Two guidance documents for the diagnosis of idiopathic pulmonary fibrosis (IPF) have been recently published by international experts representing major respiratory and radiological societies [1, 2]. Similar documents from other societies are anticipated. This is clearly a positive sign of the increasing attention being paid by the scientific community to a group of fibrotic lung diseases of which IPF is the prototype. Two new documents on the diagnosis of IPF have been published in 2018: their similarities and differences are described and discussed
No takes yet. Share an insight, caveat, or question.
Richeldi et al. (2018) studied this question.