Diagnosis and management of idiopathic pulmonary fibrosis

The Prescriber Pub Date : 2022-07-01 DOI:10.1002/psb.1998
Vijay Joshi, Zaneeta Nagji
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Abstract

Idiopathic pulmonary fibrosis (IPF) is a form of idiopathic interstitial pneumonia that currently carries a poor prognosis and remains incurable, though antifibrotic therapy can slow disease progression. This article provides an overview of its diagnosis, treatment and the management of co‐morbidities.
特发性肺纤维化的诊断和治疗
特发性肺纤维化(IPF)是一种特发性间质性肺炎,目前预后较差,仍然无法治愈,尽管抗纤维化治疗可以减缓疾病进展。本文综述了该病的诊断、治疗和并发症的管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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