DIAGNOSIS
Doctors may use a variety of tests and procedures to diagnose Johnson-Steven disease, including:
- Blood Test. A doctor may perform blood testing to verify the existence of infection and to rule out other reasons.
- Oral or Skin Culture Test. A doctor may collect a skin or mouth culture from afflicted regions to test for the condition.
- Skin Biopsy. A doctor may take a skin sample for a biopsy to indicate the existence of the condition. This test may confirm or refute the diagnosis.
- Physical Examination. A physical exam is an easy technique to check for Johnson-Steven syndrome. If your rash has advanced, a doctor will often be able to spot the indications of the condition. They will look at how much skin is damaged, how rapidly a rash spreads, and how much discomfort you are experiencing. Doctors will also look at your medical history and drug history to help them diagnose.
TREATMENT
Johnson-Steven syndrome treatments usually involve:
- Using non-adhesive dressings on the afflicted skin.
- Providing medications for pain alleviation.
- Consuming high-calorie meals to assist recovery, potentially by tube feeding.
- Utilizing intravenous (IV) fluids to replace electrolytes.
Furthermore, if you have Johnson-Steven Syndrome and your doctor says a medicine caused it, avoid that prescription and others like it. This is critical in preventing any recurrence, which is frequently more severe than the first attack and may be deadly.
