ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : -60 مورد

Antibiotic regimens for anthrax: Treatment of cutaneous infection or post-exposure prophylaxis[1]

Antibiotic regimens for anthrax: Treatment of cutaneous infection or post-exposure prophylaxis[1]
  Dosing for adults Dosing for children and adolescents (age ≥1 month through 17 years) Comments
FIRST-LINE ANTIBIOTICS
Doxycycline 100 mg orally every 12 hours
  • <45 kg: 2.2 mg/kg orally every 12 hours (max 100 mg/dose)
  • ≥45 kg: 100 mg orally every 12 hours
  • First line for empiric treatment and post-exposure prophylaxis.
  • For children ≤8 years: Although short-term exposure (<21 days) during tooth development has not been associated with staining or enamel hypoplasia, the risk with longer durations is uncertain.
Minocycline 200 mg orally once then 100 mg orally every 12 hours
  • 4 mg/kg once orally (max 200 mg) then 2 mg/kg orally every 12 hours (max 100 mg/dose)
  • First line for empiric treatment; alternative for post-exposure prophylaxis.
  • Not recommended for pregnant or lactating individuals.
  • For children ≤8 years: Prolonged exposure during tooth development may result in staining and enamel hypoplasia.
Ciprofloxacin 500 mg orally every 12 hours
  • 15 mg/kg orally every 12 hours (max 500 mg/dose)
  • First line for empiric treatment and post-exposure prophylaxis.
Levofloxacin

Post-exposure prophylaxis: 500 mg orally every 24 hours

Treatment: 750 mg orally every 24 hours
  • <50 kg post-exposure prophylaxis and treatment: 8 mg/kg orally every 12 hours (max 250 mg/dose)
  • ≥50 kg post-exposure prophylaxis: 500 mg orally every 24 hours
  • ≥50 kg treatment: 750 mg orally every 24 hours
  • First line for empiric treatment and post-exposure prophylaxis.
Penicillin VK 500 mg orally every 6 hours
  • 12.5 to 18.7 mg/kg orally every 6 hours (max 500 mg/dose)
  • Do not use for empiric therapy; only for documented penicillin-susceptible strains.
Amoxicillin 1 g orally every 8 hours
  • 25 mg/kg orally every 8 hours (max 1 g/dose)
  • Do not use for empiric therapy; only for documented penicillin-susceptible strains.
  • Ampicillin 500 mg (or 25 mg/kg; max 500 mg) orally every 6 hours is an alternative to amoxicillin.
ALTERNATIVE ANTIBIOTICS (reserve for when first-line agents cannot be used or are unavailable, as in a crisis setting; listed in descending order of preference)
Amoxicillin-clavulanate
  • 1 g/62.5 mg formulation: 2 tablets orally every 12 hours
  • 875/125 mg formulation: 1 tablet orally every 12 hours
  • For age ≥3 months:
    • 200/28.5 mg or 400/57 mg formulation: 22.5 mg/kg amoxicillin orally every 12 hours (max 875/125 mg/dose)
    • 600/42.9 mg formulation for children <40 kg: 45 mg/kg amoxicillin orally every 12 hours
    • 1 g/62.5 mg formulation for children ≥40 kg: 2 tablets (2 g amoxicillin) orally every 12 hours
  • First-line agent for post-exposure prophylaxis and treatment children.
Moxifloxacin 400 mg orally every 24 hours
  • Age ≥3 to ≥23 months: 6 mg/kg orally every 12 hours (max 200 mg/dose)
  • Age 2 to <6 years: 5 mg/kg orally every 12 hours (max 200 mg/dose)
  • Age 6 to <12 years: 4 mg/kg orally every 12 hours (max 200 mg/dose)
  • Age >12 to <18 years and <45 kg: 4 mg/kg orally every 12 hours (max 200 mg/dose)
  • Age >12 to <18 years and ≥45 kg: 400 mg every 24 hours (or 200 mg every 12 hours for those at risk for cardiac events)
 
