The Chemical Incident Management of Chemical Casualties DPT 8.0 Hospital Provider Management of Chemical Agent Casualties DPT 8.0 Chemical Warfare Agents Terminal Objective • Describe types of chemical warfare agents • Recognize signs and symptoms of exposure • Describe management of chemical agent attack victims DPT 8.0 Chemical Warfare Agents Historical Perspective • Chemicals used in military operations to kill, injure, or incapacitate • Battlefield use – World War I and Middle East conflicts • Terrorist use – Matsumoto and Tokyo, Japan DPT 8.0 Chemical Agent Terrorist Attacks • Matsumoto: – Approximately injured – 7 dead 280 • Tokyo – 12 dead – Approximately 1,000 hospitalized – 5,500 sought medical care – 10% of first responders injured DPT 8.0 Chemical Warfare Agents • Nerve Agents Tabun, Sarin, Soman, VX • Vesicants Mustard, Lewisite • Industrial Chemicals Phosgene, Chlorine, Ammonia, Cyanide • Riot Control Agents Mace®, Pepper Spray DPT 8.0 Nerve Agents • Tabun (GA), Sarin (GB), Soman (GD), VX • Most toxic of the chemical agents • Penetrate skin, eyes, lungs • Loss of consciousness, seizures, apnea, death after large amount • Diagnosis made clinically; confirmed in laboratory (cholinesterase) DPT 8.0 Normal Nerve Function ACh DPT 8.0 Normal Nerve Function ACh DPT 8.0 Normal Nerve Function AChE ACh DPT 8.0 How Nerve Agents Work AChE ACh GB DPT 8.0 Effects of Nerve Agents Organs with cholinergic receptors • Muscarinic – Smooth muscles – Glands • Nicotinic – Skeletal muscles – Ganglia DPT 8.0 Signs and Symptoms of Nerve Agents Muscarinic Sites • Increased secretions – Saliva – Tears – Runny nose – Secretions in airways – Secretions in gastrointestinal tract – Sweating DPT 8.0 Signs and Symptoms of Nerve Agents Muscarinic Sites • Smooth muscle contraction – Eyes: miosis – Airways: bronchoconstriction (shortness of breath) – Gastrointestinal: hyperactivity (nausea, vomiting, and diarrhea) DPT 8.0 Signs and Symptoms of Nerve Agents Nicotinic Sites • Skeletal muscles – – – – Fasciculations Twitching Weakness Flaccid paralysis ACh • Other (ganglionic) – Tachycardia – Hypertension GB DPT 8.0 Nerve Agents Other Signs and Symptoms • Cardiovascular – Tachycardia, bradycardia – Heart block, ventricular arrhythmias • Central Nervous System – Acute • Loss of consciousness • Seizures • Apnea – Prolonged (4-6 weeks) • Psychological effects DPT 8.0 Signs and Symptoms of Nerve Agents Vapor Exposure • Mild exposure – Miosis (dim vision, eye pain), rhinorrhea, dyspnea • Moderate exposure – Pronounced dyspnea, nausea, vomiting, diarrhea, weakness • Severe exposure – Immediate loss of consciousness, seizures, apnea, and flaccid paralysis • Vapor effects occur within seconds, peak within minutes; no late onset DPT 8.0 Signs and Symptoms of Nerve Agents Liquid Exposure • Mild exposure (to 18 hours) – Localized sweating – Fasciculations – No miosis • Moderate exposure (<LD50) (to 18 hours) – Gastrointestinal effects – Miosis uncommon • Severe exposure (LD50) (<30 minutes) – – – – – Sudden loss of consciousness Seizures Apnea Flaccid paralysis Death DPT 8.0 Diagnosis of Nerve Agent Exposure • Symptomatic – May be systemic or organ-specific – Combination of symptoms is more definitive • Situational – Multiple casualties with similar symptoms – Time or location factors in common DPT 8.0 Nerve Agent Treatment • Airway/ventilation – High resistance • Antidotes – Atropine – 2-PAMCl – Diazepam DPT 8.0 Nerve Agent Treatment • Atropine – Antagonizes muscarinic effects – Dries secretions; relaxes smooth muscles – Given IV, IM, ET • No effect on pupils • No effect on skeletal muscles • IV in hypoxic patient ventricular fibrillation DPT 8.0 Nerve Agent Treatment • Starting dose - 2 mg • Maximum