Chemical weapons: Difference between revisions
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==Background== | |||
*Can be released via unintended means such as a spill from a damaged railroad tank car or industrial explosion as well as by intentional means as chemical weapons. | |||
== | ===Pediatric considerations=== | ||
*Higher metabolic rate and faster basal respiratory rate, causing more rapid and larger exposures | |||
*Skin is thinner and more permeable | |||
*Agents heavier than air have increased concentrations closer to the ground exposing children > adults | |||
* | |||
* | |||
* | |||
==Types== | |||
{{Chemical weapon DDX}} | |||
== Cyanide Agents (CN) | ==[[Cyanide]] Agents (CN)== | ||
*AKA Hydrocyanic acid, Formonitrile, Prussic acid | *AKA Hydrocyanic acid, Formonitrile, Prussic acid | ||
*Mimics carbon monoxide poisoning | *Mimics carbon monoxide poisoning | ||
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*Can penetrate rubber and barrier fabrics | *Can penetrate rubber and barrier fabrics | ||
=== Pathophysiology === | ===Pathophysiology=== | ||
*Cyanide inhibits cytochrome oxidase on mitochondria | *Cyanide inhibits cytochrome oxidase on mitochondria | ||
*Cells unable to use oxygen in bloodstream | *Cells unable to use oxygen in bloodstream | ||
*Cellular asphyxiation | *Cellular asphyxiation | ||
=== Symptoms === | ===Symptoms=== | ||
*Symptoms can be delayed up to 60 minutes | *Symptoms can be delayed up to 60 minutes | ||
*Symptoms dependent on concentration, form of cyanide, and route of exposure | *Symptoms dependent on concentration, form of cyanide, and route of exposure | ||
Line 121: | Line 30: | ||
*Anxiety, dizziness, headache, apnea, seizures, and coma | *Anxiety, dizziness, headache, apnea, seizures, and coma | ||
=== | ===Management=== | ||
*100% oxygen and antidote therapy | *100% oxygen and antidote therapy | ||
*Sodium nitrite (IV) or amyl nitrite (inhaled) to displace cyanide from cytochrome oxidase | *Sodium nitrite (IV) or amyl nitrite (inhaled) to displace cyanide from cytochrome oxidase | ||
*Sodium thiosulfate: For conversion of cyanide to excretable thiosulfate | *Sodium thiosulfate: For conversion of cyanide to excretable thiosulfate | ||
*Repeat sodium nitrite and sodium thiosulfate in 30min at half initial dose if needed | *Repeat sodium nitrite and sodium thiosulfate in 30min at half initial dose if needed | ||
*Hydroxocobalamin (Vit B12a): makes CN water soluble and non-toxic | *[[Hydroxocobalamin]] (Vit B12a): makes CN water soluble and non-toxic | ||
*Cyanide Antidote Kit: Amyl nitrite pearls, sodium nitrite (IV), sodium thiosulfate (IV) | *Cyanide Antidote Kit: Amyl nitrite pearls, sodium nitrite (IV), sodium thiosulfate (IV) | ||
*Cyanokit: Less toxic than cyanide antidote kit and shown effective in cardiac arrest | *Cyanokit: Less toxic than cyanide antidote kit and shown effective in cardiac arrest | ||
==[[Nerve Agents]]== | |||
== Nerve Agents == | |||
*Acetylcholinesterase inhibitors | *Acetylcholinesterase inhibitors | ||
*Includes household and commercial pesticides (diazinon and parathion) | *Includes household and commercial pesticides (diazinon and parathion) | ||
*G-series (sarin, tabun, soman) and V-series (VX) | *G-series (sarin, tabun, soman) and V-series (VX) | ||
*Rapidly absorbed through skin | **G-series are volatile non-persistent agents that evaporate quickly | ||
