特发性肺纤维化
医学
肺科医生
恶化
重症监护医学
吡非尼酮
免疫抑制
内科学
肺
作者
Michael Kreuter,Markus Polke,Simon Walsh,Johannes Krisam,Harold R. Collard,Nazia Chaudhuri,С. Н. Авдеев,Jürgen Behr,Greg Calligaro,Tamera J. Corte,Kevin R. Flaherty,Manuela Funke-Chambour,Martin Kolb,Yasuhiro Kondoh,Toby M. Maher,María Molina‐Molina,António Morais,Catharina C. Moor,Julie Morisset,Carlos A.C. Pereira
出处
期刊:The European respiratory journal
[European Respiratory Society]
日期:2020-02-14
卷期号:55 (4): 1901760-1901760
被引量:115
标识
DOI:10.1183/13993003.01760-2019
摘要
Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) is an often deadly complication of IPF. No focussed international guidelines for the management of AE-IPF exist. The aim of this international survey was to assess the global variability in prevention, diagnostic and treatment strategies for AE-IPF.Pulmonologists with ILD expertise were invited to participate in a survey designed by an international expert panel.509 pulmonologists from 66 countries responded. Significant geographical variability in approaches to manage AE-IPF was found. Common preventive measures included antifibrotic drugs and vaccination. Diagnostic differences were most pronounced regarding use of Krebs von den Lungen-6 and viral testing, while high-resolution computed tomography, brain natriuretic peptide and D-dimer are generally applied. High-dose steroids are widely administered (94%); the use of other immunosuppressant and treatment strategies is highly variable. Very few (4%) responders never use immunosuppression. Antifibrotic treatments are initiated during AE-IPF by 67%. Invasive ventilation or extracorporeal membrane oxygenation are mainly used as a bridge to transplantation. Most physicians educate patients comprehensively on the severity of AE-IPF (82%) and consider palliative care (64%).Approaches to the prevention, diagnosis and treatment of AE-IPF vary worldwide. Global trials and guidelines to improve the prognosis of AE-IPF are needed.
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