An overview of international literature from cystic fibrosis registries. Part 5: Update 2012-2015 on lung disease.


Patient registry data is a tool for defining the clinical course and risk factors in patients with less common diseases like Cystic Fibrosis. Forty-one registry-based reports on lung disease in Cystic Fibrosis were published between 2011 and 2015. The aim of this review is to describe and discuss the results of these reports, focusing on the risk factors… (More)
DOI: 10.1002/ppul.23473