eMedicine Specialties > Emergency Medicine > Allergy & Immunology
Stevens-Johnson Syndrome: Follow-up
Updated: Jun 1, 2009
Follow-up
Further Inpatient Care
- Saline compresses may be applied to the eyelids, lips, and nose.
- Careful daily inspection is necessary to monitor for secondary superinfections.
- Prophylactic systemic antibiotics are not useful, especially in the current era of multiple-drug resistance.
- Antimicrobials are indicated in cases of urinary tract or cutaneous infections, either of which may lead to bacteremia.
Further Outpatient Care
- Although patients with erythema multiforme minor may be treated as outpatients with topical steroids, those with erythema multiforme major (ie, Stevens-Johnson syndrome) must be hospitalized.
- Cases of erythema multiforme minor must be followed closely. Some authors recommend daily follow-up.
Transfer
- Patients with Stevens-Johnson syndrome (SJS) are often critically ill; therefore, they must be admitted to hospitals capable of delivering critical care.
- Some patients may require the services of a burn unit.
- Transfer criteria would be the same as for patients with thermal burns.
Deterrence/Prevention
- Patients must avoid any future exposure to agent(s) implicated in the occurrence of Stevens-Johnson syndrome (SJS). Recurrences are possible.
Complications
- Ophthalmologic - Corneal ulceration, anterior uveitis, panophthalmitis, blindness
- Gastroenterologic - Esophageal strictures
- Genitourinary - Renal tubular necrosis, renal failure, penile scarring, vaginal stenosis
- Pulmonary - Tracheobronchial shedding with resultant respiratory failure
- Cutaneous - Scarring and cosmetic deformity, recurrences of infection through slow-healing ulcerations
Prognosis
- Individual lesions typically should heal within 1-2 weeks, unless secondary infection occurs. Most patients recover without sequelae.
- Development of serious sequelae, such as respiratory failure, renal failure, and blindness, determines prognosis in those affected.
- Up to 15% of all patients with Stevens-Johnson syndrome (SJS) die as a result of the condition.
- The SCORTEN score looks at a number of variables and uses them to prognosticate risk factors for death in both SJS and TEN. The variables include the following:
- Age >40 years
- Malignancy
- Heart rate >120
- Initial percentage of epidermal detachment >10%
- BUN level >10 mmol/L
- Serum glucose level >14 mmol/L
- Bicarbonate level <20 mmol/L
- Mortality rates are as follows:
- SCORTEN 0-1 >3.2%
- SCORTEN 2 >12.1%
- SCORTEN 3 >35.3%
- SCORTEN 4 >58.3%
- SCORTEN 5 or more >90%
Patient Education
- For excellent patient education resources, visit eMedicine's Skin, Hair, and Nails Center. Also, see eMedicine's patient education article Life-Threatening Skin Rashes.
Miscellaneous
Medicolegal Pitfalls
- The gravity of the diagnosis must be recognized. Because patients with Stevens-Johnson syndrome (SJS) who present early in the development of the disease may not yet be critically ill, the clinician may misdiagnose and discharge. SJS should be considered in all patients with target lesions and mucous membrane involvement.
- Provide close follow-up and clear instructions.
- When discharging a patient home, clearly document the degree (%) of skin involvement, the absence of mucous membrane lesions, and any clinical signs of toxicity.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous editor, Charles V Pollack, Jr, MD, to the development and writing of this article.
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References
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Further Reading
Keywords
Stevens-Johnson syndrome, SJS, erythema multiforme major, immune-complex–mediated hypersensitivity complex, mucosal scarring, esophageal strictures, corneal ulceration, anterior uveitis, keratitis, panophthalmitis, vaginal stenosis, penile scarring, SCORTEN score, upper respiratory tract infection,mucocutaneous lesions, rash, urticarial lesions, vulvovaginitis, balanitis, toxic epidermal necrolysis, TEN
Follow-up: Stevens-Johnson Syndrome