Cited by 173Poisoning and overdose treatmentsCassava research and cyanideHistorical and Scientific Studies

Cyanide poisoning and its treatment

Gracia, Rebeca, Shepherd, Greene·2004·Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy

Abstract

Cyanide is both widely available and easily accessible throughout the world. Although the compound is not frequently encountered, it has been used as a poison and contaminant in the past and is a potential terrorist agent. Cyanide has the ability to cause significant social disruption and demands special attention to public health preparedness. It can be obtained from a variety of sources, including industrial, medical, and even common household products. Another frequently encountered source of cyanide exposure is residential fires. Exposure to high concentrations of the chemical can result in death within seconds to minutes. Long-term effects from cyanide exposure can cause significant morbidity. The only treatment for cyanide toxicity approved for use in the United States is a kit consisting of amyl nitrite, sodium nitrite, and sodium thiosulfate. Future research aims to find a faster-acting, more effective, and better tolerated treatment for cyanide toxicity.

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Crossref · 10.1592/phco.24.14.1358.43149

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  • Therapeutic administration of sodium nitrite 30 mg/ml over 5-20 minutes (~300 mg total) significantly increases metHb levels (~20%) that can bind with cyanide to form cyanmethemoglobin thus competing with cytochrome oxidase a3.

    “Therapeutic administration of sodium nitrite 30 mg/ml over 5–20 minutes (~300 mg total) significantly increases metHb (i.e. ferric heme) levels (~20%) that can bind with cyanide to form cyanmethemoglobin thus competing with cytochrome oxidase a3 [134].”
  • The beneficial effect of sodium nitrite stems from the fact that cyanide has a high binding affinity for ferric iron, which is the basis of cyanide inhibition of cytochrome oxidase a3 thus decreasing mitochondrial respiration.

    “The beneficial effect of sodium nitrite stems from the fact that cyanide has a high binding affinity for ferric iron, which is the basis of cyanide inhibition of cytochrome oxidase a3 thus decreasing mitochondrial respiration [133].”

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References 94 · Cited by 173

Authors
Gracia, R., & Shepherd, G.
Affiliations
University of Georgia (US)
Corresponding author
Gracia, Rebeca
Venue
Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy
Publisher
Wiley
Published
2004-10
Volume
24
Issue
10
Pages
1358-1365
ISSN
  • 0277-0008 (ISSN-L)
  • 1875-9114
OpenAlex
W2017801064
Cited by
173
References
94
Citations by year
2026: 11 · 2025: 12 · 2024: 11 · 2023: 7 · 2022: 8 · 2021: 8 · 2020: 4 · 2019: 10 · 2018: 9 · 2017: 7 · 2016: 7 · 2015: 11 · 2014: 3 · 2013: 9 · 2012: 9
FWCI
1.54
Type
journal article
Language
en
Open access
closed
Locations
  • Pharmacotherapy The Journal of Human Pharmacology and Drug Therapy (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Emergency Medicine › Poisoning and overdose treatments
  • Life Sciences › Agricultural and Biological Sciences › Plant Science › Cassava research and cyanide
  • Health Sciences › Medicine › Pathology and Forensic Medicine › Historical and Scientific Studies
Keywords
cyanide poisoning, amyl nitrite, sodium nitrite, sodium thiosulfate, public health preparedness, house fires
MeSH terms
Antidotes, Charcoal, Cyanides, Gastric Lavage, Humans, Poisoning

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