In which myositis patients do you commonly use IVIG?
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Good candidates for IVIG in myositis include any patient with refractory dermatomyositis, refractory necrotizing myopathy, anti-HMGCR antibody-positive patients, as well as patients with dysphagia, pregnancy, infection or malignancy. In general, it can be added to 1st-, 2nd- or 3rd-line treatment in any form of myositis as an adjuvant therapy to boost the response rate and lower the steroid dose.
IVIG is also useful in calcinosis, malignancy and pregnancy.
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Based on the recently published ProDERM Trial, patients with dermatomyositis, especially those with muscle involvement are good candidates. However, additional published literature have demonstrated that myositis patients who have immune-mediated necrotizing myopathy (HMGCR+) in particular are good candidates for IVIG.
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Amyopathic DM, the phenotype which can look like spongiotic dermatitis histologically, consistently responds to IVIG. I have not treated patients with myositis or interstitial lung disease as I defer monitoring of response to relevant specialists. But for cutaneous symptoms, IVIG will provide months of remission, sometimes years.
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