cumulative dose - 20 mg – Total dose calculated over time; but enough must be administered to abate severe symptoms if casualty is to survive – Insecticide poisoning requires much more • Side effects in normal people – – – – Mydriasis Blurred vision Tachycardia Decreased secretions and sweating DPT 8.0 Nerve Agent Treatment • Atropine - How much to give? – Until secretions are drying or dry – Until ventilation is “easy” • If conscious or casualty is comfortable – Do not rely on heart rate/pupil size DPT 8.0 Nerve Agent Treatment • Pralidoxime Chloride (2PAM-Cl) – Remove nerve agent from AChE in absence of aging – 1 gram slowly (20-30 minutes) in IV infusion • Hypertension with rapid infusion Nerve Agent – No effects at muscarinic sites – Helps at nicotinic sites AChE 2-PAMCl DPT 8.0 Nerve Agent Treatment - Autoinjectors DPT 8.0 MARK I Injection vs. IM or IV DPT 8.0 Nerve Agent Treatment • Diazepam – Decreases seizure activity – Reduces seizureinduced brain injury – Give to severelyintoxicated casualties whether convulsing or not DPT 8.0 Nerve Agent Treatment • Treatment regimen – No signs/symptoms • Reassure • Observe – Vapor: 1 hour – Liquid: Up to 18 hours DPT 8.0 Nerve Agent Treatment • Mild vapor exposure – Miosis, rhinorrhea observation only – Increasing SOB treat • Mild liquid exposure – Localized fasiculations & sweating - treat • One MARK I kit (2 mg atropine/ 600 mg 2 PAMCl) OR • 1 gram 2-PAMCl IV • 2 mg atropine, IM or IV Parenteral atropine will not reverse miosis DPT 8.0 Nerve Agent Treatment • Moderate vapor or liquid exposure – One or two MARK I kits – Or give IV: • 2 to 4 mg atropine • 1gm 2-PAMCl (infusion) DPT 8.0 Nerve Agent Treatment • Severe - vapor or liquid – Give 3 MARK I kits or 6 mg atropine and 1 gram of 2-PAMCl as soon as possible – Airway – Ventilation/O2 – Consider diazepam 10 mg IM (2 to 5 mg IV) – Repeat atropine every 5 to10 minutes as needed – Repeat 2-PAMCl in one hour DPT 8.0 Nerve Agent Age-Related Treatment • Atropine – Infant (0 to 2) 0.5 mg IM – IV for infants and children 0.02 mg/kg – Child (2 to 10) 1.0 mg IM – Adolescent (> 10) 2.0 mg – Elderly 1.0 mg IM DPT 8.0 Nerve Agent Age-Related Treatment • 2-PAMCl – < 20 kg 15 mg/kg IV – > 20 kg 600-mg IM autoinjector – Elderly 1/2 adult dose (7.5 mg/kg IV) • 2 PAMCl-induced hypertension – Phentolamine Adult 5 mg IV Child 1 mg IV DPT 8.0 Nerve Agent Age-Related Treatment • Diazepam - Infants > 30 days old to 5 years 0.2 - 0.5 mg/kg IV q 2 to 5 min (max 5 mg) - Children > 5 years 1 mg IV q 2 to 5 min (max 10 mg) DPT 8.0 Nerve Agent Summary • Vapor exposure – Symptoms develop suddenly – Most ambulatory victims require minimal intervention – Risk of secondary contamination, which is minimized by removing the victim’s clothing – Requires immediate access to antidotes • Liquid exposure – Symptoms delayed minutes to hours – Greater need for decontamination – High risk of secondary contamination; victims require decontamination (clothing removal & washdown) – Requires immediate access to antidotes DPT 8.0 Vesicants (Blister Agents) • Vesicants - Sulfur mustard - Lewisite DPT 8.0 Mustard • Properties - Vapor & liquid threat - Latent period between exposure & effects - Systemically toxic similar to radiation DPT 8.0 Mustard Effects • Quickly cyclizes in tissue • Alkylates cell components, including DNA • DNA damage, cell death DPT 8.0 Mustard Effects Eye Injury • Mild conjunctivitis • Moderate/severe conjunctivitis, lid inflammation and edema, blepharospasm, and corneal roughening • Corneal opacification, ulceration, and/or perforation • Well over 95% had only mild to moderate conjunctivitis • Under 1% had permanent damage to cornea DPT 8.0 Mustard Effects Eye Injury DPT 8.0 Mustard