Anthrax: Difference between revisions

(anthrax)
(anthrax)
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*Transient clinical improvement followed by rapid decline
*Transient clinical improvement followed by rapid decline
====Acute phase====
====Acute phase====
*Severe respiratory distress with symptoms consisting of:
*Severe respiratory distress with symptoms consisting of<ref>[http://emedicine.medscape.com/article/212127-overview Medscape: Anthrax]</ref>:
**Hypoxia, tachypnea, cyanosis
**Hypoxia, tachypnea, cyanosis
**Severe dyspnea, chest pain
**Severe dyspnea, chest pain

Revision as of 14:53, 15 February 2016

Background

  • Gram positive rod, Bacillus anthracis, which is capable of surviving inhospitable condition through the formation of endospores. tough spores
  • Incubation period is 10 days with no ability for human to human transmission and therefore, no need for respiratory isolation
  • In general there is cutaneous, inhalational, and gastrointesinal anthrax.

Inhalational (5%)

  • Biphasic course

Prodrome Period

  • Early prodromal period often appears as an influenza like illness
  • Fever, dry cough, mylagia, malaise
  • Transient clinical improvement followed by rapid decline

Acute phase

  • Severe respiratory distress with symptoms consisting of[1]:
    • Hypoxia, tachypnea, cyanosis
    • Severe dyspnea, chest pain
    • Shock
    • Mediasitinits

Cutaneous (95%)

Cutaneous anthrax
  • The disease will start as an area of errythema and edema and progress to a vesicle which ruptures forming a central black eschar
  • Total course of lesion evolution occurs over 1 week

Gastrointestinal

  • Over the course of 7 days, nonspecific abdominal pain, nausea and vomitting with progress to severe abdominal pain, bloody emesis and diarrhea (usually bloody)[2]

Differential Diagnosis

Cutaneous (painless)

Inhalational

Lower Respiratory Zoonotic Infections


Bioterrorism Agents[3]

Category A


Category B

  • Ricin
  • Brucellosis
  • Epsilon toxin
  • Psittacosis
  • Q Fever
  • Staph enterotoxin B
  • Typhus
  • Glanders
  • Melioidosis
  • Food safety threats
  • Water safety threats
  • Viral encephalitis


Category C

Diagnosis

CXR/CT- Widened mediastinum representing hemorrhagic mediastinitis

Treatment

Contact CDC Emergency Hotline 1-707-488-7100 for all suspected bioterrorism cases

Postexposure Prophylaxis

Patient should be vaccinated at day #0, #14, #28

Cutaneous Anthrax (not systemically ill)

Inhalation or Cutaneous with systemic illness

Pediatric Postexposure Prophylaxis

Pediatric Cutaneous Anthrax (not ill)

  • Same as pediatric postexposure dosing and duration

Pediatric Inhalational or Cutaneous (systemically ill)

  • Ciprofloxacin 15mg/kg IV q12hrs OR
  • Doxycycline 2.2mg/kg IV q12hrs PLUS
  • Imipenem/Cilastatin 1g IV q6h for at least 2wk
  • Imipenem/Cilastatin Neonates >32 wk gestation; 40-75 mg/kg/day IV divided q8-12h for at least 2wk; 1 month and older; 100 mg/kg/day IV divided q6h for at least 2wk
  • Rifampin 600 mg IV q12h for at least 2 wk as part of a multi-drug regimen; Switch to PO abx x60 days total if inhalational exposure
  • Rifampin Neonates >32 wk gestation; 10-20 mg/kg/day IV divided q12-24h for at least 2 wk as part of multi-drug regimen; 1+ mo; 20 mg/kg/day IV divided q12h for at least 2 wk as part of multi-drug regimen; Max: 300 mg/dose
  • Imipenem/Cilastatin 1g IV q6h for at least 2wk
  • Imipenem/Cilastatin Neonates >32 wk gestation; 40-75 mg/kg/day IV divided q8-12h for at least 2wk; 1 month and older; 100 mg/kg/day IV divided q6h for at least 2wk
  • Rifampin 600 mg IV q12h for at least 2 wk as part of a multi-drug regimen; Switch to PO abx x60 days total if inhalational exposure
  • Rifampin Neonates >32 wk gestation; 10-20 mg/kg/day IV divided q12-24h for at least 2 wk as part of multi-drug regimen; 1+ mo; 20 mg/kg/day IV divided q12h for at least 2 wk as part of multi-drug regimen; Max: 300 mg/dose

Disposition

  • Admit

See Also

References

  1. Medscape: Anthrax
  2. CDC. Gastrointestinal anthrax after an animal-hide drumming event - New Hampshire and Massachusetts, 2009. MMWR Morb Mortal Wkly Rep. 2010 Jul 23;59(28):872-7. http://www.ncbi.nlm.nih.gov/pubmed/20651643
  3. https://www.niaid.nih.gov/topics/biodefenserelated/biodefense/pages/cata.aspx Accessed 02/26/16