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Management of
Acetaminophen
Toxicity
History

•
•
•
•

Synthesized in 1877 in U.S.
Extensive use began around 1947
Initially prescription only in the U.S.
Otc status gained in 1960

toxic effects first noted in U.S. in 1971
It’s everywhere!
• APAP is found in over 200 products
Tylenol
Tylenol cold
Contac Severe Cold
Sinutab Sinus
Sinarest
Midol PMS
Vicks 44M
Pyrroxate
Dimetapp allergy
Actifed Sinus

Anacin 3
Goody’s
Junior Strength Tylenol
Theraflu
Robitussin Cold
Sudafed Sinus
Unisom
Midol teen
Drixoral Cold
Benadryl allergy

Tempra
Comtrex multi sx
Vicks Nyquil
Sine-off
Panadol
Vanquish
Singlet
Coricidin
Alka Seltzer Plus
Panex
Actions
Analgesia
 Relieves mild to moderate pain
 Efficacy equivalent to salicylates
 Inhibits brain prostaglandin synthetase
 Blocks pain impulses peripherally
• Antipyresis
• Efficacy similar to salicylates
• Inhibits prostaglandin synthetase in the
hypothalamus
In overdose situations, liver enzymes become
saturated, glutathione is depleted, NAPQI

(N-acetyl-p-benzoquinoneimine)
accumulates, and hepatic necrosis occurs
Pharmacokinetics
• Absorption
– Rapidly absorbed from the GI tract
– Peak concentration usually occurs between 60
and 120 minutes
– Peak plasma levels almost always occur within
4 hours
Distribution
• Vd 1.0 - 2.0 L/Kg
• Approximately 20% plasma protein bound
may increase to 50% in overdose

• Has been reported to cross the placenta
Metabolism
– Occurs via several pathways in the liver
• 52% by sulfation
• 42% by glucuronidation
• 2% excreted unchanged in the urine
• 4% biotransformed by C-P450 MFO system
Excretion
• APAP’s metabolic products are excreted by
the kidneys
• Minimal excretion into breast milk
Half life
• Average 2 hours
– range 0.9 to 3.25 hours

• No age related differences
• No change in patients with renal disease
• With liver dysfunction, may increase to 17
hours
Extracorporeal elimination
• Hemodialysis
– Not proven effective in reducing or
preventing liver damage in overdose
• Peritoneal dialysis
– Not effective
Toxicity
• Factors involved in predicting hepatotoxicity
–
–
–
–
–

total quantity ingested
time from ingestion to treatment
age of the patient
alcoholism
enzyme inducing medications

♣ serum concentration in relation to Rumack
nomogram
• Toxic dose
– In adults, threshold for liver damage is 150 to
250 mg/kg
– Children under 10 appear to be more resistant
• Potential liver damage
– Adults: > 150 mg/kg in acute dose
– Adults: > 7.5 Grams in 24 hours (chronic)
– Children (<10 yrs): > 200 mg/kg
4 Stages of Acetaminophen
Poisoning
• Phase I (30 minutes to 4 hours)
– Within a few hours after ingestion, patients
experience anorexia, nausea, pallor, vomiting,
and diaphoresis. Malaise may be present.
Patient may appear normal
• Phase II (24 to 48 hours)
– Symptoms of Phase I are less severe. May seem
like a period of recovery. Right upper quadrant
pain may be present due to hepatic damage.
Blood chemistry becomes abnormal with
elevations of liver enzymes. Prothrombin times
may be prolonged. Renal function may begin
to deteriorate.
• Phase III (3 to 5 days)
– Characterized by symptoms of hepatic necrosis.
Coagulation defects, jaundice, and renal failure
have all been noted. Hepatic encephalopathy
has been noted. Hepatic biopsy at this time
would indicate centrilobular necrosis. Nausea
and vomiting may reappear. Death is due to
hepatic failure
• Phase IV (4 days to 2 weeks)
– Complete resolution or death
Treatment
• GI decontamination
– Syrup of Ipecac
• return usually 30-40% at best
• best if used early (first 1-2 hours)
– Gastric lavage
• effectiveness diminishes with time
• Activated charcoal
– Should not be witheld
– dose 50-100 Grams

