TY -的T1 -全球肺功能行动装备ations improve interpretation of FEV₁ decline among patients with cystic fibrosis JF - European Respiratory Journal JO - Eur Respir J SP - 262 LP - 264 DO - 10.1183/09031936.00187314 VL - 46 IS - 1 AU - Stanojevic, Sanja AU - Bilton, Diana AU - McDonald, Alexandra AU - Stocks, Janet AU - Aurora, Paul AU - Prasad, Ammani AU - Cole, Tim J. AU - Davies, Gwyneth Y1 - 2015/07/01 UR - //www.qdcxjkg.com/content/46/1/262.abstract N2 - The prognosis for individuals with cystic fibrosis has improved markedly over the last 50 years, with most countries now reporting that 50% of the population reach at least 35 years of age [1–3]. Despite this improvement, the average age at death is still in the late 20s and varies enormously between cystic fibrosis centres and countries [4]. To further improve the trajectory of lung disease, it is critical to identify patients that would benefit most from early intervention.Adolescent FEV1 decline in cystic fibrosis may be an artefact of the spirometry reference equations used http://ow.ly/J0com ER -