1. Management of 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 TylenolAnacin 3Tempra Tylenol coldGoody’sComtrex multi sx Contac Severe ColdJunior Strength TylenolVicks Nyquil Sinutab SinusTherafluSine-off SinarestRobitussin ColdPanadol Midol PMSSudafed SinusVanquish Vicks 44MUnisomSinglet PyrroxateMidol teenCoricidin Dimetapp allergyDrixoral ColdAlka Seltzer Plus Actifed SinusBenadryl allergyPanex

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 ( 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. mcg/ml 4 8 12 16 20 24 Hours After Acetaminophen Ingestion 150 5 10 50 500 Rumack and Matthew Nomogram 100 Late Not valid after 24 hours

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 4 or more hours since overdose Less than 2 hours More than 2 hours since overdose since overdose Gastric emptying Activated charcoal Activated charcoal Draw blood plasma 4 hours after overdose for plasma acetaminophen assay Draw blood ASAP for plasma acetaminophen assay Acetaminophen concentration available Acetaminophen concentration not within 8 hours of overdose available within 8 hours of overdose Wait for acetaminophen assay result 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.

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

54. The End