**V-series high viscosity with oily consistency | |||
*Rapidly absorbed through skin, symptoms generally develop within 1 hour | |||
*Vapors are heavier than air and tend to sink into low places | *Vapors are heavier than air and tend to sink into low places | ||
*Sarin used in Tokyo subway attack in 1995; 5,000 sought medical attention with 12 deaths. | *Sarin used in Tokyo subway attack in 1995; 5,000 sought medical attention with 12 deaths. | ||
=== Pathophysiology === | ===Pathophysiology=== | ||
* | *Inhibits acetylcholinesterase → excess acetylcholine at both nicotinic and muscarinic receptors | ||
=== Symptoms === | ===Symptoms=== | ||
*DUMBELLS | *DUMBELLS | ||
**D-Diarrhea, U-Urination, M-Miosis, B-Bronchorrhea/Bradycardia, E-Emesis, L-Lacrimation, S-Salivation/Seizures | **D-Diarrhea, U-Urination, M-Miosis, B-Bronchorrhea/Bradycardia, E-Emesis, L-Lacrimation, S-Salivation/Seizures | ||
*Cholinergic toxidrome [[Toxidromes]] | *Cholinergic toxidrome [[Toxidromes]] | ||
=== | ===Management=== | ||
*Nerve agents prolong succinylcholine's paralytic effect | *Nerve agents prolong succinylcholine's paralytic effect | ||
*Atropine for bronchorrhea and bronchoconstriction, no max dose | *Atropine for bronchorrhea and bronchoconstriction | ||
*Pralidoxime to restore function of acetylcholinesterase (given over | **Start at 2-6mg, double the dose q5-30min until control of secretions (no max dose) | ||
*Pralidoxime to restore function of acetylcholinesterase (given over approximately 30 minutes; rapid infusion can cause hypertension) | |||
**Give as soon as possible - must be given before "aging" occurs to be effective | |||
*Benzodiazepines for seizures (standard AEDs may be ineffective) | *Benzodiazepines for seizures (standard AEDs may be ineffective) | ||
*Mark 1 Nerve Agent antidote Kit (NAAK): 2 autoinjectors: | *Mark 1 Nerve Agent antidote Kit (NAAK): 2 autoinjectors: | ||
Line 159: | Line 68: | ||
**600mg pralidoxime | **600mg pralidoxime | ||
*DuoDote Autoinjector: 2.1mg atropine, 600mg pralidoxime in one autoinjector | *DuoDote Autoinjector: 2.1mg atropine, 600mg pralidoxime in one autoinjector | ||
*Prophylaxis in the military, high risk setting with [[pyridostigmine]] | |||
**Reversibly bind acetylcholinesterase before exposure to nerve agents | |||
**[[Pyridostigmine]] 30 mg PO q8<ref>Dunn MA, Sidell FR. Progress in medical defense against nerve agents. JAMA. 1989;262:649–652.</ref> | |||
==Differential Diagnosis== | |||
{{MCI types}} | |||
{{Toxic gas exposure DDX}} | |||
== | ==Management== | ||
* | *Depends on specific agent used | ||
* | *Regardless of agent, Decontamination and ABCs are of primary importance | ||
* | **Use appropriate personal protective equipment (PPE) | ||
**Decontamination (should take place pre-hospital or otherwise prior to entering the ED) | |||
***Remove all patient clothing | |||
* | ***Brush off dry agent (e.g. powders), copiously irrigate skin of any liquid contaminant | ||
* | |||
==See Also== | |||
*[[Toxicology (Main)]] | |||
*[[Weapon of mass destruction]] | |||
*[[Hazmat exposure]] | |||
== References == | ==References== | ||
<references/> | |||
[[Category: | [[Category:Toxicology]] | ||
[[Category:EMS]] |
Latest revision as of 20:34, 8 November 2023
Background
- Can be released via unintended means such as a spill from a damaged railroad tank car or industrial explosion as well as by intentional means as chemical weapons.
