What is the recommended dose of ethanol (ethyl alcohol) for treating polyethylene glycol intoxication in a patient, considering their age, weight, past medical history, and demographic information?

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Critical Clarification: Polyethylene Glycol vs. Ethylene Glycol

Polyethylene glycol (PEG) is NOT toxic and does NOT require ethanol treatment or any antidote therapy. 1

Essential Distinction

  • Polyethylene glycol is a non-toxic polymer commonly used as a laxative (e.g., MiraLAX) and does not require any specific antidote treatment 1
  • Ethylene glycol is the highly toxic component of antifreeze that requires aggressive intervention with alcohol dehydrogenase inhibitors and potentially hemodialysis 1
  • The treatment protocols for ethylene glycol poisoning (fomepizole, ethanol, or hemodialysis) are NOT indicated for polyethylene glycol exposure 1

If Ethylene Glycol Co-Ingestion is Suspected

Only if there is confirmed or suspected ethylene glycol (not polyethylene glycol) poisoning should the following ethanol dosing be considered:

Ethanol Dosing Regimen for Ethylene Glycol Poisoning

Loading Dose:

  • 10 mL/kg of 10% ethanol IV (or 0.8-1.0 g/kg) administered over 30-60 minutes to achieve target blood ethanol concentration of 100-150 mg/dL 2, 3

Maintenance Dose:

  • Non-drinkers: 66-154 mg/kg/hour (approximately 1.4 mL/kg/hour of 10% ethanol) 2
  • Chronic drinkers: Higher maintenance rates may be required due to enzyme induction 3

During Hemodialysis:

  • Increase maintenance rate to 250-350 mg/kg/hour because ethanol is readily dialyzable 2, 4
  • Monitor ethanol levels every 2-4 hours during extracorporeal treatment 2

Target Therapeutic Level

  • Maintain blood ethanol concentration at 100-150 mg/dL (22 mmol/L) throughout treatment 2, 3
  • This concentration provides adequate competitive inhibition of alcohol dehydrogenase to prevent toxic metabolite formation 3

Indications for Hemodialysis When Using Ethanol

Strong recommendations for hemodialysis with ethanol (lower thresholds than with fomepizole): 2

  • Ethylene glycol concentration >50 mmol/L (>310 mg/dL) OR osmol gap >50 2
  • Anion gap >27 mmol/L 4, 2
  • Severe clinical features: coma, seizures, or acute kidney injury (KDIGO stage 2 or 3) 2

Weaker recommendations (consider hemodialysis): 4

  • Ethylene glycol concentration 20-50 mmol/L (124-310 mg/dL) OR osmol gap 20-50 4
  • Anion gap 23-27 mmol/L 4

Rationale for Lower Thresholds with Ethanol

  • The EXTRIP workgroup uses stronger recommendations for hemodialysis when ethanol is the antidote because alcohol dehydrogenase blockade with ethanol is unpredictable compared to fomepizole 2
  • Treatment failures occur even with minimal acidosis when ethanol dosing is suboptimal 5
  • Ethanol requires intensive monitoring in a high-dependency unit due to CNS depression, dysphoria, and unpredictable pharmacokinetics 2

Duration of Treatment

  • Continue ethanol therapy until ethylene glycol concentration <4 mmol/L (25 mg/dL) 2
  • Continue until anion gap normalizes to <18 mmol/L and metabolic acidosis resolves 2

Critical Pitfalls

  • Fomepizole is strongly preferred over ethanol when available due to predictable pharmacokinetics, ease of administration, and lack of CNS depression 6
  • Ethanol should only be used when fomepizole is unavailable 2, 7
  • Subtherapeutic ethanol levels lead to continued toxic metabolite formation, so frequent monitoring is essential 5
  • Monitor for alcohol withdrawal in patients with alcohol use disorder, especially during hemodialysis 4

References

Guideline

Treatment for Polyethylene Glycol Poisoning

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Ethylene Glycol Poisoning Treatment Guidelines

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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