The impact of switching to the new global lung function initiative equations on spirometry results in the UK CF Registry

被引:30
作者
Stanojevic, Sanja [1 ]
Stocks, Janet [2 ]
Bountziouka, Vassiliki [2 ]
Aurora, Paul [2 ,3 ]
Kirkby, Jane [2 ,3 ]
Bourke, Stephen [4 ]
Carr, Siobhan B. [5 ]
Gunn, Elaine [6 ]
Prasad, Ammani [3 ]
Rosenfeld, Margaret [7 ]
Bilton, Diana [6 ]
机构
[1] Hosp Sick Children, Toronto, ON M5G 1X8, Canada
[2] UCL Inst Child Hlth, London, England
[3] Great Ormond St Hosp Sick Children, London WC1N 3JH, England
[4] Royal Victoria Infirm, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[5] Royal Brompton Hosp, London SW3 6LY, England
[6] Cyst Fibrosis Trust UK, London, England
[7] Seattle Childrens Hosp, Seattle, WA USA
基金
英国惠康基金;
关键词
Cystic fibrosis; Spirometry; Reference values; PULMONARY-FUNCTION; REFERENCE VALUES;
D O I
10.1016/j.jcf.2013.11.006
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: The Quanjer et al. Global Lung Function Initiative (GLI)-2012 multi-ethnic all-age reference equations for spirometry are endorsed by all major respiratory societies and are the new gold standard. Before the GLI equations are implemented for use in CF patients, the impact of changing equations from those. currently used needs to be better understood. Methods: Annual review data submitted to the UK CF Trust Registry between 2007 and 2011 were used to calculate %predicted FEV1, FVC and FEV1/FVC using three widely used reference equations (Wang-Hankinson and Knudson) and the new GLI-2012 equations. Results: Overall, Knudson and Wang equations overestimated %predicted values in paediatric patients, such that a greater proportion of patients had lung function values in the normal range. Within individual patients, the impact of switching equations varied greatly depending on the patients' age, and which equations were used. Conclusions: A unified approach to interpreting spirometric lung function measurements would help facilitate more appropriate comparison both within and between centres and countries. Interpretation of longitudinal measurements using a continuous referende equation across all-ages, like the GLI, may further improve our understanding of CF lung disease. (C) 2013 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:319 / 327
页数:9
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