PMID- 36251549 OWN - NLM STAT- MEDLINE DCOM- 20221019 LR - 20231106 IS - 1537-6591 (Electronic) IS - 1058-4838 (Print) IS - 1058-4838 (Linking) VI - 75 IP - Suppl 3 DP - 2022 Oct 17 TI - Safety of Antimicrobials for Postexposure Prophylaxis and Treatment of Anthrax: A Review. PG - S417-S431 LID - 10.1093/cid/ciac592 [doi] AB - BACKGROUND: Bacillus anthracis, the causative agent for anthrax, poses a potential bioterrorism threat and is capable of causing mass morbidity and mortality. Antimicrobials are the mainstay of postexposure prophylaxis (PEP) and treatment of anthrax. We conducted this safety review of 24 select antimicrobials to identify any new or emerging serious or severe adverse events (AEs) to help inform their risk-benefit evaluation for anthrax. METHODS: Twenty-four antimicrobials were included in this review. Tertiary data sources (e.g. Lactmed, Micromedex, REPROTOX) were reviewed for safety information and summarized to evaluate the known risks of these antimicrobials. PubMed was also searched for published safety information on serious or severe AEs with these antimicrobials; AEs that met inclusion criteria were abstracted and reviewed. RESULTS: A total of 1316 articles were reviewed. No consistent observations or patterns were observed among the abstracted AEs for a given antimicrobial; therefore, the literature review did not reveal evidence of new or emerging AEs that would add to the risk-benefit profiles already known from tertiary data sources. CONCLUSIONS: The reviewed antimicrobials have known and/or potential serious or severe risks that may influence selection when recommending an antimicrobial for PEP or treatment of anthrax. Given the high fatality rate of anthrax, the risk-benefit evaluation favors use of these antimicrobials for anthrax. The potential risks of antimicrobials should not preclude these reviewed antimicrobials from clinical consideration for anthrax but rather guide appropriate antimicrobial selection and prioritization across different patient populations with risk mitigation measures as warranted. CI - Published by Oxford University Press on behalf of Infectious Diseases Society of America 2022. This work is written by (a) US Government employee(s) and is in the public domain in the US. FAU - Parker, Corinne M AU - Parker CM AD - Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA. FAU - Karchmer, Adolf W AU - Karchmer AW AD - Division of Infectious Diseases, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA. FAU - Fisher, Margaret C AU - Fisher MC AD - Clinical Professor of Pediatrics, Rutgers Robert Wood Johnson School of Medicine, Monmouth Medical Center, Long Branch, New Jersey, USA. FAU - Muhammad, Kalimah M AU - Muhammad KM AD - Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA. AD - Oak Ridge Institute for Science and Education Centers for Disease Control and Prevention Fellowship Program, Atlanta, Georgia, USA. FAU - Yu, Patricia A AU - Yu PA AD - Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA. LA - eng GR - CC/CDC HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PT - Review PL - United States TA - Clin Infect Dis JT - Clinical infectious diseases : an official publication of the Infectious Diseases Society of America JID - 9203213 RN - 0 (Anti-Bacterial Agents) RN - 0 (Anti-Infective Agents) SB - IM MH - *Anthrax/drug therapy/prevention & control MH - Anti-Bacterial Agents/adverse effects MH - *Anti-Infective Agents/adverse effects MH - *Bacillus anthracis MH - Bioterrorism MH - Humans MH - Post-Exposure Prophylaxis PMC - PMC9649414 OTO - NOTNLM OT - anthrax OT - antimicrobials OT - safety EDAT- 2022/10/18 06:00 MHDA- 2022/10/20 06:00 PMCR- 2022/10/17 CRDT- 2022/10/17 13:03 PHST- 2022/10/17 13:03 [entrez] PHST- 2022/10/18 06:00 [pubmed] PHST- 2022/10/20 06:00 [medline] PHST- 2022/10/17 00:00 [pmc-release] AID - 6762170 [pii] AID - ciac592 [pii] AID - 10.1093/cid/ciac592 [doi] PST - ppublish SO - Clin Infect Dis. 2022 Oct 17;75(Suppl 3):S417-S431. doi: 10.1093/cid/ciac592.