• Cathartic
– utilized to speed transit time
• Hemodialysis
– Limited benefit
– Damage occurs quickly

• Hemoperfusion
– No benefit

• Peritoneal dialysis
– No benefit
Blood Sample

• 4 hour post ingestion APAP level
– levels drawn earlier may be
erroneous
– levels may be accurate out to 18
hours
• Plot level on Rumack-Matthews
nomogram

– 150 mg/dl at 4 hours is possibly toxic
– Do not use therapeutic “normal” values to
determine potential toxicity!
•
•
•
•

Baseline CBC
creatinine, BUN, blood sugar, electrolytes
prothrombin times
AST, ALT
– repeat q 24 hours
– elevations typically seen 24-36 hours post
ingestion
Rumack and Matthew Nomogram
500
Late

150
100
50

Not valid after
24 hours

10

5
mcg/ml

4

8

12

16

20

Hours After Acetaminophen Ingestion

24
• If APAP level plots above the possible risk
line administer N-acetylcysteine (NAC).
• If NAC is indicated, full regimen should be
followed. Do not stop NAC early if
nomogram indicates toxic possibility
N-acetylcysteine (NAC)
• Mechanism of action
– glutathione substitute
– may supply inorganic sulfur, altering
metabolism

• Route of administration
– Orally or IV
• IV not approved in the U.S.
• NAC dosing
– Oral 72 hour protocol
• Loading dose is 140 mg/kg
• Maintenance doses: 70 mg/kg
– Given every 4 hours x 17 doses starting 4 hours after
loading dose
• NAC supplied as 10 or 20% oral solution
– dilute to 5% final concentration with juice or
soft drink
– May be administered via NG tube
– If emesis occurs within 1 hour of
administration, repeat the dose
• If emesis persists, antiemetics may be used
– Reglan® (metoclopramide)
• 0.1 to 1.0 mg/kg iv is often effective

– If emesis is refractory, may consider
Zofran® (ondansetron) or Kytril® (granisetron)
• Expensive, but very effective
Pediatric overdoses
• More resistant to toxicity vs. adults
– if a child plots in the possible risk category on
the Rumack nomogram, do not resist using
NAC because of this greater tolerance to APAP
– Administer full course of NAC if nomogram
indicates that it is needed
Special considerations with NAC
• NAC administered on basis of nomogram
plot
• if initial level indicates need for NAC do

not discontinue
• subsequent APAP levels of interest only
• If NAC begun before APAP level obtained,
may DC NAC if level plots subtoxic on
nomogram
NAC side effects
• Relatively free of side effects when given
orally
• Emesis may occur
– extremely offensive sulfur odor
ED Admission
Estimate time of ingestion
Less than 4 hours since overdose
Less than 2 hours
since overdose

More than 2 hours
since overdose

Gastric emptying

4 or more hours since overdose

Activated charcoal

Activated charcoal
Draw blood plasma 4 hours after overdose for
plasma acetaminophen assay
Acetaminophen concentration available
within 8 hours of overdose
Wait for acetaminophen assay result

Draw blood ASAP for plasma
acetaminophen assay
Acetaminophen concentration not
available within 8 hours of overdose
Start NAC pending assay result
Loading does: 140 mg/kg

APAP level below risk line on nomogram

APAP level on or above risk line

DC NAC if started

Treat with full course of NAC

No further medical management needed

Daily LFT’s, prothrombin times

Treat other med or psychiatric problems

Provide supportive care
Summary
In overdose, APAP may overwhelm the liver
stores of glutathione. A rise in liver enzymes may
occur, which reflects the hepatic toxicity which
may ensue. Timely administration of NAC may
protect the patient from hepatic damage. Therapy
should be initiated as soon as possible, but NAC is
beneficial at any time. If APAP levels can not be
obtained, assume a toxic dose has been ingested,
initiate NAC, and continue until regimen
complete.
Case Studies
Case 1
A 32 year old female presents to the ED 30
minutes after taking 31 Tylenol Extra
Strength caplets in an apparent suicide
attempt. She weighs 134 pounds,
ambulated into the ED, is in no obvious
distress, has had no symptoms prior to
arrival.
Signs/symptoms
•
•
•
•
•
•

