USMLE Prep - Medical Reference Library

Toxic Epidermal Necrolysis — Immediate Drug Withdrawal, Burn‑Unit Care, and Immunomodulators

System: Dermatology • Reviewed: Sep 1, 2025 • Step 1Step 2Step 3

Synopsis:

Life‑threatening epidermal necrosis usually triggered by medications. Stop culprit drug, admit to burn/ICU, apply SCORTEN for prognosis, and provide meticulous wound, fluid, and infection care. Consider cyclosporine or etanercept in selected cases; IVIG evidence mixed.

Key Points

  • Use the highest‑yield diagnostic test early; do not let testing delay time‑critical therapy.
  • Set objective targets (hemodynamic, neurologic, respiratory) and reassess frequently.
  • Plan definitive source control or immunomodulation when indicated; document follow‑up and patient education.

Algorithm

  1. Stop suspected culprit drugs immediately; list all non‑essential meds.
  2. Admit to burn/ICU; calculate SCORTEN; begin aggressive wound and fluid management.
  3. Initiate early enteral nutrition and pain control; strict infection surveillance.
  4. Consider cyclosporine or etanercept in experienced centers; discuss IVIG on case basis.
  5. Plan ophthalmology/urogenital care to prevent sequelae; arrange rehab and dermatology follow‑up.

Clinical Synopsis & Reasoning

Life‑threatening epidermal necrosis usually triggered by medications. Stop culprit drug, admit to burn/ICU, apply SCORTEN for prognosis, and provide meticulous wound, fluid, and infection care. Consider cyclosporine or etanercept in selected cases; IVIG evidence mixed.


Treatment Strategy & Disposition

Stabilize ABCs. Initiate guideline‑concordant first‑line therapy with precise dosing and continuous monitoring. Escalate to advanced or procedural interventions based on explicit failure criteria. Define ICU, step‑down, and ward disposition triggers; involve specialty teams early.


Epidemiology / Risk Factors

  • Risk varies by comorbidity and precipitants; see citations for condition‑specific data.

Investigations

TestRole / RationaleTypical FindingsNotes
Medication history 1–3 weeks priorEtiologyHigh‑risk drugs (e.g., sulfonamides, allopurinol, anticonvulsants)Identify culprit
SCORTEN variablesPrognosisAge, TBSA, malignancy, HR, BUN, bicarb, glucoseCalculate on day 1 and 3
Cultures only if infectedInfection controlSecondary sepsis riskAvoid routine prophylactic antibiotics

Pharmacology

Medication/InterventionMechanismOnsetRole in TherapyLimitations
Cyclosporine 3–5 mg/kg/dayImmunomodulatorDaysMay reduce mortality/time to re‑epithelializationMonitor renal/BP
Etanercept 50 mg SC once (± repeat)TNF‑α inhibitorDaysEmerging evidence for benefitInfection risk
IVIG 2 g/kg total (variable)ImmunotherapyDaysMixed evidenceVolume load, cost
Supportive burn‑style careProtocolizedImmediateCore of therapyFluids, temperature, nutrition, wound care

Prognosis / Complications

  • Outcome depends on timeliness of diagnosis and definitive therapy; monitor for complications.

Patient Education / Counseling

  • Provide red‑flag education, adherence guidance, and explicit return precautions; arrange timely specialty follow‑up.

References

  1. British Association of Dermatologists Guidelines for SJS/TEN (2016) — Link
  2. Lancet Review on SJS/TEN (2021) — Link