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Paracetamol Overdose

NICE BNF Treatment summaries. Poisoning, emergency treatment. Paracetamol poisoning.

Background information added accordingly.

Date: 13/11/25

Background Information

Pathophysiology

Normal metabolism of paracetamol (under normal therapeutic dosing)

  • Main site: liver
  • ~90% of paracetamol ungoes conjugation (glucuronidation / sulfation) to form inactive, water-soluble metabolites
  • ~10% of paracetamol undergoes oxidation via CYP450 (mainly CYP2E1) to form NAPQI (a highly toxic metabolite)
    • NAPQI is usually rapidly neutralised by conjugation with glutathione, therefore is of minimal significance

 

In paracetamol overdose, the main conjugation pathway (glucuronidation and sulfation) becomes saturated

  • More paracetamol is shunted down the oxidation (CYP450) pathway → excessive NAPQI production
  • With excessive NAPQI, glutathione stores become depleted
  • Excess NAPQI binds covalently to hepatocellular proteins and lipids → oxidative stress, mitochondrial dysfunction, and cell necrosis

The antidote, N-acetylcysteine, acts by replenishing glutathione and directly detoxifying NAPQI.

Clinical Presentation

The key impact of paracetamol overdose is acute hepatocellular necrosis leading to potentially fatal acute liver failure

 

There are 3 main stages: [Ref1][Ref2]

Time from ingestion Clinical manifestation Laboratory results
0-24 hours Asymptomatic or mild non-specific symptoms

  • Nausea / vomiting
  • Anorexia
  • Malaise
  • Diaphoresis
  • Blood tests are generally normal
  • ALT may be elevated
24-72 hours Hepatic injury occurs at this point:

  • RUQ pain
  • Hepatomegaly
  • Deranged LFTs
72-96 hours Maximal liver toxicity occurs at this point

  • Jaundice
  • Hepatic encephalopathy
  • Coagulopathy
  • Hypoglycaemia
The most common stage for death to occur due to acute liver failure and subsequent multisystem organ failure
  • AST levels peak (>1,000 IU/L)
  • Signs of acute liver failure (synthetic dysfunction)
    • Hyperbilirubinaemia
    • Prolonged PT / INR
    • Hypoglycaemia
  • Lactic acidosis
  • Acute renal failure

If the patient survives stage 3, the recovery phase begins by day 4 and completes by day 7.

Classification

Paracetamol overdose can be classified by the timing of ingestion, which guides management:

Type Definition
Acute overdose Ingestion of all the paracetamol tablets within 1 hour
Staggered overdose Ingestion of the paracetamol tablets over more than 1 hour
Therapeutic excess Ingestion of potentially toxic paracetamol dose with the intent to treat pain / fever and without self-harm intent

Diagnosis

Investigation and Diagnosis

Gold standard test: serum paracetamol concentration

  • For an accurate result, the sample should be taken at least 4 hours post-ingestion, allowing for complete absorption and reliable risk stratification.
  • The test is most valid in cases of a single, acute overdose
  • See the management section below for details on when and in whom to measure the serum paracetamol concentration

 

Key laboratory features include (see clinical presentation section above regarding timing of manifestation):

Hepatitis
  • ↑↑ AST and ALT levels (often >1,000 IU/L)
Liver synthetic dysfunction (from acute liver failure)
  • Prolonged INR / PT (the earliest and most sensitive marker of loss of hepatic synthetic function)
  • ↑ Bilirubin
  • Hypoglycaemia
Systemic / secondary effects
  • Lactic acidosis → high-anion-gap metabolic acidosis
  • ↑ Urea and creatinine (from acute renal failure)

Standard blood work for paracetamol overdose:

  • Blood gas
  • FBC, U&E
  • LFT
  • Clotting profile
  • Glucose level
  • Serum paracetamol concentration

Management

Essential information to obtain from the history of ANY drug overdose cases:

  • Elicit the agent involved
  • Elicit the dose
  • Elicit the intent
  • Pattern of use (acute or staggered?)
  • Time of ingestion
  • Presence of co-ingestants
  • Presence of comorbid conditions or medications (e.g. Gilbert disease, alcohol use, antiepileptic drugs)

Antidote of choice for paracetamol overdose is N-acetylcysteine (standard 21-hour regimen, 3 consecutive IV infusions over 1 hour, 4 hours and 16 hours).