Patient is awake and alert
HEENT: normal
No GI distress
PERRLA
Temp 98.7°F
HR 84, BP 128/76, R 19
Lab results
• APAP pending
• Salicylate pending
• Tox screen Negative
Calculations
• Patient weighs 60.9 kilograms
• 15,500 mg of APAP ingested
• mg/kg = 254
– a potentially toxic “acute” dose
Treatment
• Lavage
• Activated charcoal
• Cathartic
– Hold NAC until APAP level results obtained
• can get APAP level back within 2 hours
Outcome
• APAP level 56 mg/dl drawn 4 hours post
ingestion
• ASA level 0
• patient discharged asx to mental health unit
7 hours after arrival
Case 2
A 25 year old male is brought to the ED by
his girlfriend. She states that he has taken
24 “Tylenol” tablets. She brought the bottle
with her and in fact the product is “Tylenol
ER”. He ingested the caplets approximately
5 hours ago.
Tylenol ER is a relatively new product
which throws a curve into the traditional
management of APAP overdoses. This
product releases 325 mg of APAP
immediately and 325 mg over the next 8
hours.
Tylenol “ER” is referred to by poison center
staff as

Tylenol Emergency Room
• Unsure if nomogram is useful with this
product
• 1 case demonstrated to have biphasic peaks
Signs/symptoms
•
•
•
•
•
•

Patient has vomited x 6 prior to arrival
Complaining of GI discomfort
HEENT: normal
PEERLA
Temp 98.9°F
HR 80, BP 130/78, R 20
Labs
• APAP level 110 mcg/ml at 5.0 hours post
ingestion
• ASA level 0
• Tox screen negative for other substances
Calculations
• Patient weighs 85 kilograms
• 11,050 mg APAP was ingested
• 183 mg/kg APAP ingested
– Potentially toxic amount in acute od
Treatment
• Activated charcoal with sorbitol given
• Repeat APAP level 4 hours past the 1st
level
• Strongly consider NAC with this level
– Initial 4 hour level > 100 start NAC
Outcome
• Patient was treated with full course NAC
• Liver enzymes were AST 220 U/L, and
ALT 388 U/L at 27 hours post ingestion.
• Liver enzymes returned to normal ranges
within 72 hours.
• Patient recovered uneventfully
Points to remember
•
•
•
•
•
•
•

APAP is present in many poly drug overdoses
No symptoms may be present…screen
150 mcg/ml at 4 hours is a “treat” level
NAC loading dose is 140 mg/kg
NAC maintenance doses are 70 mg/kg
Once NAC is started, DO NOT DC
Metoclopramide 0.1-1.0 mg/kg is very effective in
controlling nausea/vomiting associated with
APAP toxicity
The End

