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Reference percentiles for FEV1 and BMI in European children and adults with cystic fibrosis

Authors :
Boëlle Pierre-Yves
Viviani Laura
Busson Pierre-Francois
Olesen Hanne V
Ravilly Sophie
Stern Martin
Assael Baroukh M
Barreto Celeste
Drevinek Pavel
Thomas Muriel
Krivec Uros
Mei-Zahav Meir
Vibert Jean-François
Clement Annick
Mehta Anil
Corvol Harriet
Source :
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 64 (2012)
Publication Year :
2012
Publisher :
BMC, 2012.

Abstract

Abstract Background The clinical course of Cystic Fibrosis (CF) is usually measured using the percent predicted FEV1 and BMI Z-score referenced against a healthy population, since achieving normality is the ultimate goal of CF care. Referencing against age and sex matched CF peers may provide valuable information for patients and for comparison between CF centers or populations. Here, we used a large database of European CF patients to compute CF specific reference equations for FEV1 and BMI, derived CF-specific percentile charts and compared these European data to their nearest international equivalents. Methods 34859 FEV1 and 40947 BMI observations were used to compute European CF specific percentiles. Quantile regression was applied to raw measurements as a function of sex, age and height. Results were compared with the North American equivalent for FEV1 and with the WHO 2007 normative values for BMI. Results FEV1 and BMI percentiles illustrated the large variability between CF patients receiving the best current care. The European CF specific percentiles for FEV1 were significantly different from those in the USA from an earlier era, with higher lung function in Europe. The CF specific percentiles for BMI declined relative to the WHO standard in older children. Lung function and BMI were similar in the two largest contributing European Countries (France and Germany). Conclusion The CF specific percentile approach applied to FEV1 and BMI allows referencing patients with respect to their peers. These data allow peer to peer and population comparisons in CF patients.

Details

Language :
English
ISSN :
17501172
Volume :
7
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Orphanet Journal of Rare Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.919af9649c5544c994e236926cd0db5b
Document Type :
article
Full Text :
https://doi.org/10.1186/1750-1172-7-64