Evidence map›Paper›PMID 26690378›Full record

SynthesisHealth security

Antitoxin Treatment of Inhalation Anthrax: A Systematic Review.

Eileen Huang, Satish K Pillai, William A Bower, Katherine A Hendricks, Julie T Guarnizo, Jamechia D Hoyle, Susan E Gorman, Anne E Boyer, Conrad P Quinn, Dana Meaney-Delman

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in Health security. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Antitoxin Use in the Prevention and Treatment of Anthrax Disease: A Systematic Review.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. CDC Guidelines for the Prevention and Treatment of Anthrax, 2023.MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports · 2023
    Article
  6. Anthrax revisited: how assessing the unpredictable can improve biosecurity.Frontiers in bioengineering and biotechnology · 2023
    Article
  7. Article
  8. Welder's Anthrax: A Tale of 2 Cases.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Article
  9. PathogenicPathogens (Basel, Switzerland) · 2022
    Review
  10. Article
  11. Review
  12. American journal of physiology. Heart and circulatory physiology · 2021
    Article
  13. Article
  14. TheMicroorganisms · 2020
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 6 institutions in 1 country.

Eileen Huang
Satish K Pillai
William A Bower
Katherine A Hendricks
Julie T Guarnizo
Jamechia D Hoyle
Susan E Gorman
Anne E Boyer
Conrad P Quinn
Dana Meaney-Delman
National Center for Environmental Health · USCDC Foundation · USNational Center for Immunization and Respiratory Diseases · USAID Atlanta · USGeorge Mason University · USNational Center for Emerging and Zoonotic Infectious Diseases · US

Funding

Intramural CDC HHS CC999999
6 · The paper itself

Abstract

Concern about use of anthrax as a bioweapon prompted development of novel anthrax antitoxins for treatment. Clinical guidelines for the treatment of anthrax recommend antitoxin therapy in combination with intravenous antimicrobials; however, a large-scale or mass anthrax incident may exceed antitoxin availability and create a need for judicious antitoxin use. We conducted a systematic review of antitoxin treatment of inhalation anthrax in humans and experimental animals to inform antitoxin recommendations during a large-scale or mass anthrax incident. A comprehensive search of 11 databases and the FDA website was conducted to identify relevant animal studies and human reports: 28 animal studies and 3 human cases were identified. Antitoxin monotherapy at or shortly after symptom onset demonstrates increased survival compared to no treatment in animals. With early treatment, survival did not differ between antimicrobial monotherapy and antimicrobial-antitoxin therapy in nonhuman primates and rabbits. With delayed treatment, antitoxin-antimicrobial treatment increased rabbit survival. Among human cases, addition of antitoxin to combination antimicrobial treatment was associated with survival in 2 of the 3 cases treated. Despite the paucity of human data, limited animal data suggest that adjunctive antitoxin therapy may improve survival. Delayed treatment studies suggest improved survival with combined antitoxin-antimicrobial therapy, although a survival difference compared with antimicrobial therapy alone was not demonstrated statistically. In a mass anthrax incident with limited antitoxin supplies, antitoxin treatment of individuals who have not demonstrated a clinical benefit from antimicrobials, or those who present with more severe illness, may be warranted. Additional pathophysiology studies are needed, and a point-of-care assay correlating toxin levels with clinical status may provide important information to guide antitoxin use during a large-scale anthrax incident.

Indexed as

Administration, IntravenousAnimalsAnthraxAnti-Bacterial AgentsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, BacterialAntitoxinsBioterrorismDrug Therapy, CombinationHumansImmunoglobulin GImmunoglobulins, IntravenousMass Casualty IncidentsRabbitsRespiratory Tract InfectionsAnthrax Immune Globulin IntravenousAnti-Bacterial AgentsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, BacterialAntitoxinsImmunoglobulin GImmunoglobulins, Intravenousraxibacumab

Identifiers

PMID26690378
PMCPMC4710135
OpenAlexW2255222662

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.