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Acetaminophen toxicity

  • 2. History • • • • Synthesized in 1877 in U.S. Extensive use began around 1947 Initially prescription only in the U.S. Otc status gained in 1960 toxic effects first noted in U.S. in 1971
  • 3. It’s everywhere! • APAP is found in over 200 products Tylenol Tylenol cold Contac Severe Cold Sinutab Sinus Sinarest Midol PMS Vicks 44M Pyrroxate Dimetapp allergy Actifed Sinus Anacin 3 Goody’s Junior Strength Tylenol Theraflu Robitussin Cold Sudafed Sinus Unisom Midol teen Drixoral Cold Benadryl allergy Tempra Comtrex multi sx Vicks Nyquil Sine-off Panadol Vanquish Singlet Coricidin Alka Seltzer Plus Panex
  • 4. Actions Analgesia  Relieves mild to moderate pain  Efficacy equivalent to salicylates  Inhibits brain prostaglandin synthetase  Blocks pain impulses peripherally
  • 5. • Antipyresis • Efficacy similar to salicylates • Inhibits prostaglandin synthetase in the hypothalamus
  • 6. In overdose situations, liver enzymes become saturated, glutathione is depleted, NAPQI (N-acetyl-p-benzoquinoneimine) accumulates, and hepatic necrosis occurs
  • 7. Pharmacokinetics • Absorption – Rapidly absorbed from the GI tract – Peak concentration usually occurs between 60 and 120 minutes – Peak plasma levels almost always occur within 4 hours
  • 8. Distribution • Vd 1.0 - 2.0 L/Kg • Approximately 20% plasma protein bound may increase to 50% in overdose • Has been reported to cross the placenta
  • 9. Metabolism – Occurs via several pathways in the liver • 52% by sulfation • 42% by glucuronidation • 2% excreted unchanged in the urine • 4% biotransformed by C-P450 MFO system
  • 10. Excretion • APAP’s metabolic products are excreted by the kidneys • Minimal excretion into breast milk
  • 11. Half life • Average 2 hours – range 0.9 to 3.25 hours • No age related differences • No change in patients with renal disease • With liver dysfunction, may increase to 17 hours
  • 12. Extracorporeal elimination • Hemodialysis – Not proven effective in reducing or preventing liver damage in overdose • Peritoneal dialysis – Not effective
  • 13. Toxicity • Factors involved in predicting hepatotoxicity – – – – – total quantity ingested time from ingestion to treatment age of the patient alcoholism enzyme inducing medications ♣ serum concentration in relation to Rumack nomogram
  • 14. • Toxic dose – In adults, threshold for liver damage is 150 to 250 mg/kg – Children under 10 appear to be more resistant
  • 15. • Potential liver damage – Adults: > 150 mg/kg in acute dose – Adults: > 7.5 Grams in 24 hours (chronic) – Children (<10 yrs): > 200 mg/kg
  • 16. 4 Stages of Acetaminophen Poisoning • Phase I (30 minutes to 4 hours) – Within a few hours after ingestion, patients experience anorexia, nausea, pallor, vomiting, and diaphoresis. Malaise may be present. Patient may appear normal
  • 17. • Phase II (24 to 48 hours) – Symptoms of Phase I are less severe. May seem like a period of recovery. Right upper quadrant pain may be present due to hepatic damage. Blood chemistry becomes abnormal with elevations of liver enzymes. Prothrombin times may be prolonged. Renal function may begin to deteriorate.
  • 18. • Phase III (3 to 5 days) – Characterized by symptoms of hepatic necrosis. Coagulation defects, jaundice, and renal failure have all been noted. Hepatic encephalopathy has been noted. Hepatic biopsy at this time would indicate centrilobular necrosis. Nausea and vomiting may reappear. Death is due to hepatic failure
  • 19. • Phase IV (4 days to 2 weeks) – Complete resolution or death
  • 20. Treatment • GI decontamination – Syrup of Ipecac • return usually 30-40% at best • best if used early (first 1-2 hours) – Gastric lavage • effectiveness diminishes with time
  • 21. • Activated charcoal – Should not be witheld – dose 50-100 Grams • Cathartic – utilized to speed transit time
  • 22. • Hemodialysis – Limited benefit – Damage occurs quickly • Hemoperfusion – No benefit • Peritoneal dialysis – No benefit
  • 23. Blood Sample • 4 hour post ingestion APAP level – levels drawn earlier may be erroneous – levels may be accurate out to 18 hours
  • 24. • Plot level on Rumack-Matthews nomogram – 150 mg/dl at 4 hours is possibly toxic – Do not use therapeutic “normal” values to determine potential toxicity!
  • 25. • • • • Baseline CBC creatinine, BUN, blood sugar, electrolytes prothrombin times AST, ALT – repeat q 24 hours – elevations typically seen 24-36 hours post ingestion
  • 26. Rumack and Matthew Nomogram 500 Late 150 100 50 Not valid after 24 hours 10 5 mcg/ml 4 8 12 16 20 Hours After Acetaminophen Ingestion 24
  • 27. • If APAP level plots above the possible risk line administer N-acetylcysteine (NAC). • If NAC is indicated, full regimen should be followed. Do not stop NAC early if nomogram indicates toxic possibility
  • 28. N-acetylcysteine (NAC) • Mechanism of action – glutathione substitute – may supply inorganic sulfur, altering metabolism • Route of administration – Orally or IV • IV not approved in the U.S.
  • 29. • NAC dosing – Oral 72 hour protocol • Loading dose is 140 mg/kg • Maintenance doses: 70 mg/kg – Given every 4 hours x 17 doses starting 4 hours after loading dose
