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10.1097/BOR.0000000000000270

http://scihub22266oqcxt.onion/10.1097/BOR.0000000000000270
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C4826478!4826478!27027811
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suck abstract from ncbi


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pmid27027811      Curr+Opin+Rheumatol 2016 ; 28 (3): 236-45
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  • Management of Connective Tissue Diseases Associated Interstitial Lung Disease: A Review of the Published Literature #MMPMID27027811
  • Wallace B; Vummidi D; Khanna D
  • Curr Opin Rheumatol 2016[May]; 28 (3): 236-45 PMID27027811show ga
  • Purpose of review: Interstitial lung disease (ILD), though a common and often a severe manifestation of many connective tissue diseases (CTD), is challenging to manage due to its variable presentation and the relative lack of guidelines to assist the clinician. In this review, we discuss the approach to diagnosis, treatment, and monitoring patients with CTD-associated ILD, with a focus on systemic sclerosis (SSc), rheumatoid arthritis (RA), and idiopathic inflammatory myopathy (IIM). Recent findings: High-resolution CT scan and pulmonary function testing can be reliably used to diagnose ILD and monitor progression, and often to determine its likely histologic subtype and severity. In SSc-ILD, randomized controlled trials show ILD stabilization with cyclophosphamide treatment; preliminary data from another randomized controlled trial demonstrates similar findings with mycophenolate. There are no robust clinical trials supporting specific treatments for RA-ILD or IIM-ILD, but rituximab in RA-ILD, and cyclophosphamide, mycophenolate and calcineurin inhibitors in IIM-ILD show promise. Summary: Though ILD contributes substantially to morbidity and mortality in patients with CTD, there is minimal data to guide its management except in SSc-ILD.
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