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        ©2014 Baishideng Publishing Group Co.
    
    
        World J Crit Care Med. Feb 4, 2014; 3(1): 15-23
Published online Feb 4, 2014. doi: 10.5492/wjccm.v3.i1.15
Published online Feb 4, 2014. doi: 10.5492/wjccm.v3.i1.15
            Table 1 Pediatric specific vulnerabilities to terrorist attacks
        
    | Vulnerability | Blast Injury | Biological agents | Chemical agents | 
| Proximity to ground | Agents settle to the ground | Agents tend to pool in lower areas | |
| Increased minute ventilation | Increased exposure to inhaled agents | Increased exposure to inhaled agents | |
| Provider unfamiliarity with pediatric dosing of medications | Dosing of antibiotics different | No prepackaged store of antidotes in pediatric doses | |
| Lack of knowledge or inability to flee danger | Either unaware or unable to flee from explosion Potentially curious about ordinance | Unlikely to recognize signs/symptoms of biologic agents | Would not know to flee from strange odor or seek medical help with symptoms | 
| Lack of stockpile of pediatric dosed antidotes and vaccines | Prepackaged stockpiles of vaccines and antidotes not dosed for small children[32] | Lack of guidelines for dosing of antidotes in children | |
| Less blood volume/physiologic reserve | More rapidly develop life threatening blood loss | Prone to dehydration with illness. Lower functional residual capacity | More prone to respiratory distress/failure with nerve agents, vesicants, and pulmonary agents | 
| Thinner skin | Faster absorbtion of agents | ||
| Increased BSA to mass ratio | Prone to hypothermia during triage, evacuation and treatment | Prone to hypothermia with decontamination | |
| Developmental immaturity | Unable to follow mental status exam/communicate other injuries early | Present later in the course of biologic agents | Unable to promptly communicate symptoms | 
| Increased head size compared to body | Increased head AIS when compared to adults[2] | 
            Table 2 Management of chemical agents
        
    | Agent | Pediatric dosing | Notes | 
| Nerve agents | Atropine 0.05 mg/kg iv or im q 2-5 min (max 5 mg) Pralidoxime 25 mg/kg iv or im q 1 h (max 1 g iv or 2 g im) Benzodiazepines: Midazolam im 0.2 mg/kg (max 10 mg) (1st choice) Lorazepam iv/im 0.1 mg/kg (max 4 mg) Diazepam iv 0.3 mg/kg (max 10 mg) | Atropine should be repeated for persistent symptoms | 
| Cyanide | Hydroxocobalamin 70 mg/kg (max 5 g) or sodium nitrate; 0.33mL/kg iv (max 10 mL) followed by sodium thiosulfate (25%) 1.65 mL/kg iv (max 50 mL) | Hydroxocobalamin may be repeated × 1 if needed | 
            Table 3 Guidelines for the use of Mark I kits in pediatric patients
        
    | Pediatric patients | Mark I kits | 
| 3-7 yr (approximately 13-25 kg) | One Mark I kit as maximum dose | 
| 8-14 yr (approximately 26-50 kg) | Two Mark I kits as maximum dose | 
| > 14 yr (approximately > 51 kg) | Three Mark I kits as maximum dose | 
            Table 4 Management of biologic agents
        
    | Agent | Pediatric dosing | Notes | 
| Inhalational anthrax | Ciprofloxacin 10-15 mg/kg iv q 12 h (max 400 mg) or doxycycline 2.2 mg/kg iv q 12 h (max 100 mg) plus clindamycin 10-15 mg/kg q 8 plus penicillin G 400-600 k U/kg per day iv divided q 4 h prophylaxis for exposed contacts ciprofloxacin 15 mg/kg po q 12 h or doxycycline 2.2 mg/kg po q 12 h | Switch to oral therapy when patient shows signs of improvement At least one agent should have good CNS penetration Prophylaxis is for a 60 d course Amoxicillin or levofloxacin are second line | 
| Plague | Gentamycin 2.5 mg/kg iv q 8 h or streptomycin 15 mg/kg im q 12 h (max 2 mg/d) or doxycycline 2.2 mg/kg iv q 12 h (max 200 mg/d) or ciprofloxacin 15 mg/kg iv q 12 h prophylaxis for exposed contacts trimethoprim/sulfa 4 mg/kg po q 12 h | Chloramphenical or Levofloxacin can also be used Prophylaxis should be continued for 5-7 d | 
| Tularemia | Same as therapy for plague | |
| Botulism | Infants < 1 yr human-derived botulinum immunoglobulin children > 1 yr equine serum botulism antitoxin | In United States call 1-800-222-1222 or 770-488-7100 Outside United States contact local health agencies | 
            Table 5 Viral hemorrhagic fever, virus and disease
        
    | Family | Virus | Disease | 
| Arenaviruses | Lassa virus | Lassa fever | 
| Junin | Argentine hemorrhagic fever | |
| Machupo | Bolivian hemorrhagic fever | |
| Bunyaviruses | CCHF | Cremiean-Congo hemorrhagic fever | 
| RVF | Rift Valley fever | |
| Hantavirus | Hemorrhagic fever with renal syndrome | |
| Filoviruses | Ebola virus | Ebola hemorrhagic fever | 
| Marburg virus | Marburg hemorrhagic fever | |
| Flavivirus | Yellow fever virus | Yellow fever | 
| KFD virus | KFD | |
| OHF virus | Omsk hemorrhagic fever | |
| DENV 1-4 viruses | Dengue hemorrhagic fever | |
| Rhabdovirus | Bas-Congo virus | Bas-Congo hemorrhagic fever | 
- Citation: Hamele M, Poss WB, Sweney J. Disaster preparedness, pediatric considerations in primary blast injury, chemical, and biological terrorism. World J Crit Care Med 2014; 3(1): 15-23
 - URL: https://www.wjgnet.com/2220-3141/full/v3/i1/15.htm
 - DOI: https://dx.doi.org/10.5492/wjccm.v3.i1.15
 
