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Updated: Jul 26, 2025

Refined Murine Model of Idiopathic Pulmonary Fibrosis
07:51

Refined Murine Model of Idiopathic Pulmonary Fibrosis

Published on: June 17, 2025

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与未经治疗的患者相比,用抗纤维素药物治疗的IPF患者的生存率改善

Mark G J P Platenburg1, Coline H M van Moorsel2,3, Ivo A Wiertz2

  • 1Interstitial Lung Diseases Center of Excellence, Department of Pulmonology, St Antonius Hospital, Koekoekslaan 1, Nieuwegein, 3435CM, The Netherlands. m.platenburg@antoniusziekenhuis.nl.

Lung
|June 21, 2023
PubMed
概括

实践数据显示,抗纤维素药物可以改善异常性肺纤维化 (IPF) 患者的生存率. 这种生存益处对性别,年龄和生理学 (GAP) 阶段II和III异常性肺纤维化患者尤为重要.

关键词:
抗纤维素药物是一种抗纤维素药物.在这个问题上,GAP GAP.在IPF中,IPF是IPF.尼丁达尼比是什么意思皮尔芬尼多尼的使用方法幸存的生存方式

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