Stevens-Johnson syndrome (SJS) is a rare, serious disorder of the skin and mucous membranes. It’s usually a reaction to medication that starts with flu-like symptoms, followed by a painful rash that spreads and blisters. Then the top layer of affected skin dies, sheds and begins to heal after several days.
Stevens-Johnson syndrome is a medical emergency that usually requires hospitalization. Treatment focuses on removing the cause, caring for wounds, controlling pain and minimizing complications as skin regrows. It can take weeks to months to recover.
A more severe form of the condition is called toxic epidermal necrolysis (TEN). It involves more than 30% of the skin surface and extensive damage to the mucous membranes.
If your condition was caused by a medication, you’ll need to permanently avoid that drug and others closely related to it.
Symptoms
One to three days before a rash develops, you may show early signs of Stevens-Johnson syndrome, including:
- Fever
- A sore mouth and throat
- Fatigue
- Burning eyes
As the condition develops, other signs and symptoms include:
- Unexplained widespread skin pain
- A red or purplish rash that spreads
- Blisters on your skin and the mucous membranes of the mouth, nose, eyes and genitals
- Shedding of skin within days after blisters form
When to see a doctor
Stevens-Johnson syndrome requires immediate medical attention. Seek emergency medical care if you experience signs and symptoms of this condition. Drug-induced reactions may occur during the use of a medication or up to two weeks after discontinuing it.
Causes
Stevens-Johnson syndrome is a rare and unpredictable illness. Your doctor may not be able to identify its exact cause, but usually the condition is triggered by medication, an infection or both. You may react to medication while you’re using it or up to two weeks after you’ve stopped using it.
Drugs that can cause Stevens-Johnson syndrome include:
- Anti-gout medications, such as allopurinol
- Medications to treat seizures and mental illness (anticonvulsants and antipsychotics)
- Antibacterial sulfonamides (including sulfasalazine)
- Nevirapine (Viramune, Viramune XR)
- Pain relievers, such as acetaminophen (Tylenol, others), ibuprofen (Advil, Motrin IB, others) and naproxen sodium (Aleve)
Infections that can cause Stevens-Johnson syndrome include pneumonia and HIV.
Risk factors
Factors that increase your risk of developing Stevens-Johnson syndrome include:
- An HIV infection. Among people with HIV, the incidence of Stevens-Johnson syndrome is about 100 times greater than among the general population.
- A weakened immune system. The immune system can be affected by an organ transplant, HIV/AIDS and autoimmune diseases.
- Cancer. People with cancer, particularly blood cancer, are at increased risk of Stevens-Johnson syndrome.
- A history of Stevens-Johnson syndrome. If you’ve had a medication-related form of this condition, you are at risk of a recurrence if you use that drug again.
- A family history of Stevens-Johnson syndrome. If an immediate family member has had Stevens-Johnson syndrome, you may be more susceptible to developing it too.
- Genetic factors. Having certain genetic variations puts you at increased risk of Stevens-Johnson syndrome, especially if you’re also taking drugs for seizures, gout or mental illness.
Complications
Stevens-Johnson syndrome complications include:
- Dehydration. Areas where the skin has shed lose fluids. And sores in the mouth and throat can make fluid intake difficult, resulting in dehydration.
- Blood infection (sepsis). Sepsis occurs when bacteria from an infection enter your bloodstream and spread throughout your body. Sepsis is a rapidly progressing, life-threatening condition that can cause shock and organ failure.
- Eye problems. The rash caused by Stevens-Johnson syndrome can lead to eye inflammation, dry eye and light sensitivity. In severe cases, it can lead to visual impairment and, rarely, blindness.
- Lung involvement. The condition may lead to acute respiratory failure.
- Permanent skin damage. When your skin grows back following Stevens-Johnson syndrome, it may have abnormal bumps and coloring. And you may have scars. Lasting skin problems may cause your hair to fall out, and your fingernails and toenails may not grow normally.
Prevention
- Consider genetic testing before taking certain drugs. The U.S. Food and Drug Administration recommends screening people of Asian and South Asian ancestry for a gene variation called HLA-B*1502 before starting treatment.