Pediatric considerations
- Higher metabolic rate and faster basal respiratory rate, causing more rapid and larger exposures
- Skin is thinner and more permeable
- Agents heavier than air have increased concentrations closer to the ground exposing children > adults
Types
Chemical weapons
- Blister chemical agents (Vesicants)
- Lewisite (L)
- Sulfur mustard (H)
- Phosgene oxime (CX)
- Pulmonary chemical agents (Choking agents)
- Incendiary agents
- Cyanide chemical weapon agents (Blood agents)
- Prussic acid (AKA hydrogen cyanide, hydrocyanic acid, or formonitrile)
- Nerve Agents (organophosphates)
- Acetylcholinesterase inhibitors
- Household and commercial pesticides (diazinon and parathion)
- G-series (sarin, tabun, soman)
- V-series (VX)
- Lacrimating or riot-control agents
- Pepper spray
- Chloroacetophenone
- CS
Cyanide Agents (CN)
- AKA Hydrocyanic acid, Formonitrile, Prussic acid
- Mimics carbon monoxide poisoning
- Smell of bitter almonds but not all people can smell cyanide
- Absorbed through skin, inhaled or ingested
- Can affect individuals near fire with synthetic materials or plastics
- Can penetrate rubber and barrier fabrics
Pathophysiology
- Cyanide inhibits cytochrome oxidase on mitochondria
- Cells unable to use oxygen in bloodstream
- Cellular asphyxiation
Symptoms
- Symptoms can be delayed up to 60 minutes
- Symptoms dependent on concentration, form of cyanide, and route of exposure
- CNS and cardiovascular system most susceptible
- Initially hypertension and tachycardia progressing to bradycardia, hypotension, and arrhythmias late
- Anxiety, dizziness, headache, apnea, seizures, and coma
Management
- 100% oxygen and antidote therapy
- Sodium nitrite (IV) or amyl nitrite (inhaled) to displace cyanide from cytochrome oxidase
- Sodium thiosulfate: For conversion of cyanide to excretable thiosulfate
- Repeat sodium nitrite and sodium thiosulfate in 30min at half initial dose if needed
- Hydroxocobalamin (Vit B12a): makes CN water soluble and non-toxic
- Cyanide Antidote Kit: Amyl nitrite pearls, sodium nitrite (IV), sodium thiosulfate (IV)
- Cyanokit: Less toxic than cyanide antidote kit and shown effective in cardiac arrest
Nerve Agents
- Acetylcholinesterase inhibitors
- Includes household and commercial pesticides (diazinon and parathion)
- G-series (sarin, tabun, soman) and V-series (VX)
- G-series are volatile non-persistent agents that evaporate quickly
- V-series high viscosity with oily consistency
- Rapidly absorbed through skin, symptoms generally develop within 1 hour
- Vapors are heavier than air and tend to sink into low places
- Sarin used in Tokyo subway attack in 1995; 5,000 sought medical attention with 12 deaths.
Pathophysiology
- Inhibits acetylcholinesterase → excess acetylcholine at both nicotinic and muscarinic receptors
Symptoms
- DUMBELLS
- D-Diarrhea, U-Urination, M-Miosis, B-Bronchorrhea/Bradycardia, E-Emesis, L-Lacrimation, S-Salivation/Seizures
- Cholinergic toxidrome Toxidromes
Management
- Nerve agents prolong succinylcholine's paralytic effect
- Atropine for bronchorrhea and bronchoconstriction
- Start at 2-6mg, double the dose q5-30min until control of secretions (no max dose)
- Pralidoxime to restore function of acetylcholinesterase (given over approximately 30 minutes; rapid infusion can cause hypertension)
- Give as soon as possible - must be given before "aging" occurs to be effective
- Benzodiazepines for seizures (standard AEDs may be ineffective)
- Mark 1 Nerve Agent antidote Kit (NAAK): 2 autoinjectors:
- 2mg atropine
- 600mg pralidoxime
- DuoDote Autoinjector: 2.1mg atropine, 600mg pralidoxime in one autoinjector
- Prophylaxis in the military, high risk setting with pyridostigmine
- Reversibly bind acetylcholinesterase before exposure to nerve agents
- Pyridostigmine 30 mg PO q8[1]
Differential Diagnosis
Mass casualty incident
- Radiation exposure (disaster)
- Dirty bomb
- Bioterrorism
- Chemical weapons
- Mass shooting
- Natural Disaster (e.g. Hurricane, Earthquake, Tornado, Tsunami, etc)
- Unintentional large-scale incident (e.g. building collapse, train derailment, etc)
- Major pandemic
- Explosions
Toxic gas exposure
- Carbon monoxide toxicity
- Chemical weapons
- Cyanide toxicity
- Hydrocarbon toxicity
- Hydrogen sulfide toxicity
- Inhalant abuse
- Methane toxicity
- Smoke inhalation injury
- Ethylene dibromide toxicity
Management
- Depends on specific agent used
- Regardless of agent, Decontamination and ABCs are of primary importance
- Use appropriate personal protective equipment (PPE)
- Decontamination (should take place pre-hospital or otherwise prior to entering the ED)
- Remove all patient clothing
- Brush off dry agent (e.g. powders), copiously irrigate skin of any liquid contaminant
See Also
References
- ↑ Dunn MA, Sidell FR. Progress in medical defense against nerve agents. JAMA. 1989;262:649–652.