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- W2089821167 startingPage "417" @default.
- W2089821167 abstract "Abstract Idiopathic inflammatory myopathies, notably polymyositis and dermatomyositis are comparatively uncommon diseases and few randomised, double blind placebo controlled trials have been done. Final validation of measures to assess outcome and response to treatment is awaited. Corticosteroids are an effective initial treatment, although rarely tested in randomised controlled trials. Unfortunately, not all patients respond to them and many develop undesirable side effects. There is thus a need for second line agents notably immunosuppressives or intravenous immunoglobulin. There are no defined guidelines or best treatment protocols agreed internationally and so the medical approach must be individualised, based on the severity of clinical presentation, disease duration, presence of extramuscular features, and prior therapy and contraindications to particular agents. There is still a significant percentage of non-responders (around 25%) and clinical relapses. Novel therapeutic approaches are now directed towards cytokine modulation and the use of monoclonal antibodies targeting B and T cells." @default.
- W2089821167 created "2016-06-24" @default.
- W2089821167 creator A5065798696 @default.
- W2089821167 creator A5091255152 @default.
- W2089821167 date "2006-07-01" @default.
- W2089821167 modified "2023-10-18" @default.
- W2089821167 title "Treatment of inflammatory myopathies" @default.
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- W2089821167 doi "https://doi.org/10.1136/pgmj.2005.038455" @default.
- W2089821167 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2563757" @default.