Skip to textbook content
Doctor’s PassportTextbook
TopicsAll topics

Loading topic navigation…

Textbook navigation
TopicsAll topics

Loading topic navigation…

Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Stevens-Johnson syndrome and toxic epidermal necrolysis

Dermatology · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
!
Epidermal necrolysis emergency

Skin pain, dusky atypical targets, blistering, detachment and erosive mucositis after medicine exposure indicate potential SJS or TEN with rapidly evolving skin failure.

Action: Stop suspected non-essential medicines immediately, admit to an experienced high-dependency environment and involve dermatology, critical care, ophthalmology and affected-mucosal specialties.

Synopsis

Recognise painful mucocutaneous epidermal necrolysis early, stop culprit medicines, quantify detachment, and coordinate intensive supportive and specialist care.

  • Painful skin, fever and mucosal erosion often precede obvious detachment; do not wait for large blisters to suspect SJS or TEN.
  • SJS involves under ten percent detached or detachable body surface, overlap ten to thirty percent, and TEN more than thirty percent.
  • Stop likely culprit and non-essential medicines immediately, using a dated timeline because latency and drug half-life influence causality.
  • Transfer to an experienced intensive, burns or specialist dermatology environment according to local pathways before avoidable deterioration.
  • Support temperature, fluid, nutrition, pain, wounds and thrombosis prevention; avoid routine prophylactic systemic antibiotics without infection evidence.
  • Obtain ophthalmology review within the acute phase even when eye symptoms initially appear mild, and assess oral, genital and urinary mucosa.
  • Stevens-Johnson syndrome and toxic epidermal necrolysis must be assessed by lesion duration, onset, distribution, symptoms, mucosal findings, systemic physiology and the full medicine timeline rather than by colour alone.
  • For Stevens-Johnson syndrome and toxic epidermal necrolysis, document the working diagnosis, excluded emergencies, uncertain culprit or trigger, treatment response and the exact safety-net given.

Key red flags

Eye pain, photophobia, oral or genital erosions, skin tenderness, rapidly spreading dusky macules, blisters, positive epidermal shearing, fever, hypotension or oliguria requires emergency admission.

Pain before detachment

Marked skin tenderness or burning out of proportion to visible change is an early warning for evolving epidermal necrosis.

Physiological skin failure

Hypothermia, tachycardia, hypotension, oliguria and rising oxygen requirement indicate critical barrier and organ dysfunction.

Investigation priorities

01
Medicine chronology and culprit assessmentFirst step

Stop high-risk exposures and estimate causality from start dates, withdrawal and half-life.

Management branches

Suspected epidermal necrolysisStop drugs and transfer early

Skin pain, dusky targetoid lesions, mucosal erosions or detachment appears after a plausible medicine.

  1. Withdraw plausible culprit and non-essential medicines, document exact exposure dates and obtain emergency dermatology plus critical-care assessment.
  2. Biopsy a fresh representative edge when safe, measure detached and detachable surface and initiate physiological monitoring without awaiting pathology.
  3. Transfer early to the locally designated experienced setting because transport becomes harder after extensive skin failure develops.
Open full textbook →Answer 2 questions
Sources and review status3 sources · checked 27 Aug 2026 · clinical review pending+
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Apply principles in context and verify current guidance when a decision affects care. Source check completed 27 Aug 2026; clinical approval remains outstanding.

  • NHS Stevens-Johnson syndromeEmergency symptoms, causes and hospital treatment.
  • British Association of Dermatologists SJS and TENRecognition, intensive supportive care and sequelae.
  • NICE CG183 drug allergy diagnosis and managementAssessment, documentation, referral and future avoidance.

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom