A comparison of change point models with application to longitudinal lung function measurements in children with cystic fibrosis-Reference-Cited by-同舟云学术

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A comparison of change point models with application to longitudinal lung function measurements in children with cystic fibrosis

Published:2016-01-05 Issue:12 Volume:35 Page:2058-2073
ISSN:0277-6715
Container-title:Statistics in Medicine
language:en
Short-container-title:Statist. Med.

Author:

Moss Angela¹,Juarez-Colunga E.¹²^ORCID,Nathoo Farouk³,Wagner Brandie²^ORCID,Sagel Scott⁴

Affiliation:

1. Adult and Child Consortium for Health Outcomes and Delivery Science; University of Colorado Denver School of Medicine; Aurora 80045 CO U.S.A.

2. Department of Biostatistics and Informatics; University of Colorado Denver; Aurora 80045 CO U.S.A.

3. Department of Mathematics and Statistics; University of Victoria; Victoria V8W 3P4 BC Canada

4. Department of Pediatrics; Children's Hospital Colorado, University of Colorado School of Medicine; Aurora 80045 CO U.S.A.

Funder

Cystic Fibrosis Foundation

Publisher

Wiley

Subject

Statistics and Probability,Epidemiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/sim.6845/fullpdf

Reference36 articles.

1. Healthcare expenditures for privately insured people with cystic fibrosis;Ouyang;Pediatric Pulmonology,2009

2. Predictive 5-year survivorship model of cystic fibrosis;Liou;American Journal of Epidemiology,2001

3. Longitudinal analysis of pulmonary function decline in patients with cystic fibrosis;Corey;The Journal of Pediatrics,1997

4. Risk factors for rate of decline in forced expiratory volume in one second in children and adolescents with cystic fibrosis;Konstan;The Journal of Pediatrics,2007

5. Understanding the natural progression in %FEV1 decline in patients with cystic fibrosis: a longitudinal study;Taylor-Robinson;Thorax,2012

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