Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Apr;137(4):852-60.
doi: 10.1378/chest.09-1374. Epub 2009 Dec 4.

Influenza-associated cystic fibrosis pulmonary exacerbations

Affiliations

Influenza-associated cystic fibrosis pulmonary exacerbations

Justin R Ortiz et al. Chest. 2010 Apr.

Abstract

Background: Although cystic fibrosis (CF) is the most common inherited respiratory disease, the burden of influenza among individuals with CF is not well characterized.

Methods: We used the CF Foundation Patient Registry to determine the relationship between pulmonary exacerbation incidence rate and influenza virus season from July 2003 through June 2007. The outcome of interest, pulmonary exacerbation, was defined as treatment of a respiratory illness with IV antibiotics. Each influenza season was defined as all months during which >/= 15% of laboratory tests for influenza virus were positive in the US influenza virologic surveillance system. We calculated incidence rates of pulmonary exacerbation during the influenza and summertime seasons as well as relative rates with 95% CIs. A multivariate regression model adjusted for demographic and clinical predictors.

Results: In 2003, the patient cohort size was 21,506 patients, and 7,727 patients experienced at least one pulmonary exacerbation. The overall pulmonary exacerbation incidence rate in the influenza season was 595.0 per 10,000 person-months compared with a summertime baseline of 549.6 per 10,000 person-months. The incidence rate ratio was 1.08 (95% CI: 1.06, 1.10). Multivariate analysis did not change our estimate of risk (adjusted odds ratio: 1.07; 95% CI: 1.05, 1.10). An estimated annual excess of 147.6 per 10,000 person-months or an excess 2.1% of total exacerbations occur during the influenza season.

Conclusion: Our data demonstrate a substantial contribution of the influenza season to CF morbidity. Further studies to determine any causal link between influenza infection and CF pulmonary exacerbations are necessary.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Cystic fibrosis (CF) pulmonary exacerbation incidence rates per 10,000 person-months by age group and US influenzalike illness rates, July 2003 through June 2007. Weekly influenzalike illness rates are from US influenza surveillance data., Influenzalike illness rates are plotted on the Wednesday of each week. CF exacerbation incidence rates are plotted on the 15th day of each calendar month.
Figure 2.
Figure 2.
CF pulmonary exacerbation incidence rates per 10,000 person-months and US influenzalike illness rates among patients with < 2 pulmonary exacerbations, July 2003 through June 2007. Y-axis changed from Figure 1 to demonstrate seasonal variation. Smoothed function is a moving average of five data points: the two previous, the current, and the two subsequent incidence rates. See Figure 1 legend for expansion of abbreviation.

References

    1. Cystic Fibrosis Foundation . Patient Registry Annual Data Report 2007. Bethesda, MD: Cystic Fibrosis Foundation; 2008.
    1. Goss CH, Burns JL. Exacerbations in cystic fibrosis. 1: epidemiology and pathogenesis. Thorax. 2007;62(4):360–367. - PMC - PubMed
    1. Liou TG, Adler FR, Cahill BC, et al. Survival effect of lung transplantation among patients with cystic fibrosis. JAMA. 2001;286(21):2683–2689. - PMC - PubMed
    1. Liou TG, Adler FR, Fitzsimmons SC, Cahill BC, Hibbs JR, Marshall BC. Predictive 5-year survivorship model of cystic fibrosis. Am J Epidemiol. 2001;153(4):345–352. - PMC - PubMed
    1. Liou TG, Adler FR, Huang D. Use of lung transplantation survival models to refine patient selection in cystic fibrosis. Am J Respir Crit Care Med. 2005;171(9):1053–1059. - PubMed

MeSH terms