  • Prevents or reduces the severity of liver damage if given up to 24 hours after ingestion (possibly beyond 24 hours)
  • Most effective when given within 8 hours of ingestion, its effectiveness declines after

Guidelines regarding paracetamol overdose are complicated, therefore the author presented 2 approaches: 1) a list of indications to give N-acetylcysteine immediately, 2) management depending on the type of overdose. It is recommended to go over both and consolidate the content.

Indications to Give N-acetylcysteine Immediately

The most important and commonly examined indication to give N-acetylcysteine is if serum paracetamol concentration falls on or above the treatment line on the paracetamol treatment graph (nomogram)

 

However, there are separate indications where N-acetylcysteine should be given immediately (without waiting to measure serum paracetamol concentration or plot on the nomogram)

  • Staggered overdose (all patients)
  • Unclear / unknown timing of ingestion (all patients)
  • Selected patients in acute overdose
    • <8 hours of ingestion of >150 mg/kg + if there will be a ≥8 hours delay in obtaining paracetamol concentration
    • 8-24 hours after ingestion + >150 mg/kg / unknown dose / symptomatic with jaundice or hepatic tenderness
    • >24 hours after ingestion + >150 mg/kg / unknown dose / jaundice or hepatic tenderness / detectable paracetamol concentration
    • Biochemical tests suggest acute liver injury (e.g. ↑ ALT or INR >1.3)

Management by Type of Overdose

Unknown Ingestion Timing

Give N-acetylcysteine immediately (do not wait to measure serum paracetamol concentration or plot on the nomogram)

  • NB that paracetamol concentration should still be taken but only to guide continuation or cessation of N-acetylcysteine, NOT to decide whether to start treatment

The paracetamol overdose nomogram (Rumack–Matthew nomogram) is only valid for a single, acute ingestion of paracetamol, where the exact time of ingestion is known.

It is not valid for:

  • Unknown ingestion timing, or
  • Staggered / repeated ingestions (i.e. taken over >1 hour period)

Staggered Overdose

Give N-acetylcysteine immediately (do not wait to measure serum paracetamol concentration or plot on the nomogram)

  • NB that paracetamol concentration should still be taken but only to guide continuation or cessation of N-acetylcysteine, NOT to decide whether to start treatment

The paracetamol overdose nomogram (Rumack–Matthew nomogram) is only valid for a single, acute ingestion of paracetamol, where the exact time of ingestion is known.

It is not valid for:

  • Unknown ingestion timing, or
  • Staggered / repeated ingestions (i.e. taken over >1 hour period)

Acute Overdose

Consider activated charcoal if the patient presents within 1 hour of ingesting paracetamol (>150 mg/kg).

 

Acute overdose is a bit more complicated, with 5 main scenarios:

Scenario Management
Ingested <4 hours ago Wait until 4 hours after ingestion, then measure serum paracetamol concentration, and

  • Only give N-acetylcysteine if paracetamol level is on or above the treatment line
Ingested <8 hours ago Give N-acetylcysteine immediately (without waiting for paracetamol concentration) if

  • Dose >150 mg/kg, and
  • There will be a delay of ≥8 hours in obtaining paracetamol levels
Ingested 8-24 hours ago Give N-acetylcysteine immediately (without waiting for paracetamol concentration) if there is ANY of the following:

  • Dose >150 mg/kg
  • Unknown dose
  • Symptomatic (jaundiced or RUQ tenderness)
Ingestion >24 hours Give N-acetylcysteine if any of the following:

  • >150 mg/kg
  • Unknown dose
  • Symptomatic (jaundiced or RUQ tenderness)
  • Detectable paracetamol concentration
Biochemical tests suggest acute liver injury (e.g. ↑ ALT, INR >1.3 in the absence of other causes) Give N-acetylcysteine (even if paracetamol concentration is BELOW the treatment line)

Therapeutic Excess

If there are any clinical features of hepatic injury (e.g. jaundice / RUQ tenderness) → give N-acetylcysteine immediately

Other patients → depend on maximum dose of paracetamol ingested in any 24 hour period (BNF says use TOXBASE, so unlikely examinable)

References

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