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The Ariane-IPF ERS Clinical Research Collaboration: seeking collaboration through launch of a federation of European registries on idiopathic pulmonary fibrosis

机译:Ariane-IPF ERS临床研究合作组织:通过建立欧洲特发性肺纤维化注册机构联合会寻求合作

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Idiopathic pulmonary fibrosis (IPF) is the most prevalent of rare pulmonary diseases [1], and the most severe of the chronic forms of idiopathic interstitial pneumonias, with rising incidence and prevalence [2–4]. The prognosis for people diagnosed with IPF is a median survival of 3–3.5?years [1].Ariane-IPF is a project aimed at creating a federation of European registries for idiopathic pulmonary fibrosis, supported by an ERS Clinical Research Collaboration http://bit.ly/2J325tbWe thank Celine Genton and Elise Heuvelin from the European Respiratory Society (Lausanne, Switzerland) for their help and support and for managing the survey.
机译:特发性肺纤维化(IPF)是最普遍的罕见肺疾病[1],也是特发性间质性肺炎的最严重的慢性形式,其发病率和患病率均在上升[2-4]。诊断为IPF的人的平均生存期为3–3.5年[1]。Ariane-IPF是一个旨在建立欧洲特发性肺纤维化注册机构联盟的项目,该项目得到ERS临床研究合作小组的支持我们感谢欧洲呼吸协会(瑞士洛桑)的Celine Genton和Elise Heuvelin的帮助和支持以及对调查的管理。
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