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Comment
. 2016 May:172:228.
doi: 10.1016/j.jpeds.2016.01.035. Epub 2016 Feb 4.

Forced expiratory volume in 1 second variability in cystic fibrosis-has the clinical utility been lost in statistical translation?

Sonya L Heltshe  1 , Rhonda D Szczesniak  2
Affiliations
Comment

Forced expiratory volume in 1 second variability in cystic fibrosis-has the clinical utility been lost in statistical translation?

Sonya L Heltshe et al. J Pediatr. 2016 May.
No abstract available

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  • Reply.
    Morgan WJ, Pasta DJ, Konstan MW. Morgan WJ, et al. J Pediatr. 2016 May;172:228-9. doi: 10.1016/j.jpeds.2016.01.036. Epub 2016 Feb 9. J Pediatr. 2016. PMID: 26873654 No abstract available.

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References

    1. Taylor-Robinson D, Whitehead M, Diderichsen F, Olesen HV, Pressler T, Smyth RL, et al. Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal study. Thorax. 2012;67:860–866. - PMC - PubMed
    1. Morgan WJ, Van Devanter DR, Pasta DJ, Foreman AJ, Wagener JS, Konstan MW, et al. Forced expiratory volume in 1 second variability helps identify patients with cystic fibrosis at risk of greater loss of lung function. J Pediatr. 2016;169:116–121. e2. - PubMed
    1. Pittman JE, Davis SD. Decline in forced expiratory volume in 1 second in cystic fibrosis—watch the pendulum swing (Editorial) J Pediatr. 2016;169:7–9. - PubMed

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