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
Observational Study
. 2024 Mar;52(3):3000605241233520.
doi: 10.1177/03000605241233520.

Should atelectasis be considered a pulmonary complication and indicator of poor prognosis in cystic fibrosis?

Affiliations
Observational Study

Should atelectasis be considered a pulmonary complication and indicator of poor prognosis in cystic fibrosis?

María Martínez Redondo et al. J Int Med Res. 2024 Mar.

Abstract

Objective: This study examined whether bronchoscopy leads to clinicoradiological improvement in cystic fibrosis (CF) and the predictive factors. The study also investigated whether pulmonary atelectasis is a poor prognostic factor in CF.

Methods: This multicenter, case-control, observational, retrospective study included two groups of patients with CF: a case group (patients with persistent atelectasis who were followed-up at least for 2 years) and a control group (patients without atelectasis matched 1:1 by sex and age [±3 years]). We recorded demographic data, lung function test results, pulmonary complications, comorbidities, treatments (including bronchoscopies, surgery and transplantation), and deaths.

Results: Each group included 55 patients (case group: 20 men, mean age 25.4 ± 10.4 years; control group: 20 men, mean age 26.1 ± 11.4 years). Bronchoscopy did not lead to clinicoradiological improvement. Allergic bronchopulmonary aspergillosis (ABPA) was more frequent in the case group. Patients in the case group more frequently used inhaled steroids, their pre-atelectasis lung function was statistically worse, and they had more exacerbations during follow-up.

Conclusion: Moderate-to-severe pulmonary disease and ABPA can favor atelectasis. Pulmonary atelectasis can be a poor prognostic factor in CF because it increases exacerbations. Despite our results, we recommend enhancing treatment, including bronchoscopy, to prevent persistent atelectasis.

Keywords: Cystic fibrosis; allergic bronchopulmonary aspergillosis; atelectasis; bronchoscopy; exacerbation; prognosis; risk factor.

PubMed Disclaimer

Conflict of interest statement

Declaration of conflicting interestThe authors declare that there are no conflicts of interest.

Figures

Figure 1.
Figure 1.
Rates of patients undergoing lung surgery and lung transplantation and the rate of death.

Similar articles

References

    1. Lerín M, Prados C, Martínez MT, et al.. Cystic fibrosis in adult age. Rev Clin Esp (Barc) 2014; 214: 289–295. - PubMed
    1. Dickinson KM, Collaco JM. Cystic Fibrosis. Pediatr Rev 2021; 42: 55–67. - PMC - PubMed
    1. Huisman C, De Graaff CS, Boersma WG. Unilateral air bronchogram in a patient with cystic fibrosis. Chest 2002; 121: 1343–1344. - PubMed
    1. Flight WG, Hildage J, Webb AK. Progressive unilateral lung collapse in cystic fibrosis–a therapeutic challenge. J R Soc Med 2012; 105: S44–S49. - PMC - PubMed
    1. Martínez Redondo M, Prados Sánchez C, Salcedo Posadas A, et al.. Características de las atelectasias como complicación pulmonar en la fibrosis quística. Rev Patol Respir 2017; 20: 79–87.

Publication types