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.
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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