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
Comparative Study
. 2019 Dec 3;20(1):271.
doi: 10.1186/s12931-019-1243-3.

Mortality risk and causes of death in patients with non-cystic fibrosis bronchiectasis

Affiliations
Comparative Study

Mortality risk and causes of death in patients with non-cystic fibrosis bronchiectasis

Sooim Sin et al. Respir Res. .

Abstract

Background: All-cause mortality risk and causes of death in bronchiectasis patients have not been fully investigated. The aim of this study was to compare the mortality risk and causes of death between individuals with bronchiectasis and those without bronchiectasis.

Methods: Patients with or without bronchiectasis determined based on chest computed tomography (CT) at one centre between 2005 and 2016 were enrolled. Among the patients without bronchiectasis, a control group was selected after applying additional exclusion criteria. We compared the mortality risk and causes of death between the bronchiectasis and control groups without lung disease. Subgroup analyses were also performed according to identification of Pseudomonas or non-tuberculous mycobacteria, airflow limitation, and smoking status.

Results: Of the total 217,702 patients who underwent chest CT, 18,134 bronchiectasis patients and 90,313 non-bronchiectasis patients were included. The all-cause mortality rate in the bronchiectasis group was 1608.8 per 100,000 person-years (95% confidence interval (CI), 1531.5-1690.0), which was higher than that in the control group (133.5 per 100,000 person-years; 95% CI, 124.1-143.8; P < 0.001). The bronchiectasis group had higher all-cause (adjusted hazard ratio (aHR), 1.26; 95% CI, 1.09-1.47), respiratory (aHR, 3.49; 95% CI, 2.21-5.51), and lung cancer-related (aHR, 3.48; 95% CI, 2.33-5.22) mortality risks than the control group. In subgroup analysis, patients with airflow limitation and ever smokers showed higher all-cause mortality risk among bronchiectasis patients. Therefore, we observed significant interrelation between bronchiectasis and smoking, concerning the risks of all-cause mortality (P for multiplicative interaction, 0.030, RERI, 0.432; 95% CI, 0.097-0.769) and lung cancer-related mortality (RERI, 8.68; 95% CI, 1.631-15.736).

Conclusion: Individuals with bronchiectasis had a higher risk of all-cause, respiratory, and lung cancer-related mortality compared to control group. The risk of all-cause mortality was more prominent in those with airflow limitation and in ever smokers.

Keywords: Bronchiectasis; Cause of death; Mortality.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Flowchart for the study population
Fig. 2
Fig. 2
Bronchiectasis increased risk of all-cause mortality in comparison with the control group
Fig. 3
Fig. 3
Bronchiectasis increased risk of respiratory related death and lung cancer-related death compared with the control group. a Comparision of respiratory related mortality between bronchiectasis patients and control population b Comparison of lung cancer related mortality between bronchiectasis patients and control population
Fig. 4
Fig. 4
All-cause mortality risk according to additional risk factors. a Comparison of all-cause mortality risk between never smoker bronchiectasis patients versus ever smoker bronchiectasis patients b Comparision of all-cause mortality risk between bronchiectasis patients with airflow limitation versus bronchiectasis patients without airflow limitation

References

    1. McShane PJ, Naureckas ET, Tino G, Strek ME. Non-cystic fibrosis bronchiectasis. Am J Respir Crit Care Med. 2013;188(6):647–656. doi: 10.1164/rccm.201303-0411CI. - DOI - PubMed
    1. Venning V, Bartlett J, Jayaram L. Patients hospitalized with an infective exacerbation of bronchiectasis unrelated to cystic fibrosis: clinical, physiological and sputum characteristics. Respirology. 2017;22(5):922–927. doi: 10.1111/resp.13005. - DOI - PMC - PubMed
    1. Weycker D, Edelsberg J, Oster G, Tino G. Prevalence and economic burden of bronchiectasis. Clin Pulm Med. 2005;12(4):205–209. doi: 10.1097/01.cpm.0000171422.98696.ed. - DOI
    1. Seitz AE, Olivier KN, Adjemian J, Holland SM, Prevots DR. Trends in bronchiectasis among medicare beneficiaries in the United States, 2000 to 2007. Chest. 2012;142(2):432–439. doi: 10.1378/chest.11-2209. - DOI - PMC - PubMed
    1. Ringshausen FC, de Roux A, Pletz MW, Hamalainen N, Welte T, Rademacher J. Bronchiectasis-associated hospitalizations in Germany, 2005-2011: a population-based study of disease burden and trends. PLoS One. 2013;8(8):e71109. doi: 10.1371/journal.pone.0071109. - DOI - PMC - PubMed

Publication types

MeSH terms