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- W2188937600 abstract "Idiopathic pulmonary fibrosis (IPF) has the highest mortality rate among all interstitial lung diseases, with a mean survival time of 2 to 3 years from the time of diagnosis. Prognosis is difficult to determine, due to the recognised heterogeneous progression of the disease, as well as lack of a well recognized staging system. This in turn raises challenges when considering therapeutic options for IPF patients, such as lung transplantation, versus a more conservative approach. Multiple independent factors have been identified as prognostic indicators in IPF, and a num - ber of studies have proposed multi-dimensional indices that combine several parameters in order to achieve a more accurate delineation of disease progression. In this systematic review, the Medline database was used to identify stud - ies in the area of multi-dimensional staging of IPF. We analysed and critically appraised previously proposed prog - nostic scoring systems. Our aim is to encourage research developments in this area to help identify an optimal mul - ti-dimensional staging system for IPF.(SarcoidosisVascDiffuseLungDis2014;31:8-18)" @default.
- W2188937600 created "2016-06-24" @default.
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- W2188937600 date "2014-01-01" @default.
- W2188937600 modified "2023-09-26" @default.
- W2188937600 title "Multi-dimensional indeces to stage idiopathic pulmonary fibrosis: a systematic review" @default.
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