  • 30. • NAC supplied as 10 or 20% oral solution – dilute to 5% final concentration with juice or soft drink – May be administered via NG tube – If emesis occurs within 1 hour of administration, repeat the dose
  • 31. • If emesis persists, antiemetics may be used – Reglan® (metoclopramide) • 0.1 to 1.0 mg/kg iv is often effective – If emesis is refractory, may consider Zofran® (ondansetron) or Kytril® (granisetron) • Expensive, but very effective
  • 32. Pediatric overdoses • More resistant to toxicity vs. adults – if a child plots in the possible risk category on the Rumack nomogram, do not resist using NAC because of this greater tolerance to APAP – Administer full course of NAC if nomogram indicates that it is needed
  • 33. Special considerations with NAC • NAC administered on basis of nomogram plot • if initial level indicates need for NAC do not discontinue • subsequent APAP levels of interest only • If NAC begun before APAP level obtained, may DC NAC if level plots subtoxic on nomogram
  • 34. NAC side effects • Relatively free of side effects when given orally • Emesis may occur – extremely offensive sulfur odor
  • 35. ED Admission Estimate time of ingestion Less than 4 hours since overdose Less than 2 hours since overdose More than 2 hours since overdose Gastric emptying 4 or more hours since overdose Activated charcoal Activated charcoal Draw blood plasma 4 hours after overdose for plasma acetaminophen assay Acetaminophen concentration available within 8 hours of overdose Wait for acetaminophen assay result Draw blood ASAP for plasma acetaminophen assay Acetaminophen concentration not available within 8 hours of overdose Start NAC pending assay result Loading does: 140 mg/kg APAP level below risk line on nomogram APAP level on or above risk line DC NAC if started Treat with full course of NAC No further medical management needed Daily LFT’s, prothrombin times Treat other med or psychiatric problems Provide supportive care
  • 36. Summary In overdose, APAP may overwhelm the liver stores of glutathione. A rise in liver enzymes may occur, which reflects the hepatic toxicity which may ensue. Timely administration of NAC may protect the patient from hepatic damage. Therapy should be initiated as soon as possible, but NAC is beneficial at any time. If APAP levels can not be obtained, assume a toxic dose has been ingested, initiate NAC, and continue until regimen complete.
  • 37. Case Studies Case 1 A 32 year old female presents to the ED 30 minutes after taking 31 Tylenol Extra Strength caplets in an apparent suicide attempt. She weighs 134 pounds, ambulated into the ED, is in no obvious distress, has had no symptoms prior to arrival.
  • 38. Signs/symptoms • • • • • • Patient is awake and alert HEENT: normal No GI distress PERRLA Temp 98.7°F HR 84, BP 128/76, R 19
  • 39. Lab results • APAP pending • Salicylate pending • Tox screen Negative
  • 40. Calculations • Patient weighs 60.9 kilograms • 15,500 mg of APAP ingested • mg/kg = 254 – a potentially toxic “acute” dose
  • 41. Treatment • Lavage • Activated charcoal • Cathartic – Hold NAC until APAP level results obtained • can get APAP level back within 2 hours
  • 42. Outcome • APAP level 56 mg/dl drawn 4 hours post ingestion • ASA level 0 • patient discharged asx to mental health unit 7 hours after arrival
  • 43. Case 2 A 25 year old male is brought to the ED by his girlfriend. She states that he has taken 24 “Tylenol” tablets. She brought the bottle with her and in fact the product is “Tylenol ER”. He ingested the caplets approximately 5 hours ago.
  • 44. Tylenol ER is a relatively new product which throws a curve into the traditional management of APAP overdoses. This product releases 325 mg of APAP immediately and 325 mg over the next 8 hours.
  • 45.
  • 46. Tylenol “ER” is referred to by poison center staff as Tylenol Emergency Room
  • 47. • Unsure if nomogram is useful with this product • 1 case demonstrated to have biphasic peaks
  • 48. Signs/symptoms • • • • • • Patient has vomited x 6 prior to arrival Complaining of GI discomfort HEENT: normal PEERLA Temp 98.9°F HR 80, BP 130/78, R 20
  • 49. Labs • APAP level 110 mcg/ml at 5.0 hours post ingestion • ASA level 0 • Tox screen negative for other substances
  • 50. Calculations • Patient weighs 85 kilograms • 11,050 mg APAP was ingested • 183 mg/kg APAP ingested – Potentially toxic amount in acute od
  • 51. Treatment • Activated charcoal with sorbitol given • Repeat APAP level 4 hours past the 1st level • Strongly consider NAC with this level – Initial 4 hour level > 100 start NAC
  • 52. Outcome • Patient was treated with full course NAC • Liver enzymes were AST 220 U/L, and ALT 388 U/L at 27 hours post ingestion. • Liver enzymes returned to normal ranges within 72 hours. • Patient recovered uneventfully
  • 53. Points to remember • • • • • • • APAP is present in many poly drug overdoses No symptoms may be present…screen 150 mcg/ml at 4 hours is a “treat” level NAC loading dose is 140 mg/kg NAC maintenance doses are 70 mg/kg Once NAC is started, DO NOT DC Metoclopramide 0.1-1.0 mg/kg is very effective in controlling nausea/vomiting associated with APAP toxicity

