A patient with systemic lupus erythematosus (SLE) develops psychosis, mood lability, and cognitive decline. The psychiatrist must first differentiate primary neuropsychiatric lupus (NPSLE) from steroid-induced psychosis. Which feature FAVOURS steroid-induced psychosis?
- A Active SLE serology (elevated anti-dsDNA, low complement)
- B Cerebrospinal fluid pleocytosis
- C MRI showing white matter lesions
- D Onset within 2 weeks of starting or increasing high-dose corticosteroids ✓
Explanation
Steroid-induced psychosis typically begins within 2 weeks of starting or escalating high-dose corticosteroids (prednisone >40 mg/day equivalent) and often resolves with dose reduction. NPSLE is favoured by active serology, CSF abnormalities (pleocytosis), and neuroimaging findings (white matter lesions, vasculitis). Management differs: NPSLE may require immunosuppression; steroid psychosis requires dose reduction and possibly temporary antipsychotics.
Reference: Kaplan & Sadock's Synopsis of Psychiatry, 11th ed.
High-yield for: NEET PGINI-CETNExTFMGEUSMLEPLABMRCP
Written and medically reviewed by the StethoPrep medical team.