进行性肺纤维化(PPF)。

IF 0.7 Q4 RESPIRATORY SYSTEM
Dildar Duman
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引用次数: 1

摘要

进行性肺纤维化(PPF)的定义是,在过去一年内,除IPF外,因已知或未知原因伴有放射性肺纤维化的间质性肺病患者,至少存在三项标准中的两项,即呼吸道症状恶化、功能下降和影像学进展(1)。有条件地推荐尼达尼布治疗PPF,吡非尼酮需要进一步研究(1)。进行性肺纤维化的诊断和治疗方法,其新名称,以前被称为进行性纤维化间质性肺疾病,将进行讨论,并伴有更新。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Progressive pulmonary fibrosis (PPF).

Progressive pulmonary fibrosis (PPF) is defined as the presence of at least two of the three criteria, which are worsening respiratory symptoms, functional decline, and radiological progression in patients with interstitial lung disease with radiological pulmonary fibrosis for known or unknown reasons other than IPF, within the previous year (1). A conditional recommendation has been made for nintedanib in the treatment of PPF, and further studies are needed for pirfenidone (1). In this review, the diagnostic and therapeutic approach to progressive pulmonary fibrosis with its new name, previously known as progressive fibrotic interstitial lung diseases, will be discussed, accompanied by updates.

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来源期刊
CiteScore
1.50
自引率
9.10%
发文量
43
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