Effect of pulmonary exacerbations on long-term lung function decline in cystic fibrosis
Open accessAbstract
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.
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Pulmonary exacerbations in pwCF are associated with decreased survival.
“Pulmonary exacerbations are important life events for pwCF and are associated with a greater rate of lung function decline and decreased survival.24,26”
Pulmonary exacerbations in pwCF are associated with a greater rate of lung function decline.
“Pulmonary exacerbations are important life events for pwCF and are associated with a greater rate of lung function decline and decreased survival.24,26”
Reducing the number of pulmonary exacerbations is critical to averting the progressive lung function decline seen in patients with CF.
“Reducing the number of pulmonary exacerbations is critical to averting the progressive lung function decline seen in patients with CF [22].”
Cites
Exacerbation frequency and clinical outcomes in adult patients with cystic fibrosis
de Boer, K., Vandemheen, K. L., Tullis, E., Doucette, S., Fergusson, D., Freitag, A., Paterson, N., Jackson, M., Lougheed, M. D., Kumar, V., et al. (2011) · Thorax · doi:10.1136/thx.2011.161117 · Cited by 271 · see citing works
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Heijerman, H. G. M., McKone, E. F., Downey, D. G., Van Braeckel, E., Rowe, S. M., Tullis, E., Mall, M. A., Welter, J. J., Ramsey, B. W., McKee, C. M., et al. (2019) · The Lancet · doi:10.1016/s0140-6736(19)32597-8 · Cited by 1,414 · see citing works
Self-citationDaines, C. L., Tullis, E., Costa, S., Linnemann, R. W., Mall, M. A., McKone, E. F., Polineni, D., Quon, B. S., Ringshausen, F. C., Rowe, S. M., et al. (2023) · European Respiratory Journal · doi:10.1183/13993003.02029-2022 · Cited by 100 · see citing works
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- Authors
- Waters, V., Stanojevic, S., Atenafu, E. G., Lu, A., Yau, Y., Tullis, E., & Ratjen, F.
- Affiliations
- Hospital for Sick Children (CA)
- University Health Network (CA)
- St. Michael's Hospital (CA)
- Venue
- European Respiratory Journal
- Publisher
- European Respiratory Society (ERS)
- Published
- 2011-12-01
- Volume
- 40
- Issue
- 1
- Pages
- 61-66
- ISSN
- 0903-1936 (ISSN-L)
- 1399-3003
- OpenAlex
- W2143843692
- Cited by
- 256
- References
- 1
- Citations by year
- 2026: 9 · 2025: 15 · 2024: 22 · 2023: 23 · 2022: 23 · 2021: 16 · 2020: 20 · 2019: 15 · 2018: 25 · 2017: 20 · 2016: 17 · 2015: 24 · 2014: 11 · 2013: 13 · 2012: 3
- FWCI
- 7.00
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- European Respiratory Journal (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Cystic Fibrosis Research Advances
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
- Health Sciences › Medicine › Surgery › Transplantation: Methods and Outcomes
- Keywords
- cystic fibrosis, pulmonary exacerbations, lung function decline, FEV1 decline, hospitalization, clinical trial endpoints, lung disease progression
- MeSH terms
- Cystic Fibrosis, Female, Forced Expiratory Volume, Humans, Lung, Male, Retrospective Studies, Cohort Studies, Disease Progression
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