- If you’ve had this condition, avoid the medication that triggered it. If you’ve had Stevens-Johnson syndrome and your doctor told you it was caused by a medication, avoid that drug and others like it. This is key to preventing a recurrence, which is usually more severe than the first episode and can be fatal.Your family members also might want to avoid this drug because some forms of this condition have a genetic risk factor.
Diagnosis
Tests and procedures used to diagnose Stevens-Johnson syndrome include:
- A review of your medical history and a physical exam. Doctors often can identify Stevens-Johnson syndrome based on your medical history, including a review of your current and recently stopped medications, and a physical exam.
- Skin biopsy. To confirm the diagnosis, and rule out other possible causes, your doctor removes a sample of skin for laboratory testing (biopsy).
- Culture. Skin or oral culture or culture from other areas may be taken to confirm or rule out infection.
- Imaging. Depending on your symptoms, your doctor may have you undergo an imaging such as a chest X-ray to check for pneumonia.
- Blood tests. These are used to confirm infection or other possible causes.
Treatment
Treating Stevens-Johnson syndrome requires hospitalization, possibly in an intensive care unit or a burn unit.
Stopping nonessential medications
The first and most important step in treating Stevens-Johnson syndrome is to stop taking any medications that may be causing it. Because it’s difficult to determine exactly which drug may be causing the problem, your doctor may recommend that you stop taking all nonessential medications.
Supportive care
Supportive care you’re likely to receive while in the hospital includes:
- Fluid replacement and nutrition. Because skin loss can result in significant loss of fluid from your body, replacing fluids is an important part of treatment. You may receive fluids and nutrients through a tube inserted in the nose and guided to the stomach (nasogastric tube).
- Wound care. Cool, wet compresses might help soothe blisters while they heal. Your health care team may gently remove dead skin and put petroleum jelly (Vaseline) or a medicated dressing over affected areas.
- Eye care. You may also need care from an eye specialist (ophthalmologist).
Medications
Medications used in the treatment of Stevens-Johnson syndrome include:
- Pain medication to reduce discomfort.
- Medication to reduce inflammation of the eyes and mucous membranes (topical steroids).
- Antibiotics to control infection, when needed.
- Depending on the severity, other systemic medications can be considered, including oral corticosteroids and intravenous immune globulin, though the value of their use is debatable. Studies now show that the drugs cyclosporine (Neoral, Sandimmune) and etanercept (Enbrel) are more successful in treating this disease.
If the underlying cause of Stevens-Johnson syndrome can be eliminated and the skin reaction stopped, new skin may begin to grow within several days. In severe cases, full recovery may take several months.
Lifestyle and home remedies
If you have had Stevens-Johnson syndrome, be sure to:
- Know what caused your reaction. If your condition was caused by a medication, learn its name and that of closely related medications.
- Inform your health care providers. Tell all your health care providers that you have a history of Stevens-Johnson syndrome. If the reaction was caused by a medication, tell them which one.
- Wear a medical information bracelet or necklace. Have information about your condition and what caused it inscribed on a medical information bracelet or necklace. Always wear it.
Preparing for your appointment
Stevens-Johnson syndrome is an emergency medical condition. If you have signs and symptoms, call 911 or emergency medical help, or go to an emergency room immediately.
If you have time before you go:
- Put in a bag all the medications you’ve taken in the last three weeks, including prescription and over-the-counter (nonprescription) drugs. Take the bag with you, as it may help the doctor figure out what triggered your condition.
- Ask a family member or a friend to come along, if he or she is available immediately. You may want to share relevant health information about yourself with him or her, so this person can help you when you talk with your doctor.
Questions your doctor may ask include:
- Have you had a flu-like illness recently?
- What other medical conditions do you have?
- What medications have you taken in the last three weeks?
While you’re in the hospital, you’ll likely have questions for your doctor. It might help to keep a list of questions you have, such as:
- What caused my condition?
- How do I keep from having this reaction again?
- What restrictions do I need to follow?
- I have other medical conditions. How do I manage them together?
- How long will it take my skin to heal?
- Am I likely to have any permanent damage?
Featured Image Credit: NHS UK