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μμ© κΈ°μ : Ethanol acts by **competitively inhibiting the enzyme alcohol dehydrogenase**. - Ethylene glycol/Methanol + **Alcohol dehydrogenase** β Toxic metabolites (glycoaldehyde, glycolate, glyoxalate, and oxalic acid). - By occupying the enzyme, ethanol prevents this conversion, allowing the parent toxin (ethylene glycol or methanol) to be excreted primarily unchanged in the urine. - **Note**: For alcohol to be effective, it must be given very early after ingestion; it is seldom useful if started 8 hours after a significant ingestion.
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- Ethylene glycol poisoning Β· 5.5 mL/kg IV q4h for 5 treatments, then q6h for four additional treatments Β· IV Β· q4h then q6h Β· 9 treatments total Β· As a 20% solution; dosed as a CRI over 1 hour
- Ethylene glycol poisoning Β· 8.6 mL/kg slowly IV followed by a CRI of 1.43 mL/kg/hr Β· IV Β· CRI Β· at least 36 hours although 48 hours is probably better Β· Make a 7% ethanol solution. If EG test was positive initially, check before stopping treatment; discontinue if it reverts to negative.
- Ethylene glycol toxicity Β· 5.5 ml of 20% ethanol solution/kg Β· IV Β· q4h for 5 treatments, then q6h for 4 additional treatments Β· 9 treatments total Β· Adjust dose to maintain blood ethanol levels above 35 mg/dl.
- Ethylene glycol toxicity (CRI method) Β· Loading dose of 1.3 ml/kg of 30% solution, then 0.42 mg/kg/h Β· IV Β· CRI Β· 48 hours Β· Constant rate infusion method.
- Ethylene glycol toxicity (mild cases) Β· As directed (equivalent to IV dosing) Β· PO Β· As directed Β· Until toxicity resolves Β· For clinically mild cases with minimal CNS signs; vodka is often used.
- Ethylene glycol poisoning Β· 5 mL/kg IV q6h for 5 treatments, then q8h for four additional treatments Β· IV Β· q6h then q8h Β· 9 treatments total Β· As a 20% solution; dosed as a CRI over 1 hour
- Ethylene glycol poisoning Β· 8.6 mL/kg slowly IV followed by a CRI of 1.43 mL/kg/hr Β· IV Β· CRI Β· at least 36 hours although 48 hours is probably better Β· Make a 7% ethanol solution. If EG test was positive initially, check before stopping treatment; discontinue if it reverts to negative.
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- Concurrent use with fomepizole (usually contraindicated)
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- CNS depression
- Respiratory depression
- Diuresis
- Hypocalcemia
- Metabolic acidosis
- Pulmonary edema
- Injection site pain and infection
- Phlebitis
- Extravasation injury
- Bronchoconstriction and irritation (when aerosolized)
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- Bromocriptine Β· Alcohol may increase the severity of side effects seen with bromocriptine
- Activated Charcoal Β· Will inhibit absorption of orally administered ethanol; do not use if administering ethanol orally
- CNS Depressant Drugs (barbiturates, benzodiazepines, phenothiazines) Β· Alcohol may cause additive CNS depression
- Fomepizole (4-MP) Β· Inhibits alcohol dehydrogenase; ethanol metabolism is reduced significantly and alcohol poisoning (CNS depression, coma, death) can occur. Use together is generally not recommended.
- Insulin and antidiabetic drugs Β· Alcohol may affect glucose metabolism and the actions of insulin or oral antidiabetic agents
- Chlorpropamide, furazolidone, metronidazole Β· A disulfiram reaction (increased acetaldehyde with tachycardia, vomiting, weakness) may occur
- Fomepizole Β· Increases risk of severe alcohol toxicity; concurrent use should be avoided. Β· major
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- Alcohol blood levels (maintain at 100 to 130 mg/dL; safer to maintain >130 mg/dL than to fall below 100 mg/dL)
- Ethylene glycol or methanol levels
- Degree of CNS effect
- Fluid and electrolyte status
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If clinical signs of overdosage occur (**lateral nystagmus, respiratory depression, profound obtundation**), either slow the infusion or discontinue temporarily. Alcohol blood levels may be used to monitor both efficacy and toxicity of alcohol.
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