Progressive fibrotic interstitial lung disease

نویسندگان

چکیده

Many interstitial lung diseases (ILDs) share mechanisms that result in a progressive fibrosing phenotype. In Brazil, the most common (PF-ILDs) are chronic hypersensitivity pneumonitis, idiopathic pulmonary fibrosis, unclassified ILD, and connective tissue diseases. PF-ILD is seen approximately 30% of patients with ILD. Because characterized by disease progression after initiation appropriate treatment, diagnosis resulting fibrosis critical. Different criteria have been proposed to define disease, including worsening respiratory symptoms, function decline, radiological evidence progression. Although time elapsed between varies, can occur at any diagnosis. Several factors indicate an increased risk death. last few years, antifibrotic drugs used tested PF-ILD. The effects nintedanib placebo compared PF-ILD, mean difference 107.0 mL/year being observed, favoring nintedanib. U.S. Food Drug Administration Brazilian Health Regulatory Agency approved use such on basis this finding. Pirfenidone has evaluated ILD other ILDs, results similar those for More studies needed order identify markers determine likelihood response treatment standard or new drugs.

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ژورنال

عنوان ژورنال: Jornal Brasileiro De Pneumologia

سال: 2023

ISSN: ['1806-3713', '1806-3756']

DOI: https://doi.org/10.36416/1806-3756/e20230098