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- W3029121354 abstract "Idiopathic pulmonary fibrosis (IPF) is a chronic progressive interstitial lung disease. The prevalence of IPF is increasing year by year, and the diagnostic process is complex, the mortality rate is more than 50% in children. It has been demonstrated by multicenter, randomized, placebo-controlled trials that most of the clinical assays performed with corticosteroids, immunomodulators and antifibrotic drugs have shown inconclusive results for the treatment of IPF. To date, only pirfenidone has been proved to have significant efficacy in controlled clinical trials in the treatment of IPF. There has been an exponential increase in the number of compounds entering clinical trials for IPF in the last decade. The therapeutic use of new stem cell translantation will have a broad prospect in IPF.Key words: Pulmonary fibrosis; Idiopathic; Treatment; Children" @default.
- W3029121354 created "2020-06-05" @default.
- W3029121354 creator A5029042360 @default.
- W3029121354 date "2014-11-20" @default.
- W3029121354 modified "2023-10-15" @default.
- W3029121354 title "Progress in the treatment of idiopathic pulmonary fibrosis in children" @default.
- W3029121354 doi "https://doi.org/10.3760/cma.j.issn.1673-4912.2014.11.016" @default.
- W3029121354 hasPublicationYear "2014" @default.
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