Chemical Warfare:
Don Daniels, M.D. Chief Anesthesiologist Brooke Army Medical Center Fort Sam Houston, Texas
Anesthesia for Casualties of Nerve Agents
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Anesthesia for Casualties of Nerve Agent:
Objectives
Discuss problems posed to military Anesthesiologist and CRNAs by casualties exposed to nerve agents who require anesthesia intervention Discuss management of patients undergoing anesthesia who received pyridostigmine prophylaxis Discuss interaction with agricultural insecticide and anesthesia
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents
Alleged Uses of Chemical Warfare
Egypt
in South Yemen 1963-68 Vietnam in Laos 1975-78 Ethiopia against Eritrean & Somalia backed rebels 1976 Vietnam in Cambodia 1978 China & Vietnam 1979 Iraq against Iran 1984-88 Iraq against Kurds 1988
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents
Terriorist Attacks
1995
Tokyo subway attack (Sarin)
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents
GA: GB: GD: GF: VX
Tabun Sarin Soman no common name
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Lessons Learned from Iran-Iraq War
Troops with organophosphate exposure fell into 4 groups
1. Greatest exposure died in the field 2. Severely injured who reached medical aid were unconscious and in respiratory arrest 3. Seriously intoxicated had dizziness, disorientation, anxiety, salivation and respiratory difficulty 4. Patients with mild symptoms were physically difficult to manage due to disorientation
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Lessons Learned from Iran-Iraq War
Largest number of casualties required no treatment other than decontamination Comatose casualties of nerve agents who did not have cardiovascular problems were treated with large doses of atropine, 50 200 mg IV. Most received 2 mg q 8 hrs Comatose casualties with significant cardiovascular deterioration (such as bradycardia after 2 mg atropine) were most often found not to survive
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents
Mechanism of Action:
Organophosphorous compounds Inhibit acetylcholinesterase Accumulation of acetylcholine leads to CNS stimulation then depression, finally paralysis
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Clinical Effects
Exposure to either liquid or vapor nerve agent can cause
Muscarinic
- increase in secretions from the nose, eyes, mouth, airways and intestines. Bradycardia Nicotinic - muscle fasciculations, twitching, weakness and paralysis. Tachycardia CNS - generalized seizures
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Clinical Effects
Nerve agents are liquids, skin entry
small droplet effects onset 18 hr large exposure onset 1-30 min
At high temps or aerosolized by explosion, they may be inhaled
Small vapor exposure onset seconds - miosis, rhinorrhea, ocular pain, conjunctivitis, visual changes, bronchoconstriction & bronchial secretions Large exposure- unconsciousness in seconds, convulsions, paralysis and apnea in minutes
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Treatment
Decon - Hypochlorite or soap & water Atropine: blocks the action of excess acetylcholine at muscarinic sites 2 mg mild, 6 mg severe q 5 min until secretions minimal 15-20 mg if necessary Miosis may persist Pralidoxime Chloride - releases the inhibiting agent from acetylcholinesterase. Acts at the nicotinic site to normalize skeletal muscle activity I gram over 20 min, then q 1 hr max 3 gram Anticonvulsants: 5 - 10 mg diazepam
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Pretreatment
Pyridostigmine
Essential when GA or GD is considered imminent Reversible cholinesterase inhibitor, it binds 2030% cholinesterase so that it cannot be irreversibly inactivated by nerve agent. The bound cholinesterase is returned to normal activity after 12 hrs Alone will not entirely protect soldier from lethal effects of nerve agents 30 mg po q 8 hrs.
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Pretreatment
Pyridostigmine Side Effects Muscarinic - gastrointestinal hypermotility, cramping, nausea, vomiting, diarrhea, salivation, lacrimination, urination, sweating, increased tracheobronchial secretions, bronchoconstriction, miosis, bradycardia and atrioventricular conduction slowing Nicotinic - muscle cramps, fasciculations and weakness
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Preoperative Assessment and Examination
History of toxic exposure Type of agent, route of contamination, when and proximity Pretreatment with pyridostigmine and treatment with antimuscarinics and oximes Examination Respiratory Cardiovascular Nervous system Laboratory
Dibucaine number
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Preoperative Preparation
Cimetidine has no interactions with Pyridostigmine Diphenhydramine has antinicotinic activity and reverses organophosphate induced neuromuscular blockade Hydroxyzine does not have antinicotinic actions Promethazine anticholinergic effects should be offset by the pyridostigmine muscarinic effects. However, should use cautiously in combination with succinycholine and organophosphorous compounds Glycopyrrolate - may require larger doses to decrease oral secretions, protect against larygngeal
mediated vagal reflexes and bradyarrhytmias
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Anesthetic Induction
Thiopental can provoke asthma and pyridostigmine through its muscarinic activity may aggravate even more Ketamine will antagonize muscarinic effects
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Anesthetic Maintenance
Nondepolarizing blocking agents will be antagonized. Minimal clinical experience. Depolarizing blocking agent may be prolonged.
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Anesthesia for Casualties of Nerve Agents: Anesthetic Maintenance & Opioids
Morphine vasodilation may be accentuated in presence of pyridostigmine Meperidine tachycardia may counteract some bradycardia Fentanyl bradycardia can be treated with antimuscarinic
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Anesthesia for Casualties of Nerve Agents: Anesthetic Maintenance & Inhaled Agents
Halogenated anesthetics potentially beneficial effects in nerve injured patients
Bronchodilation Skeletal muscle relaxation
Nitrous oxide has no reported interactions with pyridostigmine
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Chemical Warfare: Anesthesia for Casualties of Nerve Agents: Postoperative Complications
Ventilatory
2
support will be required if all acetylcholinesterase is removed
- 3 hours with nerve agent Days with insecticide poisoning
High
peak pressures (50-70 cm H2O) due to bronchoconstriction
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Anesthesia for Casualties of Nerve Agents: Persian Gulf Experience
# casualties to allied forces low No nerve agent casualties 3 casualties anesthetized after pyridostigmine Ketamine, midazolam, vecuronium No extension of succinylcholine Possible increased vecuronium usage
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Anesthesia for Casualties of Nerve Agents: Conclusions
Be prepared to deliver anesthesia to patient exposed to nerve agents Be aware of prior treatment received and its potential to affect patients physiology or influence anesthetic care Be prepared for post operative ventilation Remember Anesthesia experience is virtually nonexistent Document experience in literature for others to use
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QUESTIONS?
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