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Dec 2024
28m 6s

Episode 203: Acetaminophen Toxicity

CORE EM
About this episode

We sit down with one of our toxicologists to discuss acetaminophen toxicity.

Hosts:
Marlis Gnirke, MD
Brian Gilberti, MD

Download One Comment Tags: Toxicology

Show Notes

Table of Contents

0:35 – Hidden acetaminophen toxicity in OTC products

3:24 – Pharmacokinetics and toxicokinetics 

6:06 – Clinical Course

9:22 – The antidote – NAC

11:02 – The Rumack-Matthew Nomogram 

17:36 – Treatment protocols

22:34 – Monitoring and Lab Work

23:23 – Considerations when treating pediatric patients

23:57 – IV APAP overdose, fomepizole 

25:42 – Take Home Points


Acetaminophen vs. Tylenol:

  • The importance of recognizing that acetaminophen is found in many products beyond Tylenol.
  • Common medications containing acetaminophen, such as Excedrin, Fioricet, Percocet, Dayquil/Nyquil, and others.
  • The risk of unintentional overdose due to combination products.

Prevalence of Acetaminophen Toxicity:

  • Widespread availability and under-recognition contribute to its prevalence.
  • The potential for unintentional overdose when taking multiple medications containing acetaminophen.

Pharmacokinetics and Metabolism:

  • Normal metabolism pathways of acetaminophen and the role of glutathione.
  • Formation of the toxic metabolite NAPQI during overdose situations.
  • Saturation of safe metabolic pathways leading to hepatotoxicity.

Pathophysiology of Liver Injury:

  • How excessive NAPQI leads to hepatocyte death, especially in zone III of the liver.
  • The difference between therapeutic dosing and overdose metabolism.

Clinical Stages of Acetaminophen Toxicity:

  • Stage 1: Asymptomatic or nonspecific symptoms (first 24 hours).
  • Stage 2: Onset of hepatic injury (24-72 hours), elevated AST/ALT.
  • Stage 3: Maximum hepatotoxicity (72-96 hours), signs of liver failure.
  • Stage 4: Recovery phase, complete hepatic regeneration if survived.

Antidote – N-Acetylcysteine (NAC):

  • Mechanisms of NAC in replenishing glutathione and detoxifying NAPQI.
  • The importance of early administration, ideally within 8 hours post-ingestion.
  • NAC’s role even in late presenters and in fulminant hepatic failure.

The Rumack-Matthew Nomogram:

  • How to use the nomogram for acute overdoses to determine the need for NAC.
  • Limitations in chronic overdoses and late presentations.
  • Emphasis on obtaining accurate time of ingestion and acetaminophen levels.

Treatment Protocols:

  • Standard 21-hour IV NAC protocol and dosing specifics.
  • Managing anaphylactoid reactions associated with IV NAC.
  • Criteria for extending NAC therapy beyond 21 hours.

Monitoring and Laboratory Work:

  • Importance of trending AST/ALT, INR, creatinine, lactate, and phosphate.
  • Use of the King’s College Criteria for potential liver transplant evaluation.

Special Considerations:

  • Adjustments in pediatric patients regarding NAC dosing volumes.
  • Awareness of IV acetaminophen overdoses and their management.
  • Emerging discussions on the use of fomepizole in massive overdoses.

Take-Home Points:

  • Comprehensive Medication History: Always inquire about all medications taken to assess for potential acetaminophen exposure.
  • Early Recognition and Treatment: Due to often silent initial stages, maintain a high index of suspicion and measure acetaminophen levels promptly.
  • Understanding Metabolism and Toxicity: Recognize how overdose alters metabolism, leading to toxic NAPQI accumulation.
  • N-Acetylcysteine Efficacy: NAC is most effective when administered early but remains beneficial even in advanced stages.
  • Proper Use of the Nomogram: Utilize the Rumack-Matthew Nomogram appropriately for acute ingestions and consult toxicology when in doubt.
  • Monitoring and Continuing Care: Be vigilant in monitoring laboratory values and prepared to extend NAC therapy as needed.
  • Consultation and Resources: Engage with poison control centers and utilize available resources for complex cases.

 

Resources Mentioned

Rumack-Matthew Nomogram 

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