Literature DB >> 26388208

Forced Expiratory Volume in 1 Second Variability Helps Identify Patients with Cystic Fibrosis at Risk of Greater Loss of Lung Function.

Wayne J Morgan1, Donald R VanDevanter2, David J Pasta3, Aimee J Foreman3, Jeffrey S Wagener4, Michael W Konstan2.   

Abstract

OBJECTIVE: To evaluate several alternative measures of forced expiratory volume in 1 second percent predicted (FEV1 %pred) variability as potential predictors of future FEV1 %pred decline in patients with cystic fibrosis. STUDY
DESIGN: We included 13,827 patients age ≥6 years from the Epidemiologic Study of Cystic Fibrosis 1994-2002 with ≥4 FEV1 %pred measurements spanning ≥366 days in both a 2-year baseline period and a 2-year follow-up period. We predicted change from best baseline FEV1 %pred to best follow-up FEV1 %pred and change from baseline to best in the second follow-up year by using multivariable regression stratified by 4 lung-disease stages. We assessed 5 measures of variability (some as deviations from the best and some as deviations from the trend line) both alone and after controlling for demographic and clinical factors and for the slope and level of FEV1 %pred.
RESULTS: All 5 measures of FEV1 %pred variability were predictive, but the strongest predictor was median deviation from the best FEV1 %pred in the baseline period. The contribution to explanatory power (R(2)) was substantial and exceeded the total contribution of all other factors excluding the FEV1 %pred rate of decline. Adding the other variability measures provided minimal additional value.
CONCLUSIONS: Median deviation from the best FEV1 %pred is a simple metric that markedly improves prediction of FEV1 %pred decline even after the inclusion of demographic and clinical characteristics and the FEV1 %pred rate of decline. The routine calculation of this variability measure could allow clinicians to better identify patients at risk and therefore in need of increased intervention.
Copyright © 2016 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26388208     DOI: 10.1016/j.jpeds.2015.08.042

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  14 in total

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

Authors:  Sonya L Heltshe; Rhonda D Szczesniak
Journal:  J Pediatr       Date:  2016-02-04       Impact factor: 4.406

Review 2.  Use of FEV1 in cystic fibrosis epidemiologic studies and clinical trials: A statistical perspective for the clinical researcher.

Authors:  Rhonda Szczesniak; Sonya L Heltshe; Sanja Stanojevic; Nicole Mayer-Hamblett
Journal:  J Cyst Fibros       Date:  2017-01-20       Impact factor: 5.482

3.  Seasonal variation of lung function in cystic fibrosis: longitudinal modeling to compare a Midwest US cohort to international populations.

Authors:  Emrah Gecili; Cole Brokamp; Anushka Palipana; Rui Huang; Eleni-Rosalina Andrinopoulou; Teresa Pestian; Erika Rasnick; Ruth H Keogh; Yizhao Ni; John P Clancy; Patrick Ryan; Rhonda D Szczesniak
Journal:  Sci Total Environ       Date:  2021-03-01       Impact factor: 10.753

Review 4.  Epidemiologic Study of Cystic Fibrosis: 25 years of observational research.

Authors:  Michael W Konstan; David J Pasta; Donald R VanDevanter; Jeffrey S Wagener; Wayne J Morgan
Journal:  Pediatr Pulmonol       Date:  2021-01-12

5.  Median regression spline modeling of longitudinal FEV1 measurements in cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD) patients.

Authors:  Douglas J Conrad; Barbara A Bailey; Jon A Hardie; Per S Bakke; Tomas M L Eagan; Bernt B Aarli
Journal:  PLoS One       Date:  2017-12-20       Impact factor: 3.240

6.  The Prevalence and Effect of Comorbid Cystic Fibrosis and Attention Deficit Hyperactivity Disorders on Hospitalizations: A Retrospective Analysis.

Authors:  Nicole Spitzer; Timothy B Legare; Priyanshi Patel; Nicholas Toselli; Floyd Livingston
Journal:  Cureus       Date:  2018-07-25

7.  An Animated Functional Data Analysis Interface to Cluster Rapid Lung Function Decline and Enhance Center-Level Care in Cystic Fibrosis.

Authors:  Jesse Pratt; Weiji Su; Don Hayes; John P Clancy; Rhonda D Szczesniak
Journal:  J Healthc Eng       Date:  2021-05-10       Impact factor: 2.682

8.  The importance of data issues when comparing cystic fibrosis registry outcomes between countries: Are annual review FEV1 in the UK only collected when subjects are well?

Authors:  Zhe Hui Hoo; Rachael Curley; Michael J Campbell; Stephen J Walters; Martin J Wildman
Journal:  J Eval Clin Pract       Date:  2018-06-14       Impact factor: 2.431

9.  Using different methods to process forced expiratory volume in one second (FEV 1) data can impact on the interpretation of FEV 1 as an outcome measure to understand the performance of an adult cystic fibrosis centre: A retrospective chart review.

Authors:  Zhe Hui Hoo; Muhaned S A El-Gheryani; Rachael Curley; Martin J Wildman
Journal:  F1000Res       Date:  2018-06-01

10.  Rescue therapy within the UK Cystic Fibrosis Registry: An exploration of predictors of intravenous antibiotic use amongst adults with CF.

Authors:  Zhe Hui Hoo; Martin J Wildman; Rachael Curley; Stephen J Walters; Michael J Campbell
Journal:  Respirology       Date:  2017-09-14       Impact factor: 6.424

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