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Drugs

, Volume 61, Issue 7, pp 979–988 | Cite as

Current Management of Ethylene Glycol Poisoning

  • Jeffrey BrentEmail author
Therapy in Practice

Abstract

Ethylene glycol, a common antifreeze, coolant and industrial solvent, is responsible for many instances of accidental and intentional poisoning annually. Following ingestion, ethylene glycol is first hepatically metabolised to glycoaldehyde by alcohol dehydrogenase. Glycoaldehyde is then oxidised to glycolic acid, glyoxylic acid and finally oxalic acid. While ethylene glycol itself causes intoxication, the accumulation of toxic metabolites is responsible for the potentially fatal acidosis and renal failure, which characterises ethylene glycol poisoning.

Treatment of ethylene glycol poisoning consists of emergent stabilisation, correction of metabolic acidosis, inhibition of further metabolism and enhancing elimination of both unmetabolised parent compound and its metabolites. The prevention of ethylene glycol metabolism is accomplished by the use of antidotes that inhibit alcohol dehydrogenase. Historically, this has been done with intoxicating doses of ethanol. At a sufficiently high concentration, ethanol saturates alcohol dehydrogenase, preventing it from acting on ethylene glycol, thus allowing the latter to be excreted unchanged by the kidneys. However, ethanol therapy is complicated by its own inherent toxicity, and the need to carefully monitor serum ethanol concentrations and adjust the rate of administration.

A recent alternative to ethanol therapy is fomepizole, or 4-methylpyrazole. Like ethanol, fomepizole inhibits alcohol dehydrogenase; however it does so without producing serious adverse effects. Unlike ethanol, fomepizole is metabolised in a predictable manner, allowing for the use of a standard, validated administration regimen. Fomepizole therapy eliminates the need for the haemodialysis that is required in selected patients who are non-acidotic and have adequate renal function.

Keywords

Metabolic Acidosis Calcium Oxalate Glycolic Acid Nicotinamide Adenine Dinucleotide Calcium Oxalate Crystal 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Acknowledgements

The author has accepted honoria for lecture engagements from Orphan Medical, Inc., the manufacturer and distributor of fomepizole (Amitol) in the United States. He has no current financial relationship with Orphan Medical, Inc.

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Copyright information

© Adis International Limited 2001

Authors and Affiliations

  1. 1.Section of Clinical Pharmacology and Toxicology Associates, and Division of Emergency MedicineUniversity of Colorado Health Sciences CenterDenverUSA

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