Toxic Epidermal Necrolysis (TEN) – Pathway in Korea

Toxic Epidermal Necrolysis (TEN) – Pathway in Korea

What it is

Toxic epidermal necrolysis (TEN) is the most severe form of drug-induced mucocutaneous reaction, defined by >30% body surface area (BSA) detachment with mucosal involvement.

➝ It is considered a dermatologic emergency with mortality rates of 25–35%.

➝ Common culprit drugs include allopurinol, anticonvulsants, sulfonamides, antibiotics, and NSAIDs.

➝ Management requires a structured clinical pathway, emphasizing early recognition, immediate drug withdrawal, SCORTEN-based severity assessment, intensive supportive care, and immunomodulatory therapy in selected cases.

➝ In Korea, TEN management is centralized in tertiary hospitals with dermatology, ICU, and burn-unit collaboration.

Why it’s done

→ To stabilize patients rapidly, as mortality risk increases with delayed recognition.

→ To reduce complications such as sepsis, multi-organ failure, and severe ocular/mucosal sequelae.

→ To provide standardized care across hospitals, ensuring timely referral to ICU or burn units.

→ In Korea, TEN pathways improve survival outcomes, minimize long-term disability, and reduce recurrence risk.

Alternatives to a Pathway

Ad hoc management: Historically used, but inconsistent and linked to poorer outcomes.

Dedicated clinical pathway: Ensures uniform triage, supportive care, and early involvement of multidisciplinary teams.

SCORTEN tool: Used globally (and in Korea) to predict prognosis and guide treatment intensity.

Preparation

Immediate recognition of early signs: fever, malaise, painful skin, mucosal erosions, flaccid blisters, and widespread epidermal detachment.

Medication review: Identify and stop suspected culprit drugs immediately.

Baseline investigations: CBC, renal/liver function, electrolytes, blood glucose, arterial blood gas, chest X-ray, and cultures.

→ In Korea, electronic health alerts flag high-risk drugs (e.g., allopurinol without HLA-B*58:01 screening).

How it’s Done – TEN Pathway

Step 1: Immediate Actions
→ Stop culprit medication(s) immediately.
→ Admit to hospital (ICU or burn unit for >10% BSA).
→ Initiate infection control precautions.

Step 2: SCORTEN Severity Assessment (within 24 hours)
→ Age >40 years.
→ Presence of malignancy.
→ Heart rate >120 bpm.
→ BSA detached >10%.
→ Serum urea >10 mmol/L.
→ Serum bicarbonate <20 mmol/L.
→ Serum glucose >14 mmol/L.
→ Mortality rises sharply with each additional risk factor.

Step 3: Supportive Care (Cornerstone of Therapy)
→ Fluid and electrolyte management (similar to burn protocols).
→ Nutrition: high-protein, high-calorie diet or enteral feeding.
→ Wound care: non-adhesive dressings, sterile environment.
→ Temperature regulation in warm rooms to prevent hypothermia.
→ Pain control with opioids or neuropathic pain agents.
→ Strict infection monitoring and antibiotic stewardship (no prophylactic antibiotics).

Step 4: Systemic/Immunomodulatory Therapy (Selected Cases)
Corticosteroids: controversial, but used in early severe disease in some Korean centers.
Cyclosporine: increasingly used; shown to reduce mortality by inhibiting T-cell activation.
IVIG: used variably, particularly in children or severe overlap cases.
Biologics (emerging): TNF-α inhibitors and JAK inhibitors are under study.

Step 5: Multidisciplinary Involvement
→ Dermatology: lead diagnosis and skin care.
→ Ophthalmology: urgent evaluation to prevent blindness.
→ ENT/urology/gynecology: mucosal management.
→ ICU/burn unit team: systemic stabilization.

Step 6: Long-Term Care
→ Monitor for scarring, nail loss, pigmentary changes.
→ Ophthalmology follow-up for dry eye, corneal damage, or symblepharon.
→ Psychological support for trauma and anxiety.
→ Documentation of culprit drug allergy in national medical record system.

Recovery

→ Acute stabilization usually achieved in 2–4 weeks.

→ Skin regrows but may leave scarring and pigment changes.

→ Ocular, oral, and genital mucosa may have long-term complications.

→ Mortality depends on SCORTEN score and timeliness of care; Korean centers report improved outcomes with rapid ICU/burn unit referral.

Complications

Acute: sepsis, pneumonia, multi-organ failure, electrolyte imbalance.

Chronic: ocular sequelae (dry eye, corneal blindness), genital adhesions, nail dystrophy, pigmentation changes, psychological trauma.

Treatment-related: risks of systemic steroids (infection), cyclosporine (renal toxicity), IVIG (thrombosis risk).

Treatment Options in Korea

→ Korea follows structured TEN pathways in major hospitals, using SCORTEN-based triage.

ICU and burn-unit referrals are standard for severe cases, with dermatology as lead.

Cyclosporine is increasingly used in Korean centers, often preferred over corticosteroids alone.

HLA-B*58:01 screening is mandatory before allopurinol, reducing TEN incidence significantly.

→ Hospitals use electronic drug safety alerts to prevent re-exposure.

→ Patients receive integrated rehabilitation, including wound healing, ocular care, and psychological support.

→ With Korea’s structured approach, outcomes are among the best globally, with lower recurrence and improved survival.

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