Effects Skin Injury • Erythema • Small vesicles; later coalesce • Blisters/bulla • Possible coagulation necrosis with liquid DPT 8.0 Mustard Effects Airway Injury • Upper: nose sinuses, pharynx – (epistaxis, sore throat, hacking cough) • Mid: Larynx (hoarseness) • Lower: Bronchioles (dyspnea, productive cough) • Pulmonary edema is rare DPT 8.0 Mustard Effects GI Injury • Gastrointestinal – Within 24 hours • Nausea and vomiting • Cholinergic effects • After 3 to 5 days – Tissue destruction DPT 8.0 Mustard Effects Bone Marrow Damage • Damages stem cells • Decreased WBC, RBC, platelets after 3 - 5 days • Survival rare if WBC < 200 DPT 8.0 Skin Treatment • Decontamination must be done within minutes to reduce damage • Delays in decontamination will not prevent illness, but will prevent cross-contamination • Supportive care - soothing lotions, frequent irrigation, topical antibiotics, pain medication • Do NOT overhydrate; not a thermal burn DPT 8.0 Eye Treatment • Topical mydriatics • Topical antibiotics • Vaseline on lid edges • Topical steroids (only in the first 24 hrs) DPT 8.0 Airway Treatment • Cool mist, cough suppressants for mild symptoms • Oxygen • Assisted ventilation • Early intubation • Bronchodilators (steroids) • Antibiotics AFTER organism identified DPT 8.0 Lewisite Effects • Causes severe irritation to eyes, skin, and airways IMMEDIATELY on exposure (no delay) • Tissue necrosis, pseudomembranes • Increased capillary permeability • No bone marrow effects DPT 8.0 Lewisite - Treatment • Immediate decontamination • British anti-Lewisite (BAL) for systemic effects • Supportive Care – Oxygen DPT 8.0 Vesicant Agent Summary • Agents damage eyes, skin, respiratory system; cause additional systemic effects – Mustard • Fast acting; symptoms delayed, no specific antidote – Lewisite • Fast acting, symptoms immediate, BAL antidote available • Decontamination is best initial treatment DPT 8.0 Phosgene • At high concentrations: – Irritates eyes, nose, upper airways; possible laryngospasm Cl • Toxic to lungs by inhalation C=O • Carbonyl group damages alveolar-capillary membrane • Non-cardiac pulmonary edema: onset 2 to 12 hours Cl – Dyspnea, cough with sputum • Management of non-cardiac pulmonary edema – Hypoxia, fluid loss; requires pulmonary care, careful fluid replacement • ABSOLUTE REST POST-EXPOSURE DPT 8.0 Chlorine • High concentration or prolonged exposure – Pulmonary edema, sudden death • Eye irritation, cough, dyspnea • More severe airway and lung damage with high concentration • Management – Remove from exposure; manage airway • Oxygen, ventilation, PEEP • Intubation, bronchodilators DPT 8.0 Ammonia • Anhydrous Ammonia – pH>12; (household ammonia pH < 12) – Wide industrial use • Plastics, fertilizer, explosives – Irritating, corrosive; causes necrosis, severe pain – Serious injury to eyes, lungs, skin, GI tract • Management – Remove from exposure, decontaminate – Symptomatic; maintain airway DPT 8.0 Riot Control Agents • Irritating agents, lacrimators, “tear gas” • Cause reaction in – Eyes: burning, tearing, eyelid spasm, redness – Airways: burning, coughing, dyspnea – Skin: burning, erythema • Eye irrigation and supportive care DPT 8.0 Chemical Agent Summary • Vapor exposure – Nerve agent symptoms develop suddenly, mustard and phosgene symptoms are delayed – Most ambulatory victims require minimal intervention – Risk of secondary contamination – Requires airway management; antidotes for nerve agents and Lewisite DPT 8.0 Chemical Agent Summary • Liquid exposure – Symptoms delayed minutes to hours – Greater need for decontamination – Risk of secondary contamination, victims require clothing removal & decontamination – Requires immediate access to antidotes DPT 8.0