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特发性肺纤维化急性加重:国际调查与协调呼吁

Acute exacerbation of idiopathic pulmonary fibrosis: international survey and call for harmonisation.

作者信息

Kreuter Michael, Polke Markus, Walsh Simon L F, Krisam Johannes, Collard Harold R, Chaudhuri Nazia, Avdeev Sergey, Behr Jürgen, Calligaro Gregory, Corte Tamera, Flaherty Kevin, Funke-Chambour Manuela, Kolb Martin, Kondoh Yasuhiro, Maher Toby M, Molina Molina Maria, Morais Antonio, Moor Catharina C, Morisset Julie, Pereira Carlos, Quadrelli Silvia, Selman Moises, Tzouvelekis Argyrios, Valenzuela Claudia, Vancheri Carlo, Vicens-Zygmunt Vanesa, Wälscher Julia, Wuyts Wim, Wijsenbeek Marlies, Cottin Vincent, Bendstrup Elisabeth

机构信息

Center for Interstitial and Rare Lung Diseases, Pneumology, Thoraxklinik, University of Heidelberg, Heidelberg, Germany

Member of the German Center for Lung Research (DZL), Germany.

出版信息

Eur Respir J. 2020 Apr 3;55(4). doi: 10.1183/13993003.01760-2019. Print 2020 Apr.

Abstract

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.

摘要

特发性肺纤维化急性加重(AE-IPF)是IPF一种常致命的并发症。目前尚无针对AE-IPF管理的专门国际指南。这项国际调查的目的是评估AE-IPF预防、诊断和治疗策略的全球差异。邀请了具有间质性肺疾病专业知识的肺科医生参与由一个国际专家小组设计的调查。来自66个国家的509名肺科医生做出了回应。发现管理AE-IPF的方法存在显著的地域差异。常见的预防措施包括抗纤维化药物和疫苗接种。在使用克雷布斯-冯-登-卢肯斯-6和病毒检测方面,诊断差异最为明显,而高分辨率计算机断层扫描、脑钠肽和D-二聚体通常被应用。大剂量类固醇广泛使用(94%);其他免疫抑制剂和治疗策略的使用差异很大。很少有(4%)受访者从不使用免疫抑制。67%的患者在AE-IPF期间开始使用抗纤维化治疗。有创通气或体外膜肺氧合主要用作移植的桥梁。大多数医生会全面告知患者AE-IPF的严重程度(82%)并考虑姑息治疗(64%)。全球范围内,AE-IPF的预防、诊断和治疗方法各不相同。需要开展全球试验并制定指南以改善AE-IPF的预后。

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