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Anthrax

Last reviewed: 21 Oct 2024
Last updated: 03 Jun 2024
03 Jun 2024

CDC updates advice for prevention and treatment of anthrax

​The Centers for Disease Control and Prevention (CDC) has updated its 2014 recommendations for the post-exposure prophylaxis (PEP) and treatment of anthrax. The CDC based the updates on systematic reviews of studies involving in vitro antimicrobial drug activity against Bacillus anthracis, in vivo antimicrobial drug efficacy for PEP and treatment, in vivo and human anthrax antitoxin efficacy for PEP and treatment, and survival data.

The updated recommendations include an expanded list of alternative antimicrobial drugs that can be used if first-line drugs are contraindicated, not tolerated, ineffective, or unavailable.

The CDC has also issued new recommendations for the management of anthrax meningitis which includes the use of mannitol or hypertonic saline for cerebral oedema, corticosteroids as clinically indicated, and therapies that target intracranial bleeding and swelling.

No changes were made to previously published recommendations for critical care measures and clinical assessment tools or procedures, or to recommendations for the use of the anthrax vaccine.

The updated guidance highlights the recent approval of the adjuvanted anthrax vaccine adsorbed for PEP. The vaccine has the advantage of a reduced number of doses compared to the traditional anthrax vaccine adsorbed (AVA) vaccine.

Anthrax still occurs in agricultural regions of the Americas, southern and eastern Europe, central and southwestern Asia, and sub-Saharan Africa. A large-scale outbreak of anthrax is currently ongoing in Zambia.​[1]

See Management: approach

See Management: treatment algorithm

Original source of update

Summary

Definition

History and exam

Key diagnostic factors

  • presence of risk factors
  • necrotic skin lesions (cutaneous)
  • painless lesions (cutaneous)
  • oedema (cutaneous)
  • influenza-like illness (inhalation)
  • respiratory symptoms (inhalation)
  • oropharyngeal ulceration (ingestion)
Full details

Other diagnostic factors

  • lymphadenopathy
  • signs of meningitis
  • hypotension
  • gastrointestinal symptoms (ingestion)
Full details

Risk factors

  • environmental exposure
  • occupational exposure
  • biological terrorism
  • under-cooked meat ingestion
  • heroin use
Full details

Diagnostic investigations

1st investigations to order

  • culture and Gram stain
  • real-time polymerase chain reaction (RT-PCR)
  • serology
  • anthrax lethal factor (LF) toxin mass spectrometry
  • biopsy
  • FBC
  • chest x-ray
Full details

Investigations to consider

  • CT chest
Full details

Treatment algorithm

ACUTE

cutaneous anthrax without signs/symptoms of meningitis

systemic anthrax with or without meningitis

Contributors

Authors

Kari Simonsen, MD, MBA

Professor of Pediatric Infectious Diseases

University of Nebraska Medical Center

Omaha

NE

Disclosures

KS declares that she has organisational financial interests for sponsored clinical trials for COVID-19 vaccines (Pfizer/BioNTech), investigational antibiotics (Melinta Therapeutics), and RSV vaccine (Sanofi/AstraZeneca), none of which are related to anthrax.

Clayton Mowrer, DO, MBA

Fellow

Division of Internal Medicine/Pediatric Infectious Diseases

University of Nebraska Medical Center

Omaha

NE

Disclosures

CM declares that he has no competing interests.

Acknowledgements

Dr Kari Simonsen and Dr Clayton Mowrer would like to gratefully acknowledge Dr Daniel Boyle, Dr Brian Wolf, Dr Teresa Zembower, and Dr Pavani Reddy, previous contributors to this topic.

Disclosures

DB, BW, TZ, and PR declare that they have no competing interests.

Peer reviewers

Timothy Benton, MD

Regional Chairman

Residency Program Director

Associate Professor

Family and Community Medicine

Texas Tech University Health Sciences Center at the Permian Basin

Odessa

TX

Disclosures

TB declares that he has no competing interests.

Raffaele D’Amelio, MD

Professor of Internal Medicine

Director: Unit Clinical Immunology and Allergy

Department of Clinical and Molecular Medicine

Sapienza University of Rome, S. Andrea University Hospital

Rome

Italy

Disclosures

RD declares that he has no competing interests.

Ali Hassoun, MD, FACP, FIDSA, AAHIVS

Infectious Disease Specialist

Alabama Infectious Diseases Center

Huntsville

AL

Disclosures

AH declares that he has no competing interests.

Tim Brooks, MA, LMSSA, MB BChir, MSc, FRCPath, FRSPH

Head of Novel & Dangerous Pathogens

Novel and Dangerous Pathogens

HPA Centre for Emergency Preparedness and Response

Salisbury

UK

Disclosures

TB declares that he has no competing interests.

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