Template:Cholinergic Toxicity Treatment: Difference between revisions
(Add MedicationDose templates for atropine and pralidoxime in cholinergic toxicity) |
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*'''Must give atropine BEFORE pralidoxime''' to prevent worsening of muscarinic symptoms | *'''Must give atropine BEFORE pralidoxime''' to prevent worsening of muscarinic symptoms | ||
*'''Must be given before aging occurs''' (see [[#Aging and Oxime Window|aging table above]]) | *'''Must be given before aging occurs''' (see [[#Aging and Oxime Window|aging table above]]) | ||
* | *{{MedicationDose|drug=Pralidoxime|dose=1-2 g IV over 15-30 min, then 8-10 mg/kg/hr infusion (or repeat bolus in 1 hr)|route=IV|context=Cholinergic toxicity (oxime reactivator)|indication={{PAGENAME}}|population=Adult}} | ||
*Pediatric: {{MedicationDose|drug=Pralidoxime|dose=20-50 mg/kg IV, then 5-10 mg/kg/hr infusion|route=IV|context=Cholinergic toxicity (oxime reactivator)|indication={{PAGENAME}}|population=Pediatric}} | *Pediatric: {{MedicationDose|drug=Pralidoxime|dose=20-50 mg/kg IV, then 5-10 mg/kg/hr infusion|route=IV|context=Cholinergic toxicity (oxime reactivator)|indication={{PAGENAME}}|population=Pediatric}} | ||
*Continue until clinical improvement or patient is off ventilator | *Continue until clinical improvement or patient is off ventilator | ||
Revision as of 22:39, 20 March 2026
Decontamination
- Providers should wear appropriate PPE during decontamination.
- Neoprene or nitrile gloves and gown (latex and vinyl are ineffective)
- Dispose of all clothes in biohazard container
- Wash patient with soap and water
Supportive Care
- IVF, O2, Monitor
- Aggressive airway management is of utmost importance.
- Intubation often needed due to significant respiratory secretions / bronchospasm.
- Use nondepolarizing agent (Rocuronium or Vecuronium)
- Succinylcholine is absolutely contraindicated
- Benzodiazepines for seizures
Antidotes
- Dosing with atropine and pralidoxime are time dependent and provides ability to reverse symptoms while awaiting agent metabolism
- For exposure to nerve agents, manufactured IM autoinjectors are available for rapid administration:
- Mark 1
- Contains 2 separate cartridges: atropine 2 mg + 2-PAM 600 mg
- Being phased out with newer kits
- DuoDote
- Single autoinjector containing both medications
- Same doses as Mark 1: atropine 2 mg + 2-PAM 600 mg
- Mark 1
Antidotes
Atropine
- First-line antidote — muscarinic antagonist; treats bronchorrhea, bronchospasm, bradycardia, and secretions[1]
- Does NOT reverse nicotinic symptoms (weakness, fasciculations, paralysis)
- Starting dose: Atropine 1-2 mg IV (double q5min until atropinization) IV — May need 100+ mg in first 24h; endpoint is drying of secretions
- Pediatric: Atropine 0.02-0.05 mg/kg IV (min 0.1 mg), double q5min IV
- Doubling protocol: If inadequate response after 5 minutes, double the dose (1 → 2 → 4 → 8 → 16 mg...) until atropinization is achieved[1]
- Massive doses may be required — total doses of 100+ mg in the first 24 hours have been reported[2]
- Endpoints of adequate atropinization (goal of therapy):
- Drying of bronchial secretions (most important endpoint)
- Heart rate >80 bpm
- Systolic BP >80 mmHg
- Do NOT target: Fully dilated pupils, absent bowel sounds, or HR >150 — these indicate atropine toxicity[3]
- After initial atropinization: Consider atropine infusion (10-20% of loading dose per hour) to maintain effect
- Optimize oxygenation before giving atropine to reduce risk of dysrhythmias (though in resource-limited settings, do not withhold atropine waiting for oxygen)[2]
Pralidoxime
- AKA 2-PAM
- Oxime that reactivates phosphorylated AChE → primarily reverses nicotinic symptoms (weakness, fasciculations, respiratory muscle paralysis)[4]
- Must give atropine BEFORE pralidoxime to prevent worsening of muscarinic symptoms
- Must be given before aging occurs (see aging table above)
- Pralidoxime 1-2 g IV over 15-30 min, then 8-10 mg/kg/hr infusion (or repeat bolus in 1 hr) IV
- Pediatric: Pralidoxime 20-50 mg/kg IV, then 5-10 mg/kg/hr infusion IV
- Continue until clinical improvement or patient is off ventilator
- Controversies:
- Evidence for benefit of pralidoxime is inconsistent; several meta-analyses have not shown clear mortality benefit when added to atropine[5]
- However, per AHA 2023 guidelines and expert consensus, oximes should still be given for significant OP poisoning, particularly when fasciculations, weakness, or paralysis are present[1]
- Efficacy depends on timing (before aging), dose, and the specific OP compound involved
- Caution: Administer slowly — rapid IV push can cause hypertensive crisis, cardiac arrest
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