Notas do Editor

  1. APAP (N-acetyl-p-aminophenol_ Paracetamol in the UK, Mexico, many other countries Now surpasses ASA as a major cause of poisoning in US Use incr. Dramatically as Reyes syndrome was linked to salicylate use. Now considered “safed” than aspirin One of the most commonly used analgesic/antipyretic agents in the US Has none of ASA’sunderirable side effects when used in therapeutic dose Due to this increased availability and use, toxic exposures have also increased. Toxic effects seen in great Britain in late 1960’s. In each of the last few years, over 60,ooo queries related to APAP thru TESS each year
  2. In over 50 “Trade” name products Some are APAP alone, many others in combo with other agents. Most pain meds today contain APAP Codeine/APAP, Hcodone/APAP, Oxycodone/APAP Suppositories, elixirs, tablets, caplets, geltabs, capsules, powdered (Tylenol Cold?Flu) some up to 1000 mg/dose
  3. Peripheral action is blockade of Pain Impulse generation Less effect on peripheral enzyme Studies have shown that both apap and asa have equal effects on pain when given in equiv. Doses when the pain in non inflammatory in origin For inflammatory pain, salicylates are superior. They also inhibit prostaglandin synthetase peripherally, resulting in anti inflammatory activity.
  4. Inhib. Prost. Snythetase in the hypothalamus, altering response of the heat regulating center. Studies comparing APAP and ASA have shown no significant difference in temperature response, time of onset, time of peak activity, or duration of antipyretic activity
  5. Peak concentration occur even more quickly with liquid formulations Bezoar formation has not been seen with APAP like it has with ASA
  6. The 4% metab by the P450 system is an active intermediate (NAPQI) Normally, this minor metabolite of hydroxylation is detoxified by conjugation with hepatic glutathione, with the conjugated products mercapturic acid and cysteine excreted in the urine When large doses of APAP are ingested, both the glucoronidation and sulfation pathways become saturated, shunting more APAP toward the P-450 system and increasing NAPQI formation. When glutathione depletes to 30% of normal, NAPQI accumulates. The NAPQI arylates to protein in the cytosol and endoplasmic reticulum in the centrilobular zone of the liver, producing cell necrosis and death. NAPQI is neutralized by glutathione NAPQI contains a sulfhydryl group. If all glutathione is used up, other sulfhydryl groups in the liver are attacked and cells are damaged or destroyed
  7. Haemodialysis readily removes APAP, but the toxic metabolite is formed rapidly Peritoneal dialysis- Protein binding may increase up to 50% in overdose Forced diuresis- Not effective because of small amount excreted unchanged in the urine.