Transcription of 1. 1 特発性肺線維症 IPF) の管理と治療
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1. 1 特発性肺線維症 IPF) の管理と治療
1.. 1.. 1 (idiopathicpulmonaryfibrosis :I. PF) .. (I. PF) 3 . 5 20 40% . CT. (HRCT ) KL 6 SP D 6 .. N . ( ) . (QOL) QOL .. 1) 2) 3) 4) QOL. ( 49: 1 14 2. 010. ). TreatmentandManagementofIdiopathicPulmon aryFibrosis H. iro miTomioka D. epa rtm ento fRe spi rat oryM. edi cin e KobeC. ityM. edi calC. ent erWestH. osp ita l Kobe . Jap an A. bst rac t I. dio pat hicp ulm ona ryf ibr osi s(I. PF)i sap rog res siv edi sea set hati sse ver elyd ebi lit ati nga ndn g ati vel yaf fec tsq ual ityo fli fe (QOL). Thep rog nos iso fIP. Fisv eryp oo . rwi thmedians urv iva lof2. 4y raf tert hed iag nos atu ralh ist oryo fth isd ise asemayi nvo lve p eri odso fre lat ives tab ili typ unc tua tedbya cut eex ace rba tio nst hatr esu lti nsu bst ant ialm orb idi tyo rde ath .Va rio usc lin ica lan dra dio . l ogi cva ria ble spr edi cti ngp rog nos ish aveb eeni den tif ied .Al tho ughc urr ent lya vai lab lem edi cat ios.
Idiopathic pulmonary fibrosis (IPF) is a progressive disease that is severely debilitating and n巴gatively affects quality oflife (QOL). The prognosis of IPF is very poor， with median survival of 2-4yr after the diagnosis.
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