimuscarinic· Brands: Atropine Sulfate, Atropine, AtroPen, Isopto AtropineIMIVNEBPOSCTOP
Symptomatic bradycardia (e.g., acute myocardial infarction, perioperative)
Repeat until adequate heart rate; total max 3 mg.
- adult · IV: 0.5–1 mg every 3-5 min PRN · Repeat until adequate heart rate; total max 3 mg.
Organophosphate or carbamate insecticide poisoning
Titrate to atropinization; doses may exceed standard.
- adult · IV: 2 mg every 5-10 min · Titrate to atropinization; doses may exceed standard.
Preoperative reduction of secretions (e.g., salivation, bronchial secretions)
Given 30-60 min preoperatively.
- adult · IM: 0.3–0.6 mg single dose · Given 30-60 min preoperatively.
Symptomatic bradycardia in children
Minimum single dose 0.1 mg; maximum single dose 0.5 mg (1 mg in adolescents).
- pediatric · IV: 0.02 mg/kg every 5 min · Minimum single dose 0.1 mg; maximum single dose 0.5 mg (1 mg in adolescents).
Uveitis and cycloplegic refraction (ophthalmic)
Use atropine sulfate 1% eye drops.
- adult · TOP: 1–2 drops twice daily · Use atropine sulfate 1% eye drops.
- Angle-closure glaucoma · Atropine can precipitate acute glaucoma by increasing intraocular pressure.
- Paralytic ileus · Atropine reduces gastrointestinal motility and may worsen obstruction.
- Prostatic hyperplasia with urinary retention · May cause or worsen urinary retention due to increased bladder sphincter tone.
- Tachyarrhythmias · Atropine may increase heart rate and worsen existing arrhythmias.
- Use with caution in the elderly due to increased risk of confusion, constipation, and urinary retention.
- Use with caution in patients with cardiovascular disease, especially coronary artery disease, as tachycardia may increase myocardial oxygen demand.
- Avoid in hot environments or during strenuous exercise because reduced sweating can precipitate heat stroke.
- Use with caution in children, who are more susceptible to atropine toxicity including excitement and hallucinations.
- Use with caution in pregnancy and during lactation; atropine crosses the placenta and appears in breast milk.
- Use with caution in severe hepatic impairment as atropine is metabolised in the liver.
- Dry mouth
- Blurred vision
- Tachycardiaserious
- Constipation
- Urinary retentionserious
- Confusion and agitation in the elderlyserious
- eGFR 0–30: Use with caution; consider dose reduction due to reduced clearance.
- Hepatic impairment (severe): Use with caution; consider dose reduction due to reduced metabolism.
- Heart rate · After administration
- Blood pressure · After administration
- ECG · Baseline and during therapy
- Signs of anticholinergic toxicity (dry mouth, blurred vision, urinary retention, confusion) · Regularly during therapy
- Pregnancy: Atropine should be used during pregnancy only if clearly needed, as it crosses the placenta and may cause fetal tachycardia and anticholinergic effects. Consider alternative antimuscarinics if available.
- Toxicity: Anticholinergic syndrome: dry mouth, dilated pupils, blurred vision, tachycardia, urinary retention, confusion, hallucinations, seizures, hyperthermia. · Supportive care: airway management, cooling, cardiovascular support. In severe cases, physostigmine may be used cautiously under specialist supervision.
- Toxicity: CNS excitation: agitation, delirium, seizures. · Benzodiazepines for agitation or seizures. Avoid phenothiazines.
- Toxicity: Hyperthermia from impaired sweating. · Active cooling; avoid anticholinergic drugs.
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BNF; local formulary