Effect of pulmonary exacerbations on long-term lung function decline in cystic fibrosis
- PMID: 22135280
- DOI: 10.1183/09031936.00159111
Effect of pulmonary exacerbations on long-term lung function decline in cystic fibrosis
Abstract
It is unknown what proportion of long-term lung function decline in cystic fibrosis (CF) is explained by pulmonary exacerbations. The aim of this study was to determine how exacerbations requiring hospitalisation contribute to the course of CF lung disease. This was a retrospective cohort study. The primary outcome was the rate of decline of forced expiratory volume in 1 s (FEV(1)) % predicted. Out of 851 subjects, 415 (48.8%) subjects had ≥ 1 exacerbation. After adjustment for confounders, the annual rate of FEV(1) decline in those without an exacerbation was 1.2% per yr (95% CI 1.0-1.5), compared with 2.5% per yr (95% CI 2.1-2.8) in those with an exacerbation. The proportion of overall FEV(1) decline associated with ≥ 1 exacerbation was 52% (95% CI 35.0-68.9). For a given number of exacerbations, the annual rate of FEV(1) decline was greatest in subjects with ≤ 6 months between exacerbations. Half of FEV(1) decline seen in CF patients was associated with pulmonary exacerbations. Time between exacerbations, specifically ≤ 6 months between exacerbations, plays an important contribution to overall lung function decline. These findings support using time to next exacerbation as a clinical end-point for CF trials.
Similar articles
-
Chronic Stenotrophomonas maltophilia infection and exacerbation outcomes in cystic fibrosis.J Cyst Fibros. 2012 Jan;11(1):8-13. doi: 10.1016/j.jcf.2011.07.008. Epub 2011 Aug 16. J Cyst Fibros. 2012. PMID: 21849265
-
Exacerbation frequency and clinical outcomes in adult patients with cystic fibrosis.Thorax. 2011 Aug;66(8):680-5. doi: 10.1136/thx.2011.161117. Epub 2011 Jun 15. Thorax. 2011. PMID: 21680566
-
Recurrent exacerbations affect FEV(1) decline in adult patients with cystic fibrosis.Respir Med. 2009 Mar;103(3):407-13. doi: 10.1016/j.rmed.2008.09.024. Epub 2008 Nov 22. Respir Med. 2009. PMID: 19027279
-
Power considerations for studies of lung function in cystic fibrosis.Proc Am Thorac Soc. 2007 Aug 1;4(4):334-7. doi: 10.1513/pats.200611-176HT. Proc Am Thorac Soc. 2007. PMID: 17652496 Review.
-
Pulmonary exacerbations in cystic fibrosis.Curr Opin Pulm Med. 2011 Nov;17(6):442-7. doi: 10.1097/MCP.0b013e32834b8c04. Curr Opin Pulm Med. 2011. PMID: 21881509 Review.
Cited by
-
Clinical outcomes of adults and children with cystic fibrosis during the COVID-19 pandemic.J Cyst Fibros. 2023 May;22(3):581-586. doi: 10.1016/j.jcf.2022.09.006. Epub 2022 Sep 16. J Cyst Fibros. 2023. PMID: 36163166 Free PMC article.
-
Clinician's Commentary on Morgan et al.(1).Physiother Can. 2015 Fall;67(4):327-8. doi: 10.3138/ptc.2014-64-CC. Physiother Can. 2015. PMID: 27504747 Free PMC article. No abstract available.
-
Sweat metabolomics before and after intravenous antibiotics for pulmonary exacerbation in people with cystic fibrosis.Respir Med. 2022 Jan;191:106687. doi: 10.1016/j.rmed.2021.106687. Epub 2021 Nov 23. Respir Med. 2022. PMID: 34864373 Free PMC article.
-
Efficacy and safety profile of elexacaftor-tezacaftor-ivacaftor triple therapy on cystic fibrosis: a systematic review and single arm meta-analysis.Front Pharmacol. 2023 Dec 14;14:1275470. doi: 10.3389/fphar.2023.1275470. eCollection 2023. Front Pharmacol. 2023. PMID: 38186649 Free PMC article.
-
Static mucus impairs bacterial clearance and allows chronic infection with Pseudomonas aeruginosa in the cystic fibrosis rat.Eur Respir J. 2022 Sep 7;60(3):2101032. doi: 10.1183/13993003.01032-2021. Print 2022 Sep. Eur Respir J. 2022. PMID: 35115338 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical