Episode 162.0 – Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis

A look at this deadly mucocutaneous reaction and how to best manage these patients in the ED

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Show Notes

Episode Produced by Audrey Bree Tse, MD


  • Rash with dysuria should raise concern for SJS with associated urethritis
    • Dysuria present in a majority of cases
  • SJS is a mucocutaneous reaction caused by Type IV hypersensitivity
    • Cytotoxic t-lymphocytes apoptose keratinocytes → blistering, bullae formation, and sloughing of the detached skin
  • Disease spectrum
    • SJS =
    • TEN = >30% TBSA
    • SJS/ TEN Overlap = 10-30% TBSA
  • Incidence is estimated at around 9 per 1 million people in the US
  • Mortality is 10% for SJS and 30-50% for TEN
    • Mainly 2/2 sepsis and end organ dysfunction.
  • SJS can occur even without a precipitating medication
    • Infection can set it off especially in patients with risk factors including HIV, lupus, underlying malignancy, and genetic factors
    • SATAN for the most common drugs
      • Sulfa, Allopurinol, Tetracyclines, Anticonvulsants, and NSAIDS
    • Anti-epileptics include carbamazepine, lamictal, phenobarb, and phenytoin
  • Can have a curious course
    • Hypersensitivity reaction can develop while taking medication, or even one to four weeks after exposure
    • In pediatric population, mycoplasma pneumonia and herpes simplex have been identified as precipitating infections
  • Patients often have a prodrome 1-3 days prior to the skin lesions appearing
    • May complain of fever,

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