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===Treatment for Cutaneous Anthrax without Systemic Involvement===
===Treatment for Cutaneous Anthrax without Systemic Involvement===
==Antitoxins==
An [[antitoxin]] should be added to combination [[antibiotic]] treatment for any patient for whom there is a high level of clinical suspicion for systemic [[anthrax]]. Given that systemic [[anthrax]] has a high case-fatality rate and the risk for [[antitoxin]] treatment appears to be low, the potential benefit achieved by adding [[antitoxin]] to combination [[antibiotic]] treatment outweighs the potential risk.
Currently there are 2 antitoxins in the CDC Strategic National Stockpile: [[raxibacumab]] and [[Anthrax Immune Globulin Intravenous]] ([[AIGIV]]). Both [[antitoxins]] inhibit binding of Protective Antigen (PA) to [[anthrax toxin]] receptors and translocation of the 2 primary toxins (Lethal Toxin (LT) and Edema Toxin (ET)) into [[cells]].
===Raxibacumab===
[[Raxibacumab]] is a recombinant, fully humanized, IgG1λ [[monoclonal antibody]]. It appeared safe and well tolerated in 333 healthy adults who received the recommended dose of 40 mg/kg.
Most [[adverse events]] were transient and mild to moderate in severity. [[Pruritis]] was noted in 2.1% of persons treated with [[raxibacumab]] and in none treated with [[placebo]]. Although [[raxibacumab]] has not been given to patients with systemic anthrax, it is FDA-approved for postexposure [[prophylaxis]] PEP and treatment for anthrax under the Animal Rule Summary
===Anthrax Immune Globulin===
AIGIV is a human polyclonal [[antiserum]] made from [[plasma]] of persons [[Immunization|immunized]] with Anthrax Vaccine Absorbed (AVA), which might have some direct effect on Lethal Factor (LF) and Edema Factor (EF). It was evaluated in 74 healthy adult volunteers and appears safe and well tolerated at all doses tested.
The most frequently reported [[adverse events]] were [[headache]]  pharyngolaryngeal pain, and [[nausea]].
AIGIV is not [[FDA]] approved and could be made available under an Investigational New Drug protocol or an Emergency Use Authorization during a declared emergency.


==Supportive Treatment==
==Supportive Treatment==

Revision as of 15:51, 17 July 2014

Medical Therapy

The treatment of anthrax infection includes antimicrobial and antitoxin agents. This treatment and postexposure prophylaxis differs from other bacterial infections because:

Hospitalized patients for systemic anthrax should be immediately treated with a combination of broad-spectrum intravenous antimicrobial drug treatment pending confirmatory test results because any delay may prove fatal.

Because meningitis and hemorrhagic brain parenchymal infection was observed in ≤50% of cases, meningitis must be considered in all cases of systemic anthrax. Therefore antibiotics to treat possible meningitis must have good penetration of the central nervous system (CNS).

Empiric therapy for anthrax in which anthrax meningitis is suspected or cannot be ruled out should include ≥3 antibiotics with activity against Bacillus anthracis, in which:

  • ≥1 drug should have bactericidal activity
  • ≥1 should be a protein synthesis inhibitor
  • All should have good CNS penetration

Given the high mortality rate associated with meningitis, 3 weeks of treatment for patients in whom meningitis could not be ruled out, is preferred. Because of the presence of a spore form of Bacillus anthracis, antibiotic therapy should be continued for 60 days to clear germinating organisms.

Antimicrobial Treatment

Antimicrobial Treatment for Systemic Disease with Possible Meningitis

Antimicrobial Treatment for Systemic Disease If Meningitis Is Ruled Out

Follow-up Oral Treatment for Systemic Disease

Once patients with systemic illness who were exposed to aerosolized spores have completed initial combination treatment, they should be transitioned to single-agent oral treatment to prevent relapse from surviving Bacillus anthracis spores.

Treatment for Cutaneous Anthrax without Systemic Involvement

Supportive Treatment