Post TB Bronchiectasis:a distinct phenotype

<bold>Introduction:</bold> Bronchiectasis occurs frequently as a consequence of pulmonary tuberculosis. We investigated whether TB associated bronchiectasis has a distinct clinical phenotype using the EMBARC bronchiectasis registry. <bold>Methods:</bold> EMBARC is a prospective observational registry of adult patients with bronchiectasis from 31 countries. Patients were classified into two groups based on whether or not they had a history of pulmonary tuberculosis. Factors associated with pulmonary TB history were evaluated using logistic regression. <bold>Results:</bold> 19324 patients were included. Pulmonary TB was associated with a large number of individual factors in multivariate analysis including older age (OR 1.01 95%CI 1.01-1.02), a higher risk of P.aeruginosa infection (OR 1.18 95%CI 1.03-1.35), and a lower risk of H. influenzae infection (OR 0.69 95%CI 0.57-0.83). FEV1 was lower in TB patients (p<0.0001) and MRC dyspnoea score was higher (OR 1.07 95%CI 1.02-1.12). TB was associated with greater extent of radiological bronchiectasis in the right upper lobe (OR 1.36 95%CI 1.28-1.44) and left upper lobe (1.27 95%CI 1.19-1.35) with corresponding less severe bronchiectasis in the middle and lower lobes (all p<0.0001). Compared to the UK (reference), all other regions had a higher incidence of TB, Northern and Western Europe (OR 1.32 95%CI 1.10-1.59), Southern Europe (OR 1.83 95%CI 1.59-2.11), Eastern Europe (OR 2.32 95%CI 1.88-2.86) and Asia (OR 8.92 95%CI 7.63-10.42). Post-TB bronchiectasis was not associated with increased exacerbations or mortality during 5 years follow-up. <bold>Conclusion:</bold> Post TB bronchiectasis is associated with a clinical phenotype of older age, P. aeruginosa infection, worse lung function and dyspnoea, and upper lobar cystic lung disease.

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Published
2024-09-14
DOI
https://doi.org/10.1183/13993003.congress-2024.pa2390
Primary Topic
Cystic Fibrosis Research Advances
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article
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article

Post TB Bronchiectasis:a distinct phenotype

Rajesh Swarnakar, Felix C. Ringshausen, Raja Dhar, Eva Polverino et al.
Cystic Fibrosis Research Advances
article

Post TB Bronchiectasis:a distinct phenotype

Rajesh Swarnakar, Felix C. Ringshausen, Raja Dhar, Eva Polverino, James Duncan Chalmers, Montserrat Vendrell, Anthony De Soyza, Megan Crichton, Deepak Talwar, Sheetu Singh, Murali Mohan
article en

Abstract

<bold>Introduction:</bold> Bronchiectasis occurs frequently as a consequence of pulmonary tuberculosis. We investigated whether TB associated bronchiectasis has a distinct clinical phenotype using the EMBARC bronchiectasis registry. <bold>Methods:</bold> EMBARC is a prospective observational registry of adult patients with bronchiectasis from 31 countries. Patients were classified into two groups based on whether or not they had a history of pulmonary tuberculosis. Factors associated with pulmonary TB history were evaluated using logistic regression. <bold>Results:</bold> 19324 patients were included. Pulmonary TB was associated with a large number of individual factors in multivariate analysis including older age (OR 1.01 95%CI 1.01-1.02), a higher risk of P.aeruginosa infection (OR 1.18 95%CI 1.03-1.35), and a lower risk of H. influenzae infection (OR 0.69 95%CI 0.57-0.83). FEV1 was lower in TB patients (p<0.0001) and MRC dyspnoea score was higher (OR 1.07 95%CI 1.02-1.12). TB was associated with greater extent of radiological bronchiectasis in the right upper lobe (OR 1.36 95%CI 1.28-1.44) and left upper lobe (1.27 95%CI 1.19-1.35) with corresponding less severe bronchiectasis in the middle and lower lobes (all p<0.0001). Compared to the UK (reference), all other regions had a higher incidence of TB, Northern and Western Europe (OR 1.32 95%CI 1.10-1.59), Southern Europe (OR 1.83 95%CI 1.59-2.11), Eastern Europe (OR 2.32 95%CI 1.88-2.86) and Asia (OR 8.92 95%CI 7.63-10.42). Post-TB bronchiectasis was not associated with increased exacerbations or mortality during 5 years follow-up. <bold>Conclusion:</bold> Post TB bronchiectasis is associated with a clinical phenotype of older age, P. aeruginosa infection, worse lung function and dyspnoea, and upper lobar cystic lung disease.

University of Dundee (GB), King George's Medical University (IN), Narayana Health (IN), Medizinische Hochschule Hannover (DE), Vall d'Hebron Hospital Universitari (ES), Calvary Mater Newcastle Hospital (AU), Hospital Universitari de Girona Doctor Josep Trueta (ES), Getwell Hospital and Research Institute (IN), Centre for Sight (IN), Rajasthan Dental College and Hospital (IN), AMRI Hospitals (IN)
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Cystic Fibrosis Research Advances
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