Atropine Intramuscular Dosing
For adults, administer atropine 0.4 to 0.6 mg IM every 4 to 6 hours for standard antimuscarinic indications, with context-specific dosing ranging from 1 mg IM for gastrointestinal radiography to 2-5 mg IM for organophosphate poisoning. 1
Adult IM Dosing by Indication
Standard Antimuscarinic Use
- Dose: 400 to 600 mcg (0.4 to 0.6 mg) IM every 4 to 6 hours 1
- This represents the FDA-approved baseline dosing for routine antimuscarinic effects 1
Preanesthesia (Antisialagogue)
- Dose: 200 to 600 mcg (0.2 to 0.6 mg) IM administered 30 to 60 minutes before surgery 1
- Timing is critical—administration 15 minutes before entering the operating room optimizes effect while minimizing excessive sedation when combined with other agents 2
Gastrointestinal Radiography
- Dose: 1 mg IM 1
Organophosphate/Nerve Agent Poisoning
- Initial dose: 2 to 5 mg IM, repeated every 20 to 30 minutes until muscarinic symptoms resolve 3, 4, 1
- Escalation: Double the dose with each administration if inadequate response 3
- No arbitrary maximum: Cumulative doses may reach 10-20 mg in the first 2-3 hours, with total 24-hour doses up to 50 mg or more 3
- Endpoints of adequate atropinization: Clear chest on auscultation, heart rate >80/min, systolic BP >80 mmHg, drying of secretions, and resolution of miosis 3, 4
Critical pitfall: In organophosphate poisoning, underdosing is more dangerous than overdosing—aggressive titration is essential and standard cardiac dose limits do not apply 3
Muscarine Poisoning (Mushrooms)
- Dose: 1 to 2 mg IM every hour until respiratory effects subside 1
Pediatric IM Dosing
Standard Antimuscarinic Use
- Dose: 10 mcg (0.01 mg)/kg IM, not to exceed 400 mcg (0.4 mg), or 300 mcg (0.3 mg)/m² body surface area, every 4 to 6 hours 1
Weight-Based Preanesthesia Dosing (Subcutaneous/IM)
- Up to 3 kg: 100 mcg (0.1 mg) 1
- 7 to 9 kg: 200 mcg (0.2 mg) 1
- 12 to 16 kg: 300 mcg (0.3 mg) 1
- 20 to 27 kg: 400 mcg (0.4 mg) 1
- 32 kg: 500 mcg (0.5 mg) 1
- 41 kg: 600 mcg (0.6 mg) 1
Organophosphate Poisoning (Pediatric)
- Initial dose: 0.02 to 0.05 mg/kg IV (preferred route), but can be given IM if IV access unavailable 4
- Maximum single dose: Typically 2-3 mg 4
- Repeat dosing: 0.5 to 1 mg every 5 to 10 minutes until muscarinic symptoms disappear or signs of atropine toxicity appear 1
Administration Technique & Pharmacokinetics
IM Injection Considerations
- Absorption enhancement: Automatic injector devices substantially enhance drug absorption rate compared to manual IM injection 5
- Site selection matters: Devices that deliver atropine into separate IM sites (away from pralidoxime when co-administered) produce faster absorption in the first 30 minutes 5
- Onset: IM atropine has slower onset than IV (which peaks within 3 minutes), making IV the preferred route for emergencies 3
When IM Is Appropriate
- Moderately ill victims who don't require IV access for other care 6
- Mass casualty scenarios where IM administration is faster and easier than establishing IV access 6
- Preanesthesia antisialagogue use where rapid onset is not critical 1
Critical Dosing Warnings
Paradoxical Bradycardia
- Doses below 0.5 mg can paradoxically worsen bradycardia through central vagal stimulation in adults 3
- This warning applies primarily to IV administration; IM dosing of 0.4-0.6 mg is FDA-approved but should be used cautiously in bradycardic patients 1
Pediatric Minimum Dose Controversy
- Older guidelines recommended a minimum dose of 0.1 mg to avoid paradoxical bradycardia 7
- 2015 American Heart Association guidelines eliminated this minimum dose requirement after evidence showed 0.02 mg/kg without a minimum is effective and safe 7
- For neonates specifically, use 0.01-0.03 mg/kg IV/IO without a minimum dose 7
Contraindications
- Heart transplant recipients: Atropine is contraindicated for treating bradycardia in denervated hearts without autonomic re-innervation 3
Monitoring Parameters
- Continuous ECG monitoring during administration for cardiac indications 3
- Heart rate, blood pressure, pupil size (resolution of miosis indicates adequate dosing in poisoning) 3, 4
- Respiratory status and secretion clearance in organophosphate poisoning 3
- Signs of excessive dosing: tachycardia >120/min, anticholinergic toxicity (fever, delirium, urinary retention, dry flushed skin) 3
Practical Considerations for Mass Casualty Preparedness
- Stock augmentation: Existing 0.4 mg/mL or 1 mg/mL atropine can be fortified with pharmaceutical-grade atropine powder to 2 mg/mL concentration, facilitating IM administration of larger doses 6
- Stability: Compounded high-concentration atropine maintains potency for 8 weeks refrigerated or 4 weeks at room temperature 6
- Compounding time: Approximately 1 hour to prepare fortified stocks once materials are available 6