Clindamycin 600 mg orally every 8 hours
  • 10 mg/kg orally every 8 hours (max 600 mg/dose)
  • First-line agent for post-exposure prophylaxis and treatment in children.
Ofloxacin 400 mg orally every 12 hours
  • 11.25 mg/kg orally every 12 hours
 
Omadacycline 450 mg orally every 12 hours for 2 days then 300 mg orally every 24 hours
  • Age >8 years: 450 mg orally every 24 hours for 2 days then 300 mg orally every 24 hours orally
  • Children ≤8 years: Prolonged exposure during tooth development may result in staining and enamel hypoplasia.
Linezolid 600 mg orally every 12 hours
  • Age <12 years: 10 mg/kg orally every 8 hours (max 600 mg/dose)
  • Age ≥12 years: 600 mg orally every 12 hours
  • Extended use (eg, >2 weeks) warrants monitoring for cytopenias or neurotoxicity.
Tetracycline 500 mg orally every 6 hours
  • 12.5 mg/kg orally every 6 hours (max 500 mg/dose)
  • Not recommended for pregnant or lactating individuals.
  • Children ≤8 years: Prolonged exposure during tooth development may result in staining and enamel hypoplasia.
Clarithromycin 500 mg orally every 12 hours
  • 7.5 mg/kg orally every 12 hours (max 500 mg/dose)
  • Only initiate after at least 3 days of treatment with any of the other agents listed.
Dalbavancin 1 g intravenously once then 500 mg intravenously weekly
  • Age ≥3 months to <6 years: 22.5 mg/kg intravenously every 2 weeks for post-exposure prophylaxis or once weekly for treatment (max 1.5 g/dose)
  • Age ≥6 to <18 years: 18 mg/kg intravenously every 2 weeks for post-exposure prophylaxis or once weekly for treatment (max 1.5 g/dose)
 
Imipenem-cilastatin 2 g intravenously every 8 hours
  • 25 mg/kg every 6 hours (max 1 g/dose)
  • Not recommended for post-exposure prophylaxis.
Meropenem 2 g intravenously every 8 hours
  • 20 mg/kg intravenously every 8 hours (max 2 g/dose)
  • Not recommended for post-exposure prophylaxis.
Vancomycin 15 mg/kg intravenously over 1 to 2 hours every 12 hours
  • 20 mg/kg intravenously over 1 to 2 hours every 8 hours
  • Not recommended for post-exposure prophylaxis.
  • For critically ill adults: Loading dose of 20 to 35 mg/kg (max 3 g) once.
  • Target AUC of 400 to 600 mcg × h/mL (preferred) or trough concentration 15 to 20 mcg/mL.

These agents can be used as monotherapy for post-exposure prophylaxis or for patients with cutaneous anthrax, with or without systemic symptoms, as long as they do not have evidence of meningitis. If an antibiotic is selected empirically, susceptibility testing of the isolate should be performed whenever possible to confirm that the selected agent is active.

  • When used for treatment of cutaneous anthrax, the duration is 7 to 10 days, as long as clinical improvement is documented. Patients with cutaneous anthrax and a suspected aerosol exposure to B. anthracis spores should continue the antibiotic after the treatment course for post-exposure prophylaxis.
  • When used for post-exposure prophylaxis, the duration depends on the age, immune status, pregnancy status, and vaccination status; for individuals who have not previously received anthrax vaccine, the duration generally ranges from 42 to 60 days from the time of aerosol exposure. Shorter durations are used if there was only cutaneous exposure. Refer to other UpToDate content on prevention of anthrax for additional details.

The doses recommended above are intended for patients with normal kidney function; the doses of some of these agents must be adjusted in patients with kidney insufficiency.

Refer to other UpToDate content on management of patients with suspected inhalational, gastrointestinal, or injection anthrax, or anthrax meningitis.

These recommendations are consistent with those from the Centers for Disease Control and Prevention (CDC) in the United States. For dosing in neonates, refer directly to CDC documents.
AUC: area under the curve.
Reference:
  1. Bower WA, Yu Y, Person MK, et al. CDC Guidelines for the Prevention and Treatment of Anthrax, 2023. MMWR Recomm Rep 2023; 72:1.
Graphic 144947 Version 3.0