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Please select the option that best describes you:
Topics:
General Internal Medicine
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Rheumatology
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Systemic lupus erythematosus
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Neurology
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Neuro-immunology
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lupus
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Neuropsychiatric Lupus
What is your treatment approach to neuropsychiatric symptoms secondary to lupus?
Related Questions
What is your workup and treatment approach for cranial neuropathies in patients with lupus?
How do you approach new onset idiopathic intracranial hypertension (IIH) with someone who has history of systemic lupus erythematosus? Would you consider this to be neuropsychiatric SLE (NPSLE) manifesting as IIH?
What is your approach when surgeons want to stop hydroxychloroquine prior to surgery?
Should IVIG dosing in patients with autoimmune disease (i.e., dermatomyositis) who become pregnant continue to be based on actual weight at the time of each infusion, or should it be limited to pre-pregnancy weight?
How do you approach managing nausea and GI side effects when initiating methotrexate?
Do you generally prefer to continue hydroxychloroquine in lupus patients who develop ESRD despite the low likelihood of clinically active disease in this patient population?
What is the clinical significance of a low titer RNP, negative Sm, but Sm/RNP that is very high titer?
Would you accept the diagnosis of SLE on the basis of an AVISE CTD panel where the results just showed a positive EC4d or BC4d, positive ANA>1/80 + one clinical criteria such as multiple tender joints but did otherwise not fulfill criteria for SLE?
How would you work up splenomegaly and abdominal pain in a patient with primary antiphospholipid syndrome and a high + ANA, but no other serological or clinical SLE symptoms?
For patients with SLE, is there an ANC level for which you would hold or adjust hydroxychloroquine in an asymptomatic patient?