特发性肺纤维化
肺科医生
医学
病因学
肺康复
基督教牧师
特发性间质性肺炎
俄罗斯联邦
重症监护医学
物理疗法
病理
内科学
康复
肺
业务
哲学
经济政策
神学
作者
S. N. Avdeev,З. Р. Айсанов,А. С. Белевский,Mikhail M. Ilkovich,Evgeniya Kogan,Zamira M. Merzhoeva,D Petrov,M. V. Samsonova,С. А. Терпигорев,Natalia V. Trushenko,И. Н. Трофименко,I. E. Tyurin,A. L. Chernyaev,B. A. Chernyak,А. В. Черняк,С. Ю. Чикина,A. G. Chuchalin,E. I. Shmelev
出处
期刊:Pulʹmonologiâ
[Scientific and Practical Reviewed Journal Pulmonology]
日期:2022-07-14
卷期号:32 (3): 473-495
被引量:3
标识
DOI:10.18093/0869-0189-2022-32-3-473-495
摘要
Idiopathic pulmonary fibrosis (IPF) is a specific form of chronic fibrotic interstitial pneumonia with a progressive course and poor prognosis. The prevalence of IPF in the Russian Federation is about 8 – 12 cases per 100,000 population. The basic treatment of IPF is antifibrotic agents. Methodology . The target audience of these clinical recommendations are therapists, general practitioners, pulmonologists, pathologists, radiologists, and medical rehabilitation doctors. Each thesis-recommendation about diagnostic and therapeutic procedures has been scored according to the scale of classes of recommendations from 1 to 5 and A, B, C scale of the levels of evidence. Clinical recommendations also contain comments and explanations to the theses, algorithms for the diagnosis and treatment of idiopathic pulmonary fibrosis, and reference materials. Conclusion . The presented clinical guidelines cover current information about the etiology and pathogenesis, clinical manifestations, diagnosis, treatment, and prevention of idiopathic pulmonary fibrosis. These guidelines were approved by the Scientific and Practical Council of the Ministry of Health of the Russian Federation in 2021.
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